CN101175508A - 表皮葡萄球菌多肽抗原的免疫原性组合物 - Google Patents
表皮葡萄球菌多肽抗原的免疫原性组合物 Download PDFInfo
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Abstract
本发明涉及免疫原性组合物,其包含从表皮葡萄球菌(Staphylococcus epidermidis)分离的多肽。本发明还涉及编码表皮葡萄球菌多肽的聚核苷酸和其于免疫原性组合物中的用途。此外,本发明涉及使用所述表皮葡萄球菌多肽和聚核苷酸的免疫原性组合物诱导哺乳动物对表皮葡萄球菌和金黄葡萄球菌(Staphylococcus aureus)的免疫反应的方法。本发明还涉及用于检测生物样本中的表皮葡萄球菌的方法。
Description
技术领域
本发明涉及免疫原性组合物,其包含从表皮葡萄球菌(Staphylococcus epidermidis)分离的多肽。本发明还涉及编码表皮葡萄球菌多肽的聚核苷酸和其于免疫原性组合物中的用途。此外,本发明涉及使用所述表皮葡萄球菌多肽和聚核苷酸的免疫原性组合物诱导哺乳动物对抗表皮葡萄球菌和金黄葡萄球菌(Staphylococcus aureus)的免疫反应的方法。本发明还涉及用于检测生物样本中的表皮葡萄球菌的方法。
背景技术
表皮葡萄球菌是皮肤和粘膜上正常人类微生物集落的主要组成部分,且曾经认为其只是由受感染患者培养得到的污染物。参看Heilmann,C.和G.Peters,Biology andpathogenicity of Staphylococcus epidermidis,in Gram-positive pathogens,V.A.Fischetti编辑,2000,American Society for Microbiology:Washington,D.C.第442-449页;von Eiff,C等人,Lancet Infect Dis,2(11):第677-85页(2002)。现已广泛承认表皮葡萄球菌是一种极其重要的条件致病菌和引起医院血流感染的主要原因。参看Am J Infect Control,27:第520-32页(1999);Diekema,D.J.等人,Int J Antimicrob Agents,20(6):第412-8页(2002);Edmond,M.B.等人,Clin Infect Dis,29(2):第239-44页(1999)。这些感染主要与诸如静脉导管、人工关节或人工心脏瓣膜等留置外来聚合物体的存在有关。参看Heilmann,C.和G.Peters,Biology and pathogenicity of Staphylococcus epidermidis,in Gram-positivepathogens,V.A.Fischetti,编辑2000,American Society for Microbiology:Washington,D.C.第442-449页;von Eiff,C等人,Lancet Infect Dis,2(11):第677-85页(2002)。认为感染是在插入人工装置时从患者的皮肤引入表皮葡萄球菌引起的。定殖和随后生物膜的形成可导致可能血行播散(hematogenous spread)到体内其它部位的菌血症。这些感染通常因抗生素和临床分离株抗生素抗性增加于生物膜内引起的杀菌作用降低而难以进行治疗。参看Diekema,D.J.等人,Int J Antimicrob Agents,20(6):第412-8页(2002);Edmond,M.B.等人,Clin Infect Dis,29(2):第239-44页(1999);Lewis,K.,Antimicrob Agents Chemother,45(4):第999-1007页(2001);Raad,I.等人,Clin Infect Dis,26(5):第1182-7页(1998)。已报导对万古霉素(vancomycin)具有降低的易感性的表皮葡萄球菌。参看Sanyal,D.和D.Greenwood,J Med Microbiol,.39(3):第204-10页(1993);Sanyal,D.等人,Lancet,337(8732):第54页(1991)。治疗这些感染的困难使得使用免疫法作为预防感染的方式成为必要。
生物膜形成是表皮葡萄球菌感染的主要毒力决定因素。因此,有关表皮葡萄球菌表面蛋白的研究已集中于在生物膜形成中所涉及的那些蛋白。基于生物膜形成的两个主要步骤中涉及蛋白,已将这些蛋白再分成以下群组:1)起始附着,葡萄球菌表面蛋白-1(SSP-1)、自溶素(AtlE)、Fbe(SdrG)和GehD;和2)细菌细胞聚集,Bap同源蛋白(Bhp)、聚集相关蛋白(AAP)和自溶素(AtlE)。参看von Eiff,C等人,Lancet Infect Dis,2002.2(11):第677-85页;Vuong,C等人,J Infect Dis,188(5):第706-18页(2003);Veenstra,G.J.等人,J Bacteriol.,178(2):第537-41页(1996);Rupp,M.E.等人,J Infect Dis,183(7):第1038-42页(2001);Hussain,M.等人,Infect Immun,65(2):第519-24页(1997);Nilsson,M.等人,Infect Immun,66(6):第2666-73页(1998);Davis,S.L.等人,J Biol Chem,276(30):第27799-805页(2001);和Bowden,M.G.等人,J Biol Chem,277(45):第43017-43023页(2002)。对于暴露到宿主内的环境暗示(environmental cue)时所表达的表面蛋白或宿主-寄生物相互作用中所涉及的蛋白的鉴别已进行比较少的尝试。
表皮葡萄球菌必须经历从共生体到致病菌的转变且适应宿主内的微环境。为使共生体转变成致病菌,其必须进入宿主组织,感觉其环境的改变,改变基因表达,从而使其能够避开宿主防御,附着和粘附到宿主因子上,在不同养分和宿主防御的存在下生长并分裂。细菌表面上的蛋白使其与宿主内的新环境初始接触。这些蛋白的多种功能包括感觉环境;净化和转运养分;抵抗宿主免疫系统;和结合宿主蛋白。表面暴露蛋白也可用作宿主免疫系统的接触点或识别点,且可为对抗细菌的体液免疫反应的目标。Josefsson,E.等人,J Infect Dis,184(12):第1572-80页(2001);Swiatlo,E.等人,Infect Immun,71(12):第7149-53页(2003);Grifantini,R.等人,Nat Biotechnol,20(9):第914-21页(2002)。因此,迫切需要鉴别用于免疫原性组合物中的表皮葡萄球菌蛋白中的有前途候选物,所述免疫原性组合物将诱导对于表皮葡萄球菌中引起疾病的血清型的免疫反应。
发明内容
本发明提供一种免疫原性组合物,其包含具有选自一或多个SEQ ID NO:1到SEQ IDNO:32、其生物等效物或其片段的氨基酸序列的多肽。在特定实施例中,多肽与受表皮葡萄球菌感染的兔的血清中的抗体具免疫反应性。在另一实施例中,多肽与一或多种兔血清蛋白结合。
在某些实施例中,免疫原性组合物另外包含医药学上可接受的载剂。在其它实施例中,本发明的免疫原性组合物还包含一或多种佐剂。在另一实施例中,免疫原性组合物另外包含表皮葡萄球菌多糖抗原。在又一实施例中,免疫原性组合物另外包含金黄葡萄球菌多糖或多肽抗原。
本发明提供免疫原性组合物,其包含从表皮葡萄球菌分离的多肽。
本发明提供一种包含表皮葡萄球菌多肽的免疫原性组合物,其中所述多肽另外包含异源氨基酸。在特定实施例中,多肽是融合多肽。在另一实施例中,多肽是重组多肽。在又一实施例中,本发明提供一种包含表皮葡萄球菌多肽的免疫原性组合物,其中所述多肽包含表皮葡萄球菌的中和表位。在某些实施例中,多肽为脂蛋白。
本发明另外提供包含表皮葡萄球菌多肽的免疫原性组合物,其中所述多肽是由聚核苷酸编码,所述聚核苷酸包含与选自SEQ ID NO:33到SEQ ID NO:64其中之一或其简并变异体或其片段的核苷酸序列。在特定实施例中,表皮葡萄球菌聚核苷酸序列选自由SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:43、SEQ ID NO:44、SEQ ID NO:46、SEQID NO:50、SEQ ID NO:51、SEQ ID NO:52、SEQ ID NO:55、SEQ ID NO:58、SEQ ID NO:59和SEQ ID NO:62或其简并变异体或其片段组成的群组。
本发明提供一种免疫原性组合物,其中聚核苷酸是得自表皮葡萄球菌。在特定实施例中,聚核苷酸另外包含异源核苷酸。在另一实施例中,聚核苷酸是在表达载体中。在又一实施例中,表达载体为质粒DNA。在某些实施例中,聚核苷酸为重组聚核苷酸。在另一实施例中,聚核苷酸可操作地连接到一个或多个基因表达调控元件。在又一实施例中,聚核苷酸引导表皮葡萄球菌中和表位的表达。
本发明还提供一种包含由聚核苷酸编码的表皮葡萄球菌多肽的免疫原性组合物,其中所述免疫原性组合物另外包含转染促进剂。在特定实施例中,所述转染促进剂为布比卡因(bupivicaine)。
本发明还提供一种诱导对抗表皮葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:具有选自一或多个SEQ ID NO:1到SEQ ID NO:32或其生物等效物或其片段的氨基酸序列的多肽,和医药学上可接受的载剂。
此外,本发明提供一种诱导对抗表皮葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:具有选自一或多个SEQ ID NO:33到SEQID NO:64或其简并变异体或其片段的核苷酸序列的聚核苷酸,和医药学上可接受的载剂。
在一实施例中,本发明提供一种包含聚核苷酸的免疫原性组合物,所述聚核苷酸具有选自SEQ ID NO:33到SEQ ID NO:64其中之一、其简并变异体或其片段的核苷酸序列,且其包含于表达载体中。在另一实施例中,所述聚核苷酸是得自表皮葡萄球菌。在又一实施例中,所述聚核苷酸包含异源核苷酸。
在某一实施例中,本发明提供一种用于检测和/或鉴别生物样本中的表皮葡萄球菌的方法,其包含(a)在允许杂交的条件下,使所述样本与聚核苷酸的寡核苷酸探针接触,所述聚核苷酸包含选自SEQ ID NO:33到SEQ ID NO:64其中之一或其简并变异体或其片段的核苷酸序列;和(b)检测所述样本中杂交复合物的存在,其中杂交复合物表明所述样本中存在表皮葡萄球菌。
在其它实施例中,本发明提供一种用于检测和/或鉴别生物样本中抗表皮葡萄球菌的抗体的方法,其包含(a)在允许形成免疫复合物的条件下,使所述样本与多肽接触,所述多肽包含选自SEQ ID NO:1到SEQ ID NO:32其中之一或其生物等效物或其片段的氨基酸序列;和检测所述样本中免疫复合物的存在,其中免疫复合物表明所述样本中存在肺炎链球菌(streptococcus pneumoniae)。
在特定实施例中,免疫原性组合物包含选自由SEQ ID NO:8、SEQ ID NO:10、SEQID NO:11、SEQ ID NO:12、SEQ ID NO:14、SEQ ID NO:18、SEQ ID NO:19、SEQ ID NO:20、SEQ ID NO:23、SEQ ID NO:26、SEQ ID NO:27、SEQ ID NO:30、其生物等效物或其片段组成的群组的表皮葡萄球菌多肽序列。在另一实施例中,免疫原性组合物包含选自由SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:43、SEQ ID NO:44、SEQ ID NO:46、SEQ ID NO:50、SEQ ID NO:51、SEQ ID NO:52、SEQ ID NO:55、SEQ ID NO:58、SEQID NO:59、SEQ ID NO:62或其简并变异体或其片段组成的群组的表皮葡萄球菌聚核苷酸序列。
在又一实施例中,本发明提供一种诱导对抗金黄葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:选自由SEQ ID NO:8、SEQ IDNO:10、SEQ ID NO:11、SEQ ID NO:12、SEQ ID NO:14、SEQ ID NO:18、SEQ ID NO:19、SEQ ID NO:20、SEQ ID NO:23、SEQ ID NO:26、SEQ ID NO:27、SEQ ID NO:30、其生物等效物或其片段组成的群组的表皮葡萄球菌多肽序列。
在特定实施例中,本发明提供一种诱导对抗金黄葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:选自由SEQ ID NO:40、SEQID NO:42、SEQ ID NO:43、SEQ ID NO:44、SEQ ID NO:46、SEQ ID NO:50、SEQ ID NO:51、SEQ ID NO:52、SEQ ID NO:55、SEQ ID NO:58、SEQ ID NO:59、SEQ ID NO:62或其简并变异体或其片段组成的群组的表皮葡萄球菌聚核苷酸序列。
附图说明
图1绘示通过2D凝胶电泳比较的在TSB(1A和1C)或70%兔血清(1B和1D)中生长的表皮葡萄球菌0-47的细胞壁片断的蛋白质表达概况。在第一维中于pH 4-7的IPG条带上分离蛋白质,随后在第二维中以SDS-PAGE进行分离,将其转移到硝酸纤维素上,并通过荧光染色进行检测(1A和1C)。以受表皮葡萄球菌0-47感染的兔的免疫血清(1B和ID)显现免疫反应性蛋白。分子量标记标于左侧。
图2绘示生长于70%兔血清中的表皮葡萄球菌0-47的细胞表面片断的荧光染色印迹(2A)和免疫印迹(2B),所述细胞表面片断是在第一维中于pH 4-7的IPG条带上分离且在第二维中以SDS-PAGE分离。通过质谱分析鉴别斑点中的蛋白质。
图3绘示从生长于TSB或70%兔血清中的表皮葡萄球菌0-47的表面用增加浓度的NaCl或4.0M尿素洗脱的蛋白质。星号表明从在血清存在下生长的表皮葡萄球菌的表面洗脱的富集蛋白质。用TBS随后依次以0.5M和1.0M NaCl和4.0M尿素洗涤细菌3次。测定每一样本的蛋白质浓度,并于4-20%梯度凝胶上跑胶0.75μg。通过蛋白质检定,在从TSB中生长的细菌的表面洗脱的样本(第2-5道)中未检测到蛋白质,故将25μl装载于凝胶上。第1道,兔血清;第2道和第6道-0.15M NaCl洗出液;第3道和第7道-0.5M NaCl;第4道和第8道-1.0M NaCl;第5道和第9道-4.0M尿素。
图4绘示细胞表面蛋白从表皮葡萄球菌的2D转移,针对蛋白质(4A)对所述表皮葡萄球菌荧光染色,并且以从生长于70%兔血清中的表皮葡萄球菌洗脱的生物素化血清蛋白(4B)进行探测。用抗生蛋白链菌素-碱性磷酸酶接合物显现斑点。通过质谱法鉴别所述斑点中的蛋白质。
具体实施方式
暴露到宿主的血流中之后,入侵细菌遇到对新环境特异的环境暗示。通过细胞壁纯化蛋白中可检测的蛋白质表达中的细菌和信号适应性改变来检测这些暗示。通常,细菌细胞壁处的蛋白质和碳水化合物是用于包涵于治疗或预防细菌感染的免疫原性组合物中的候选物。无论上调的蛋白质是与宿主相互作用还是在养分获取中起到作用对于细菌而言都极为重要,且因此在细菌存活和发病机理中起到作用。已将细菌于体液(即,血清、腹膜透析液和尿液)中的生长用作模仿细菌在宿主内遇到的某些信号的模型系统。参看Wiltshire,M.D.和S.J.Foster,Infect Immun,69(8):第5198-202页(2001);Shepard,B.D.和M.S.Gilmore,Infect Immun,70(8):第4344-52页(2002);Smith,D.G.等人,Infect Immun,59(2):第617-24页(1991);McDermid,K.P.等人,Infect Immun,61(5):第1743-9页(1993)。已发现一或多种所述培养条件改变粪肠球菌(Enterococcus faecalis)、金黄葡萄球菌和表皮葡萄球菌中的基因表达,并且发现经鉴别在变化的培养条件下表达增加的那些蛋白质属于不同种类的具有多种功能的蛋白质。参看Wiltshire,M.D.和S.J.Foster,Infect Immun,69(8):第5198-202页(2001);Shepard,B.D.和M.S.Gilmore,Infect Immun,70(8):第4344-52页(2002)。
表皮葡萄球菌感染的最常见易感因素是植入人工装置。所植入的人工装置经血浆蛋白和基质蛋白包覆,所述血浆蛋白和基质蛋白包括纤维蛋白原、玻连蛋白(vitronectin)、von Willebrand氏因子和粘连蛋白。参看von Eiff,C等人,.Eur J Clin Microbiol Infect Dis,18(12):第843-6页(1999)。这些蛋白通常充当表皮葡萄球菌表面蛋白的配体,由此使细菌与人工装置结合并定殖于人工装置上。已知表皮葡萄球菌表达与纤维蛋白原、玻连蛋白和粘连蛋白结合的蛋白质。参看Nilsson,M.等人,A fibrinogen-binding protein ofStaphylococcus epidermidis.Infect Immun,66(6),第2666-73页(1998);Davis,S.L.等人,JBiol Chem,276(30),第27799-805页(2001);Williams,R.J.等人,Infect Immun,.70(12),第6805-10页(2002);Heilmann,C等人,Mol Microbiol,24(5),第1013-24页(1997)。预期表皮葡萄球菌将结合使共生体转换成致病菌的其它血清蛋白是合乎情理的。
下文所述的本发明解决对于表皮葡萄球菌免疫原性组合物的需求,所述免疫原性组合物有效预防或治疗由表皮葡萄球菌血清型所引起的大部分或所有疾病。本发明另外解决对于诊断表皮葡萄球菌感染的方法的需求。本发明已鉴别出编码抗原多肽的表皮葡萄球菌开放阅读框(下文的ORF)。更具体说来,表皮葡萄球菌ORF编码用作免疫原性组合物中的潜在抗原多肽的多肽。在某些实施例中,本发明包含编码表面定位、暴露、分泌或膜相关的多肽抗原的表皮葡萄球菌聚核苷酸ORF。
在其它实施例中,本发明包含含有ORF序列的载体和经这些载体转化、转染或感染的宿主细胞或动物。本发明还包含表皮葡萄球菌ORF的转录基因产物,诸如mRNA、反义RNA、反义寡核苷酸和核糖酶分子,其可用于抑制或控制微生物的生长。本发明还涉及检测这些核酸或多肽的方法和诊断表皮葡萄球菌感染的试剂盒。本发明还涉及用于预防和/或治疗细菌感染、尤其是由表皮葡萄球菌引起或因其而恶化的感染的免疫原性组合物。在特定实施例中,使用免疫原性组合物治疗或预防由表皮葡萄球菌引起或因其而恶化的全身性疾病。在其它实施例中,使用免疫原性组合物治疗或预防由表皮葡萄球菌引起或因其而恶化的非全身性疾病。
A.表皮葡萄球菌ORF聚核苷酸和多肽
鉴别用于产生供包涵于免疫原性组合物中之用的表皮葡萄球菌多肽的经分离和纯化的表皮葡萄球菌ORF聚核苷酸。更具体说来,在某些实施例中,ORF编码表皮葡萄球菌表面定位、暴露、膜相关或分泌的多肽、尤其是抗原多肽。因此,一方面,本发明鉴别经分离和纯化的聚核苷酸(ORF),其编码用于包涵于免疫原性组合物中的表皮葡萄球菌表面定位、暴露、膜相关或分泌的多肽。在特定实施例中,本发明的聚核苷酸为DNA分子,其中DNA可为基因组DNA、染色体DNA、质粒DNA或cDNA。在另一实施例中,聚核苷酸为重组聚核苷酸,其编码表皮葡萄球菌多肽,所述多肽包含与SEQ ID NO:1到SEQ ID NO:32其中之一或其片段的氨基酸序列。在另一实施例中,经分离和纯化的ORF聚核苷酸包含与SEQ ID NO:33到SEQ ID NO:64、其简并变异体或其补体的ORF核苷酸序列其中之一具有至少95%同一性的核苷酸序列。在一实施例中,SEQ ID NO:33到SEQ ID NO:64其中之一的ORF聚核苷酸是包含于质粒载体中,且在原核宿主细胞中得以表达。
如下文所使用,术语“聚核苷酸”意思是由磷酸二酯键连接的核苷酸序列。下文是以5′到3′方向的方向呈现聚核苷酸。本发明的聚核苷酸可包含约10个到约数十万个碱基对。在一实施例中,聚核苷酸包含约10个到约3,000个碱基对。特定聚核苷酸的长度实例陈述于下文中。
本文所述的聚核苷酸可为脱氧核糖核酸(DNA)分子、核糖核酸(RNA)分子或使用核苷酸类似物产生的DNA或RNA的类似物。核酸分子可为单链或双链,但优选为双链DNA。在聚核苷酸为DNA分子的情况下,所述分子可为基因、cDNA分子或基因组DNA分子。下文通过单字母密码指示核苷酸碱基:腺嘌呤(A)、鸟嘌呤(G)、胸腺嘧啶(T)、胞嘧啶(C)、肌苷(I)和尿嘧啶(U)。
“经分离”意思是“通过人工”从其天然状态变化而来。如果组合物或物质存在于自然界中,那么为了认为其“经分离”,其必须已经改变或从其原始环境中移除,或两者皆有。举例说来,当将术语用于下文中时,天然存在于活动物中的聚核苷酸或多肽未经“分离”,但与其天然状态的共存物质分离的相同聚核苷酸或多肽“经分离”。
如本文所使用,“经分离”聚核苷酸不含天然与得到核酸的生物体的基因组DNA中的核酸侧接的序列(即,位于所述核酸5′端和3′端的序列)。举例说来,在各种实施例中,经分离表皮葡萄球菌核酸分子可含有小于约5kb、4kb、3kb、2kb、1kb、0.5kb或0.1kb的天然与得到核酸的细胞的基因组DNA中的核酸侧接的核苷酸序列。然而,表皮葡萄球菌核酸分子可与其它蛋白质编码序列或调控序列融合,且仍认为其经分离。
可使用标准克隆和筛选技术从得自mRNA的cDNA文库获得本文所述的ORF聚核苷酸且从而获得多肽。也可从诸如基因组DNA文库(例如,表皮葡萄球菌文库)的天然来源获得本发明的聚核苷酸,或可使用众所周知和市面有售的技术进行合成。
本文还涵盖因遗传密码的简并性而与SEQ ID NO:33到SEQ ID NO:64(和其片段)所示的核苷酸序列不同且因此编码与SEQ ID NO:33到SEQ ID NO:64中所示的核苷酸序列所编码的多肽相同的表皮葡萄球菌多肽的核酸分子。
可使用此项技术中众所周知的方法轻易地鉴别表皮葡萄球菌聚核苷酸的直系同源物(orthologue)和等位基因变异体。聚核苷酸的等位基因变异体和直系同源物将包含通常至少约70-75%、更通常至少约80-85%且最通常至少约90-95%或95%以上与SEQ IDNO:33到SEQ ID NO:64或这些核苷酸序列的片段同源的核苷酸序列。可轻易鉴别所述核酸分子能够在严格条件下与SEQ ID NO:33到SEQ ID NO:64或这些核苷酸序列的片段所示的核苷酸序列杂交。
而且,聚核苷酸可仅包含表皮葡萄球菌聚核苷酸或基因的编码区的片段,诸如SEQID NO:33到SEQ ID NO:64其中之一的片段。在某些实施例中,所述片段编码免疫原性片段。
当使用本发明的这些表皮葡萄球菌ORF聚核苷酸重组产生用于包涵于免疫原性组合物中的表皮葡萄球菌多肽时,所述聚核苷酸可包括成熟多肽的编码序列;其本身;或阅读框中的成熟多肽的编码序列;和其它编码序列,诸如编码前导序列或分泌序列、前蛋白序列或前体蛋白序列或原前体蛋白序列或其它融合肽部分的编码序列。举例说来,可将有助于融合多肽纯化的标记序列与编码序列连接(参看Gentz等人,Proc.Natl.Acad.Sci.USA,86:821-824,1989,其是以全文引用的方式并入下文中)。因此,本文涵盖编码允许表达产物的His标签纯化的融合多肽的聚核苷酸的制备。聚核苷酸还可含有非编码5′和3′序列,诸如已转录序列、未翻译序列、剪接信号和聚腺苷酸化信号。
因此,可通过一种方法获得编码用于包涵于本发明的免疫原性组合物中的多肽的聚核苷酸,包括来自除表皮葡萄球菌外的物种(诸如金黄葡萄球菌)的同源物和直系同源物,所述方法包含以下步骤:在严格杂交条件下,用具有SEQ ID NO:33到SEQ ID NO:64其中之一、其片段的序列的经标记探针筛选适当文库;和分离含有所述聚核苷酸序列的全长cDNA和基因组克隆。所述杂交技术已为所属领域技术人员众所周知。所属领域技术人员将认识到,在许多情况下,经分离cDNA序列将是不完整的,这是因为编码多肽的区域在cDNA的5′端被切短。这是反转录酶作用的结果,使得无法在第一条cDNA链合成期间完成mRNA模板的DNA拷贝,所述反转录酶是一种具有固有地低“处理能力(processivity)”(聚合反应期间酶保持附着到模板上的能力的度量)的酶。
因此,在某些实施例中,本文所提供的聚核苷酸序列信息允许制备能够与下文所公开的所选聚核苷酸基因序列特异性杂交的相对短的DNA(或RNA)寡核苷酸序列。如下文所使用,术语“寡核苷酸”是定义为包含2个或2个以上脱氧核糖核苷酸或核糖核苷酸、通常大于3个且通常大于10个且多达100个或100个以上(但优选介于20个与30个之间)脱氧核糖核苷酸或核糖核苷酸的分子。确切尺寸将视许多因素而定,于是其视所述寡核苷酸的最终功能或用途而定。因此,在特定实施例中,适当长度的核酸探针是基于所选核苷酸序列(例如,诸如SEQ ID NO:33到SEQ ID NO:64所示的序列的序列)的考虑进行制备。所述核酸探针与编码表皮葡萄球菌多肽的聚核苷酸特异性杂交的能力使其在多个实施例中特别有用。最重要的是,可将所述探针用于多种用于检测给定样本中互补序列的存在的检定中。
在某些实施例中,使用寡核苷酸引物是有利的。可以任何方式产生这些引物,包括化学合成、DNA复制、反转录或其组合。使用本文所述的聚核苷酸设计所述引物的序列以用于使用聚合酶链式反应(PCR)技术检测、扩增或突变编码来自原核细胞的表皮葡萄球菌多肽的ORF聚核苷酸的规定区段。
在某些实施例中,使用本文所述的聚核苷酸与用于检测杂交体形成的适当标记的组合是有利的。此项技术中已知广泛多种能够提供可检测信号的适当标记,包括放射性、酶或其它配体,诸如亲和素/生物素。
可将与SEQ ID NO:33到SEQ ID NO:64其中之一或其片段中所含的核苷酸序列相同或足够相同的聚核苷酸用作cDNA和基因组DNA的杂交探针或用作核酸扩增(PCR)反应的引物,以分离编码本文所述的多肽的全长cDNA和基因组克隆并分离与SEQ IDNO:33到SEQ ID NO:64或其片段中所述的聚核苷酸序列具有高度序列相似度的其它基因(包括编码除表皮葡萄球菌外的物种的同源物和直系同源物的基因)的cDNA和基因组克隆。这些核苷酸序列通常与参考聚核苷酸序列至少约70%相同到至少约95%相同。探针或引物一般将包含至少15个核苷酸,优选至少30个核苷酸,且可具有至少50个核苷酸。特别优选的探针将具有介于30个与50个之间的核苷酸。
存在数种可用且所属领域技术人员众所周知的获得全长cDNA或延长短cDNA的方法,例如基于cDNA末端快速扩增(RACE)法的方法。参看Frohman等人,Proc.Natl.Acad.Sci.USA 85,8998-9002,1988。举例说来,近来对MarathonTM技术(Clontech LaboratoriesInc.)所例示的技术的改进已显著简化有关较长cDNA的研究。在MarathonTM技术中,已由从所选组织提取的mRNA和接合于每一端上的“接头”序列制备cDNA。随后,进行核酸扩增(PCR)以使用基因特异性与接头特异性寡核苷酸引物的组合扩增cDNA“缺失”的5′端。接着,使用“套式”引物重复PCR反应,所述套式引物为经设计以于经扩增产物内退火的引物(通常为在接头序列中3′处进一步退火的接头特异性引物和在已知基因序列中5′处进一步退火的基因特异性引物)。可随后通过DNA测序分析这一反应的产物,且全长cDNA可通过将所述产物直接与现存cDNA接合以得到完整序列来构建,或使用有关设计5′引物的新序列信息进行单独的全长PCR来构建。
为提供本发明的某些优点,用于杂交研究或检定的优选核酸序列包括与至少10个到约70个核苷酸长的聚核苷酸区段互补的探针分子,所述聚核苷酸编码表皮葡萄球菌多肽,诸如SEQ ID NO:33到SEQ ID NO:64其中之一中所示的多肽。至少10个核苷酸长的尺寸有助于确保片段将具有足够长度以形成稳定且具选择性的双链体分子。然而,一般优选在大于10个碱基长的区段上具有互补序列的分子,以便增加杂交体的稳定性和选择性,且借此改良所获得的特异性杂交体分子的品质和等级。一般将优选设计具有25个到40个核苷酸、55个到70个核苷酸或视需要甚至更长的基因互补区段的核酸分子。可例如通过以化学方式直接合成片段、通过应用诸如PCR技术(美国专利4,683,202,其是以引用的方式并入本文)的核酸复制技术或通过从含有适当插入物和适当限制性酶位点的重组质粒切除所选DNA片段来容易地制备所述片段。
在另一实施例中,预期经分离和纯化的聚核苷酸包含与SEQ ID NO:33到SEQ ID NO:64其中之一的至少10个相邻碱基的区段相同或互补的核苷酸序列,其中所述聚核苷酸与编码表皮葡萄球菌多肽的聚核苷酸杂交。经分离和纯化的聚核苷酸优选包含与SEQ IDNO:33到SEQ ID NO:64其中之一的至少25个到约70个相邻碱基的区段相同或互补的碱基序列。举例说来,聚核苷酸可包含与已公开核苷酸序列的40个或55个相邻碱基相同或互补的碱基区段。
因此,可使用聚核苷酸探针分子与互补基因区段选择性形成双链体分子的能力。视所预想的应用而定,将需要使用不同杂交条件以达成探针对目标序列的不同选择性程度(参看下表1)。对于需要高选择性程度的应用而言,通常将需要使用相对严格的条件形成杂交体。对于一些应用而言,例如,当需要使用与基础模板杂交的突变体引物链制备突变体时,或当设法从其它细胞、功能性等效物等分离表皮葡萄球菌同源多肽编码序列时,通常需要较低严格度杂交条件以允许形成异源双链体(参看表1)。因此,可相对于对照杂交容易地将交叉杂交物质鉴别为阳性杂交信号。由此,易于操纵杂交条件且因此一般将为视所需结果选择的方法。
对于某些应用而言,例如当需要使用与基础模板杂交的突变体引物链制备突变体时,或当设法从其它细胞、功能性等效物等分离同源多肽编码序列时,通常需要较低严格度杂交条件以允许形成异源双链体。因此,可相对于对照杂交容易地将交叉杂交物质鉴别为阳性杂交信号。在任何情况下,一般应了解,可通过加入渐增量的甲酰胺使条件更为严格,所述渐增量的甲酰胺是用于以与上升温度相同的方式使杂交双链体去稳定。因此,易于操纵杂交条件,且由此一般将为视所需结果选择的方法。
本文中还描述能够在低严格度条件下、更优选在严格条件下且最优选在高度严格的条件下与下文所述的聚核苷酸杂交的聚核苷酸。严格度条件的实例展示于下表1中:高严格度条件为至少与(例如)条件A-F同样严格的条件;严格条件至少与(例如)条件G-L同样严格;且低严格度条件至少与(例如)条件M-R同样严格。
表1
严格度条件
严格度条件 | 聚核苷酸杂交体 | 杂交体长度(bp)1 | 杂交温度和缓冲液H | 洗涤温度和缓冲液H |
A | DNA:DNA | >50 | 65℃;1×SSC或42℃;1×SSC,50%甲酰胺 | 65℃;0.3×SSC |
B | DNA:DNA | <50 | TB;1×SSC | TB;1×SSC |
C | DNA:RNA | >50 | 67℃;1×SSC或45℃;1×SSC,50%甲酰胺 | 67℃;0.3×SSC |
D | DNA:RNA | <50 | TD;1×SSC | TD;1×SSC |
E | RNA:RNA | >50 | 70℃;1×SSC或50℃;1×SSC,50%甲酰胺 | 70℃;0.3×SSC |
F | RNA:RNA | <50 | TF;1×SSC | TF;1×SSC |
G | DNA:DNA | >50 | 65℃;4×SSC或42℃;4×SSC;50%甲酰胺 | 65℃;1×SSC |
H | DNA:DNA | <50 | TH;4×SSC | TH;4×SSC |
I | DNA:RNA | >50 | 67℃;4×SSC或45℃;4×SSC,50%甲酰胺 | 67℃;1×SSC |
J | DNA:RNA | <50 | TJ;4×SSC | TJ;4×SSC |
K | RNA:RNA | >50 | 70℃;4×SSC或50℃;4×SSC;50%甲酰胺 | 67℃;1×SSC |
L | RNA:RNA | <50 | TL;2×SSC | TL;2×SSC |
M | DNA:DNA | >50 | 50℃;4×SSC或40℃;6×SSC,50%甲酰胺 | 50℃;2×SSC |
N | DNA:DNA | <50 | TN;6×SSC | TN;6×SSC |
O | DNA:RNA | >50 | 55℃;4×SSC或42℃;6×SSC,50%甲酰胺 | 55℃;2×SSC |
P | DNA:RNA | <50 | TP;6×SSC | TP;6×SSC |
Q | RNA:RNA | >50 | 60℃;4×SSC或45℃;6×SSC,50%甲酰胺 | 60℃,2×SSC |
R | RNA:RNA | <50 | TR;4×SSC | TR;4×SSC |
(bp)1:杂交体长度为所预期的杂交聚核苷酸中杂交区域的长度。当使聚核苷酸与具有未知序列的目标聚核苷酸杂交时,假定杂交体长度为杂交聚核苷酸的长度。当与具有已知序列的聚核苷酸杂交时,可通过对准聚核苷酸的序列并鉴别具有最佳序列互补性的区域来测定杂交体长度。
缓冲液H:在杂交和洗涤缓冲液中,SSPE(1×SSPE为0.15M NaCl、10mM NaH2PO4和1.25mM EDTA,pH 7.4)可经SSC(1×SSC为0.15M NaCl和15mM柠檬酸钠)替换;在杂交完成后进行洗涤15分钟。
TB到TR:预期小于50个碱基对长的杂交体的杂交温度应比杂交体的熔解温度(Tm)低5-10℃,其中Tm是根据以下等式确定。对于小于18个碱基对长的杂交体而言,Tm(℃)=2(A+T碱基数)+4(G+C碱基数)。对于介于18个与49个碱基对长度之间的杂交体而言,Tm(℃)=81.5+16.6(log10[Na+])+0.41(%G+C)-(600/N),其中N为杂交体中的碱基数,且[Na+]为杂交缓冲液中钠离子的浓度(1×SSC中[Na+]=0.165M)。
聚核苷酸杂交的严格度条件的其它实例提供于Sambrook等人,1989,MolecularCloning:A Laboratory Manual,Cold Spring Harbor Laboratory Press,Cold Spring Harbor,NY,第9章和第11章;和Ausubel等人,1995,Current Protocols in Molecular Biology编辑,John Wiley&Sons,Inc.,第2.10节和第6.3-6.4节中,所述文献是以引用的方式并入下文中。
B.表皮葡萄球菌多肽
在特定实施例中,本发明提供用于免疫原性组合物中的经分离和纯化的表皮葡萄球菌多肽。用于本发明的免疫原性组合物中的表皮葡萄球菌多肽优选为重组多肽。在某些实施例中,表皮葡萄球菌多肽包含与SEQ ID NO:1到SEQ ID NO:32其中之一、其生物等效物或其片段的氨基酸序列具有至少95%同一性的氨基酸序列。
用于本发明的免疫原性组合物中的表皮葡萄球菌多肽涵盖包含以下各物的多肽:1)SEQ ID NO:1到SEQ ID NO:32其中之一中所示的氨基酸序列;2)天然存在的SEQ ID NO:1到SEQ ID NO:32的表皮葡萄球菌多肽的功能性和非功能性变异体或生物等效物;3)SEQ ID NO:1到SEQ ID NO:32的表皮葡萄球菌多肽的重组产生变异体或生物等效物;和4)从除表皮葡萄球菌外的生物体分离的多肽(表皮葡萄球菌多肽的直系同源物)。
所述表皮葡萄球菌多肽的生物等效物或变异体涵盖:1)从表皮葡萄球菌分离的多肽;和2)实质上含有与表皮葡萄球菌多肽的同源性的多肽。
表皮葡萄球菌的生物等效物或变异体包括功能性与非功能性表皮葡萄球菌多肽。功能性生物等效物或变异体为保持在受试者体内引发免疫或抗原反应的能力的表皮葡萄球菌多肽的天然存在的氨基酸序列变异体。功能性变异体通常将仅含有SEQ ID NO:1到SEQ ID NO:32其中之一的一个或多个氨基酸的保守取代或所述多肽的非关键区域中(例如,不是在含有抗原决定簇或保护性抗原表位的区域中)非关键残基的取代、缺失或插入。
本发明另外提供表皮葡萄球菌多肽的非表皮葡萄球菌直系同源物。表皮葡萄球菌多肽的直系同源物是从非表皮葡萄球菌生物体分离且具有表皮葡萄球菌多肽的抗原能力的多肽。可容易地鉴别表皮葡萄球菌多肽的直系同源物包含与SEQ ID NO:1到SEQ ID NO:32其中之一实质同源的氨基酸序列。
可对本发明的多肽的结构进行改进和改变,且仍获得具有表皮葡萄球菌抗原性的分子。举例说来,可在序列中以其它氨基酸取代某些氨基酸而不明显损失抗原性。由于多肽的相互作用能力和性质界定所述多肽的生物功能活性,故可在多肽序列(或当然其基础DNA编码序列)中进行某些氨基酸序列的取代,且仍然获得具类似特性的多肽。
在进行所述改变时,可考虑氨基酸的水合指数(hydropathic index)。此项技术中一般理解氨基酸水合指数于赋予多肽相互作用的生物功能中的重要性(Kyte和Doolittle,JMol Biol,157:第105-132页,1982)。已知某些氨基酸可经具有类似水合指数或得分的其它氨基酸取代且仍产生具有类似生物活性的多肽。已基于氨基酸的疏水性和电荷特性指派每一氨基酸的水合指数。这些指数为:异亮氨酸(+4.5);缬氨酸(+4.2);亮氨酸(+3.8);苯丙氨酸(+2.8);半胱氨酸/胱氨酸(+2.5);甲硫氨酸(+1.9);丙氨酸(+1.8);甘氨酸(-0.4);苏氨酸(-0.7);丝氨酸(-0.8);色氨酸(-0.9);酪氨酸(-1.3);脯氨酸(-1.6);组氨酸(-3.2);谷氨酸(-3.5);谷氨酰胺(-3.5);天冬氨酸(-3.5);天冬酰胺酸(-3.5);和精氨酸(-4.5)。
认为氨基酸残基的相对水合特性决定所得多肽的二级和三级结构,其接着界定所述多肽与诸如酶、底物、受体、抗体、抗原等其它分子的相互作用。此项技术中已知,氨基酸可经另一具有相似水合指数的氨基酸取代且仍获得功能相当的多肽。在所述改变中,优选水合指数在+/-2以内的氨基酸的取代,特别优选水合指数在+/-1以内的氨基酸的取代,且甚至更特别优选在+/-0.5以内的氨基酸的取代。
也可基于亲水性、尤其在意欲将由此产生的生物功能相当的多肽或肽用于免疫实施例中的情况下对相似氨基酸进行取代。以引用的方式并入下文中的美国专利4,554,101声明,如受相邻氨基酸的亲水性影响的多肽的最大局部平均亲水性与其免疫原性和抗原性相关,即与所述多肽的生物学特性相关。
如美国专利4,554,101中所详述,已将以下亲水性值指派给氨基酸残基:精氨酸(+3.0);赖氨酸(+3.0);天冬氨酸(+3.0±1);谷氨酸(+3.0±1);丝氨酸(+3.0);天冬酰胺酸(+0.2);谷氨酰胺(+0.2);甘氨酸(0);脯氨酸(-0.5±1);苏氨酸(-0.4);丙氨酸(-0.5);组氨酸(-0.5);半胱氨酸(-1.0);甲硫氨酸(-1.3);缬氨酸(-1.5);亮氨酸(-1.8);异亮氨酸(-1.8);酪氨酸(-2.3);苯丙氨酸(-2.5);色氨酸(-3.4)。应了解,氨基酸可经另一具有相似亲水性值的氨基酸取代且仍获得生物学上相当且尤其是免疫学上相当的多肽。在所述改变中,优选亲水性值在±2以内的氨基酸的取代,特别优选亲水性值在±1以内的氨基酸的取代,且甚至更特别优选亲水性值在±0.5以内的氨基酸的取代。
如上文所述,因此,氨基酸取代一般是基于氨基酸侧链取代基(例如)疏水性、亲水性、电荷、尺寸等的相对相似度。所属领域技术人员众所周知考虑到多种上述特性的示范性取代,且其包括:精氨酸与赖氨酸;谷氨酸与天冬氨酸;丝氨酸与苏氨酸;谷氨酰胺与天冬酰胺酸;和缬氨酸、亮氨酸与异亮氨酸(参看下表2)。因此,本发明涵盖包含如上文所述的表皮葡萄球菌多肽的功能性或生物等效物的免疫原性组合物。
表2
氨基酸取代
原始残基示范性残基取代
也可使用位点特异性突变诱发制备多肽的生物等效物或功能性等效物。位点特异性突变诱发是可通过编码DNA的特异性突变诱发来制备衍生自其序列的第二代多肽或生物功能相当的多肽或肽的有用技术。如上文所述,在需要氨基酸取代的地方可能需要所述改变。所述技术另外提供通过将一或多种核苷酸序列改变引入DNA中来制备和测试序列变异体(例如,并有一或多种前述考虑因素)的现成能力。位点特异性突变诱发允许通过使用编码具有所需突变和足够数量相邻核苷酸的DNA序列的特异性寡核苷酸序列提供具有足够长度和序列复杂度的引物序列以于横越缺失接点两侧上形成稳定双链体,来产生突变体。通常,优选长度为约17个到25个核苷酸的引物,且序列接合点两侧上约5个到10个残基是变化的。
一般说来,此项技术中众所周知位点特异性突变诱发的技术。如将了解的,所述技术通常使用可以单链和双链形式存在的噬菌体载体。通常,通过首先获得序列内包括编码所有或一部分所选表皮葡萄球菌多肽序列的DNA序列的单链载体来进行根据本文的定点突变诱发。制备(例如,合成)具有所需突变序列的寡核苷酸引物。随后,使这一引物与单链载体退火,并通过使用诸如大肠杆菌聚合酶I Klenow片段的酶进行延长,以完成具有突变的链的合成。因此,形成异源双链体,其中一条链编码未突变的原始序列,且另一条链具有所需突变。随后,使用这一异源双链体载体转化适当的细胞(诸如,大肠杆菌细胞),并且选择包括具有突变的重组载体的克隆。一起提供市面有售的试剂盒与所有必需的试剂,但寡核苷酸引物除外。
应将用于本发明的免疫原性组合物中的表皮葡萄球菌多肽或多肽抗原理解为任何表皮葡萄球菌多肽,其包含与包含SEQ ID NO:1到SEQ ID NO:32其中之一的氨基酸序列的表皮葡萄球菌多肽的实质序列相似性、结构相似性和/或功能相似性。此外,所述表皮葡萄球菌多肽或多肽抗原不限于特定来源。因此,本发明提供对于各种来源的多肽的通用检测和分离技术。
本发明预期可有利地将表皮葡萄球菌多肽分裂成片段以用于进一步结构或功能分析中或用于产生诸如表皮葡萄球菌相关多肽和表皮葡萄球菌特异性抗体的试剂。这可通过用诸如内切蛋白酶glu-C(Boehringer,Indianapolis,IN)的肽酶处理经纯化或未经纯化的表皮葡萄球菌多肽实现。用CNBr处理是可由天然表皮葡萄球菌多肽产生肽片段的另一种方法。也可使用重组技术产生表皮葡萄球菌多肽的特定片段。
本发明的免疫原性组合物中还包括表皮葡萄球菌多肽的片段。片段是具有完全与氨基酸序列的部分(但非全部)相同的氨基酸序列的多肽。所述片段可包含SEQ ID NO:1到SEQ ID NO:32其中之一的氨基酸序列的(例如)至少7个或7个以上(例如,8、10、12、14、16、18、20或20个以上)相邻氨基酸。片段可为“独立式(freestanding)”或包含在其形成一部分或区域、最优选作为单一连续区域的较大多肽内。在一实施例中,所述片段包括成熟多肽序列的至少一个抗原表位。
“融合蛋白”是指由两个通常不相关的融合基因或其片段编码的蛋白质或多肽。举例说来,已描述包含免疫球蛋白分子恒定区中多个部分连同另一人类蛋白或其部分的融合蛋白或多肽。在许多情况下,使用免疫球蛋白Fc区作为融合蛋白或多肽的一部分对于用于引起(例如)药代动力学特性改良的治疗和诊断中是有利的(例如,参看国际专利申请案EP-A 0232 2621)。另一方面,对于某些用途而言,需要能够在表达、检测和纯化融合蛋白或多肽之后缺失Fc部分。
预期可从表皮葡萄球菌分离或如本文所述重组制备表皮葡萄球菌多肽。
C.表皮葡萄球菌聚核苷酸和多肽变异体
如下文所使用的术语“变异体”是一种分别不同于参考聚核苷酸或多肽但保持基本特性的聚核苷酸或多肽。聚核苷酸的典型变异体的核苷酸序列与另一参考聚核苷酸的核苷酸序列不同。所述变异体核苷酸序列的改变可能改变或可能不改变由参考聚核苷酸编码的多肽的氨基酸序列。如下文所讨论,核苷酸改变可导致由参考序列编码的多肽中氨基酸取代、添加、缺失、融合和截断。多肽的典型变异体的氨基酸序列与另一参考多肽的氨基酸序列不同。一般会对差异加以限制,从而使参考多肽和变异体的全部序列紧密类似且在许多区域中相同。变异体多肽与参考多肽的不同之处可在于氨基酸序列中一个或多个取代、添加、缺失的任何组合。经取代或插入的氨基酸残基可能是或可能不是遗传密码所编码的氨基酸残基。聚核苷酸或多肽的变异体可天然存在,诸如等位基因变异体;或者其可为并未已知天然存在的变异体。可通过突变诱发技术或通过直接合成制得聚核苷酸和多肽的非天然存在的变异体。
如此项技术中已知,“同一性”是如通过比较两个或两个以上多肽序列或两个或两个以上聚核苷酸序列所确定的所述序列之间的关系。在此项技术中,“同一性”还指,视情况如通过匹配多肽或聚核苷酸序列链所确定的所述序列之间的序列相关程度。可通过已知方法容易地计算“同一性”和“相似度”,所述方法包括(但不限于)(ComputationalMolecular Biology,Lesk,A.M.,编辑,Oxford University Press,New York,1988;Biocomputing:Informatics and Genome Projects,Smith,D.W.,编辑,Academic Press,NewYork,1993;Computer Analysis of Sequence Data,第I部,Griffin,A.M.和Griffin,H.G.,编辑,Humana Press,New Jersey,1994;Sequence Analysis in Molecular Biology,yon Heinje,G.,Academic Press,1987;和Sequence Analysis Primer,Gribskov,M.和Devereux,J.,编辑,MStockton Press,New York,1991;和Carillo,H.和Lipman,D.,SIAM J.Applied Math.,48:1073(1988))中所述的方法。设计测定同一性的方法以得到经测试序列之间的最大匹配。将测定同一性和相似度的方法编程成为公开可用的计算机程序。测定两个序列之间的同一性和相似度的计算机程序方法包括(但不限于)GCG程序包(Devereux等人,Nucleic Acids Research 12(1):387,1984)、BLASTP、BLASTN、TBLASTN和FASTA(Altschul等人,J.Molec.Biol.215:403-410,1990)。BLASTX程序是从NCBI和其它来源公开可用(BLAST Manual,Altschul,S.等人,NCBI NLM NIH Bethesda,Md.20894;Altschul等人,J.Molec.Biol.215:403-410,1990)。众所周知的Smith-Waterman算法也可用于测定同一性。
举例说来,本文所述的聚核苷酸序列可与SEQ ID NO:33到SEQ ID NO:64其中之一的参考序列相同,即100%相同;或如与参考序列相比较,其可包括至多特定整数个数的核苷酸变化。所述变化选自由至少一个核苷酸缺失、取代(包括转换和颠换)或插入组成的群组,且其中所述变化可发生于参考核苷酸序列的5′或3′末端位置,或所述末端位置之间的任何地方,独立地分散于参考序列中的核苷酸之间或参考序列内一个或多个相邻基团中。通过使SEQ ID NO:33到SEQ ID NO:64其中之一中的核苷酸总数乘以个别同一性百分数的数字百分数(除以100),并以所述SEQ ID NO:33到SEQ ID NO:64其中之一的核苷酸总数减去所述乘积来确定核苷酸变化数。
举例说来,经分离的表皮葡萄球菌聚核苷酸包含与SEQ ID NO:33到SEQ ID NO:64其中之一、其简并变异体或其片段的核苷酸序列具有至少70%同一性的聚核苷酸序列,其中所述聚核苷酸序列可包括SEQ ID NO:33到SEQ ID NO:64其中之一的核酸序列的整个聚核苷酸区域内至多nn个核酸变化,其中nn为最大变化数,且其是通过下式计算:
nn≤xn-(xn·y),
其中,xn为SEQ ID NO:33到SEQ ID NO:64其中之一的核酸总数,且y值为0.70,其中将xn与y的任何非整数乘积都四舍五入成最接近的整数,随后用xn减去所述乘积。当然,y值也可为0.80(80%)、0.85(85%)、0.90(90%)、0.95(95%)等。编码SEQ IDNO:1到SEQ ID NO:32中的一个多肽的聚核苷酸序列的变化可在这一编码序列中产生无义、错义或移码突变,且因此改变由所述变化后的聚核苷酸编码的多肽。
类似地,本文所述的多肽序列可与SEQ ID NO:1到SEQ ID NO:32的参考序列相同,即100%相同;或如与参考序列相比较,其可包括至多特定整数个数的氨基酸变化,从而使同一性%小于100%。所述变化选自由至少一个氨基酸缺失、取代(包括保守和非保守取代)或插入组成的群组,且其中所述变化可发生于参考多肽序列的氨基末端或羧基末端位置,或所述末端位置之间的任何地方,独立地分散于参考序列中的氨基酸之间或参考序列内一个或多个相邻基团中。通过使SEQ ID NO:1到SEQ ID NO:32其中之一中的氨基酸总数乘以个别同一性百分数的数字百分数(除以100),且随后以所述SEQ ID NO:1到SEQ ID NO:32其中之一的氨基酸总数减去所述乘积或以下式来确定指定同一性%下氨基酸的变化数:
na≤xa-(xa·y),
其中,na为氨基酸变化的数量,xa为SEQ ID NO:1到SEQ ID NO:32其中之一的氨基酸总数,且y为(例如)0.70(70%)、0.80(80%)、0.85(85%)等,且其中将xa与y的任何非整数乘积四舍五入成最接近的整数,随后用xa减去所述乘积。
D.载体、宿主细胞和重组表皮葡萄球菌多肽
在一实施例中,本发明提供包含ORF聚核苷酸的表达载体,所述ORF聚核苷酸编码用于免疫原性组合物中的表皮葡萄球菌多肽。表皮葡萄球菌表达载体包含编码表皮葡萄球菌多肽的ORF聚核苷酸,所述表皮葡萄球菌多肽包含SEQ ID NO:1到SEQ ID NO:32其中之一的氨基酸残基序列。或者,表达载体包含具有SEQ ID NO:33到SEQ ID NO:64其中之一的核苷酸碱基序列的聚核苷酸。在其它实施例中,本发明的表达载体包含可操作地连接到增强子-启动子的聚核苷酸。在其它实施例中,表达载体包含可操作地连接到原核启动子的聚核苷酸。或者,表达载体包含可操作地连接到为真核启动子的增强子-启动子的聚核苷酸。表达载体另外包含定位于羧基端氨基酸的3′处且在经编码多肽的转录单元内的聚腺苷酸化信号。
原核生物中蛋白质的表达最常是在大肠杆菌中以含有引导融合或非融合蛋白表达的组成性或可诱导启动子的载体进行。融合载体将多个氨基酸添加到其中编码的蛋白质上,通常添加到重组蛋白的氨基端。所述融合载体通常用于三个目的:1)增加重组蛋白的表达;2)增加重组蛋白的溶解性;和3)通过充当亲和纯化中的配体来辅助重组蛋白的纯化。通常,在融合表达载体中,在融合部分与重组蛋白的接合处引入蛋白水解分裂位点,以使重组蛋白与融合部分能够分离,随后进行融合蛋白的纯化。所述酶和其同源识别序列包括因子Xa、凝血酶和肠激酶。
典型的融合表达载体包括pGEX(Pharmacia Biotech Inc;Smith和Johnson,Gene67:31-40,1988)、pMAL(New England Biolabs,Beverly;MA)和pRIT5(Pharmacia,Piscataway,NJ),其将谷胱甘肽S转移酶(GST)、麦芽糖E结合蛋白或蛋白A分别与目标重组蛋白融合。
在一实施例中,将表皮葡萄球菌聚核苷酸的编码序列克隆到pGEX表达载体中以产生编码融合蛋白的载体,所述融合蛋白从N末端到C末端包含GST-凝血酶分裂位点-表皮葡萄球菌多肽。可使用谷胱甘肽-琼脂糖树脂通过亲和色谱纯化融合蛋白。未与GST融合的重组表皮葡萄球菌多肽可通过用凝血酶分裂融合蛋白来进行回收。
适当的可诱导非融合型大肠杆菌表达载体的实例包括pTrc(Amann等人,Gene69:301-315,1988)、pET lld(Studier等人,″Gene Expression Technology″Methods inEnzymology 185,60-89,1990)、pBAD和pCRT7。pTrc载体的目标基因表达依赖于从杂交体trp-lac融合启动子的宿主RNA聚合酶转录。pET lld载体的目标基因表达依赖于由共表达的病毒RNA聚合酶J7gnl介导的从T7gnl 0-lac融合启动子起始的转录。这一病毒聚合酶是由具有处于lacUV 5启动子转录控制下的T7gnl基因的常驻原噬菌体(residentprophage)的宿主菌株BL21(DE3)或HMS I 74(DE3)提供。
一种使大肠杆菌中重组蛋白的表达最大化的策略是,在具有削弱的蛋白水解分裂重组蛋白的能力的宿主细菌中表达蛋白质。另一策略是,改变待插入表达载体中的核酸的核酸序列,从而使每一氨基酸的个别密码子都是大肠杆菌中优先利用的密码子。所述本发明核酸序列的变化可通过标准DNA突变诱发或合成技术进行。
在另一实施例中,表皮葡萄球菌聚核苷酸表达载体为酵母表达载体。用于在酵母酿酒酵母(S.cerevisiae)中表达的载体的实例包括pYepSec I(Baldari等人,Embo J,6:第229-234页,1987)、pMFa(Kurjan和Herskowitz,Cell,第933-943页,1982)、pJRY88(Schultz等人,Gene,54:第113-123页,1987)和pYES2(Invitrogen Corporation,San Diego,CA)。
或者,可在昆虫细胞中(例如)使用杆状病毒表达载体表达表皮葡萄球菌聚核苷酸。可用于在所培养的昆虫细胞(例如,Sf9细胞)中表达蛋白质的杆状病毒载体包括pAc系列(Smith等人,Mol Cell Biol,3:第2156-2165页,1983)和pVL系列(Lucklow和Summers,Virology,170:第31-39页,1989)。
在另一实施例中,本发明的核酸是在哺乳动物细胞中使用哺乳动物表达载体进行表达。哺乳动物表达载体的实例包括pCDM8(Seed,Nature,329:第840页,1987)和pMT2PC(Kaufman等人,EMBO J,6:第187-195页,1987)。当用于哺乳动物细胞中时,表达载体的控制功能通常是由病毒调控元件提供。
如下文所使用,启动子是通常在转录起始点(即,转录起始位点)前(上游)约100个核苷酸对以内的DNA分子区域。这一区域通常含有在不同基因中位于类似相对位置中的数类DNA序列元件。如下文所使用,术语“启动子”包括此项技术中称为通用真核RNA聚合酶II转录单元的上游启动子区、启动子区或启动子的物质。
另一类不连续转录调控序列元件是增强子。增强子对特定编码区(例如,基因)提供时间、位置和表达水平的特异性。增强子的主要功能是增加细胞中含有一个或多个与所述增强子结合的转录因子的编码序列的转录水平。与启动子不同,只要存在启动子,那么当增强子位于距离转录起始位点不定距离处时都可起作用。
如下文所使用,短语“增强子-启动子”意思是含有增强子元件与启动子元件的复合单元。增强子-启动子可操作地连接到编码至少一种基因产物的编码序列。如下文所使用,短语“可操作地连接”意思是,增强子-启动子是以使所述编码序列的转录受所述增强子-启动子控制和调控的方式与编码序列连接。此项技术中众所周知使增强子-启动子与编码序列可操作地连接的方式。如此项技术中众所周知,相对于转录受控制的编码序列的精确方向和位置特别视增强子-启动子的特殊性质而定。因此,TATA框的最小启动子通常位于转录起始位点上游约25个到约30个碱基对处,且上游启动子元件通常位于转录起始位点上游约100个到约200个碱基对处。相比之下,增强子可位于起始位点下游且可在距离所述位点合理的距离处。
用于本文所述的载体构建体中的增强子-启动子可为驱动待转染的细胞中的表达的任何增强子-启动子。通过使用具有众所周知的特性的增强子-启动子,可使基因产物的表达水平和模式最佳化。
举例说来,常用启动子是得自多瘤病毒、腺病毒2、巨细胞病毒和猿猴病毒40。关于其它用于原核和真核细胞的适当表达系统请参看Sambrook等人,″Molecular Cloning:ALaboratory Manual″第2版,Cold Spring Harbor Laboratory,Cold Spring Harbor LaboratoryPress,Cold Spring Harbor,NY,1989第16章和第17章,所述文献是以引用的方式并入下文。
在另一实施例中,重组哺乳动物表达载体能够引导核酸优先在特定细胞类型中表达(例如,组织特异性调控元件用于表达核酸)。此项技术中已知组织特异性调控元件。适当组织特异性启动子的非限制性实例包括白蛋白启动子(肝脏特异性;Pinkert等人,GenesDev,1:第268-277页,1987)、淋巴特异性启动子(Calame和Eaton,Adv Immunol,43:第235-275页,1988)(尤其是T细胞受体(Winoto和Baltimore,EMBO J,8:第729-733页,1989)和免疫球蛋白(Banerji等人,Cell,33:第729-740页,1983)(Queen和Baltimore,Cell,33:第741-748页,1983)的启动子)、神经元特异性启动子(例如,神经丝启动子;Byrne和Ruddle,PNAS,86:第5473-5477页,1989)、胰腺特异性启动子(Edlund等人,Science,230:第912-916页,1985)和乳腺特异性启动子(例如,乳清启动子;美国专利4,873,316和国际专利申请案EP 264,166)。也涵盖发育调控的启动子,例如鼠类hox启动子(Kessel和Gruss,Science,249:第374-379页,1990)和甲胎蛋白启动子(Campes和Tilghman,Genes Dev,3:第537-546页,1989)。
本文还提供一种重组表达载体,其包含以反义方向克隆到表达载体中的编码表皮葡萄球菌多肽的DNA分子。也就是说,DNA分子以允许与表皮葡萄球菌mRNA反义的RNA分子表达(通过转录DNA分子)的方式与调控序列可操作地连接。可选择可操作地连接到以反义方向克隆的核酸的调控序列,其引导反义RNA分子在多种细胞类型中连续表达。举例说来,可选择引导反义RNA组成性、组织特异性或细胞类型特异性表达的病毒启动子和/或增强子或调控序列。反义表达载体可为反义核酸是在高效调控区的控制下产生的重组质粒、噬菌粒或减毒病毒的形式,其活性可通过引入载体的细胞类型确定。
可将本文所述的重组表达载体插入到任何适当的宿主细胞中。术语“宿主细胞”与“重组宿主细胞”在下文中可互换使用。应了解,所述术语不仅是指特定的受试者细胞,而且也指所述细胞的后代或可能的后代。由于在随后的数代中因突变或环境影响而可能出现某些改变,故实际上,所述后代可能与亲代细胞不同,但仍包括于如下文所使用的术语的范围内。宿主细胞可为任何原核或真核细胞。举例说来,表皮葡萄球菌多肽可在细菌细胞(诸如,大肠杆菌)、昆虫细胞(诸如Sf9、Sf21)、酵母或哺乳动物细胞(诸如,中国仓鼠卵巢细胞(CHO)、VERO、鸡胚成纤维细胞(chick embryo fibroblast)、BHK细胞或COS细胞)中表达。所属领域技术人员已知其它适当的宿主细胞。
载体DNA是通过常规转化、感染或转染技术引入原核或真核细胞。如下文所使用,术语“转化”和“转染”旨在是指将外来核酸(例如,DNA)引入宿主细胞中的各种技术公认的技术,包括磷酸钙或氯化钙共沉淀、DEAE-葡聚糖介导的转染、脂质体转染(lipofection)、超声波处理或电穿孔。用于转化或转染宿主细胞的适当方法可见于Sambrook等人(″Molecular Cloning:A Laboratory Manual″第2版,Cold Spring HarborLaboratory,Cold Spring Harbor Laboratory Press,Cold Spring Harbor,NY,1989)和其它实验室手册中。
使用本文所述的宿主细胞(诸如培养中的原核或真核宿主细胞)产生(即,表达)表皮葡萄球菌多肽。因此,本文也描述使用所述宿主细胞产生表皮葡萄球菌多肽的方法。在一实施例中,所述方法包含在适当培养基中培养宿主细胞(其中已引入编码表皮葡萄球菌多肽的重组表达载体)直到产生表皮葡萄球菌多肽。在另一实施例中,所述方法另外包含将表皮葡萄球菌多肽从培养基或宿主细胞中分离。
使表达载体的编码序列可操作地连接到转录终止区。RNA聚合酶经由发生聚腺苷酸化的位点转录编码DNA序列。通常,位于聚腺苷酸化位点下游数百碱基对处的DNA序列用于终止转录。这些DNA序列在下文中被称为转录终止区。这些区域为有效聚腺苷酸化经转录信使RNA(mRNA)所必需。此项技术中众所周知转录终止区。所述转录终止区的实例为SV40和鱼精蛋白基因的聚腺苷酸化信号。
表达载体包含编码表皮葡萄球菌多肽的聚核苷酸。所述多肽意欲包括编码表皮葡萄球菌多肽的核苷酸碱基序列,所述表皮葡萄球菌多肽的长度足以使所述区段与编码非表皮葡萄球菌多肽的聚核苷酸区段相区别。所述多肽还可编码生物功能性多肽或肽,其具有诸如具有基于(诸如)所交换的氨基酸的相对水合得分的考虑因素而选择的改变的变异体氨基酸序列。这些变异体序列是从天然来源分离或使用诸如定点突变诱发的突变诱发程序在下文所公开的序列中诱导的序列。
在某些实施例中,本文所述的表达载体包含编码多肽的聚核苷酸,所述多肽包含SEQID NO:1到SEQ ID NO:32其中之一的氨基酸残基序列。表达载体可包括上文所示的任何表皮葡萄球菌多肽的表皮葡萄球菌多肽编码区本身,或者其可含有在所述表皮葡萄球菌多肽的基础编码区中具有所选变化或修饰的编码区。或者,所述载体或片段可编码较大多肽或仍包括基础编码区的多肽。在任何情况下,都应了解,归因于密码子冗余和生物功能的等效性,这一方面不限于与上文所示的多肽序列对应的特定DNA分子。
示范性载体包括pCMV家族的哺乳动物表达载体,包括pCMV6b和pCMV6c(ChironCorp.,Emeryville CA.)。在某些情况下且尤其在这些个别哺乳动物表达载体的情况下,所得构建体可能必需与含有诸如pSV2neo的可选择标记的载体共转染。通过共转染到二氢叶酸还原酶缺陷型中国仓鼠卵巢细胞系(诸如DG44)中,依靠并入所述表达载体中的DNA表达表皮葡萄球菌多肽的克隆可得以检测。
可通过多种此项技术中众所周知的技术将DNA分子并入载体中。举例说来,已证实载体pUC18对于克隆和表达基因特别有价值。同样,可在本发明的某些实施例中、尤其是在进行双脱氧测序时使用相关载体M13mp18和M13mp19。
本文所述的表达载体可用作制备大量表皮葡萄球菌多肽编码DNA本身的方式,而且也可用作制备经编码多肽和肽的方式。预期当以重组方式制得表皮葡萄球菌多肽时,可使用原核或真核表达载体作为穿梭系统(shuttle system)。
另一方面,重组宿主细胞为原核宿主细胞。本发明的重组宿主细胞优选为大肠杆菌(Escherichia coli)DH5α菌株的细菌细胞。一般说来,优选原核生物起始克隆DNA序列并构建可用于本发明中的载体。举例说来,大肠杆菌K12菌株可特别有用。可使用的其它微生物菌株包括E.coli B和E.colix 1976(ATCC编号31537)。当然,这些实例旨在进行说明而非限制。
可使用上文所提及的菌株,和大肠杆菌W3110(ATCC编号273325)、大肠杆菌BL21(DE3)、大肠杆菌Top10;杆状菌(bacilli),诸如枯草芽胞杆菌(Bacillus subtilis);或其它肠杆菌(enterobacteriaceae),诸如鼠伤寒沙门氏菌(Salmonella typhimurium)(或如美国专利4,837,15中所述的其它减毒沙门氏菌属菌株)或粘质沙雷氏菌(Serratiamarcesans)和各种假单胞菌属。
一般说来,含有得自与宿主细胞可相容的种属的复制子和控制序列的质粒载体可与这些宿主组合使用。所述载体通常具有复制位点和能够在经转化细胞中提供表型选择的标记序列。举例说来,可使用pBR322(即,一种得自大肠杆菌种属的质粒)转化大肠杆菌(Bolivar等人,1977)。pBR322含有用于氨比西林(ampicillin)和四环素(tetracycline)抗性的基因,且因此提供鉴别经转化细胞的简便方式。pBR质粒或其它微生物质粒或噬菌体也必须含有或经修饰而含有可由微生物生物体用于表达其自身多肽的启动子。
最常用于重组DNA构建中的那些启动子包括β-内酰胺酶(青霉素酶)和乳糖启动子系统(Chang等人,1978;Itakura.等人,1977;Goeddel等人,1979;Goeddel等人,1980)和色氨酸(TRP)启动子系统(EP 0036776;Siebwenlist等人,1980)。尽管这些启动子最常使用,但已发现并利用其它微生物启动子,且已公开有关其核苷酸序列的细节,使得所属领域技术人员能够将功能性启动子引入质粒载体中(Siebwenlist等人,1980)。
除原核生物外,还可使用真核微生物,诸如酵母。酿酒酵母或普通面包酵母是最常用的真核微生物,但许多其它菌株通常可用。对于酵母菌中的表达而言,例如,通常使用质粒YRp7(Stinchcomb等人,1979;Kingsman等人,1979;Tschemper等人,1980)。这一质粒已含有trpl基因,其提供用于缺乏在色氨酸中生长的能力的酵母突变体菌株(例如,ATCC编号44076或PEP4-1)的选择标记(Jones,1977)。随后,作为酵母宿主细胞基因组特征的trpl损伤的存在为通过不存在色氨酸时的生长检测转化提供有效环境。
酵母载体中的适当启动子序列包括用于3-磷酸甘油酸激酶(Hitzeman.等人,1980)或其它糖酵解酶(Hess等人,1968;Holland等人,1978)(诸如烯醇酶、甘油醛-3-磷酸脱氢酶、己糖激酶、丙酮酸脱羧酶、磷酸果糖激酶、葡萄糖-6-磷酸异构酶、3-磷酸甘油酸变位酶、丙酮酸激酶、磷酸丙糖异构酶、磷酸葡糖异构酶和葡糖激酶)的启动子。在构建适当表达质粒时,也将与这些基因有关的终止序列引入待表达序列下游的表达载体中,以使mRNA聚腺苷酸化和终止。具有转录受生长条件控制的其它优势的其它启动子为用于醇脱氢酶2、异细胞色素C(isocytochrome C)、酸性磷酸酶、与氮代谢有关的降解酶和上文提及的甘油醛-3-磷酸脱氢酶和负责麦芽糖和半乳糖利用的酶的启动子区。含有酵母可相容启动子、复制起点和终止序列的任何质粒载体都是适合的。
除微生物外,还可将得自多细胞生物体的细胞的培养物用作宿主。原则上,任何所述细胞培养物都可使用,无论是来自脊椎动物还是来自非脊椎动物的培养物。然而,脊椎动物细胞已引起极大兴趣,且近年来,用培养(组织培养)使脊椎动物细胞繁殖已变成常规程序。所述有用的宿主细胞系的实例为AtT-20、VERO、HeLa、NSO、PER C6、中国仓鼠卵巢(CHO)细胞系和W138、BHK、COSM6、COS-7、293和MDCK细胞系。用于所述细胞的表达载体通常包括(必要时)复制起点、位于待表达的基因上游的启动子连同任何必需的核糖体结合位点、RNA剪接位点、聚腺苷酸化位点和转录终止子序列。
在需要表达重组表皮葡萄球菌多肽且涵盖真核宿主的情况下,使用并有真核复制起点的载体(诸如质粒)是最合乎需要的。此外,出于在真核系统中表达的目的,需要将表皮葡萄球菌编码序列定位于邻近+.o且处于有效的真核启动子(诸如与中国仓鼠卵巢细胞组合使用的启动子)控制下。为使编码序列处于启动子(无论是真核启动子还是原核启动子)的控制下,必须将多肽的适当翻译阅读框的翻译起始区的5′端定位于距离所选启动子3′端或下游约1个与约50个核苷酸之间。而且,当预期进行真核表达时,通常需要将编码表皮葡萄球菌多肽的聚核苷酸并入转录单元中。
此项技术中众所周知用外源聚核苷酸(诸如DNA分子)转化或转染细胞的方式,且其包括诸如磷酸钙介导或DEAE-葡聚糖介导的转染、原生质体融合、电穿孔、脂质体介导的转染、直接显微注射和腺病毒感染等技术(例如,参看Sambrook,Fritsch和Maniatis,1989)。
最常用的方法是由磷酸钙或DEAE-葡聚糖介导的转染。尽管相关机制尚不明了,但认为经转染DNA通过内吞作用进入细胞的细胞质并转运到细胞核中。视细胞类型而定,可在任一时间转染多达90%的培养细胞集群。归因于其高效率,由磷酸钙或DEAE-葡聚糖介导的转染成为用于需要在大量细胞中瞬时表达外来DNA的实验的所选方法。磷酸钙介导的转染也用于建立整合外来DNA拷贝的细胞系,所述DNA拷贝通常是以头尾串联阵列排列于宿主细胞基因组中。
在原生质体融合方法中,将得自细菌的具有大量所关注质粒拷贝的原生质体直接与所培养的哺乳动物细胞混合。在细胞膜融合(通常使用聚乙二醇)后,将所述细菌的内容物传递到哺乳动物细胞的细胞质中,且将质粒DNA转运到细胞核中。对于瞬时表达检定常用的许多细胞系而言,原生质体融合不如转染有效,但其对于DNA内吞作用不能有效发生的细胞系有用。原生质体融合经常得到多个串联整合于宿主染色体中的质粒DNA拷贝。
将简短、高电压电子脉冲施加于多种哺乳动物和植物细胞会导致在质膜中形成纳米尺寸的孔。使DNA通过这些孔或因伴随所述孔封闭的膜组份再分布而直接进入细胞质中。电穿孔可极为有效,且可用于瞬时表达经克隆基因和用于建立携带已整合的所关注基因拷贝的细胞系。相比磷酸钙介导的转染和原生质体融合,电穿孔经常使细胞系携带一个或至多数个已整合的外来DNA拷贝。
脂质体转染涉及将DNA和RNA封装于脂质体内,随后使脂质体与细胞膜融合。如何将DNA传递到细胞中的机制尚不明了,但转染效率可高达90%。
将DNA分子直接显微注射到细胞核中具有不将DNA暴露给诸如低pH值内体的细胞区室的优势。因此,显微注射主要用作建立携带已整合的所关注DNA拷贝的细胞系的方法。
此项技术中众所周知使用腺病毒作为细胞转染的载体。已关于多种细胞报导腺病毒载体介导的细胞转染(Stratford-Perricaudet等人,1992)。
经转染细胞可为原核或真核细胞。本发明的宿主细胞优选原核宿主细胞。当希望产生表皮葡萄球菌多肽时,经培养的原核宿主细胞特别引人关注。
本文还涵盖一种制备表皮葡萄萄球菌多肽的工艺或方法,其包含用编码表皮葡萄球菌多肽的聚核苷酸转化、转染或感染细胞以产生经转化宿主细胞;和在足以表达所述多肽的生物学条件下维持所述经转化宿主细胞。在特定实施例中,经转化宿主细胞为原核细胞。或者,所述宿主细胞为真核细胞。更具体说来,原核细胞为大肠杆菌DH5-α菌株的细菌细胞。或者,转染到经转化细胞中的聚核苷酸包含SEQ ID NO:33到SEQ ID NO:64其中之一的核酸序列。此外,使用上文所公开的表达载体实现转染。用于所述工艺中的宿主细胞能够表达功能性重组表皮葡萄球菌多肽。
转染后,在培养条件下维持所述细胞一段足以表达表皮葡萄球菌多肽的时间。此项技术中众所周知培养条件,且其包括离子组成和浓度、温度、pH值等。通常,在培养条件下于培养基中维持经转染细胞。此项技术中众所周知用于各种细胞类型的适当培养基。在某些实施例中,培养温度为约20℃到约50℃,更优选约30℃到约40℃且甚至更优选约37℃。
pH值优选为约6.0的值到约8.0的值、更优选为约6.8的值到约7.8的值且最优选为约7.4。摩尔渗透压浓度优选为约每升200毫渗克分子(mosm/L)到约400mosm/L且更优选为约290mosm/L到约310mosm/L。此项技术中众所周知转染和表达经编码蛋白质所需的其它生物学条件。
将经转染细胞维持一段足以表达表皮葡萄球菌多肽的时间。适当时间特别视所使用的细胞类型而定且易于由所属领域技术人员确定。通常,维持时间为约2天到约14天。
从经转染细胞或培养这些细胞的培养基中回收或收集重组表皮葡萄球菌多肽。回收包含分离和纯化表皮葡萄球菌多肽。此项技术中众所周知用于多肽的分离和纯化技术,且其包括诸如沉淀、过滤、色谱、电泳等程序。
E.免疫原性组合物
本发明提供免疫原性组合物,其包含一或多种如下述实例中所述选择的表皮葡萄球菌多肽和生理学上可接受的载剂。在某些实施例中,免疫原性组合物包含一或多种包含一或多个SEQ ID NO:1到SEQ ID NO:32的氨基酸残基序列的表皮葡萄球菌多肽。在其它实施例中,本发明的免疫原性组合物包含编码表皮葡萄球菌多肽的聚核苷酸和生理学上可接受的载剂。举例说来,本发明的免疫原性组合物包含含有一或多个SEQ ID NO:1到SEQ ID NO:32的氨基酸序列的表皮葡萄球菌多肽。或者,免疫原性组合物包含含有一或多个SEQ ID NO:33到SEQ ID NO:64的核苷酸序列的聚核苷酸。
使用多种测试评定本发明多肽的体外免疫原性。举例说来,通过一起培育表皮葡萄球菌细胞、含有抗所讨论的多肽的特异性抗体的热灭活人类血清和外源补体源的混合物来进行体外调理素检定(opsonic assay)。调理吞噬是在培育新近分离的人类多形核细胞(PMN)和抗体/补体/葡萄球菌细胞混合物过程中进行。调理吞噬后,包覆有抗体和补体的细菌细胞被杀死。通过用检定混合物涂布平板来测定幸免于调理吞噬的存活细菌的集落形成单位(cfu)。如通过与检定对照相比较所测定,将滴度报导为得到≥50%细菌杀死率的最大稀释率的倒数。将在所测试的最低血清稀释率(1∶8)下证实小于50%杀死率的试样报导为具有为4的OPA滴度。所测试的最大稀释率为1∶2560。以较高初始稀释率开始,重复在最高稀释率下具有≥50%杀死率的样本。上述方法为Gray法(Gray,ConjugateVaccines Supplement,第694-697页,1990)的改进方法。
每一个别血清中都包括含有测试血清加细菌细胞和热灭活补体的测试血清对照。所述对照是用于评定抗生素的存在或其它血清组份的存在是否能够直接(即,不存在补体或PMN)杀死细菌菌株。将具有已知调理素滴度的人类血清用作阳性人类血清对照。将每一未知血清的调理素抗体滴度都计算为与无血清的对照相比得到50%cfu降低的初始血清稀释率的倒数。
还使用全细胞ELISA检定评定多肽抗原的体外免疫原性和表面暴露,其中将所关注的细菌菌株(表皮葡萄球菌)涂覆于诸如96孔板的平板上,且使来自免疫动物的测试血清与细菌细胞反应。如果对测试多肽抗原具特异性的任何抗体都可与多肽抗原表面暴露的抗原表位反应,那么其可通过所属领域技术人员已知的标准方法加以检测。
随后,在体内动物激发模型中测试证实所需体外活性的任何多肽。在某些实施例中,通过所属领域技术人员已知的免疫方法和途径(例如,鼻内、不经肠、经口、直肠、阴道、经皮、腹膜内、静脉内、皮下等)将免疫原性组合物用于动物(例如,小鼠)免疫中。在用特定表皮葡萄球菌免疫原性组合物使动物免疫后,用表皮葡萄球菌激发动物,并检定对表皮葡萄球菌感染的抗性。
将表皮葡萄球菌聚核苷酸和多肽并入适于投与受试者(例如,人类)的免疫原性组合物中。所述组合物通常包含核酸分子或蛋白质连同医药学上可接受的载剂。如下文所使用,术语“医药学上可接受的载剂”旨在包括可与医药投药相容的任何和所有溶剂、分散介质、涂料、抗菌剂和抗真菌剂、等渗剂和吸收延迟剂等。此项技术中众所周知医药活性物质的所述介质和试剂的使用。除非任何常规介质或试剂与活性化合物不相容,否则所述介质都可用于本发明的组合物中。也可将辅助活性化合物并入组合物中。
对本发明的免疫原性组合物加以调配以使其与预期的投药途径相容。投药途径的实例包括不经肠(例如,静脉内、皮内、皮下、腹膜内)、经粘膜(例如,经口、直肠、鼻内、阴道、呼吸)和经皮(局部)。用于不经肠、皮内或皮下施用的溶液或悬浮液可包括以下组份:无菌稀释剂,诸如注射用水、生理盐水溶液、非挥发性油、聚乙二醇、甘油、丙二醇或其它合成溶剂;抗菌剂,诸如苯甲醇或对羟基苯甲酸甲酯;抗氧化剂,诸如抗坏血酸或亚硫酸氢钠;螯合剂,诸如乙二胺四乙酸;缓冲剂,诸如乙酸盐、柠檬酸盐或磷酸盐;和调节渗透压的试剂,诸如氯化钠或右旋糖。可用诸如盐酸或氢氧化钠的酸或碱调节pH值。可将不经肠制剂密封于由玻璃或塑料制成的安瓿、一次性注射器或多剂量瓶中。
适于注射使用的医药组合物包括无菌水溶液(在水溶情况下)或分散液和用于临时制备无菌可注射溶液或分散液的无菌粉末。对于静脉内投药而言,适当载剂包括生理盐水、抑菌水、Cremophor ELTM(BASF,Parsippany,NJ)或磷酸盐缓冲生理盐水(PBS)。在所有情况下,组合物都必须无菌且应具有足够流动性以易于注射。其必须在制造和储存条件下稳定,且必须防止诸如细菌和真菌的微生物的污染作用。载剂可为含有例如水、乙醇、多元醇(例如,甘油、丙二醇和液态聚乙二醇等)和其适当混合物的溶剂或分散介质。举例说来,可通过使用诸如卵磷脂的涂料、通过在分散液情况下维持所需粒度和通过使用表面活性剂来维持适当的流动性。可通过多种抗菌剂和抗真菌剂实现对于微生物作用的预防,所述抗菌剂和抗真菌剂例如为对羟基苯甲酸酯、氯丁醇、苯酚、抗坏血酸等。在许多情况下,组合物中包括例如糖、多元醇(诸如甘露醇、山梨醇)、氯化钠的等渗剂。可通过在组合物中包括延迟吸收的试剂(例如,单硬脂酸铝和明胶)来引起对于可注射组合物的延缓吸收。
可通过将所需量的活性化合物(例如,表皮葡萄球菌多肽或抗表皮葡萄球菌抗体)并入具有上文所列举的一种成分或成分组合的适当溶剂中,视需要随后过滤杀菌来制备无菌可注射溶液。一般说来,通过将活性化合物并入含有基础分散介质和所需来自上文所列举的成分中的其它成分的无菌媒剂中来制备分散液。在用于制备无菌可注射溶液的无菌粉末的情况下,优选的制备方法为真空干燥和冷冻干燥,其将得到活性成分加上来自其先前经无菌过滤的溶液的任何其它所需成分的粉末。
口服组合物一般包括惰性稀释剂或可食用载剂。可将其密封于明胶胶囊中或压制成片剂。出于经口治疗投与的目的,可将活性化合物与赋形剂合并,并以片剂、锭剂或胶囊的形式使用。也可使用用作漱口药的流体载剂制备口服组合物,其中所述流体载剂中的化合物是经口施用且漱口并吐出或咽下。可包括医药学上可相容的粘合剂和/或佐剂材料作为组合物的部分。片剂、丸剂、胶囊、锭剂等都可含有下述具有类似性质的成分或化合物中的任一种:粘合剂,诸如微晶纤维素、黄芪胶或明胶;赋形剂,诸如淀粉或乳糖;崩解剂,诸如褐藻酸、Primogel或玉米淀粉;润滑剂,诸如硬脂酸镁或Sterotes;助流剂,诸如胶状二氧化硅;甜味剂,诸如蔗糖或糖精;或调味剂,诸如薄荷油、水杨酸甲酯或橙类调味剂。
对于吸入投药而言,化合物是以气雾剂喷雾形式从含有适当推进剂(例如,气体,诸如二氧化碳)的加压容器或分配器或喷雾器传递。全身投药也可通过经粘膜或经皮方式进行。对于经粘膜或经皮投药而言,将适于透过屏障的渗透剂用于配方中。所述渗透剂一般为此项技术中所知,且包括(例如)用于经粘膜投药的清洁剂、胆汁盐和梭链孢酸衍生物。可通过使用鼻喷雾或栓剂实现经粘膜投药。对于经皮投药而言,将活性化合物调配成如此项技术中一般已知的油膏、药膏、凝胶或乳膏。
还可制备栓剂(例如,具有常规栓剂基质,诸如可可油和其它甘油酯)或保留灌肠剂形式的化合物以用于直肠传递。
在一实施例中,将活性化合物与将保护化合物免于经身体快速去除的载剂一起制备,诸如受控释放配方,包括植入物和微胶囊传递系统。
可使用生物可降解型生物可相容聚合物,诸如乙烯乙酸乙烯酯、聚酸酐、聚乙醇酸、胶原蛋白、聚原酸酯和聚乳酸。制备所述配方的方法将为所属领域技术人员显而易见。所述材料也可从Alza Corporation和Nova Pharmaceuticals,Inc购得。也可将脂质体悬浮液(包括以具有抗病毒抗原的单克隆抗体的经感染细胞为目标的脂质体)用作医药学上可接受的载剂。这些悬浮液可根据所属领域技术人员已知的方法制备,例如,如美国专利4,522,811中所述,所述专利是以引用的方式并入下文中。
将口服或不经肠组合物调配成剂量单位形式对于简化投药和使剂量均匀特别有利。如下文所使用的剂量单位形式是指适于作为整体剂量用于待治疗的受试者的实体离散单位;每一单位都含有经计算以产生所需治疗作用的预定量的活性化合物以及所需医药载剂。本发明的剂量单位形式的规格是通过且直接视活性化合物的独特特性和将达成的特殊治疗作用和复合所述治疗个体的活性化合物的技术的固有局限性而指示。
通过包括两种或两种以上本发明的多肽,以及通过使一或多种本发明的多肽与一或多种已知的非表皮葡萄球菌多肽(诸如,金黄葡萄球菌多肽)组合来提供组合免疫原性组合物。
下述十二种表皮葡萄球菌多肽序列SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO:11、SEQ ID NO:12、SEQ ID NO:14、SEQ ID NO:18、SEQ ID NO:19、SEQ ID NO:20、SEQID NO:23、SEQ ID NO:26、SEQ ID NO:27和SEQ ID NO:30具有与来自金黄葡萄球菌的同源物具至少90%同一性的多肽序列。因此,这十二种多肽也可用于对抗金黄葡萄球菌的免疫原性组合物中。此外,下述十二种编码与金黄葡萄球菌同源物具有至少90%同一性的多肽的表皮葡萄球菌聚核苷酸序列也可用于免疫原性组合物中:SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:43、SEQ ID NO:44、SEQ ID NO:46、SEQ ID NO:50、SEQID NO:51、SEQ ID NO:52、SEQ ID NO:55、SEQ ID NO:58、SEQ ID NO:59和SEQ IDNO:62或其简并变异体或其片段。
在其它实施例中,通过使一或多种本发明的多肽与一或多种已知的表皮葡萄球菌多糖或多糖-蛋白质接合物组合来提供组合免疫原性组合物。例如,参看表皮葡萄球菌和金黄葡萄球菌荚膜多糖粘合素PNSG,即聚N-琥珀酰β-1-6N-乙酰葡糖胺(也称为PIA、PS/A、PNAG)。参看Mckenney,D.等人,Infect.Immun.66:4711(1998)和Mckenney,D.等人,Science 284:1523(1998),所述文献的公开内容都是以全文引用的方式并入本文中。
在其它实施例中,通过使一或多种本发明的多肽与一或多种已知的金黄葡萄球菌多糖或金黄葡萄球菌多糖-蛋白质接合物组合来提供组合免疫原性组合物。举例说来,在12种已知的金黄葡萄球菌荚膜血清型中,血清型5(CP5)和血清型8(CP8)占所有临床分离株的约85-90%。大部分耐甲氧西林(methicillin)金黄葡萄球菌分离株表达CP5。抗CP5和CP8的抗体通过人类中性多形核白细胞体外诱导类型特异性调理吞噬杀死作用,并且使动物得到保护[Karakawa,W.W.,Sutton,A.等人,Infect Immun 56(5):1090-1095(1988);Fattom,A.I.,Sarwar,J.等人,Infection&Immunity64(5):1659-1665(1996)]。一些实验室已合成由共价连接到蛋白质的CP5和CP8组成的免疫原性接合物。这些接合物在小鼠和人类体内具有高度免疫原性,且诱导调理微胶囊化金黄葡萄球菌吞噬作用的抗体[Fattom,A.,Schneerson,R等人,Infect Immun 61(3):1023-1032(1993);Gilbert,F.B.,Poutrel,B.等人,Vaccine 12(4):369-374(1994);Reynaud-Rondier,L,Voiland,A.等人,FEMSMicrobiol Immunol 3(4):193-199(1991)]。含有接合到铜绿假单胞菌(Pseudomonasaeruginosa)重组外毒素A的CP5的单价免疫原性组合物具免疫原性且在健康成人和晚期肾病患者体内良好耐受[Welch,P.G.,Fattom,A.,Moore,J.Jr.等人,J.Am.Soc.Nephrol.7:247-253[Abstract](1996)]。在涉及接收血液透析的晚期肾病患者的双盲试验中,由共价结合到铜绿假单胞菌重组外毒素A的CP5和CP8构成的二价接合疫苗赋予对抗金黄葡萄球菌菌血症的部分免疫性持续约40周,此后,保护作用随抗体含量的降低而降低[Shinefield,H.,Black,S.等人,NEngl J Med 346(7):491-496(2002)]。这一试验的结果表明需要一种可有助于更广泛和更完全保护的改良型免疫原性组合物。
如上文所述,在某些实施例中,通过使一或多种本发明的多肽与一或多种已知的金黄葡萄球菌多糖-蛋白质接合物组合来提供组合免疫原性组合物。碳水化合物-蛋白质接合物的“蛋白质组份”被称为载体蛋白。总的来说,术语“载体蛋白”优选为无毒且无致反应性且可以充足量和纯度获得的蛋白质。载体蛋白应遵从标准接合程序。在本发明的特定实施例中,将CRM197用作载体蛋白。CRM197(Wyeth,Sanford,NC)是从在以酪蛋白氨基酸和酵母提取物为主的培养基中生长的白喉杆菌(Corynebacterium diphtheria)菌株C7(β197)培养物中分离的白喉毒素的无毒变异体(即,类毒素)。CRM197是通过超滤、硫酸铵沉淀和离子交换色谱加以纯化。其它白喉类毒素也适用作载体蛋白。免疫原性组合物可另外包含佐剂,诸如铝基佐剂,诸如磷酸铝、硫酸铝和氢氧化铝。
其它适当的载体蛋白包括已灭活的细菌毒素,诸如破伤风类毒素、百日咳类毒素、霍乱类毒素(例如,如国际专利申请案WO2004/083251[38]中所述)、大肠杆菌LT、大肠杆菌ST和来自铜绿假单胞菌的外毒素A。也可使用细菌外膜蛋白,诸如外膜复合物c(OMPC)、孔蛋白(porin)、转铁结合蛋白(transferrin binding protein)、肺松解术(pneumolysis)、肺炎球菌表面蛋白A(PspA)、肺炎球菌粘附蛋白(PsaA)或流感嗜血杆菌(Haemophilus influenzae)蛋白D。也可将其它蛋白用作载体蛋白,诸如卵清蛋白、钥孔血蓝蛋白(keyhole limpet hemocyanin,KLH)、胎牛血清白蛋白(BSA)或结核菌素的经纯化蛋白衍生物(PPD)。
通过多种载体和表达系统将包含聚核苷酸的免疫原性组合物传递到接受者。所述系统包括染色体系统、附加体系统和得自病毒的系统,例如得自以下各物的载体:细菌质粒;减毒细菌,诸如沙门氏菌属(Salmonella)(美国专利4,837,151);噬菌体;转座子;酵母附加体;插入元件;酵母染色体元件;病毒,诸如牛痘和其它痘病毒、腺病毒、杆状病毒、乳多空病毒(诸如SV40)、禽痘病毒、伪狂犬病病毒和逆转录酶病毒、α病毒(诸如委内瑞拉马脑炎病毒(Venezuelan equine encephalitis virus)(美国专利5,643,576)、辛德毕斯病毒(sindbis virus)和西门利克病毒(semiliki forest virus))、不分节段负链RNA病毒(nonsegmented negative-stranded RNA virus)(诸如水疱性口炎病毒(美国专利6,168,94));和得自其组合的载体,诸如得自质粒和噬菌体遗传元件的载体,诸如柯斯质粒(cosmid)和噬粒。表达系统应包括调控和引起表达的控制区域,诸如启动子和其它调控元件(诸如聚腺苷酸化信号)。一般说来,可使用适于维持、繁殖或表达聚核苷酸以于宿主中产生多肽的任何系统或载体。可通过多种众所周知和常规技术中的任一种将适当的核苷酸序列插入到表达系统中,所述技术诸如Sambrook等人,″Molecular Cloning:ALaboratory Manual″第2版,Cold Spring Harbor Laboratory,Cold Spring Harbor LaboratoryPress,Cold Spring Harbor,NY,1989中所述的技术。
医药学上可接受的媒剂应理解为表示进入医药组合物或免疫原性组合物中的化合物或化合物组合,其不引起副作用且使得可能(例如)有助于投与活性化合物、增加其在体内的寿命和/或功效、增加其在溶液中的溶解性或者增强其保存。众所周知这些医药学上可接受的媒剂,且所属领域技术人员将根据所选活性化合物的性质和投药模式对其进行调适。
如下文所定义,“佐剂”是一种用于增强“抗原”或免疫原性组合物的免疫原性的物质,所述免疫原性组合物包含一或多种具有选自SEQ ID NO:1到SEQ ID NO:32其中之一的氨基酸序列的多肽抗原。因此,佐剂通常用于激发或调节免疫反应且为所属领域技术人员众所周知。本发明所涵盖的佐剂的实例包括(但不限于)铝盐(明矾),诸如磷酸铝和氢氧化铝;结核分枝杆菌(Mycobacterium tuberculosis);细菌脂多糖;氨基烷基葡糖胺磷酸酯化合物(AGP)或其衍生物或类似物,其是从Corixa(Hamilton,MT)购得,且其描述于美国专利第6,113,918号中,一种所述AGP为2-[(R)-3-十四烷酰氧基十四烷酰基氨基]乙基2-脱氧-4-O-膦酰基-3-O-[(R)-3-十四烷酰氧基十四烷酰基]-2-[(R)-3-十四烷酰氧基十四烷酰基氨基]-b-D-吡喃葡萄糖苷,其也称为529(先前称为RC529),其经调配为水溶液形式或稳定乳液形式;美国专利第4,912,094号中所述的MPLTM(3-O-脱酰化单磷酰脂A)(Corixa);合成聚核苷酸,诸如含有CpG基序的寡核苷酸(美国专利第6,207,646号);多肽;皂角苷,诸如Quil A或STIMULONTM QS-21(Antigenics,Framingham,Massachusetts),其描述于美国专利第5,057,540号中;百日咳毒素(PT)或大肠杆菌不耐热毒素(LT),尤其是LT-K63、LT-R72、CT-S109、PT-K9/G129,例如,参看国际专利公开案第WO 93/13302号和第WO 92/19265号;霍乱毒素(野生型或突变体形式,例如,根据已公开的国际专利申请案第WO 00/18434号,其中氨基酸第29位的谷氨酸经另一氨基酸、优选是组氨酸置换)。类似的霍乱毒素突变体描述于已公开的国际专利申请案第WO 02/098368号中(其中仅氨基酸第16位的异亮氨酸经另一氨基酸置换,或连同氨基酸第68位的丝氨酸经另一氨基酸置换;和/或其中氨基酸第72位的缬氨酸经另一氨基酸置换)。其它霍乱毒素突变体描述于已公开的国际专利申请案第WO 02/098369号中(其中氨基酸第25位的精氨酸经另一氨基酸置换;和/或将一个氨基酸插入到氨基酸第49位;和/或将两个氨基酸插入到氨基酸第35位和第36位)。
多种细胞因子和淋巴因子适于用作佐剂。一种所述佐剂为粒细胞-巨噬细胞集落刺激因子(GM-CSF),其具有如美国专利第5,078,996号中所述的核苷酸序列。已将含有GM-CSF cDNA的质粒转化到大肠杆菌中,且已由美国典型培养物保藏中心(AmericanType Culture Collection,ATCC)(1081University Boulevard,Manassas,VA 20110-2209)以寄存编号39900予以保藏。细胞因子白细胞介素-12(IL-12)是描述于美国专利第5,723,127号中的另一种佐剂。已展示其它细胞因子或淋巴因子具有免疫调节活性,包括(但不限于)白细胞介素1-α、1-β、2、4、5、6、7、8、10、13、14、15、16、17和18、干扰素-α、β和γ、粒细胞集落刺激因子和肿瘤坏死因子α和β,且其都适于用作佐剂。
通常以含有标准、众所周知的生理学上可接受的无毒载剂、佐剂和媒剂(视需要)的单位剂量配方形式不经肠投与本发明的组合物。
可注射制剂(例如,无菌可注射水性或油性悬浮液)是根据已知技术使用适当的分散剂或润湿剂和悬浮剂加以调配。无菌可注射制剂也可为无毒不经肠可接受的稀释剂或溶剂中的无菌可注射溶液或悬浮液,例如1,3-丁二醇中的溶液。
可使用的可接受的媒剂和溶剂为水、林格氏溶液(Ringer′s solution)和等渗氯化钠溶液。此外,常规使用无菌的非挥发性油作为溶剂或悬浮介质。出于这一目的,可使用包括合成单甘油酯或二甘油酯的任何温和非挥发性油。另外,诸如油酸的脂肪酸也可用于制备可注射物。
优选载剂包括经磷酸盐、乳酸盐、Tris等缓冲的中性生理盐水溶液。当然,当投与病毒载体时,需充分纯化载体以使其基本上无不合需要的污染物(诸如缺陷型干扰腺病毒粒子或内毒素和其它热原质),从而不会于接收载体构建体的个体体内引起任何不恰当的反应。纯化载体的优选方式包括使用浮力密度梯度,诸如氯化铯梯度离心。
载体也可为脂质体。此项技术中众所周知使用脂质体作为传递工具的方式(例如,参看Gabizon等人,1990;Ferruti等人,1986;和Ranade,1989)。
本发明的免疫原性组合物还包含可操作地与控制基因表达的调控序列缔合的本发明的聚核苷酸序列。在将促进DNA表达的调控元件(即,启动子和/或增强子元件)的控制下,将所关注的聚核苷酸序列工程设计到诸如质粒的表达载体中。在优选实施例中,使用人类巨细胞病毒即刻早期启动子/增强子(美国专利5,168,062)。启动子可具有细胞特异性且仅允许在预定细胞中实质上转录聚核苷酸。
将本发明的聚核苷酸直接引入宿主中,所述聚核苷酸为“裸”DNA(美国专利5,580,859)或与诸如布比卡因和其它局部麻醉剂(美国专利5,593,972)和阳离子聚胺(美国专利6,127,170)的促进剂一起调配成组合物,所述专利是以全文引用的方式并入本文中。
在这一聚核苷酸免疫程序中,本发明的多肽是在体内瞬时表达;并未将遗传物质插入或整合到宿主染色体中。这一程序将与目的是将所关注遗传物质插入或整合到染色体中的基因疗法相区别。使用检定确认通过免疫投与的聚核苷酸不会在宿主中产生经转化表型(美国专利6,168,918)。
H.本发明的用途和方法
在免疫方法中使用本文所述的表皮葡萄球菌聚核苷酸、多肽和多肽同源物。经分离的聚核苷酸将用于表达表皮葡萄球菌多肽(例如,经由用于宿主细胞中或聚核苷酸免疫应用中的重组表达载体)。
如本文的实例中所详细描述,表皮葡萄球菌是在血清存在下生长以刺激可对全身细菌感染具重要意义的细菌细胞壁上蛋白质和碳水化合物表达。结果,将三十二种多肽和对应的聚核苷酸确定为当表皮葡萄球菌于70%血清中生长时由表皮葡萄球菌所表达。此外,已发现这些蛋白质中有二十四种与来自经表皮葡萄球菌感染的兔的免疫血清具反应性。
克隆对应于当表皮葡萄球菌在血清中生长时所表达的蛋白质的基因,并将其用于重组表达蛋白质。使用重组蛋白使小鼠免疫,且二十六种蛋白质中有二十五种将诱导与表皮葡萄球菌的全细胞溶解物反应的抗体。此外,这些血清中有十八种还与金黄葡萄球菌的全细胞溶解物反应。最后,当用表皮葡萄球菌激发经免疫小鼠时,发现十一种所述蛋白质已诱导降低激发后脾中所发现的可检测细菌的量的抗体。
本发明另外提供包含一或多种所述多肽的免疫原性组合物,所述多肽具有选自SEQID NO:1到SEQ ID NO:32其中之一、其生物等效物或其片段的氨基酸序列。免疫原性组合物可另外包含医药学上可接受的载剂。在某些实施例中,免疫原性组合物将包含一或多种佐剂。
在另一实施例中,本发明提供免疫原性组合物,其包含具有选自SEQ ID NO:33到SEQ ID NO:64其中之一的核苷酸序列的聚核苷酸,其中所述聚核苷酸是包含于重组表达载体中。所述载体优选为质粒DNA。聚核苷酸可另外包含异源核苷酸,例如聚核苷酸是可操作地连接到一或多种基因表达调控元件,且另外包含一或多种佐剂。在优选实施例中,免疫原性聚核苷酸组合物引导表皮葡萄球菌的一或多种中和表位的表达。
还提供使宿主免疫以对抗表皮葡萄球菌感染的方法。在优选实施例中,宿主为人类。因此,向宿主或受试者投与免疫量的免疫原性组合物,其包含具有选自SEQ ID NO:1到SEQ ID NO:32其中之一、其生物等效物或其片段的氨基酸序列的多肽,和医药学上可接受的载剂。免疫原性组合物的免疫量是通过进行剂量反应研究而确定,在所述剂量反应研究中,以逐渐增加量的免疫原性组合物使受试者免疫,且分析免疫反应以确定最佳剂量。所述研究的起始点是由动物模型中的免疫数据推定。剂量可视个体的特定情形而变化。所述量是在常规试验中通过所属领域技术人员已知的方式加以确定。
将免疫学上有效量的免疫原性组合物以适当数量的剂量投与受试者以引发免疫反应。如本文所使用的免疫学上有效量的意思是,将所述作为单一剂量或连续剂量一部分的量投与哺乳动物宿主(优选人类)足以至少引起待治疗个体的免疫系统产生降低细菌感染的临床影响的反应。理想地,所治疗的个体将不会展现出更严重的表皮葡萄球菌或金黄葡萄球菌感染的临床表现。剂量可视个体的特定情形(诸如年龄和体重)而变化。所述量可在常规试验中通过所属领域技术人员已知的方式加以确定。
本文所引用的所有专利和公开案都是以引用的方式并入本文。
实例
以下实例是使用标准技术进行,除此处详细描述的技术外,所述标准技术是众所周知的技术且对于所属领域技术人员而言为常规技术。除非另作说明,否则所有化学制品都是从Sigma(Sigma Chemical Co.,St.Louis,MO)获得。以下实例是出于说明目的提供,且不应将其解释为以任何方式限制本发明的范围。
实例1
在70%血清中的细菌生长
使用临床分离株表皮葡萄球菌0-47进行以下实例。这一分离株中未加注释的基因组序列可得自Incyte Corporation,Palo Alto,CA。参看Heilmann,C等人,Infect Immun,64(1):第277-82页(1996)。为刺激可与致病性临床相关的蛋白质的表达,37℃下,于振荡(200rpm)下,使细菌培养物在100%胰蛋白酶大豆肉汤(TSB)或70:30兔血清:TSB中生长整夜。兔血清是从Life Technologies,Rockville,MD获得。将整夜培养的细菌稀释到OD600约为0.1,并且使其生长4h直到对数生长中期。在对数生长中期,通过离心采集细胞,并如以下实例中所述进行进一步处理。
实例2
制备用于2-D凝胶电泳的细胞壁片断
分离如实例1所述生长的表皮葡萄球菌0-47的细胞壁,且随后对其进行制备以用于二维凝胶电泳。再悬浮细菌小球直到OD600约为20,并在4℃下使用Tris缓冲生理盐水(TBS、20mM Tris(pH 8.0)、150mM NaCl)摇动洗涤两次历时15分钟。通过在4℃下用含有1M NaCl的20mM Tris(pH 8.0)洗涤15分钟来除去结合到细菌表面的血清蛋白。以与处理在血清中生长的细菌的方式相同的方式处理在TSB中生长的细菌。通过离心使细菌再次粒化。为产生原生质体,随后将细菌再悬浮于含有30%蔗糖、100μg/ml溶葡球菌酶、10μg/ml DNase、1μg/ml Pefablock(Boehringer Mannheim,Indianapolis,IN)、10μg/ml溶菌酶和100单位/毫升变溶菌素的TBS中直到OD600约为40,且在37℃下培育1小时。通过在5000rpm下离心10分钟使所得原生质体粒化,且倾析出含有细胞壁材料的上清液。向所倾析的含有细胞壁片断的上清液中补充Complete Mini蛋白酶抑制剂片剂(Roche Diagnostics,Indianapolis,IN)并在4℃下使用10,000kD MWCO透析膜(PierceBiotechnology,Inc.,Rockford,IL)对水透析整夜。透析后,于-20℃下冷冻细胞壁片断。
分离后,如下制备用于2-D凝胶电泳的细胞壁片断样本:使冷冻细胞壁提取物解冻,且在冰上用70%丙酮使其沉淀4小时。使蛋白质沉淀物粒化,在SpeedVac(Thermo Savant,Holbrook,NY)中干燥且用含有5M尿素、2M硫脲、2%(w/v)CHAPS、2%(w/v)SB3-10、40mM Tris和0.2%Bio-Lyte 3/10的ReadyPrep(BioRad)SEQUENTIALEXTRACTION REAGENT 3溶解。
在室温下整夜培育期间,通过使各样本再水合凝胶条带来将所制备的细胞壁片断样本装载于11cm固定化pH梯度(IPG)条带pH 4-7(BioRad)上。样本尺寸为200μl总体积中250μg。整夜培育期间,用矿物油(BioRad)覆盖所述条带以防止蒸发。完成所述条带的再水合后,将过量矿物油移到已经水饱和的吸墨纸(blotting paper)上,且随后将已水合的条带装载于移相器等电聚焦(pHaser Isoelectric focusing,IEF)设备(GenomicSolutions Inc.,Ann Arbor,Ml)中。在50毫安/条带的电流极限下,以逐渐从250V增加到5,000V的电压使所述条带预先聚焦。接着,使电压在5,000V下保持恒定共计50kVh(约16h)。使用12.5%Criterion预制凝胶(BioRad)进行第二维SDS-PAGE。为进行质谱分析,根据制造商的说明书,用Sypro Ruby蛋白质凝胶染色剂(BioRad)对凝胶染色。
比较在TSB或70%兔血清中生长的表皮葡萄球菌中细胞壁相关蛋白的二维(2D)凝胶概况。参看图1。在70%兔血清中生长导致表皮葡萄球菌中细胞壁相关蛋白的蛋白质表达概况改变,所述改变易于在经荧光染色的2D凝胶转移中检测到(图1A和1B)。
通过荧光染色检测八种在TSB中或在兔血清存在下生长的表皮葡萄球菌之间经差异调控的蛋白质。参看表3和图1。最值得关注的是在70%血清中生长的细胞中介于25kDa与37kDa之间的三种蛋白质条纹带的荧光染色增加(图1B,斑点e、g和h)。
表3
经鉴别的斑点列表a
b斑点编号 | 蛋白质 | c检测 |
SEQ ID NO: | 方法 | |
1,2 | 12 | I,S |
3 | 12 | I,S |
3 | 19 | I,S |
4c | 11 | I,S |
4 | 18 | I,S |
5-7,9 | 11 | I,S |
8 | 21 | I |
10c | 11 | I,S |
10 | 18 | I,S |
10 | 28 | I,S |
11 | 3 | I,S |
12 | 10 | I,S |
13 | 10 | I,S |
13 | 26 | I,S |
14 | dNGID | I,S |
15-16 | 10 | I,S |
17 | 25 | I |
18 | 4 | I |
19 | 17 | I,S |
19 | 23 | I,S |
20-23,25 | 17 | I,S |
24 | 30 | I,S |
26 | 30 | I,S |
26 | 8 | I,S |
26 | 7 | I,S |
27,30-32 | 2 | I,S |
28,33 | 22 | I,S |
29 | 5 | I,S |
34 | 13 | I,S |
35 | NGID | I |
36 | NGID | I |
37 | NGID | I,S |
38 | 29 | I,S |
38 | 3 | I,S |
39 | 32 | I,S |
40 | 14 | S |
40 | 20 | S |
40 | 27 | S |
41 | 14 | S |
42 | 6 | |
43 | 32 | S |
43 | 16 | S |
43 | 24 | S |
44 | 15 | S |
a通过与免疫血清的反应性或与血清组份的结合在2D印迹上检测的斑点列表。
b某些斑点含有一种以上蛋白质。
c在转移到硝酸纤维素之后检测斑点的方法,受感染兔的反应性免疫血清为I或结合血清组份为S。
dNGID=数据库中无基因
实例3
免疫血清和生物素化血清蛋白与细胞壁蛋白质的结合
完成第一维和第二维电泳后,将所述凝胶的蛋白质内容物转移到硝酸纤维素上供结合检定。具体说来,使用半干印迹设备(semi-dry blotting apparatus)(Owl SeparationsSystems,Portsmouth,NH)在12V下将所述凝胶的蛋白质内容物电印迹到硝酸纤维素膜(BioRad)上历时1小时。随后遵循制造商的说明书,用Sypro Ruby蛋白质印迹染色剂(BioRad)对含有蛋白质的硝酸纤维素膜(印迹)染色,且在FluorS Imager(BioRad)中显现。室温下在阻断缓冲液(具有0.05%Tween 20和5%奶粉的PBS)中培育每一印迹,随后与1∶2000稀释的免疫血清(Western印迹法)或40μg/ml生物素化血清蛋白(参看下文)一起培育整夜。培育整夜后,用洗涤缓冲液(具有0.5%Tween 20的PBS)洗涤印迹三次,且在室温下,在阻断缓冲液中与山羊抗兔IgG碱性磷酸酶接合物(BiosourceInternational,Camarillo,CA)或抗生蛋白链菌素碱性磷酸酶接合物(Biosource)一起培育2小时。用洗涤缓冲液再次洗涤印迹三次,并用BCIP/NBT膜磷酸酶底物系统(KPL,Inc.,Gaithersburg,MD)显现。在FluorS中取得图像。2D凝胶的所有分析都是使用Melanie 3.0软件进行。
使用BioRad蛋白质检定试剂盒(BioRad)检定蛋白质浓度。
通过考察含有从2D凝胶上转移的蛋白质的硝酸纤维素膜的Western印迹,能够使细胞壁相关蛋白的蛋白质表达概况的改变更为明确。在Western印迹法中,将硝酸纤维素膜与从经表皮葡萄球菌0-47反复感染的兔汇集的免疫血清一起培育。参看图1C和1D。这些经上调的蛋白质也具有强免疫反应性,表明其在所述兔感染期间得到表达。在TSB中生长的细胞中,五种来自血清生长细胞的其它免疫反应性条纹带或斑点以较低或不可检测的水平表达。参看图1,斑点a、b、c、d和f。
实例4
分析与表皮葡萄球菌细胞壁相关蛋白质相互作用的血清蛋白
洗脱表皮葡萄球菌的血清蛋白
37℃下,使表皮葡萄球菌0-47在70%兔血清中生长直到OD600约为0.8,并使细胞粒化。在OD600约为20时使细胞再悬浮,并在4℃下,在摇动下用TSB洗涤三次。4℃下,在摇动下依次用含有0.5M NaCl、1.0M NaCl或4.0M尿素的20mM Tris(pH 8.0)洗脱已结合的血清蛋白历时1小时。随后通过离心除去细菌,并收集上清液。上清液含有从细菌表面洗脱的血清蛋白。通过SDS-PAGE使用4-20%梯度Tris-甘氨酸凝胶(Cambrex Biosciences Rockland,Inc.,Rockland,ME)分析在不同条件下洗脱的蛋白质。
生物素化血清蛋白
4℃下,对PBS透析所洗脱的血清蛋白整夜。通过在4℃下与蛋白质G琼脂糖凝胶(Amersham-Pharmacia,Piscataway,NJ)培育整夜耗尽IgG。假设在洗脱部分中平均蛋白质质量为50kDa,在4℃下用15摩尔过量的NHS-生物素(Pierce Biotechnology)标记所述蛋白质1.5小时。用过量的甘氨酸中止反应,并对PBS透析整夜(10,0000MWCO,Pierce)。
鉴别与表皮葡萄球菌表面结合的血清蛋白
通过SDS-PAGE将在这些条件下从细菌洗脱的血清蛋白与正常的兔血清和从在TSB中生长的表皮葡萄球菌表面洗脱的细菌蛋白相比较。参看图3。用含有0.5NaCl、1M NaCl和4M尿素的缓冲液各自从细菌细胞中洗脱已结合的血清蛋白。这些经洗脱的血清蛋白表示从富集血清蛋白的细菌表面洗脱的蛋白质池。某些细菌蛋白质很可能存在于这一池中,然而,并未从生长于TSB中的细菌洗脱出可通过蛋白质检定检测的细菌蛋白质。尽管通过银染色检测出从生长于TSB中的细菌洗脱出的某些模糊的蛋白质带,但其与从生长于血清中的细菌表面洗脱的经更强烈染色的蛋白质并不对应。用1M NaCl洗脱是洗脱大部分蛋白质的最低变性条件,且用于洗脱以下实例中的蛋白质。
为鉴别结合血清组份中所涉及的细胞壁相关蛋白,使用生物素化血清蛋白通过培育经标记蛋白与从2D凝胶转移的与硝酸纤维素结合的细胞壁蛋白的溶液探测2D转移。为分离与表皮葡萄球菌结合的血清蛋白,用1M NaCl洗涤在70%兔血清中生长的细菌。收集经洗脱的血清蛋白并将其透析到PBS中。然后,通过与蛋白质G琼脂糖凝胶一起培育来耗尽可能存在于经洗脱血清蛋白中的天然存在的免疫IgG。除去IgG会减少鉴别出与宿主抗体具反应性的蛋白质的可能性。随后,如上文所述,以生物素标记已洗脱的血清蛋白,并将其用于探测表皮葡萄球菌细胞表面蛋白的2D印迹。参看图4A和4B。通过这一方法显现三十四个斑点和区域,且可能涉及表皮葡萄球菌与宿主血清蛋白相互作用。始终发现34个斑点都与血清组份相互作用,但发现其中有4个斑点与来自受感染兔的免疫血清反应。参看图2和表3。
生长于血清中的表皮葡萄球菌具有以0.5M和1M NaCl洗脱的与细菌表面蛋白结合的血清蛋白。在相同条件下,从生长于TSB中的细菌中洗脱出极少葡萄球菌蛋白,然而,通过高盐处理洗脱出仅在血清中表达的葡萄球菌蛋白是可能的。
实例5
血清上调蛋白质的质谱鉴别
在随后的蛋白质组学实验和分析中使用在70%血清中生长的细菌,假定改变是在血清中生长期间检测的情况下进行的操作可更为准确地反映因细菌对宿主内所见的环境线索起反应而产生的基因表达的变化。在随后的质谱研究中,首先使从2D凝胶电泳分离上的斑点分离的蛋白质经历飞行时间质谱分析(time-of-flight mass spectroscopy)。如果呈正数,那么获得明确的鉴别,无需进行进一步质谱分析。参看表4。在进行飞行时间质谱分析后仍保留一些不明确部分的情况下,诸如当多种蛋白质在2D凝胶上解析成相同斑点时,则进行电喷雾质谱分析以解析所述不明确部分。参看表4。
表4
通过质谱法鉴别的蛋白质
蛋白质 | DNA | 2-D凝胶 | |
Orf | SEQ ID NO: | SEQ ID NO: | 斑点编号 |
121 | 1 | 33 | 38 |
305 | 2 | 34 | 27,30-32 |
321 | 3 | 35 | 11 |
373 | 4 | 36 | 18 |
554 | 5 | 37 | 29 |
639 | 6 | 38 | 42 |
608 | 7 | 39 | 26, |
702 | 8 | 40 | 26 |
793 | 9 | 41 | 39 |
847 | 10 | 42 | 12,13,15,16 |
854 | 11 | 43 | 4,5-7,9,10 |
1015 | 12 | 44 | 1,2,3 |
1069 | 13 | 45 | 34 |
1238 | 14 | 46 | 40,41 |
1382 | 15 | 47 | 44 |
1405 | 16 | 48 | 43 |
1450 | 17 | 49 | 19,20-23,25 |
1522 | 18 | 50 | 4,10 |
1545 | 19 | 51 | 3 |
1653 | 20 | 52 | 40, |
1690 | 21 | 53 | 8 |
1703 | 22 | 54 | 28,33 |
2006 | 23 | 55 | 19 |
2180 | 24 | 56 | 43 |
2214 | 25 | 57 | 17 |
2482 | 26 | 58 | 13 |
2580 | 27 | 59 | 40 |
2649 | 28 | 60 | 10 |
2653 | 29 | 61 | 38 |
2736 | 30 | 62 | 24,26 |
2907 | 31 | 63 | |
2975 | 32 | 64 | 39,43 |
样本制备
在进行质谱分析之前,使目标蛋白质斑点经历胶内胰蛋白酶消化(in-gel trypticdigestion)。将蛋白质斑点从凝胶除去,并切成约1mm的小片。在偶尔涡旋下,用10mM碳酸氢铵(J.T.Baker,Phillipsburg,NJ)中的0.2ml 50%(v/v)乙腈(Burdick&Jackson,Muskegon,Ml)洗涤凝胶片三次历时15分钟。用乙腈使凝胶片脱水5分钟,冻干,且在-20℃下冷冻储存。随后,在37℃下,用50μl 12ng/ml测序级经修饰胰蛋白酶(PromegaCorporation,Madison,WI)消化凝胶中的蛋白质整夜。接着,除去胰蛋白酶溶液,且于50μl乙腈中使凝胶再次脱水。接着,在室温下,于超声波仪水浴(Branson CleaningEquipment Co.,Shelton,CT)中,除去含肽乙腈,且在50μl 5%甲酸(Riedel-de ,Seelze,Germany)中洗涤凝胶片15分钟。除去含肽上清液并使其与最初的乙腈洗涤液合并。在乙腈中再次洗涤凝胶,并使上清液与两个先前提取步骤合并,且在SpeedVac(ThermoSavant)中干燥到约10μl,随后用0.1%(v/v)甲酸水溶液稀释到100μl。接着,将样本装载于Zip-TipC18P10柱(Waters Corporation,Milford,MA)上,并于50μl 50%乙腈/0.1%甲酸中洗脱。将样本转移到96×2孔涂覆有特氟隆(Teflon)的不锈钢板(PerSeptiveBiosystems,Framingham,MA)上以用于在将喷雾于离子阱质谱仪(ion trap massspectrometer)的孔中的MALDI-ToF仪器(PerSeptive Biosystems)玻璃制纳米喷雾喷嘴(glass nanospray tip)(New Objective Inc.,Woburn,MA)上进行的质量指纹分析。
使用ToF质谱法进行的肽质量指纹分析
将各样本施加到经特氟隆涂覆的涂敷有α-氰基-4-羟基肉桂酸薄层的不锈钢96×2孔板上。使样本在室温下干燥。于装备有延迟提取技术(delayed extraction technology)和反射器的Voyager DE-STR MALDI-ToF质谱仪(PerSeptive Biosystems)上获取质谱数据。质谱仪上装备有337nm和具有3Hz激光速率(laser rate)的氮分子激光器。加速电压设置为20kV,操作模式(反射器),提取模式(延迟),极性(正),栅极电压(65%),反射电压比率(mirror voltage ratio)(1.12),提取延迟时间(200nsec),质量范围(800-3500Da)和每频谱激光发射数(laser shots per spectrum)(200)。
静态纳米喷雾离子阱质谱法(Static Nanospray Ion Trap-Mass Spectrometry)
在装备有纳米-电喷雾界面的ThermoFinnigan LCQ DECA四级离子阱质谱仪(ThermoFinnigan,San Jose,CA)上获取质谱数据。纳米-电喷雾界面是由二氧化硅喷雾针(New Objective Inc.)组成,所述喷雾针为约27mm长、约120/69μm OD/ID、2μm孔径。将玻璃喷嘴安装于固定在定位于质谱仪检测器前面的基座上的x、y、z轴固定器(ThermoFinnigan)中。将电流施加到玻璃喷嘴的标准涂层上以通过静态电喷雾探针(ThermoFinnigan)上的金属接面给电喷雾界面提供电连接。电喷雾传递20-80nl/min的流量。
使用直接喷雾于质谱仪孔中的电喷雾玻璃喷嘴分析2到5微升胰蛋白酶消化液。在约1kV的易变喷雾电压下操作的LCQ-DECA离子阱质谱仪(Thermofinnigan)上且使用200℃热毛细管温度进行肽分析。使用随所述仪器提供的数据获取软件获取自动化MS/MS模式中的数据组。获取方法包括1MS扫描(400-1800m/z),随后是对所述MS扫描中前三个最富有离子的部分进行MS/MS扫描。使用动态排除功能增加经分析的肽离子的数量(设置:3amu=排除宽度,0.5分钟=排除持续时间)。在样本组中且以手工方式对当前实验进行分析。
使用MSFIT(Protein Prospector)和MASCOT(Matrix Science)软件数据库搜索引擎(其使用Incyte的PathoSeq(c)表皮葡萄球菌0-47数据库)进行质量指纹数据的自动化分析。在利用所述搜索引擎之前,用基线校正、噪声除去和峰去同位素(peak de-isotoping)来处理所得频谱。将数据库搜索参数设置为如下水平:MW(1000-150kDa)、pI(3-10)、消化液(胰蛋白酶)、最大错误分裂数量(2)、错误分裂pfactor(0.4)、静态修饰(经丙烯酰胺修饰的半胱氨酸)、N末端(氢)、C末端(游离酸)、易变模数(甲硫氨酸氧化、N末端乙酰化、丝氨酸、苏氨酸和酪氨酸磷酸化)、质量(单一同位素)、以300ppm的质量公差进行匹配所需的最小的肽数量(4),和以15ppm质量公差的反复校准(Intelcast)的应用。通过MOWSE得分和分别通过MS-FIT与MASCOT的95%置信得分确定蛋白质的鉴别。
使用已并入Finnigan Bioworks数据分析包(ThermoFinnigan)的SEQUEST进行MS/MS的自动化分析。参看Eng,J.K.等人,J AmerSoc Mass Spec,5(11):第976-89页(1994)。软件中允许进行以下可变修饰:半胱氨酸丙烯酰胺修饰和甲硫氨酸氧化。将搜索参数设置在以下规定:质量范围(400-3500Da)、较低强度MS信号(1e+5)、肽公差(2.0Da)、最小片段离子数量(15)、群组中最小扫描数量(1)和错误分裂的最大数量(2)。手工检验所有蛋白质鉴别的准确性。
通过质谱法鉴别蛋白质
定位在生长于70%血清中的表皮葡萄球菌的荧光与免疫染色转移上都检测到的斑点,并对其进行标记以供质谱法鉴别。参看图2A和2B。切下总计40个免疫反应性斑点,并使其经历质谱分析以供鉴别。参看表4。将完整蛋白质序列展示于序列表(SEQ ID NO:1-32)中。将含有蛋白质的凝胶斑点从凝胶上切下,并使用MALDI-TOF进行质量指纹分析,随后搜索Incyte的PathSeq(c)表皮葡萄球菌0-47数据库中对应的编码区来加以鉴别。参看表4。使用静态纳米喷雾进一步分析具有多种蛋白质采样数或可疑信号的斑点。鉴别出总计32种蛋白质,其中某些斑点含有一种以上蛋白质。参看表3和4。24种经鉴别的蛋白质具免疫反应性,26种与血清组份结合,且20种蛋白质具免疫反应性与血清结合性。当结合血清因子所涉及的表皮葡萄球菌表面上大部分蛋白质将可能引发免疫反应时,可预期这一极大重叠。
六种蛋白质始终存在于经免疫染色的印迹中,但荧光染色的转移上并不存在对应的斑点。参看图2B中白色圆形和箭状物。尽管这些蛋白质可能在感染期间表达并引发免疫反应,但在这些实验中所使用的条件下,其不以允许其通过荧光蛋白质染色的水平表达。
实例6
预测蛋白质功能
通过与ATCC12228的完整基因组同源物比较确定预测的蛋白质功能。参看Zhang,Y.Q.等人,Mol Microbiol,49(6),第1577-93页(2003)。表5所示的预测功能是归因于涉及特定蛋白质的先前公开案或与其它生物体中存在的先前经表征的蛋白质同源的个别ORF。
表5
表皮葡萄球菌蛋白的预测功能
斑点# | a预测功能 | 蛋白质SEQID NO: | b检测方法 |
1,2 | 二氢硫辛酰胺脱氢酶 | 12 | I,S |
3 | ″ | 12 | I,S |
谷氨酸-1-半醛2,1-氨基变位酶 | 19 | I,S | |
4 | 烯醇酶 | 11 | I,S |
延伸因子TU(EF-TU) | 18 | I,S | |
5-7,9 | 烯醇酶 | 11 | I,S |
8 | 磷酸葡萄糖酸脱氢酶 | 21 | I |
10 | 烯醇酶 | 11 | I,S |
延伸因子TU(EF-TU) | 18 | I,S | |
Na+/H+逆向转运蛋白 | 28 | I,S | |
11 | 丙氨酸脱氢酶 | 3 | I,S |
12 | 甘油醛-3-磷酸脱氢酶(GAPDH) | 10 | I,S |
13 | ″ | ″ | I,S |
延伸因子TU(EF-TS) | 26 | I,S | |
14 | 不匹配 | I,S | |
15-16 | 甘油醛-3-磷酸脱氢酶(GAPDH) | 10 | I,S |
17 | 乙酰辅酶A C-乙酰转移酶 | 25 | I |
18 | 胱硫醚γ-合酶 | 4 | I |
19 | 铁色素结合脂蛋白 | 17 | I,S |
寡肽通透酶 | 23 | I,S | |
20-23,25 | 铁色素结合脂蛋白 | 17 | I,S |
24 | 果糖二磷酸醛缩酶 | 30 | I,S |
26 | ″ | ″ | I,S |
假设性蛋白 | 8 | I,S | |
假设性蛋白 | 7 | I,S | |
27,30-32 | 脂蛋白(SitC) | 2 | I,S |
28,33 | 氨基酸结合脂蛋白 | 22 | I,S |
29 | 推定的己酮糖-6-磷酸合酶 | 5 | I,S |
34 | 硫辛酸连接酶 | 13 | I,S |
35 | 不匹配 | I | |
36 | 不匹配 | I | |
37 | 不匹配 | I,S | |
38 | 免疫优势抗原A | 29 | I,S |
推定的蛋白 | 1 | I,S | |
39 | 胞外基质结合蛋白(Embp) | 32 | I,S |
40 | 半胱氨酸合酶 | 14 | S |
果糖二磷酸醛缩酶同源物 | 20 | S | |
硫氧还蛋白还原酶 | 27 | S | |
41 | 半胱氨酸合酶 | 14 | S |
42 | 推定的转醛醇酶 | 6 | I |
43 | 胞外基质结合蛋白(Embp) | 32 | S |
转酮醇酶 | 16 | S | |
假设性蛋白 | 24 | S | |
44 | 谷氨酰-tRNA Gln酰胺转移酶亚单元 | 15 | S |
a蛋白质的预测功能是通过与ATCC12228的完整基因组同源物比较确定。
b检测斑点的方法接着转移到硝酸纤维,来自受感染兔的反应性免疫血清I或结合血清组份S。
如上文所讨论,通过2D凝胶电泳分析在70%兔血清中生长的表皮葡萄球菌0-47的细胞壁相关蛋白的表达概况。确定血清中的总体表达概况显著不同于随后在TSB中发生的生长的概况。通过质谱法鉴别在血清中生长期间上调的多种蛋白质,并通过序列比较预测其功能。参看表5。预测养分获取所涉及的三种蛋白质305、1450和1703都显著增加。参看表4和5。所有三种蛋白质都形成横过凝胶的条纹。参看图4。在不受理论束缚的情况下,这可能是多种电荷异构体的结果或可能与其预测的脂蛋白组成有关。此外,所有三种蛋白质都与经表皮葡萄球菌0-47感染的兔的免疫血清具有高度反应性,表明感染期间宿主中也表达这些蛋白质。参看图2和表5。总起来说,这些蛋白质中有24种鉴别为与来自受感染兔的免疫血清具有反应性。这些蛋白质不仅在血清中生长期间表达,而且其还引起受感染动物的免疫反应。参看实例8。总的说来,这些数据表明在感染期间所有这些抗原都表达。受感染小鼠血流内这些ORF的转录本的表达是通过所有经鉴别蛋白质的RT-PCR确认(数据未图示)。
实例7
重组蛋白的克隆和表达
使用基于已表达的蛋白质的质谱所鉴别的蛋白质和表皮葡萄球菌0-47数据库设计的引物克隆基因。使用Pfu Turbo DNA聚合酶(Stratagene,La Jolla,CA)通过聚合酶链式反应(PCR)扩增个别基因,并且用Taq DNA聚合酶(Roche Diagnostics)添加腺嘌呤悬突。遵循制造商的说明书,将反应产物克隆到pCRT7/NT-TOPO或pBAD/TOPOThio(Invitrogen,Carlsbad,CA)中,并将其转化到大肠杆菌Top10(Invitrogen)中。使用ReddyMix PCR mastermix(ABgene,Rochester,NY)通过集落PCR检测阳性克隆,并且进行测序以确保无假突变出现。纯化来自pCRT7克隆的质粒,并将其转化到大肠杆菌BL21(DE3)(Invitrogen)中以供使用T7聚合酶进行表达。37℃下,通过在振荡下(200rpm)使阳性克隆在补充有100μg/ml氨比西林的HySoy肉汤(1%HySoy(Quest Intl,Stockbridge,GA)、0.5%酵母提取物、100mM NaCl、50mM Na2HPO4-7H2O、40mMNaH2PO4-H2O)中生长直到OD600约为1.0来表达蛋白质。用1mM IPTG(pCRT7)或0.2%阿拉伯糖(pBAD)诱导蛋白质表达,并使培养物再生长3小时。接着,通过离心采集细胞,并通过全细胞溶解物的SDS-PAGE评定表达。
纯化重组蛋白质
使细胞小球再悬浮于100ml TBS(20mM Tris(pH 8.0)、150mM NaCl)中,并通过使其通过法氏压力室(French pressure cell)(SLM-Aminco,Rochester,NY)一次将其溶解。随后,通过在10,000×g下离心10分钟将样本分成可溶部分或不可溶小球。通过SDS-PAGE评定重组蛋白的位置。如果重组蛋白在可溶部分中,那么将蛋白质装载于负载有Ni2+的亚氨基二乙酸琼脂糖树脂上。参看表6。接着,用TBS中的30mM咪唑洗涤柱。用TBS中的300mM咪唑洗脱已结合的蛋白质。如果需要额外的纯化步骤,那么将蛋白质透析到含有50mM NaCl的20mM Tris(pH 8.0)和1mM EDTA中,并将其装载于填充有POROS-Q树脂(Applied Biosystems,Foster City,CA)的柱上。用20mM Tris(pH 8.0)中的50mM到500mM梯度NaCl和0.1mM EDTA洗脱已结合的蛋白质。通过SDS-PAGE测定含有所关注的蛋白质的部分,并在-20℃下冷冻。
如果发现重组蛋白在不可溶部分中,那么在4℃下用TBS中的100ml1%Triton X-100将不可溶部分处理4小时。参看表6。通过离心使不可溶蛋白质粒化并丢弃上清液。随后,在室温下,用100ml TBS中的8M尿素提取不可溶小球历时至少8小时。使不可溶碎片粒化,并如上所述纯化蛋白质,但所有缓冲液中都含有2M尿素。纯化后,加入TritonX-100直到0.1%的最终浓度。随后,将蛋白质透析到含有0.1%Triton的TBS中,并且在-20℃下储存。
所有的液相色谱都是使用AKTA探察器(Amersham-Pharmacia Biotech,Piscataway,NJ)进行。所有的SDS-PAGE都是使用4-20%梯度Tris-甘氨酸凝胶(Cambrex)进行。
表6
重组蛋白的溶解性
X表示蛋白质是在所述部分中发现。NT表示未测试。
实例8
使用重组表皮葡萄球菌蛋白的免疫原性组合物
在第0、3和6周时,通过皮下注射用与20μgSTIMULONTM QS-21一起调配的10μg重组蛋白使四周龄的雌性Balb/C小鼠(Charles River Laboratories,Wilmington,MA)免疫。在第一次免疫前0周时和第8周时对所述小鼠抽血。最后一次抽血两天后,通过腹膜内注射在哥伦比亚盐琼脂(Columbia salt agar)(1×哥伦比亚琼脂、0.1%葡萄糖、1%酵母提取物、0.5%NaCl)上生长整夜的5×108cfu表皮葡萄球菌0-47激发小鼠。激发24小时后,处死小鼠并对脾和血液中的细菌计数。
用重组蛋白使小鼠主动免疫
从表皮葡萄球菌0-47克隆27个编码血清结合或免疫反应性蛋白的开放阅读框,并在具有六聚组氨酸标签的大肠杆菌中表达重组蛋白(His标签是为方便起见而使用;本发明的免疫原性组合物将含有在无His标签情况下表达的蛋白质)。参看表7。使用Ni2+螯合柱随后使用离子交换色谱纯化这些蛋白。克隆三个剩余的经克隆的开放阅读框(2006、2975和2907),但不以足以纯化的水平表达。在第0、3和6周时,用个别重组蛋白使Balb/C小鼠免疫。在第0周和第8周对动物抽血,并在第8周用表皮葡萄球菌0-47激发(腹膜内)。激发24小时后,对动物施以安乐死,并计数血液和脾中存在的细菌数量。对5个动物的群组进行这一免疫原性组合物候选物的初始筛选以能够筛选多种蛋白质。所得数据在统计学上不显著,但其仍提供关于大量候选物的免疫原性组合物可能性的有价值信息。27种重组蛋白中有8种使从脾和/或血液回收的细菌数量降低1个对数或更多。参看表7(NT=未测试)。
表7
免疫后细菌总数降低
NT表示未测试。
评估从经免疫小鼠获得的血清对细菌蛋白的抗体反应性。参看表8。如通过在兔血清中生长到对数生长中期的表皮葡萄球菌的全细胞溶解物的Western印迹法所测定,所测试的24份免疫血清中有23份与天然蛋白质反应。参看表8(NT=未测试)。
表8
与葡萄球菌蛋白的抗体反应性
NT表示未测试。
如表8所示,许多经表皮葡萄球菌抗原免疫的动物也对金黄葡萄球菌显现出抗体反应。
因此,对抗表皮葡萄球菌抗原的免疫原性组合物可有效治疗或预防金黄葡萄球菌和表皮葡萄球菌。参看表8。
将用于上述免疫原性组合物中的一分组重组蛋白用于使较大的小鼠群组免疫。通过皮下注射生理盐水或10μg抗原和作为佐剂的20μgSTIMULONTM QS-21使10只雌性(4周龄)Balb/C小鼠的群组免疫。最后一次免疫2周后,通过腹膜内注射用约5×108cfu表皮葡萄球菌0-47激发小鼠。激发后24小时,对血液和脾中的细菌计数。参看表9。与生理盐水中的STIMULONTM QS-21对照相比较,测定log CFU的降低。通过Student′s-T检验分析数据,且得到*0.05或**0.01的p值。
表9
免疫原性组合物中所使用的蛋白质
*p值<0.05
**p值<0.01
表9中所示的表皮葡萄球菌蛋白展示出当用于免疫原性组合物中时降低随后激发后细菌感染的严重程度的极高效用。
实例9
经表皮葡萄球菌蛋白免疫后防止金黄葡萄球菌激发
如实例8(表8)中的抗体结合数据所表明,对抗表皮葡萄球菌抗原的免疫原性组合物可对治疗或预防金黄葡萄球菌有效。因此,使用经表皮葡萄球菌抗原的免疫原性组合物免疫后的金黄葡萄球菌进行激发。
在第0、3和6周时,通过皮下注射以20μg STIMULONTM QS-21中的10μg重组蛋白使四周龄的雌性CD-1小鼠(Charles River Laboratories,Wilmington,MA)免疫。在第一次免疫前0周时和第8周时对所述小鼠抽血。最后一次抽血两天后,通过腹膜内注射在哥伦比亚盐琼脂(1×哥伦比亚琼脂、0.1%葡萄糖、1%酵母提取物、0.5%NaCl)上生长整夜的3×108cfu金黄葡萄球菌Reynolds激发小鼠。激发24小时后,处死小鼠并对肾中的细菌计数。
表10
以金黄葡萄球菌激发
蛋白 | 预期 | CFU | |
ORF | SEQ ID NO: | 功能 | 降低 |
2653 | 29 | 免疫优势Ag A | 0.9log |
321 | 3 | 丙氨酸脱氢酶 | 0.7log |
1015 | 12 | 二氢硫辛酰胺脱氢酶 | 无 |
608 | 7 | 未知 | 0.6log |
1069 | 13 | 硫辛酸连接酶 | 1.7log |
639 | 6 | 假设 | 无 |
如表10所示,某些表皮葡萄球菌抗原能够有效诱导识别金黄葡萄球菌并与其结合的抗体。此外,所诱导的抗体对于降低金黄葡萄球菌激发后所计数的细菌含量具有有益作用。
将SEQ ID NO:1到SEQ ID NO:32的表皮葡萄球菌多肽抗原的氨基酸序列的同一性百分数与其来自金黄葡萄球菌的同源物的氨基酸序列相比较。结果展示于表11中。
表11
表皮葡萄球菌与金黄葡萄球菌之间的同一性
多肽 | a与金黄葡萄球菌同源物的 | |
Orf | SEQ ID NO: | 同一性% |
121 | 1 | 33% |
305 | 2 | 76% |
321 | 3 | 85% |
373 | 4 | 81% |
554 | 5 | 87% |
639 | 6 | 62% |
608 | 7 | 89% |
702 | 8 | 97% |
793 | 9 | 23% |
847 | 10 | 95% |
854 | 11 | 94% |
1015 | 12 | 96% |
1069 | 13 | 82% |
1238 | 14 | 94% |
1382 | 15 | 93% |
1405 | 16 | 82% |
1450 | 17 | 71% |
1522 | 18 | 96% |
1545 | 19 | 91% |
1653 | 20 | 95% |
1690 | 21 | 89% |
1703 | 22 | 82% |
2006 | 23 | 90% |
2180 | 24 | 87% |
2214 | 25 | 73% |
2482 | 26 | 91% |
2580 | 27 | 91% |
2649 | 28 | 78% |
2653 | 29 | 62% |
2736 | 30 | 92% |
2907 | 31 | |
2975 | 32 | 32% |
测定多肽序列之间的同源性。
序列表
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245 250 255
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260 265 270
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290 295 300
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Gly Arg Ala Leu Val Pro Ser Gly Ala Ser Thr Gly Glu His Glu Ala
35 40 45
Val Glu Leu Arg Asp Gly Asp Lys Ser Arg Tyr Leu Gly Lys Gly Val
50 55 60
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Glu Gly Glu Phe Ser Val Leu Asp Gln Val Ser Ile Asp Lys Met Met
85 90 95
Ile Gln Leu Asp Gly Thr His Asn Lys Gly Lys Leu Gly Ala Asn Ala
100 105 110
Ile Leu Gly Val Ser Ile Ala Val Ala Arg Ala Ala Ala Asp Leu Leu
115 120 125
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Pro Val Pro Met Met Asn Ile Val Asn Gly Gly Ser His Ser Asp Ala
145 150 155 160
Pro Ile Ala Phe Gln Glu Phe Met Ile Leu Pro Val Gly Ala Glu Ser
165 170 175
Phe Lys Glu Ser Leu Arg Trp Gly Ala Glu Ile Phe His Asn Leu Lys
180 185 190
Ser Ile Leu Ser Glu Arg Gly Leu Glu Thr Ala Val Gly Asp Glu Gly
195 200 205
Gly Phe Ala Pro Arg Phe Glu Gly Thr Glu Asp Ala Val Glu Thr Ile
210 215 220
Ile Lys Ala Ile Glu Lys Ala Gly Tyr Lys Pro Gly Glu Asp Val Phe
225 230 235 240
Leu Gly Phe Asp Cys Ala Ser Ser Glu Phe Tyr Glu Asn Gly Val Tyr
245 250 255
Asp Tyr Thr Lys Phe Glu Gly Glu His Gly Ala Lys Arg Ser Ala Ala
260 265 270
Glu Gln Val Asp Tyr Leu Glu Glu Leu Ile Gly Lys Tyr Pro Ile Ile
275 280 285
Thr Ile Glu Asp Gly Met Asp Glu Asn Asp Trp Glu Gly Trp Lys Gln
290 295 300
Leu Thr Asp Arg Ile Gly Asp Lys Val Gln Leu Val Gly Asp Asp Leu
305 310 315 320
Phe Val Thr Asn Thr Glu Ile Leu Ser Lys Gly IIle Glu Gln Gly Ile
325 330 335
Gly Asn Ser Ile Leu Ile Lys Val Asn Gln Ile Gly Thr Leu Thr Glu
340 345 350
Thr Phe Asp Ala Ile Glu Met Ala Gln Lys Ala Gly Tyr Thr Ala Val
355 360 365
Val Ser His Arg Ser Gly Glu Thr Glu Asp Thr Thr Ile Ala Asp Ile
370 375 380
Ala Val Ala Thr Asn Ala Gly Gln Ile Lys Thr Gly Ser Leu Ser Arg
385 390 395 400
Thr Asp Arg Ile Ala Lys Tyr Asn Gln Leu Leu Arg Ile Glu Asp Glu
405 410 415
Leu Tyr Glu Thr Ala Lys Phe Glu Gly Ile Lys Ser Phe Tyr Asn Leu
420 425 430
Asp Lys
<210>12
<211>468
<212>PRT
<213>表皮葡萄球菌
<400>12
Met Val Val Gly Asp Phe Pro Ile Glu Thr Asp Thr Ile Val Ile Gly
1 5 10 15
Ala Gly Pro Gly Gly Tyr Val Ala Ala Ile Arg Ala Ala Gln Leu Gly
20 25 30
Gln Lys Val Thr Ile Val Glu Lys Gly Asn Leu Gly Gly Val Cys Leu
35 40 45
Asn Val Gly Cys Ile Pro Ser Lys Ala Leu Leu His Ala Ser His Arg
50 55 60
Phe Val Glu Ala Gln Asn Ser Glu Asn Leu Gly Val Ile Ala Glu Ser
65 70 75 80
Val Ser Leu Asn Tyr Gln Lys Val Gln Glu Phe Lys Thr Ser Val Val
85 90 95
Asn Lys Leu Thr Gly Gly Val Glu Gly Leu Leu Lys Gly Asn Lys Val
100 105 110
Glu Ile Val Arg Gly Glu Ala Tyr Phe Val Asp Asn Asn Ser Leu Arg
115 120 125
Val Met Asp Glu Lys Ser Ala Gln Thr Tyr Asn Phe Lys His Ala Ile
130 135 140
Ile Ala Thr Gly Ser Arg Pro Ile Glu Ile Pro Asn Phe Glu Phe Gly
145 150 155 160
Lys Arg Val Ile Asp Ser Thr Gly Ala Leu Asn Leu Gln Glu Val Pro
165 170 175
Asn Lys Leu Val Val Val Gly Gly Gly Tyr Ile Gly Ser Glu Leu Gly
180 185 190
Thr Ala Phe Ala Asn Phe Gly Ser Glu Val Thr Ile Leu Glu Gly Ala
195 200 205
Lys Asp Ile Leu Gly Gly Phe Glu Lys Gln Met Thr Gln Pro Val Lys
210 215 220
Lys Gly Met Lys Glu Lys Gly Ile Glu Ile Val Thr Glu Ala Met Ala
225 230 235 240
Lys Ser Ala Glu Glu Thr Glu Asn Gly Val Lys Val Thr Tyr Glu Ala
245 250 255
Lys Gly Glu Glu Gln Thr Ile Glu Ala Asp Tyr Val Leu Val Thr Val
260 265 270
Gly Arg Arg Pro Asn Thr Asp Glu Leu Gly Leu Glu Glu Leu Gly Leu
275 280 285
Lys Phe Ala Asp Arg Gly Leu Leu Glu Val Asp Lys Gln Ser Arg Thr
290 295 300
Ser Ile Glu Asn Ile Phe Ala Ile Gly Asp Ile Val Pro Gly Leu Pro
305 310 315 320
Leu Ala His Lys Ala Ser Tyr Glu Gly Lys Val Ala Ala Glu Ala Ile
325 330 335
Asp Gly Gln Ala Ala Glu Val Asp Tyr Ile Gly Met Pro Ala Val Cys
340 345 350
Phe Thr Glu Pro Glu Leu Ala Gln Val Gly Tyr Thr Glu Ala Gln Ala
355 360 365
Lys Glu Glu Gly Leu Ser Ile Lys Ala Ser Lys Phe Pro Tyr Ala Ala
370 375 380
Asn Gly Arg Ala Leu Ser Leu Asp Asp Thr Asn Gly Phe Val Lys Leu
385 390 395 400
Ile Thr Leu Lys Glu Asp Asp Thr Leu Ile Gly Ala Gln Val Val Gly
405 410 415
Thr Gly Ala Ser Asp Ile Ile Ser Glu Leu Gly Leu Ala Ile Glu Ser
420 425 430
Gly Met Asn Ala Glu Asp Ile Ala Leu Thr Val His Ala His Pro Thr
435 440 445
Leu Gly Glu Met Thr Met Glu Ala Ala Glu Lys Ala Ile Gly Tyr Pro
450 455 460
Ile His Thr Met
465
<210>13
<211>279
<212>PRT
<213>表皮葡萄球菌
<400>13
Met Asp Leu Ala Thr Lys Tyr Phe Asn Gln Ile Asn Trp Arg Tyr Val
1 5 10 15
Asp His Ser Ser Gly Leu Glu Pro Met Gln Ser Phe Ala Phe Asp Asp
20 25 30
Thr Phe Ser Glu Ser Val Gly Lys Asp Leu Ser Cys Asn Val Val Arg
35 40 45
Thr Trp Ile His Gln His Thr Val Ile Leu Gly Ile His Asp Ser Arg
50 55 60
Leu Pro Phe Leu Ser Asp Gly Ile Arg Phe Leu Thr Asp Glu Gln Gly
65 70 75 80
Tyr Asn Ala Ile Val Arg Asn Ser Gly Gly Leu Gly Val Val Leu Asp
85 90 95
Gln Gly Ile Leu Asn Ile Ser Leu Ile Phe Lys Gly Gln Thr Glu Thr
100 105 110
Thr Ile Asp Glu Ala Phe Thr Val Met Tyr Leu Leu Ile Asn Lys Met
115 120 125
Phe Glu Asp Glu Asp Val Ser Ile Asp Thr Lys Glu Ile Glu Gln Ser
130 135 140
Tyr Cys Pro Gly Lys Phe Asp Leu Ser Ile Asn Asp Lys Lys Phe Ala
145 150 155 160
Gly Ile Ser Gln Arg Arg Val Arg Gly Gly Ile Ala Val Gln Ile Tyr
165 170 175
Leu Cys Ile Glu Gly Ser Gly Ser Glu Arg Ala Leu Met Met Gln Gln
180 185 190
Phe Tyr Gln Arg Ala Leu Lys Gly Glu Thr Thr Lys Phe His Tyr Pro
195 200 205
Asp Ile Asp Pro Ser Cys Met Ala Ser Leu Glu Thr Leu Leu Asn Arg
210 215 220
Glu Ile Lys Val Gln Asp Val Met Phe Leu Leu Leu Tyr Ala Leu Lys
225 230 235 240
Asp Leu Gly Ala Asn Leu Asn Met Asp Pro Ile Thr Glu Asp Glu Trp
245 250 255
Thr Arg Tyr Glu Gly Tyr Tyr Asp Lys Met Leu Glu Arg Asn Ala Lys
260 265 270
Met Asn Glu Lys Leu Asp Phe
275
<210>14
<211>310
<212>PRT
<213>表皮葡萄球菌
<400>14
Met Ala Gln Lys Pro Val Asp Tyr Val Thr Gln Ile Ile Gly Asn Thr
1 5 10 15
Pro Val Val Lys Leu Arg Asn Val Val Asp Asp Asp Ala Ala Asp Ile
20 25 30
Tyr Val Lys Leu Glu Tyr Gln Asn Pro Gly Gly Ser Val Lys Asp Arg
35 40 45
Ile Ala Leu Ala Met Ile Glu Lys Ala Glu Arg Glu Gly Lys Ile Lys
50 55 60
Pro Gly Asp Thr Ile Val Glu Pro Thr Ser Gly Asn Thr Gly Ile Gly
65 70 75 80
Leu Ala Phe Val Cys Ala Ala Lys Gly Tyr Lys Ala Val Phe Thr Met
85 90 95
Pro Glu Thr Met Ser Gln Glu Arg Arg Asn Leu Leu Lys Ala Tyr Gly
100 105 110
Ala Glu Leu Val Leu Thr Pro Gly Ser Glu Ala Met Lys Gly Ala Ile
115 120 125
Lys Lys Ala Lys Glu Leu Lys Glu Glu His Gly Tyr Phe Glu Pro Gln
130 135 140
Gln Phe Glu Asn Pro Ala Asn Pro Glu Ile His Glu Leu Thr Thr Gly
145 150 155 160
Pro Glu Leu Val Glu Gln Phe Glu Gly Arg Gln Ile Asp Ala Phe Leu
165 170 175
Ala Gly Val Gly Thr Gly Gly Thr Leu Ser Gly Val Gly Lys Val Leu
180 185 190
Lys Lys Glu Tyr Pro Asn Val Glu Ile Val Ala Ile Glu Pro Glu Ala
195 200 205
Ser Pro Val Leu Ser Gly Gly Glu Pro Gly Pro His Lys Leu Gln Gly
210 215 220
Leu Gly Ala Gly Phe Val Pro Asp Thr Leu Asn Thr Glu Val Tyr Asp
225 230 235 240
Ser Ile Ile Lys Val Gly Asn Asp Thr Ala Met Asp Met Ala Arg Arg
245 250 255
Val Ala Arg Glu Glu Gly Ile Leu Ala Gly Ile Ser Ser Gly Ala Ala
260 265 270
Ile Tyr Ala Ala Ile Gln Lys Ala Lys Glu Leu Gly Lys Gly Lys Thr
275 280 285
Val Val Thr Val Leu Pro Ser Asn Gly Glu Arg Tyr Leu Ser Thr Pro
290 295 300
Leu Tyr Ser Phe Asp Asn
305 310
<210>15
<211>475
<212>PRT
<213>表皮葡萄球菌
<400>15
Met His Phe Glu Thr Val Ile Gly Leu Glu Val His Val Glu Leu Lys
1 5 10 15
Thr Asp Ser Lys Met Phe Ser Pro Ser Pro Ala His Phe Gly Ala Glu
20 25 30
Pro Asn Ser Asn Thr Asn Val Ile Asp Leu Ala Tyr Pro Gly Val Leu
35 40 45
Pro Val Val Asn Arg Arg Ala Val Asp Trp Ala Met Arg Ala Ser Met
50 55 60
Ala Leu Asn Met Asp Ile Ala Thr Asn Ser Lys Phe Asp Arg Lys Asn
65 70 75 80
Tyr Phe Tyr Pro Asp Asn Pro Lys Ala Tyr Gln Ile Ser Gln Phe Asp
85 90 95
Gln Pro Ile Gly Glu Asn Gly Tyr Ile Asp Ile Glu Val Asp Gly Glu
100 105 110
Thr Lys Arg Ile Gly Ile Thr Arg Leu His Met Glu Glu Asp Ala Gly
115 120 125
Lys Ser Thr His Lys Asp Gly Tyr Ser Leu Val Asp Leu Asn Arg Gln
130 135 140
Gly Thr Pro Leu Ile Glu Ile Val Ser Glu Pro Asp Ile Arg Ser Pro
145 150 155 160
Lys Glu Ala Tyr Ala Tyr Leu Glu Lys Leu Arg Ser Ile Ile Gln Tyr
165 170 175
Thr Gly Val Ser Asp Cys Lys Met Glu Glu Gly Ser Leu Arg Cys Asp
180 185 190
Ala Asn Ile Ser Leu Arg Pro Tyr Gly Gln Lys Glu Phe Gly Thr Lys
195 200 205
Thr Glu Leu Lys Asn Leu Asn Ser Phe Asn Tyr Val Lys Lys Gly Leu
210 215 220
Glu Tyr Glu Glu Lys Arg Gln Glu Glu Glu Leu Leu Asn Gly Gly Glu
225 230 235 240
Ile Gly Gln Glu Thr Arg Arg Phe Asp Glu Ser Thr Gly Lys Thr Ile
245 250 255
Leu Met Arg Val Lys Glu Gly Ser Asp Asp Tyr Arg Tyr Phe Pro Glu
260 265 270
Pro Asp Ile Val Pro Leu Tyr Val Asp Glu Asp Trp Lys Ala Arg Val
275 280 285
Arg Glu Thr Ile Pro Glu Leu Pro Asp Glu Arg Lys Ala Lys Tyr Val
290 295 300
Asn Asp Leu Gly Leu Pro Glu Tyr Asp Ala His Val Leu Thr Leu Thr
305 310 315 320
Lys Glu Met Ser Asp Phe Phe Glu Gly Ala Ile Asp His Gly Ala Asp
325 330 335
Val Lys Leu Thr Ser Asn Trp Leu Met Gly Gly Val Asn Glu Tyr Leu
340 345 350
Asn Lys Asn Gln Val Glu Leu Lys Asp Thr Gln Leu Thr Pro Glu Asn
355 360 365
Leu Ala Gly Met Ile Lys Leu Ile Glu Asp Gly Thr Met Ser Ser Lys
370 375 380
Ile Ala Lys Lys Val Phe Pro Glu Leu Ala Glu Asn Gly Gly Asp Ala
385 390 395 400
Lys Gln Ile Met Glu Asp Lys Gly Leu Val Gln Ile Ser Asp Glu Ala
405 410 415
Thr Leu Leu Lys Phe Val Thr Asp Ala Leu Asp Asn Asn Pro Gln Ser
420 425 430
Ile Glu Asp Tyr Lys Asn Gly Lys Gly Lys Ala Mer Gly Phe Leu Val
435 440 445
Gly Gln Ile Met Lys Ala Ser Lys Gly Gln Ala Asn Pro Gln Lys Val
450 455 460
Asn Ser Leu Leu Lys Gln Glu Leu Asp Asn Arg
465 470 475
<210>16
<211>364
<212>PRT
<213>表皮葡萄球菌
<400>16
Met Leu Lys Arg Ala Asn Glu Asn Glu Glu Ala Trp Asn Asn Met Leu
1 5 10 15
Lys Asn Tyr Ser Glu Ala Tyr Pro Glu Leu Ala Glu Glu Phe Lys Leu
20 25 30
Ala Met Ser Gly Lys Leu Pro Asn Asn Tyr Ala Asp Ala Leu Pro Glu
35 40 45
Tyr Asp Leu Asn His Ser Gly Ala Ser Arg Ala Asp Ser Gly Glu Ile
50 55 60
Ile Gln Lys Leu Ser Glu Phe Val Pro Ser Phe Phe Gly Gly Ser Ala
65 70 75 80
Asp Leu Ala Gly Ser Asn Lys Ser Asn Val Lys Glu Ala Lys Asp Tyr
85 90 95
Asn Lys Asp Thr Pro Glu Gly Lys Asn Val Trp Phe Gly Val Arg Glu
100 105 110
Phe Ala Met Gly Ala Ala Ile Asn Gly Met Ala Ala His Gly Gly Leu
115 120 125
His Pro Tyr Ala Ala Thr Phe Phe Val Phe Ser Asp Tyr Leu Lys Pro
130 135 140
Ala Leu Arg Leu Ser Ser Ile Met Gly Leu Asn Ser Thr Phe Ile Phe
145 150 155 160
Thr His Asp Ser Ile Ala Val Gly Glu Asp Gly Pro Thr His Glu Pro
165 170 175
Ile Glu Gln Leu Ala Gly Leu Arg Ala Ile Pro Asn Met Asn Val Ile
180 185 190
Arg Pro Ala Asp Gly Asn Glu Thr Arg Val Ala Trp Glu Val Ala Leu
195 200 205
Glu Ser Glu Gln Thr Pro Thr Ser Leu Val Leu Thr Arg Gln Asn Leu
210 215 220
Pro Thr Leu Asp Val Asp Lys Gln Thr Val Glu Asn Gly Val Arg Lys
225 230 235 240
Gly Ala Tyr Ile Val Phe Glu Thr Glu Gln Gln Leu Glu Tyr Leu Leu
245 250 255
Leu Ala Ser Gly Ser Glu Val Asn Leu Ala Val Glu Ala Ala Lys Glu
260 265 270
Leu Glu Gln Gln Gly Lys Gly Val Arg Val Ile Ser Met Pro Asn Trp
275 280 285
Tyr Ala Phe Glu Gln Gln Ser Ser Glu Tyr Lys Glu Ser Ile Leu Pro
290 295 300
Ser Asp Val Thr Lys Arg Ile Ala Ile Glu Met Ala Ser Pro Leu Gly
305 310 315 320
Trp His Lys Tyr Val Gly Ile Glu Gly Lys Val Ile Gly Ile Asn Ser
325 330 335
Phe Gly Ala Ser Ala Pro Gly Asp Leu Val Val Glu Lys Tyr Gly Phe
340 345 350
Thr Lys Glu Asn Ile Leu Lys Gln Val Arg Ser Leu
355 360
<210>17
<211>334
<212>PRT
<213>表皮葡萄球菌
<400>17
Val Glu Ser Val Arg Gly Leu Lys Ile Leu Ser Val Ile Gly Leu Leu
1 5 10 15
Phe Val Leu Ile Ala Thr Ala Ala Cys Gly Asn Asn Ser Ser Ser Asn
20 25 30
Ser Ser Lys Glu Ser Ser Lys Asp Gly Val Glu Ile Lys His Glu Glu
35 40 45
Gly Thr Thr Lys Val Pro Lys His Pro Lys Arg Val Val Val Leu Glu
50 55 60
Tyr Ser Phe Val Asp Ala Leu Val Ala Leu Asp Val Lys Pro Val Gly
65 70 75 80
Ile Ala Asp Asp Asn Lys Lys Asn Arg Ile Ile Lys Pro Leu Arg Asp
85 90 95
Lys Ile Gly Lys Tyr Thr Ser Val Gly Thr Arg Lys Pro Pro Asn Leu
100 105 110
Glu Glu Ile Ser Lys Leu Lys Pro Asp Leu Ile Ile Ala Asp Asn Asn
115 120 125
Arg His Lys Gly Ile Tyr Lys Asp Leu Asn Lys Ile Ala Pro Thr Ile
130 135 140
Glu Leu Lys Ser Phe Asp Gly Asp Tyr Asn Glu Asn Ile Asp Ala Phe
145 150 155 160
Lys Thr Ile Ser Lys Ala Leu Gly Lys Glu Glu Glu Gly Lys Lys Arg
165 170 175
Leu Glu Glu His Asp Lys Lys Ile Glu Glu Tyr Lys Lys Glu Ile Thr
180 185 190
Met Asp Lys Asn Gln Lys Val Leu Pro Ala Val Ala Ala Lys Ser Gly
195 200 205
Leu Leu Ala His Pro Ser Asn Ser Tyr Val Gly Gln Phe Leu Ser Gln
210 215 220
Leu Gly Phe Lys Glu Ala Leu Ser Asp Asp Val Thr Lys Gly Leu Ser
225 230 235 240
Lys Tyr Leu Lys Gly Pro Tyr Leu Gln Met Asn Thr Glu Thr Leu Ser
245 250 255
Gln Val Asn Pro Glu Arg Met Phe Ile Met Thr Asn Lys Ala Ser Ser
260 265 270
Asn Glu Pro Ser Leu Lys Glu Leu Glu Lys Asp Pro Val Trp Lys Lys
275 280 285
Leu Asn Ala Val Lys Asn Gln Arg Val Asp Ile Leu Asp Arg Asp Leu
290 295 300
Trp Ala Arg Ser Arg Gly Leu Ile Ser Ser Glu Glu Met Ala Lys Glu
305 310 315 320
Leu Val Glu Leu Ser Lys Thr Asp Ser Lys Lys Asp Asn Lys
325 330
<210>18
<211>411
<212>PRT
<213>表皮葡萄球菌
<400>18
Met Arg Asp Lys Phe Glu Ile Thr Phe Ile Lys Asn Arg Arg Asp Leu
1 5 10 15
Ile Met Ala Lys Glu Lys Phe Asp Arg Ser Lys Glu His Ala Asn Ile
20 25 30
Gly Thr Ile Gly His Val Asp His Gly Lys Thr Thr Leu Thr Ala Ala
35 40 45
Ile Ala Thr Val Leu Ala Lys Asn Gly Asp Thr Val Ala Gln Ser Tyr
50 55 60
Asp Met Ile Asp Asn Ala Pro Glu Glu Lys Glu Arg Gly Ile Thr Ile
65 70 75 80
Asn Thr Ala His Ile Glu Tyr Gln Thr Asp Lys Arg His Tyr Ala His
85 90 95
Val Asp Cys Pro Gly His Ala Asp Tyr Val Lys Asn Met Ile Thr Gly
100 105 110
Ala Ala Gln Met Asp Gly Gly Ile Leu Val Val Ser Ala Ala Asp Gly
115 120 125
Pro Met Pro Gln Thr Arg Glu His Ile Leu Leu Ser Arg Asn Val Gly
130 135 140
Val Pro Ala Leu Val Val Phe Leu Asn Lys Val Asp Met Val Asp Asp
145 150 155 160
Glu Glu Leu Leu Glu Leu Val Glu Met Glu Val Arg Asp Leu Leu Ser
165 170 175
Glu Tyr Asp Phe Pro Gly Asp Asp Val Pro Val Ile Ala Gly Ser Ala
180 185 190
Leu Lys Ala Leu Glu Gly Asp Ala Glu Tyr Glu Gln Lys Ile Leu Asp
195 200 205
Leu Met Gln Ala Val Asp Asp Tyr Ile Pro Thr Pro Glu Arg Asp Ser
210 215 220
Asp Lys Pro Phe Met Met Pro Val Glu Asp Val Phe Ser Ile Thr Gly
225 230 235 240
Arg Gly Thr Val Ala Thr Gly Arg Val Glu Arg Gly Gln Ile Lys Val
245 250 255
Gly Glu Glu Val Glu Ile Ile Gly Met His Glu Thr Ser Lys Thr Thr
260 265 270
Val Thr Gly Val Glu Met Phe Arg Lys Leu Leu Asp Tyr Ala Glu Ala
275 280 285
Gly Asp Asn Ile Gly Ala Leu Leu Arg Gly Val Ala Arg Glu Asp Val
290 295 300
Gln Arg Gly Gln Val Leu Ala Ala Pro Gly Ser Ile Thr Pro His Thr
305 310 315 320
Lys Phe Lys Ala Glu Val Tyr Val Leu Ser Lys Asp Glu Gly Gly Arg
325 330 335
His Thr Pro Phe Phe Thr Asn Tyr Arg Pro Gln Phe Tyr Phe Arg Thr
340 345 350
Thr Asp Val Thr Gly Val Val Asn Leu Pro Glu Gly Thr Glu Met Val
355 360 365
Met Pro Gly Asp Asn Val Glu Met Thr Val Glu Leu Ile Ala Pro Ile
370 375 380
Ala Ile Glu Asp Gly Thr Arg Phe Ser Ile Arg Glu Gly Gly Arg Thr
385 390 395 400
Val Gly Ser Gly Val Val Thr Glu Ile Phe Glu
405 410
<210>19
<211>428
<212>PRT
<213>表皮葡萄球菌
<400>19
Met Met Ser Phe Glu Lys Ser Ile Lys Ala Met Glu Gln Ala Glu Lys
1 5 10 15
Leu Met Pro Gly Gly Val Asn Ser Pro Val Arg Ala Phe Lys Ser Val
20 25 30
Asp Thr Pro Ala Ile Phe Met Asp His Gly Glu Gly Ser Lys Ile Tyr
35 40 45
Asp Ile Asp Gly Asn Glu Tyr Ile Asp Tyr Val Leu Ser Trp Gly Pro
50 55 60
Leu Ile Leu Gly His Lys Asn Gln Gln Val Ile Ser Lys Leu His Glu
65 70 75 80
Ala Val Asp Lys Gly Thr Ser Phe Gly Ala Ser Thr Leu Gln Glu Asn
85 90 95
Lys Leu Ala Glu Leu Val Ile Asp Arg Val Pro Ser Ile Glu Lys Val
100 105 110
Arg Met Val Ser Ser Gly Thr Glu Ala Thr Leu Asp Thr Leu Arg Leu
115 120 125
Ala Arg Gly Tyr Thr Gly Arg Asn Lys Ile Ile Lys Phe Glu Gly Cys
130 135 140
Tyr His Gly His Ser Asp Ser Leu Leu Ile Lys Ala Gly Ser Gly Val
145 150 155 160
Ala Thr Leu Gly Leu Pro Asp Ser Pro Gly Val Pro Glu Gly Ile Ala
165 170 175
Lys Asn Thr Ile Thr Val Pro Tyr Asn Asp Leu Asp Ser Leu Lys Leu
180 185 190
Ala Phe Glu Lys Tyr Gly Asp Asp Ile Ala Gly Val Ile Val Glu Pro
195 200 205
Val Ala Gly Asn Met Gly Val Val Pro Pro Val Asn Gly Phe Leu Gln
210 215 220
Gly Leu Arg Asp Ile Thr Asn Glu Tyr Gly Ala Leu Leu Ile Phe Asp
225 230 235 240
Glu Val Met Thr Gly Phe Arg Val Gly Tyr Asn Cys Ala Gln Gly Tyr
245 250 255
Phe Gly Val Thr Pro Asp Leu Thr Cys Leu Gly Lys Val Ile Gly Gly
260 265 270
Gly Leu Pro Val Gly Ala Phe Gly Gly Lys Lys Glu Ile Met Asp Tyr
275 280 285
Ile Ala Pro Val Gly Thr Ile Tyr Gln Ala Gly Thr Leu Ser Gly Asn
290 295 300
Pro Leu Ala Met Thr Ser Gly Tyr Glu Thr Leu Ser Gln Leu Thr Pro
305 310 315 320
Glu Ser Tyr Glu Tyr Phe Asn Ser Leu Gly Asp Ile Leu Glu Lys Gly
325 330 335
Leu Lys Glu Val Phe Ala Lys Tyr Asn Val Pro Ile Thr Val Asn Arg
340 345 350
Ala Gly Ser Met Ile Gly Tyr Phe Leu Asn Glu Gly Pro Val Thr Asn
355 360 365
Phe Glu Glu Ala Asn Lys Ser Asp Leu Lys Leu Phe Ser Asn Met Tyr
370 375 380
Arg Glu Met Ala Lys Glu Gly Val Tyr Ile Pro Pro Ser Gln Phe Glu
385 390 395 400
Gly Thr Phe Leu Ser Thr Ala His Thr Lys Asp Asp Ile Glu Lys Thr
405 410 415
Ile Gln Ala Phe Asp Asn Ala Leu Ser Arg Ile Val
420 425
<210>20
<211>286
<212>PRT
<213>表皮葡萄球菌
<400>20
Met Pro Leu Val Ser Met Lys Glu Met Leu Ile Asp Ala Lys Glu Asn
1 5 10 15
Gly Tyr Ala Val Gly Gln Tyr Asn Leu Asn Asn Leu Glu Phe Thr Gln
20 25 30
Ala Ile Leu Glu Ala Ser Gln Glu Glu Asn Ala Pro Val Ile Leu Gly
35 40 45
Val Ser Glu Gly Ala Ala Arg Tyr Met Ser Gly Phe Tyr Thr Val Val
50 55 60
Lys Met Val Glu Gly Leu Met His Asp Leu Asn Ile Thr Ile Pro Val
65 70 75 80
Ala Ile His Leu Asp His Gly Ser Ser Phe Glu Lys Cys Lys Glu Ala
85 90 95
Ile Asp Ala Gly Phe Thr Ser Val Met Ile Asp Ala Ser His Ser Pro
100 105 110
Phe Glu Glu Asn Val Glu Ile Thr Ser Lys Val Val Glu Tyr Ala His
115 120 125
Asp Arg Gly Val Ser Val Glu Ala Glu Leu Gly Thr Val Gly Gly Gln
130 135 140
Glu Asp Asp Val Val Ala Asp Gly Val Ile Tyr Ala Asp Pro Lys Glu
145 150 155 160
Cys Gln Glu Leu Val Glu Lys Thr Gly Ile Asp Thr Leu Ala Pro Ala
165 170 175
Leu Gly Ser Val His Gly Pro Tyr Lys Gly Glu Pro Lys Leu Gly Phe
180 185 190
Lys Glu Met Glu Glu Ile Gly Ala Ser Thr Gly Leu Pro Leu Val Leu
195 200 205
His Gly Gly Thr Gly Ile Pro Thr Lys Asp Ile Gln Lys Ala Ile Pro
210 215 220
Tyr Gly Thr Ala Lys Ile Asn Val Asn Thr Glu Asn Gln Ile Ala Ser
225 230 235 240
Ala Lys Ala Val Arg Glu Val Leu Asn Asn Asp Lys Asp Val Tyr Asp
245 250 255
Pro Arg Lys Tyr Leu Gly Pro Ala Arg Glu Ala Ile Lys Glu Thr Val
260 265 270
Lys Gly Lys Ile Arg Glu Phe Gly Thr Ser Asn Arg Ala Lys
275 280 285
<210>21
<211>468
<212>PRT
<213>表皮葡萄球菌
<400>21
Met Thr Gln Gln Ile Gly Val Val Gly Leu Ala Val Met Gly Lys Asn
1 5 10 15
Leu Ala Trp Asn Ile Glu Ser Arg Gly Tyr Ser Val Ser Val Tyr Asn
20 25 30
Arg Ser Arg Gln Lys Thr Asp Glu Met Val Lys Glu Ser Pro Gly Arg
35 40 45
Glu Ile Tyr Pro Thr Tyr Ser Leu Glu Glu Phe Val Glu Ser Leu Glu
50 55 60
Lys Pro Arg Lys Ile Leu Leu Met Val Lys Ala Gly Pro Ala Thr Asp
65 70 75 80
Ala Thr Ile Asp Gly Leu Leu Pro Leu Leu Asp Asp Asp Asp Ile Leu
85 90 95
Ile Asp Gly Gly Asn Thr Asn Tyr Gln Asp Thr Ile Arg Arg Asn Lys
100 105 110
Ala Leu Ala Glu Ser Ser Ile Asn Phe Ile Gly Met Gly Val Ser Gly
115 120 125
Gly Glu Ile Gly Ala Leu Thr Gly Pro Ser Leu Met Pro Gly Gly Gln
130 135 140
Lys Asp Ala Tyr Asn Lys Val Ser Asp Ile Leu Asp Ala Ile Ala Ala
145 150 155 160
Lys Ala Gln Asp Gly Ala Ser Cys Val Thr Tyr Ile Gly Pro Asn Gly
165 170 175
Ala Gly His Tyr Val Lys Met Val His Asn Gly Ile Glu Tyr Ala Asp
180 185 190
Met Gln Leu Ile Ala Glu Ser Tyr Ala Met Met Lys Asp Leu Leu Gly
195 200 205
Met Ser His Lys Glu Ile Ser Gln Thr Phe Lys Glu Trp Asn Ala Gly
210 215 220
Glu Leu Glu Ser Tyr Leu Ile Glu Ile Thr Gly Asp Ile Phe Asn Lys
225 230 235 240
Leu Asp Asp Asp Asn Glu Ala Leu Val Glu Lys Ile Leu Asp Thr Ala
245 250 255
Gly Gln Lys Gly Thr Gly Lys Trp Thr Ser Ile Asn Ala Leu Glu Leu
260 265 270
Gly Val Pro Leu Thr Ile Ile Thr Glu Ser Val Phe Ala Arg Phe Ile
275 280 285
Ser Ser Ile Lys Glu Glu Arg Val Thr Ala Ser Lys Ser Leu Lys Gly
290 295 300
Pro Lys Ala His Phe Glu Gly Asp Lys Lys Thr Phe Leu Glu Lys Ile
305 310 315 320
Arg Lys Ala Leu Tyr Met Ser Lys Ile Cys Ser Tyr Ala Gln Gly Phe
325 330 335
Ala Gln Met Arg Lys Ala Ser Glu Asp Asn Glu Trp Asn Leu Lys Leu
340 345 350
Gly Glu Leu Ala Met Ile Trp Arg Glu Gly Cys Ile Ile Arg Ala Gln
355 360 365
Phe Leu Gln Lys Ile Lys Asp Ala Tyr Asp Asn Asn Glu Asn Leu Gln
370 375 380
Asn Leu Leu Leu Asp Pro Tyr Phe Lys Asn Ile Val Met Glu Tyr Gln
385 390 395 400
Asp Ala Leu Arg Glu Val Val Ala Thr Ser Val Tyr Asn Gly Val Pro
405 410 415
Thr Pro Gly Phe Ser Ala Ser Ile Asn Tyr Tyr Asp Ser Tyr Arg Ser
420 425 430
Glu Asp Leu Pro Ala Asn Leu Ile Gln Ala Gln Arg Asp Tyr Phe Gly
435 440 445
Ala His Thr Tyr Glu Arg Lys Asp Arg Glu Gly Ile Phe His Thr Gln
450 455 460
Trp Val Glu Glu
465
<210>22
<211>262
<212>PRT
<213>表皮葡萄球菌
<400>22
Met Lys Arg Leu Leu Leu Cys Ile Val Ala Leu Val Phe Val Leu Ala
1 5 10 15
Ala Cys Gly Asn Asn Ser Ser Asn Asn Lys Asp Asn Gln Ser Ser Ser
20 25 30
Lys Asp Lys Asp Thr Leu Arg Val Gly Thr Glu Gly Thr Tyr Ala Pro
35 40 45
Phe Thr Tyr His Asn Lys Lys Asp Gln Leu Thr Gly Tyr Asp Ile Asp
50 55 60
Val Ile Lys Ala Val Ala Lys Glu Glu Asn Leu Lys Leu Lys Phe Asn
65 70 75 80
Glu Thr Ser Trp Asp Ser Met Phe Ala Gly Leu Asp Ala Gly Arg Phe
85 90 95
Asp Val Ile Ala Asn Gln Val Gly Val Asn Lys Asp Arg Glu Lys Lys
100 105 110
Tyr Lys Phe Ser Glu Pro Tyr Thr Tyr Ser Ser Ala Val Leu Val Val
115 120 125
Arg Glu Asn Glu Lys Asp Ile Thr Ser Phe Asn Asp Val Lys Gly Lys
130 135 140
Lys Leu Ala Gln Thr Phe Thr Ser Asn Tyr Gly Gln Leu Ala Lys Asp
145 150 155 160
Lys Gly Ala Asp Ile Thr Lys Val Asp Gly Phe Asn Gln Ser Met Asp
165 170 175
Leu Leu Leu Ser Lys Arg Val Asp Gly Thr Phe Asn Asp Ser Leu Ser
180 185 190
Tyr Leu Asp Tyr Arg Lys Gln Lys Pro Asn Ala Lys Ile Lys Ala Ile
195 200 205
Lys Gly His Ala Glu Gln Asn Lys Ser Ala Phe Ala Phe Ser Lys Lys
210 215 220
Val Asp Glu Lys Thr Ile GluLys Phe Asn Lys Gly Leu Glu Lys Ile
225 230 235 240
Arg Asp Asn Gly Glu Leu Ala Lys Ile Gly Lys Lys Trp Phe Gly Gln
245 250 255
Asp Val Ser Lys Pro Glu
260
<210>23
<211>310
<212>PRT
<213>表皮葡萄球菌
<400>23
Val Tyr Met Thr Lys Tyr Val Leu Lys Arg Leu Cys Tyr Met Phe Val
1 5 10 15
Ser Leu Phe Ile Val Ile Thr Ile Thr Phe Phe Leu Met Lys Leu Met
20 25 30
Pro Gly Ser Pro Phe Asn Asp Thr Lys Leu Asn Ala Gln Gln Lys Glu
35 40 45
Ile Leu Asn Glu Lys Tyr Gly Leu Asn Asp Pro Val Ala Leu Gln Tyr
50 55 60
Val Asn Tyr Leu Lys Asn Val Val Thr Gly Asp Phe Gly Asn Ser Phe
65 70 75 80
Gln Tyr His Asn Met Pro Val Trp Asp Leu Val Lys Pro Arg Leu Ile
85 90 95
Pro Ser Met Glu Met Gly Ile Thr Ala Met Val Ile Gly Val Val Leu
100 105 110
Gly Leu Val Leu Gly Val Ala Ala Ala Thr Lys Gln Asn Thr Trp Val
115 120 125
Asp Tyr Thr Thr Thr Ile Ile Ser Val Ile Ala Val Ser Val Pro Ser
130 135 140
Phe Val Leu Ala Val Leu Leu Gln Tyr Val Phe Ala Val Lys Leu Glu
145 150 155 160
Trp Phe Pro Val Ala Gly Trp Glu Gly Phe Ser Thr Ala Ile Leu Pro
165 170 175
Ser Leu Ala Leu Ser Ala Thr Val Leu Ala Thr Val Ala Arg Tyr Ile
180 185 190
Arg Ala Glu Met Ile Glu Val Leu Ser Ser Asp Tyr Ile Leu Leu Ala
195 200 205
Arg Ala Lys Gly Asn Ser Thr Leu Lys Val Leu Phe Gly His Ala Leu
210 215 220
Arg Asn Ala Leu Ile Pro Ile Ile Thr Ile Ile Val Pro Met Leu Ala
225 230 235 240
Gly Ile Leu Thr Gly Thr Leu Thr Ile Glu Asn Ile Phe Gly Val Pro
245 250 255
Gly Leu Gly Asp Gln Phe Val Arg Ser Ile Thr Thr Asn Asp Phe Ser
260 265 270
Val Ile Met Ala Thr Thr Ile Leu Phe Ser Thr Leu Phe Ile Val Ser
275 280 285
Ile Phe Ile Val Asp Ile Leu Tyr Gly Val Ile Asp Pro Arg Ile Arg
290 295 300
Val Gln Gly Gly Lys Lys
305 310
<210>24
<211>514
<212>PRT
<213>表皮葡萄球菌
<400>24
Val Asn Glu Glu Gln Arg Lys Ala Gly Thr Ile Asn Ile Leu Ala Glu
1 5 10 15
Arg Asp Arg Lys Ala Glu Lys Asp Tyr Ser Lys Tyr Phe Glu Gln Val
20 25 30
Tyr Gln Pro Pro Ser Leu Lys Glu Ala Lys Lys Arg Gly Lys Gln Glu
35 40 45
Val Gln Tyr Asn Arg Asp Phe His Ile Asp Glu Lys Tyr Lys Gly Met
50 55 60
Gly Lys Gly Arg Thr Phe Leu Ile Lys Thr Tyr Gly Cys Gln Met Asn
65 70 75 80
Ala His Asp Thr Glu Val Met Ala Gly Ile Leu Asn Ala Leu Gly Tyr
85 90 95
Ser Ala Thr Ser Asp Ile Asn Glu Ala Asp Val Ile Leu Ile Asn Thr
100 105 110
Cys Ala Ile Arg Glu Asn Ala Glu Asn Lys Val Phe Ser Glu Ile Gly
115 120 125
Asn Leu Lys His Leu Lys Lys Glu Arg Pro Asp Cys Leu Ile Gly Val
130 135 140
Cys Gly Cys Met Ser Gln Glu Glu Ser Val Val Asn Lys Ile Leu Lys
145 150 155 160
Ser Tyr Gln Asn Val Asp Met Val Phe Gly Thr His Asn Ile His His
165 170 175
Leu Pro Glu Ile Leu Glu Glu Ala Tyr Leu Ser Lys Ala Met Val Val
180 185 190
Glu Val Trp Ser Lys Glu Gly Asp Ile Ile Glu Asn Leu Pro Lys Val
195 200 205
Arg Asp Gly His Ile Lys Ala Trp Val Asn Ile Met Tyr Gly Cys Asp
210 215 220
Lys Phe Cys Thr Tyr Cys Ile Val Pro Phe Thr Arg Gly Lys Glu Arg
225 230 235 240
Ser Arg Arg Pro Glu Asp Ile Ile Asp Glu Val Arg Glu Leu Ala Arg
245 250 255
Glu Gly Tyr Gln Glu Ile Thr Leu Leu Gly Gln Asn Val Asn Ser Tyr
260 265 270
Gly Lys Asp Ile Glu Gly Leu Asp Tyr Glu Leu Gly Asp Leu Leu Glu
275 280 285
Asp Ile Ser Lys Ile Asp Ile Pro Arg Val Arg Phe Thr Thr Ser His
290 295 300
Pro Trp Asp Phe Thr Asp Arg Met Ile Glu Val Ile Ala Lys Gly Gly
305 310 315 320
Asn Ile Val Pro His Ile His Leu Pro Val Gln Ser Gly Asn Asn Gln
325 330 335
Val Leu Lys Ile Met Gly Arg Lys Tyr Thr Arg Glu Ser Tyr Leu Asp
340 345 350
Leu Val Ser Arg Ile Lys Glu Ala Ile Pro Asn Val Ala Leu Thr Thr
355 360 365
Asp Ile Ile Val Gly Tyr Pro Asn Glu Thr Val Glu Gln Phe Glu Glu
370 375 380
Thr Leu Ser Leu Tyr Asp Asp Val Gln Phe Glu His Ala Tyr Thr Tyr
385 390 395 400
Leu Tyr Ser Gln Arg Asp Gly Thr Pro Ala Ala Lys Met Lys Asp Asn
405 410 415
Val Pro Leu Glu Val Lys Lys Glu Arg Leu Gln Arg Leu Asn Lys Lys
420 425 430
Val Gly Ile Tyr Ser Gln Gln Ala Met Ser Gln Tyr Glu Gly Lys Ile
435 440 445
Val Thr Val Leu Cys Glu Gly Ser Ser Lys Lys Asp GluAsn Val Leu
450 455 460
Ala Gly Tyr Thr Asp Lys Asn Lys Leu Val Asn Phe Lys Gly Pro Arg
465 470 475 480
Glu Ser Ile Gly Lys Leu Val Asp Val Lys Ile Asp Glu Ala Lys Gln
485 490 495
Tyr Ser Leu Asn Gly Thr Phe Ile Gln Glu His Gln Arg Ser Met Val
500 505 510
Thr Gln
<210>25
<211>394
<212>PRT
<213>表皮葡萄球菌
<400>25
Met Ser Arg Ile Val Leu Ala Glu Ala Tyr Arg Thr Pro Ile Gly Val
1 5 10 15
Phe Gly Gly Val Phe Lys Asp Ile Pro Ala Tyr Glu Leu Gly Ala Thr
20 25 30
Val Ile Arg Gln Ile Leu Glu His 5er Gln Ile Asp Pro Asn Glu Ile
35 40 45
Asn Glu Val Ile Leu Gly Asn Val Leu Gln Ala Gly Gln Gly Gln Asn
50 55 60
Pro Ala Arg Ile Ala Ala Ile His Gly Gly Val Pro Glu Ala Val Pro
65 70 75 80
Ser Phe Thr Val Asn Lys Val Cys Gly Ser Gly Leu Lys Ala Ile Gln
85 90 95
Leu Ala Tyr Gln Ser Ile Val Ala Gly Asp Asn Glu Ile Val Ile Ala
100 105 110
Gly Gly Met Glu Ser Met Ser Gln Ser Pro Met Leu Leu Lys Asn Ser
115 120 125
Arg Phe Gly Phe Lys Met Gly Asn Gln Thr Leu Glu Asp Ser Met Ile
130 135 140
Ala Asp Gly Leu Thr Asp Lys Phe Asn Asp Tyr His Met Gly Ile Thr
145 150 155 160
Ala Glu Asn Leu Val Glu Gln Tyr Gln Ile Ser Arg Lys Glu Gln Asp
165 170 175
Gln Phe Ala Phe Asp Ser Gln Gln Lys Ala Ser Arg Ala Gln Gln Ala
180 185 190
Gly Val Phe Asp Ala Glu Ile Val Pro Val Glu Val Pro Gln Arg Lys
195 200 205
Gly Asp Pro Leu Ile Ile Ser Gln Asp Glu Gly Ile Arg Pro Gln Thr
210 215 220
Thr Ile Asp Lys Leu Ala Gln Leu Arg Pro Ala Phe Lys Lys Asp Gly
225 230 235 240
Ser Val Thr Ala Gly Asn Ala Ser Gly Ile Asn Asp Gly Ala Ala Ala
245 250 255
Met Leu Val Met Thr Glu Asp Lys Ala Lys Ala Leu Gly Leu Gln Pro
260 265 270
Ile Ala Val Leu Asp Ser Phe Gly Ala Ser Gly Val Ala Pro Ser Ile
275 280 285
Met Gly Ile Gly Pro Val Glu Ala Ile His Lys Ala Leu Lys Arg Ser
290 295 300
Asn Lys Val Ile Asn Asp Val Asp Ile Phe Glu Leu Asn Glu Ala Phe
305 310 315 320
Ala Ala Gln Ser Ile Ala Val Asn Arg Glu Leu Gln Leu Pro Gln Asp
325 330 335
Lys Val Asn Val Asn Gly Gly Ala Ile Ala Leu Gly His Pro Ile Gly
340 345 350
Ala Ser Gly Ala Arg Thr Leu Val Ser Leu Leu His Gln Leu Ser Asp
355 360 365
Ala Lys Pro Thr Gly Val Ala Ser Leu Cys Ile Gly Gly Gly Gln Gly
370 375 380
Ile Ala Thr Val Val Ser Lys Tyr Glu Val
385 390
<210>26
<211>292
<212>PRT
<213>表皮葡萄球菌
<400>26
Met Ala Ile Ser Ala Lys Leu Val Lys Glu Leu Arg Glu Lys Thr Gly
1 5 10 15
Ala Gly Met Met Asp Cys Lys Lys Ala Leu Thr Glu Thr Asp Gly Asp
20 25 30
Ile Asp Lys Ala Ile Asp Tyr Leu Arg Glu Lys Gly Ile Ala Lys Ala
35 40 45
Ala Lys Lys Ala Asp Arg Ile Ala Ala Glu Gly Leu Val His Val Glu
50 55 60
Val Lys Asp Asn Glu Ala Ala Ile Val Glu Ile Asn Ser Glu Thr Asp
65 70 75 80
Phe Val Ala Arg Asn Glu Gly Phe Gln Glu Leu Val Lys Glu Ile Ala
85 90 95
Asn His Ile Leu Asp Ser Lys Val Glu Thr Val Asp Ala Leu Met Glu
100 105 110
Ser Lys Leu Ser Ser Gly Lys Thr Val Asp Glu Arg Met Lys Glu Ala
115 120 125
Ile Ser Thr Ile Gly Glu Lys Leu ser Ile Arg Arg Phe ser Ile Arg
130 135 140
Thr Lys Thr Asp Asn Asp Ala Phe Gly Ala Tyr Leu His Met Gly Gly
145 150 155 160
Arg Ile Gly Val Leu Thr Val Val Glu Gly Thr Thr Asp Glu Glu Ala
165 170 175
Ala Lys Asp Val Ala Met His Ile Ala Ala Ile Asn Pro Lys Tyr Val
180 185 190
Ser Ser Glu Gln Val 5er Glu Glu Glu Ile Asn His Glu Arg Glu Val
195 200 205
Leu Lys Gln Gln Ala Leu Asn Glu Gly Lys Pro Glu Lys Ile Val Glu
210 215 220
Lys Met Val Glu Gly Arg Leu Arg Lys Tyr Leu Gln Glu Ile Cys Ala
225 230 235 240
Val Asp Gln Asn Phe Val Lys Asn Pro Asp Glu Thr Val Glu Ala Phe
245 250 255
Leu Lys Ala Lys Gly Gly Lys Leu Thr Asp Phe Val Arg Tyr Glu Val
260 265 270
Gly Glu Gly Met Glu Lys Arg Glu Glu Asn Phe Ala Glu Glu Val Lys
275 280 285
Gly Gln Met Lys
290
<210>27
<211>310
<212>PRT
<213>表皮葡萄球菌
<400>27
Met Thr Glu Val Asp Phe Asp Val Ala Ile Ile Gly Ala Gly Pro Ala
1 5 10 15
Gly Met Thr Ala Ala Val Tyr Ala Ser Arg Ala Asn Leu Lys Thr Val
20 25 30
Met Ile Glu Arg Gly Met Pro Gly Gly Gln Met Ala Asn Thr Glu Glu
35 40 45
Val Glu Asn Phe Pro Gly Phe Glu Met Ile Thr Gly Pro Asp Leu Ser
50 55 60
Thr Lys Met Phe Glu His Ala Lys Lys Phe Gly Ala Glu Tyr Gln Tyr
65 70 75 80
Gly Asp Ile Lys Ser Val Glu Asp Lys Gly Asp Tyr Lys Val Ile Asn
85 90 95
Leu Gly Asn Lys Glu Ile Thr Ala His Ala Val Ile Ile Ser Thr Gly
100 105 110
Ala Glu Tyr Lys Lys Ile Gly Val Pro Gly Glu Gln Glu Leu Gly Gly
115 120 125
Arg Gly Val Ser Tyr Cys Ala Val Cys Asp Gly Ala Phe Phe Lys Asn
130 135 140
Lys Arg Leu Phe Val Ile Gly Gly Gly Asp Ser Ala Val Glu Glu Gly
145 150 155 160
Thr Phe Leu Thr Lys Phe Ala Asp Lys Val Thr Ile Val His Arg Arg
165 170 175
Asp Glu Leu Arg Ala Gln Asn Ile Leu Gln Glu Arg Ala Phe Lys Asn
180 185 190
Asp Lys Val Asp Phe Ile Trp Ser His Thr Leu Lys Thr Ile Asn Glu
195 200 205
Lys Asp Gly Lys Val Gly Ser Val Thr Leu Glu Ser Thr Lys Asp Gly
210 215 220
Ala Glu Gln Thr Tyr Asp Ala Asp Gly Val Phe Ile Tyr Ile Gly Met
225 230 235 240
Lys Pro Leu Thr Ala Pro Phe Lys Asn Leu Gly Ile Thr Asn Asp Ala
245 250 255
Gly Tyr Ile Val Thr Gln Asp Asp Met Ser Thr Lys Val Arg Gly Ile
260 265 270
Phe Ala Ala Gly Asp Val Arg Asp Lys Gly Leu Arg Gln Ile Val Thr
275 280 285
Ala Thr Gly Asp Gly Ser Ile Ala Ala Gln Ser Ala Ala Asp Tyr Ile
290 295 300
Thr Glu Leu Lys Asp Asn
305 310
<210>28
<211>465
<212>PRT
<213>表皮葡萄球菌
<400>28
Met Thr Gln Lys Tyr Arg Tyr Pro Thr Phe Leu Glu Ser Ile Ser Thr
1 5 10 15
Ile Leu Val Met Val Val Val Val Val Ile Gly Phe Val Phe Phe Asn
20 25 30
Val Pro Ile Gln Ile Leu Leu Leu Ile Ser Ser Ala Tyr Ala Ala Leu
35 40 45
Ile Ala His Arg Val Gly Leu Lys Trp Lys Asp Leu Glu Glu Gly Ile
50 55 60
Thr His Arg Leu Ser Thr Ala Met Pro Ala Ile Phe Ile Ile Leu Ala
65 70 75 80
Val Gly Ile Ile Val Gly Ser Trp Met Tyr Ser Gly Thr Val Pro Ala
85 90 95
Leu Ile Tyr Tyr Gly Leu Lys Phe Leu Asn Pro Ser Tyr Leu Leu Val
100 105 110
Ser Ala Phe Ile Ile Ser Ala Met Thr Ser Ile Ala Thr Gly Thr Ala
115 120 125
Trp Gly Ser Ala Ser Thr Ala Gly Ile Ala Leu Ile Ser Ile Ala Asn
130 135 140
Gln Leu Gly Val Pro Ala Gly Met Ala Ala Gly Ala Ile Ile Ala Gly
145 150 155 160
Ala Val Phe Gly Asp Lys Met Ser Pro Leu Ser Asp Thr Thr Asn Leu
165 170 175
Ala Ala Leu Val Thr Lys Val Asn Ile Phe Ala His Ile Lys Ser Met
180 185 190
Met Trp Thr Thr Ile Pro Ala Ser Ile Ile Gly Leu Ala Ile Trp Phe
195 200 205
Ile Val Gly Leu Gln Tyr Lys Gly Asp Ala Asn Thr Gln Gln Ile Gln
210 215 220
Asn Leu Leu Lys Glu Leu Thr Thr Ile Tyr Asn Leu Asn Phe Trp Val
225 230 235 240
Trp Ile Pro Leu Ile Ile Ile Val Leu Cys Leu Ile Phe Arg Ile Ser
245 250 255
Thr Val Pro Ser Met Leu Ile Ser Ser Ile Ser Ala Leu Val Ile Gly
260 265 270
Thr Phe Asp His Gln Phe Asn Met Lys Asp Gly Phe Lys Ala Ser Phe
275 280 285
Asp Gly Phe Asn His Thr Met Leu His Gln Ser His Ile Ser Asp Asn
290 295 300
Ala Lys Thr Leu Ile Glu Gln Gly Gly Met Met Ser Met Thr Gln Ile
305 310 315 320
Ile Val Thr Ile Phe Cys Gly Tyr Ala Phe Ala Gly Ile Val Glu Lys
325 330 335
Ala Gly Cys Leu Asp Val Ile Leu Glu Thr Ile Ala Lys Gly Val Lys
340 345 350
Ser Val Gly Thr Leu Ile Leu Ile Thr Val Val Cys Ser Ile Met Leu
355 360 365
Val Phe Ala Ala Gly Val Ala Ser Ile Val Ile Ile Met Val Gly Val
370 375 380
Leu Met Lys Asp Met Phe Glu Lys Met Asn Val Ser Lys Ser Val Leu
385 390 395 400
Ser Arg Thr Leu Glu Asp Ser Ser Thr Met Val Leu Pro Leu Ile Pro
405 410 415
Trp Gly Thr Ser Gly Ile Tyr Tyr Ala His Gln Leu Asn Val Ser Val
420 425 430
Asp Gln Phe Phe Ile Trp Ala Ile Pro Cys Tyr Leu Cys Ala Phe Ile
435 440 445
Ala Ile Ile Tyr Gly Phe Thr Gly Ile Gly Ile Lys Lys Ile Ser Arg
450 455 460
Lys
465
<210>29
<211>235
<212>PRT
<213>表皮葡萄球菌
<400>29
Met Lys Lys Thr Val Ile Ala Ser Thr Leu Ala Val SerLeu Gly Ile
1 5 10 15
Ala Gly Tyr Gly Leu Ser Gly His Glu Ala His Ala Ser Glu Thr Thr
20 25 30
Asn Val Asp Lys Ala His Leu Val Asp Leu Ala Gln His Asn Pro Glu
35 40 45
Glu Leu Asn Ala Lys Pro Val Gln Ala Gly Ala Tyr Asp Ile His Phe
50 55 60
Val Asp Asn Gly Tyr Gln Tyr Asn Phe Thr Ser Asn Gly Ser Glu Trp
65 70 75 80
Ser Trp Ser Tyr Ala Val Ala Gly Ser Asp Ala Asp Tyr Thr Glu Ser
85 90 95
Ser Ser Asn Gln Glu Val Ser Ala Asn Thr Gln Ser Ser Asn Thr Asn
100 105 110
Val Gln Ala Val Ser Ala Pro Thr Ser Ser Glu Ser Arg Ser Tyr Ser
115 120 125
Thr Ser Thr Thr Ser Tyr Ser Ala Pro Ser His Asn Tyr Ser Ser His
130 135 140
Ser Ser Ser Val Arg Leu Ser Asn Gly Asn Thr Ala Gly Ser Val Gly
145 150 155 160
Ser Tyr Ala Ala Ala Gln Met Ala Ala Arg Thr Gly Val Ser Ala Ser
165 170 175
Thr Trp Glu His Ile Ile Ala Arg Glu Ser Asn Gly Gln Leu His Ala
180 185 190
Arg Asn Ala Ser Gly Ala Ala Gly Leu Phe Gln Thr Met Pro Gly Trp
195 200 205
Gly Ser Thr Gly Ser Val Asn Asp Gln Ile Asn Ala Ala Tyr Lys Ala
210 215 220
Tyr Lys Ala Gln Gly Leu Ser Ala Trp Gly Met
225 230 235
<210>30
<211>296
<212>PRT
<213>表皮葡萄球菌
<400>30
Met Asn Lys Glu Gln Leu Glu Lys Met Thr His Gly Lys Gly Phe Ile
1 5 10 15
Ala Ala Leu Asp Gln Ser Gly Gly Ser Thr Pro Lys Ala Leu Lys Glu
20 25 30
Tyr Gly Val Asn Glu Asp Gln Tyr Ser Asn Glu Asp Glu Met Phe Gln
35 40 45
Leu Val His Asp Met Arg Thr Arg Val Val Thr Ser Pro Ser Phe Ser
50 55 60
Pro Asp Lys Ile Leu Gly Ala Ile Leu Phe Glu Gln Thr Met Asp Arg
65 70 75 80
Glu Val Glu Gly Lys Tyr Thr Gly Asp Tyr Leu Ala Asp Lys Gly Val
85 90 95
Val Pro Phe Leu Lys Val Asp Lys Gly Leu Ala Glu Glu Lys Asn Gly
100 105 110
Val Gln Leu Met Lys Pro Ile Asp Asp Leu Asp Glu Thr Leu Asp Arg
115 120 125
Ala Asn Glu Arg His Ile Phe Gly Thr Lys Met Arg Ser Asn Ile Leu
130 135 140
Glu Leu Asn Glu Gln Gly Ile Lys Asp Val Val Glu Gln Gln Phe Glu
145 150 155 160
Phe Ala Lys Lys Ile Ile Ala Lys Gly Leu Val Pro Ile Ile Glu Pro
165 170 175
Glu Val Asn Ile Asn Ala Lys Asp Lys Ser Glu Ile Glu Lys Val Leu
180 185 190
Lys Ala Glu Ile Lys Lys Gly Leu Asp Ser Leu Asn Asp Asp Gln Leu
195 200 205
Val Met Leu Lys Leu Thr Ile Pro Thr Glu Ala Asn Leu Tyr Lys Asp
210 215 220
Leu Ala Asp His Pro Asn Val Val Arg Val Val Val Leu Ser Gly Gly
225 230 235 240
Tyr Ser Arg Asp Glu Ala Asn Lys Leu Leu Lys Asp Asn Asp Glu Leu
245 250 255
Ile Ala Ser Phe Ser Arg Ala Leu Ala Ser Asp Leu Arg Ala Ser Gln
260 265 270
Ser Gln Glu Glu Phe Asp Lys Ala Leu Gly Asp Ala Val Asp Ser Ile
275 280 285
Tyr Asp Ala Ser Val Asn Lys Asn
290 295
<210>31
<211>263
<212>PRT
<213>表皮葡萄球菌
<400>31
Leu Lys Glu Arg Phe Ile Lys Lys Thr His Tyr Leu Asp Tyr Gln Phe
1 5 10 15
Asp Glu Pro Thr Asp Ile Lys Leu Gly Phe Thr Thr Arg Glu Asn Gly
20 25 30
Leu Ser Pro Tyr Pro Asn His Ser Phe Asn Met Ala Arg Tyr Ile Ser
35 40 45
Asp Ser Ala His His Ile Thr His His Gln Asp Ile Leu Ala Asn Leu
50 55 60
Ile Gly Tyr Pro Arg Asp Glu Trp Val Phe Pro Ile Gln Thr His Asp
65 70 75 80
Ser Arg Ile Val Glu Val Thr Ser Glu His Lys Gly Thr Asn Ile Asp
85 90 95
Glu Leu Thr Asp Asp Leu His Gly Ile Asp Gly Met Tyr Thr Phe Asp
100 105 110
Ser His Ile Leu Leu Thr Met Cys Tyr Ala Asp Cys Val Pro Val Tyr
115 120 125
Phe Tyr Ser Glu Pro His Gly Tyr Ile Gly Leu Ala His Ala Gly Trp
130 135 140
Arg Gly Thr Tyr Gly Gln Ile Val Lys Asp Met Leu Lys Lys Val Asp
145 150 155 160
Phe Asp Tyr Glu Asp Leu Lys Ile Val Ile Gly Pro Ala Thr Ser Asn
165 170 175
Ser Tyr Glu Ile Asn Asp Asp Ile Lys Asn Lys Phe Glu Glu Leu Thr
180 185 190
Ile Asp Ser Thr Leu Tyr Ile Glu Thr Arg Gly Lys Asn Gln His Gly
195 200 205
Ile Asp Leu Lys Asn Ala Asn Ala Leu Leu Leu Glu Glu Ala Gly Val
210 215 220
Pro Ser Lys Asn Ile Tyr Val Thr Glu Tyr Ala Ihr Ser Glu Asn Leu
225 230 235 240
Asp Leu Phe Phe Ser Tyr Arg Val Glu Lys Gly Gln Thr Gly Arg Met
245 250 255
Leu Ala Phe Ile Gly Arg Lys
260
<210>32
<211>10203
<212>PRT
<213>表皮葡萄球菌
<400>32
Met Lys Ser Lys Pro Lys Leu Asn Gly Arg Asn Ile Cys Ser Phe Leu
1 5 10 15
Leu Ser Lys Cys Met Ser Tyr Ser Leu Ser Lys Leu Ser Thr Leu Lys
20 25 30
Thr Tyr Asn Phe Gln Ile Thr Ser Asn Asn Lys Glu Lys Thr Ser Arg
35 40 45
Ile Gly Val Ala Ile Ala Leu Asn Asn Arg Asp Lys Leu Gln Lys Phe
50 55 60
Ser Ile Arg Lys Tyr Ala Ile Gly Thr Phe Ser Thr Val Ile Ala Thr
65 70 75 80
Leu Val Phe Met Gly Ile Asn Thr Asn His Ala Ser Ala Asp Glu Leu
85 90 95
Asn Gln Asn Gln Lys Leu Ile Lys Gln Leu Asn Gln Thr Asp Asp Asp
100 105 110
Asp Ser Asn Thr His Ser Gln Glu Ile Glu Asn Asn Lys Gln Asn Ser
115 120 125
Ser Gly Gln Thr Glu Ser Leu Arg Ser Ser Thr Ser Gln Asn Gln Ala
130 135 140
Asn Ala Arg Leu Ser Asp Gln Phe Lys Asp Thr Asn Glu Thr Ser Gln
145 150 155 160
Gln Leu Pro Thr Asn Val Ser Asp Asp Ser Ile Asn Gln Ser His Ser
165 170 175
Glu Ala Asn Met Asn Asn Glu Pro Leu Lys Val Asp Asn Ser Thr Met
180 185 190
Gln Ala His Ser Lys Ile Val Ser Asp Ser Asp Gly Asn Ala Ser Glu
195 200 205
Asn Lys His His Lys Leu Thr Glu Asn Val Leu Ala Glu Ser Arg Ala
210 215 220
Ser Lys Asn Asp Lys Glu Lys Glu Asn Leu Gln Glu Lys Asp Lys Ser
225 230 235 240
Gln Gln Val His Pro Pro Leu Asp Lys Asn Ala Leu Gln Ala Phe Phe
245 250 255
Asp Ala Ser Tyr His Asn Tyr Arg Met Ile Asp Arg Asp Arg Ala Asp
260 265 270
Ala Thr Glu Tyr Gln Lys Val Lys Ser Thr Phe Asp Tyr Val Asn Asp
275 280 285
Leu Leu Gly Asn Asn Gln Asn Ile Pro Ser Glu Gln Leu Val Ser Ala
290 295 300
Tyr Gln Gln Leu Glu Lys Ala Leu Glu Leu Ala Arg Thr Leu Ser Gln
305 310 315 320
Arg Ser Thr Thr Glu Lys Arg Gly Arg Arg Ser Thr Arg Ser Val Val
325 330 335
Glu Asn Arg Ser Ser Arg Ser Asp Tyr Leu Asp Ala Arg Thr Glu Tyr
340 345 350
Tyr Val Ser Lys Asp Asp Asp Asp Ser Gly Phe Pro Pro Gly Thr Phe
355 360 365
Phe His Ala Ser Asn Arg Arg Trp Pro Tyr Asn Leu Pro Arg Ser Arg
370 375 380
Asn Ile Leu Arg Ala 5er Asp Val Gln Gly Asn Ala Tyr Ile Thr Thr
385 390 395 400
Lys Arg Leu Lys Asp Gly Tyr Gln Trp Asp Ile Leu Phe Asn Ser Asn
405 410 415
His Lys Gly His Glu Tyr Met Tyr Tyr Trp Phe Gly Leu Pro Ser Asp
420 425 430
Gln Thr Pro Thr Gly Pro Val Thr Phe Thr Ile Ile Asn Arg Asp Gly
435 440 445
Ser Ser Thr Ser Thr Gly Gly val Gly Phe Gly Ser Gly Ala Pro Leu
450 455 460
Pro Gln Phe Trp Arg Ser Ala Gly Ala Ile Asn Ser Ser Val Ala Asn
465 470 475 480
Asp Phe Lys His Gly Ser Ala Thr Asn Tyr Ala Phe Tyr Asp Gly Val
485 490 495
Asn Asn Phe Ser Asp Phe Ala Arg Gly Gly Glu Leu Tyr Phe Asp Arg
500 505 510
Glu Gly Ala Thr Gln Thr Asn Lys Tyr Tyr Gly Asp Glu Asn Phe Ala
515 520 525
Leu Leu Asn Ser Glu Lys Pro Asp Gln Ile Arg Gly Leu Asp Thr Ile
530 535 540
Tyr Ser Phe Lys Gly Ser Gly Asp Val Ser Tyr Arg Ile Ser Phe Lys
545 550 555 560
Thr Gln Gly Ala Pro Thr Ala Arg Leu Tyr Tyr Ala Ala Gly Ala Arg
565 570 575
Ser Gly Glu Tyr Arg Gln Ala Thr Asn Tyr Asn Gln Leu Tyr Val Glu
580 585 590
Pro Tyr Lys Asn Tyr Arg Asn Arg Val Gln Ser Asn Val Gl nVal Lys
595 600 605
Asn Arg Thr Leu His Leu Lys Arg Thr Ile Arg Gln Phe Asp Pro Thr
610 615 620
Leu Gln Arg Thr Thr Asp Val Pro Ile Leu Asp Ser Asp Gly Ser Gly
625 630 635 640
Ser Ile Asp Ser Val Tyr Asp Pro Leu Ser Tyr Val Lys Asn Val Thr
645 650 655
Gly Thr Val Leu Gly Ile Tyr Pro Ser Tyr Leu Pro Tyr Asn Gln Glu
660 665 670
Arg Trp Gln Gly Ala Asn Ala Met Asn Ala Tyr Gln Ile Glu Glu Leu
675 680 685
Phe Ser Gln Glu Asn Leu Gln Asn Ala Ala Arg Ser Gly Arg Pro Ile
690 695 700
Gln Phe Leu Val Gly Phe Asp Val Glu Asp Ser His His Asn Pro Glu
705 710 715 720
Thr Leu Leu Pro Val Asn Leu Tyr Val Lys Pro Glu Leu Lys His Thr
725 730 735
Ile Glu Leu Tyr His Asp Asn Glu Lys Gln Asn Arg Lys Glu Phe Ser
740 745 750
Val Ser Lys Arg Ala Gly His Gly Val Phe Gln Ile Met Ser Gly Thr
755 760 765
Leu His Asn Thr Val Gly Ser Gly Ile Leu Pro Tyr Gln Gln Glu Ile
770 775 780
Arg Ile Lys Leu Thr Ser Asn Glu Pro Ile Lys Asp Ser Glu Trp Ser
785 790 795 800
Ile Thr Gly Tyr Pro Asn Thr Leu Thr Leu Gln Asn Ala Val Gly Arg
805 810 815
Thr Asn Asn Ala Thr Glu Lys Asn Leu Ala Leu Val Gly His Ile Asp
820 825 830
Pro Gly Asn Tyr Phe Ile Thr Val Lys Phe Gly Asp Lys Val Glu Gln
835 840 845
Phe Glu Ile Arg Ser Lys Pro Thr Pro Pro Arg Ile Ile Thr Thr Ala
850 855 860
Asn Glu Leu Arg Gly Asn Pro Asn His Lys Pro Glu Ile Arg Val Thr
865 870 875 880
Asp Ile Pro Asn Asp Thr Thr Ala Lys Ile Lys Leu Val Met Gly Gly
885 890 895
Thr Asp Gly Asp His Asp Pro Glu Ile Asn Pro Tyr Thr Val Pro Glu
900 905 910
Asn Tyr Thr Val Val Ala Glu Ala Tyr His Asp Asn Asp Pro Ser Lys
915 920 925
Asn Gly Val Leu Thr Phe Arg Ser Ser Asp Tyr Leu Lys Asp Leu Pro
930 935 940
Leu Ser Gly Glu Leu Lys Ala Ile Val Tyr Tyr Asn Gln Tyr Val Gln
945 950 955 960
Ser Asn Phe Ser Asn Ser Val Pro Phe Ser Ser Asp Thr Thr Pro Pro
965 970 975
Thr Ile Asn Glu Pro Ala Gly Leu Val His Lys Tyr Tyr Arg Gly Asp
980 985 990
His Val Glu Ile Thr Leu Pro Val Thr Asp Asn Thr Gly Gly Ser Gly
995 1000 1005
Leu Arg Asp Val Asn Val Asn Leu Pro Gln Gly Trp Thr Lys Thr
1010 1015 1020
Phe Thr Ile Asn Pro Asn Asn Asn Thr Glu Gly Thr Leu Lys Leu
1025 1030 1035
Ile Gly Asn Ile Pro Ser Asn Glu Ala Tyr Asn Thr Thr Tyr His
1040 1045 1050
Phe Asn Ile Thr Ala Thr Asp Asn Ser Gly Asn Thr Thr Asn Pro
1055 1060 1065
Ala Lys Thr Phe Ile Leu Asn Val Gly Lys Leu Ala Asp Asp Leu
1070 1075 1080
Asn Pro Val Gly Leu Ser Arg Asp Gln Leu Gln Leu Val Thr Asp
1085 1090 1095
Pro Ser Ser Leu Ser Asn Ser Glu Arg Glu Glu Val Lys Arg Lys
1100 1105 1110
Ile Ser Glu Ala Asn Ala Asn Ile Arg Ser Tyr Leu Leu Gln Asn
1115 1120 1125
Asn Pro Ile Leu Ala Gly Val Asn Gly Asp Val Thr Phe Tyr Tyr
1130 1135 1140
Arg Asp Gly Ser Val Asp Val Ile Asp Ala Glu Asn Val Ile Thr
1145 1150 1155
Tyr Glu Pro Glu Arg Lys Ser Ile Phe Ser Glu Asn Gly Asn Thr
1160 1165 1170
Asn Lys Lys Glu Ala Val Ile Thr Ile Ala Arg Gly Gln Asn Tyr
1175 1180 1185
Thr Ile Gly Pro Asn Leu Arg Lys Tyr Phe Ser Leu Ser Asn Gly
1190 1195 1200
Ser Asp Leu Pro Asn Arg Asp Phe Thr Ser Ile Ser Ala Ile Gly
1205 1210 1215
Ser Leu Pro Ser Ser Ser Glu Ile Ser Arg Leu Asn Val Gly Asn
1220 1225 1230
Tyr Asn Tyr Arg Val Asn Ala Lys Asn Ala Tyr His Lys Thr Gln
1235 1240 1245
Gln Glu Leu Asn Leu Lys Leu Lys Ile Val Glu Val Asn Ala Pro
1250 1255 1260
Thr Gly Asn Asn Arg Val Tyr Arg Val Ser Thr Tyr Asn Leu Thr
1265 1270 1275
Asn Asp Glu Ile Asn Lys Ile Lys Gln Ala Phe Lys Ala Ala Asn
1280 1285 1290
Ser Gly Leu Asn Leu Asn Asp Asn Asp Ile Thr Val Ser Asn Asn
1295 1300 1305
Phe Asp His Arg Asn Val Ser Ser Val Thr Val Thr Ile Arg Lys
1310 1315 1320
Gly Asp Leu Ile Lys Glu Phe Ser Ser Asn Leu Asn Asn Met Asn
1325 1330 1335
Phe Leu Arg Trp Val Asn Ile Arg Asp Asp Tyr Thr Ile Ser Trp
1340 1345 1350
Thr Ser Ser Lys Ile Gln Gly Arg Asn Thr Asp Gly Gly Leu Glu
1355 1360 1365
Trp Ser Pro Asp His Lys Ser Leu Ile Tyr Lys Tyr Asp Ala Thr
1370 1375 1380
Leu Gly Arg Gln Ile Asn Thr Asn Asp Val Leu Thr Leu Leu Gln
1385 1390 1395
Ala Thr Ala Lys Asn Ser Asn Leu Arg Ser Asn Ile Asn Ser Asn
1400 1405 1410
Glu Lys Gln Leu Ala Glu Arg Gly Ser Asn Gly Tyr Ser Lys Ser
1415 1420 1425
Ile Ile Arg Asp Asp Gly Glu Lys Ser Tyr Leu Leu Asn Ser Asn
1430 1435 1440
Pro Ile Gln Val Leu Asp Leu Val Glu Pro Asp Asn Gly Tyr Gly
1445 1450 1455
Gly Arg Gln Val Ser His Ser Asn Val Ile Tyr Asn Glu Lys Asn
1460 1465 1470
Ser Ser Ile Val Asn Gly Gln Val Pro Glu Ala Asn Gly Ala Ser
1475 1480 1485
Ala Phe Asn Ile Asp Lys Val Val Lys Ala Asn Ala Ala Asn Asn
1490 1495 1500
Gly Ile Met Gly Val Ile Tyr Lys Ala Gln Leu Tyr Leu Ala Pro
1505 1510 1515
Tyr Ser Pro L ys Gly Tyr Ile Glu Lys Leu Gly Gln Asn Leu Ser
1520 1525 1530
Asn Thr Asn Asn Val Ile Asn Val Tyr Phe Val Pro Ser Asp Lys
1535 1540 1545
Val Asn Pro Ser Ile Thr Val Gly Asn Tyr Asp His His Thr Val
1550 1555 1560
Tyr Ser Gly Glu Thr Phe Lys Asn Thr Ile Asn Val Asn Asp Asn
1565 1570 1575
Tyr Gly Leu Asn Thr Val Ala Ser Thr Ser Asp Ser Ala Ile Thr
1580 1585 1590
Met Thr Arg Asn Asn Asn Glu Leu Val Gly Gln Ala Pro Asn Val
1595 1600 1605
Thr Asn Ser Thr Asn Lys Ile Val Lys Val Lys Ala Thr Asp Lys
1610 1615 1620
Ser Gly Asn Glu Ser Ile Val Ser Phe Thr Val Asn Ile Lys Pro
1625 1630 1635
Leu Asn Glu Lys Tyr Arg Ile Thr Thr Ser Ser Ser Asn Gln Thr
1640 1645 1650
Pro Val Arg Ile Ser Asn Ile Gln Asn Asn Ala Asn Leu Ser Ile
1655 1660 1665
Glu Asp Gln Asn Arg Val Lys Ser Ser Leu Ser Met Thr Lys Ile
1670 1675 1680
Leu Gly Thr Arg Asn Tyr Val Asn Glu Ser Asn Asn Asp Val Arg
1685 1690 1695
Ser Gln Val Val Ser Lys Val Asn Arg Ser Gly Asn Asn Ala Thr
1700 1705 1710
Val Asn Val Thr Thr Thr Phe Ser Asp Gly Thr Thr Asn Thr Ile
1715 1720 1725
Thr Val Pro Val Lys His Val Leu Leu Glu Val Val Pro Thr Thr
1730 1735 1740
Arg Thr Thr Val Arg Gly Gln Gln Phe Pro Thr Gly Lys Gly Thr
1745 1750 1755
Ser Pro Asn Asp Phe Phe Ser Leu Arg Thr Gly Gly Pro Val Asp
1760 1765 1770
Al a Arg Il e Val Trp Val Asn Asn Gl n Gl y Pro Asp Il e Asn Ser
1775 1780 1785
Asn Gln Ile Gly Arg Asp Leu Thr Leu His Ala Glu Ile Phe Phe
1790 1795 1800
Asp Gly Glu Thr Thr Pro Ile Arg Lys Asp Thr Thr Tyr Lys Leu
1805 1810 1815
Ser Gln Ser Ile Pro Lys Gln Ile Tyr Glu Thr Thr Ile Asn Gly
1820 1825 1830
Arg Phe Asn Ser Ser Gly Asp Ala Tyr Pro Gly Asn Phe Val Gln
1835 1840 1845
Ala Val Asn Gln Tyr Trp Pro Glu His Met Asp Phe Arg Trp Ala
1850 1855 1860
G1n Gly Ser Gly Thr Pro Ser Ser Arg Asn Ala Gly Ser Phe Thr
1865 1870 1875
Lys Thr Val Thr Val Val Tyr Gln Asn Gly Gln Thr Glu Asn Val
1880 1885 1890
Asn Val Leu Phe Lys Val Lys Pro Asn Lys Pro Val Ile Asp Ser
1895 1900 1905
Asn Ser Val Ile Ser Lys Gly Gln Leu Asn Gly Gln Gln Ile Leu
1910 1915 1920
Val Arg Asn Val Pro Gln Asn Ala Gln Val Thr Leu Tyr Gln Ser
1925 1930 1935
Asn Gly Thr Val Ile Pro Asn Thr Asn Thr Thr Ile Asp Ser Asn
1940 1945 1950
Gly Ile Ala Thr Val Thr Ile Gln Gly Thr Leu Pro Thr Gly Asn
1955 1960 1965
Ile Thr Ala Lys Thr Ser Met Thr Asn Asn Val Thr Tyr Thr Lys
1970 1975 1980
Gln Asn Ser Ser Gly Ile Ala Ser Asn Thr Thr Glu Asp Ile Ser
1985 1990 1995
Val Phe Ser Glu Asn Ser Asp Gln Val Asn Val Thr Ala Gly Met
2000 2005 2010
Gln Ala Lys Asn Asp Gly Ile Lys Ile Ile Lys Gly Thr Asn Tyr
2015 2020 2025
Asn Phe Asn Asp Phe Asn Ser Phe Ile Ser Asn Ile Pro Ala His
2030 2035 2040
Ser Thr Leu Thr Trp Asn Glu Glu Pro Asn Ser Trp Lys Asn Asn
2045 20502055
Ile Gly Thr Thr Thr Lys Thr Val Thr Val Thr Leu Pro Asn His
2060 2065 2070
Gln Gly Thr Arg Thr Val Asp Ile Pro Ile Thr Ile Tyr Pro Thr
2075 2080 2085
Val Thr Ala Lys Asn Pro Val Arg Asp Gln Lys Gly Arg Asn Leu
2090 2095 2100
Thr Asn Gly Thr Asp Val Tyr Asn Tyr Ile Ile Phe Glu Asn Asn
2105 2110 2115
Asn Arg Leu Gly Gly Thr Ala Ser Trp Lys Asp Asn Arg Gln Pro
2120 2125 2130
Asp Lys Asn Ile Ala Gly Val Gln Asn Leu Ile Ala Leu Val Asn
2135 2140 2145
Tyr Pro Gly Ile Ser Thr Pro Leu Glu Val Pro Val Lys Val Trp
2150 2155 2160
Val Tyr Asn Phe Asp Phe Thr Gln Pro Ile Tyr Lys Ile Gln Val
2165 2170 2175
Gly Asp Thr Phe Pro Lys Gly Thr Trp Ala Gly Tyr Tyr Lys His
2180 2185 2190
Leu Glu Asn Gly Glu Gly Leu Pro Ile Asp Gly Trp Lys Phe Tyr
2195 2200 2205
Trp Asn Gln Gln Ser Thr Gly Thr Thr Ser Asp Gln Trp Gln Ser
2210 2215 2220
Leu Ala Tyr Thr Arg Thr Pro Phe Val Lys Thr Gly Thr Tyr Asp
2225 2230 2235
Val Val Asn Pro Ser Asn Trp Gly Val Trp Gln Thr Ser Gln Ser
2240 2245 2250
Ala Lys Phe Ile Val Thr Asn Ala Lys Pro Asn Gln Pro Thr Ile
2255 2260 2265
Thr Gln Ser Lys Thr Gly Asp Val Thr Val Thr Pro Gly Ala Val
2270 2275 2280
Arg Asn Ile Leu Ile Ser Gly Thr Asn Asp Tyr Ile Gln Ala Ser
2285 2290 2295
Ala Asp Lys Ile Val Ile Asn Lys Asn Gly Asn Lys Leu Thr Thr
2300 2305 2310
Phe Val Lys Asn Asn Asp Gly Arg Trp Thr Val Glu Thr Gly Ser
2315 2320 2325
Pro Asp Ile Asn Gly Ile Gly Pro Thr Asn Asn Gly Thr Ala Ile
2330 2335 2340
Ser Leu Ser Arg Leu Ala Val Arg Pro Gly Asp Ser Ile Glu Ala
2345 2350 2355
Ile Ala Thr Glu Gly Ser Gly Glu Thr Ile Ser Thr Ser Ala Thr
2360 2365 2370
Ser Glu Ile Tyr Ile Val Lys Ala Pro Gln Pro Glu Gln Val Ala
2375 2380 2385
Thr His Thr Tyr Asp Asn Gly Thr Phe Asp Ile Leu Pro Asp Asn
2390 2395 2400
Ser Arg Asn Ser Leu Asn Pro Thr Glu Arg Val Glu Ile Asn Tyr
2405 2410 2415
Thr Glu Lys Leu Asn Gly Asn Glu Thr Gln Lys Ser Phe Thr Ile
2420 2425 2430
Thr Lys Asn Asn Asn Gly Lys Trp Thr Ile Asn Asn Lys Pro Asn
2435 2440 2445
Tyr Val Glu Phe Asn Gln Asp Asn Gly Lys Val Val Phe Ser Ala
2450 2455 2460
Asn Thr Ile Lys Pro Asn Ser Gln Ile Thr Ile Thr Pro Lys Ala
2465 2470 2475
Gly Gln Gly Asn Thr Glu Asn Thr Asn Pro Thr Val Ile Gln Ala
2480 2485 2490
Pro Ala Gln His Thr Leu Thr Ile Asn Glu Ile Val Lys Glu Gln
2495 2500 2505
Gly Gln Asn Val Thr Asn Asp Asp Ile Asn Asn Ala Val Gln Val
2510 2515 2520
Pro Asn Lys Asn Arg Val Ala Ile Lys Gln Gly Asn Ala Leu Pro
2525 2530 2535
Thr Asn Leu Ala Gly Gly Ser Thr Ser His Ile Pro Val Val Ile
2540 2545 2550
Tyr Tyr Ser Asp Gly Ser Ser Glu Glu Ala Thr Glu Thr Val Arg
2555 2560 2565
Thr Lys Val Asn Lys Thr Glu Leu Ile Asn Ala Arg Arg Arg Leu
2570 2575 2580
Asp Glu Glu Ile Ser Lys Glu Asn Lys Thr Pro Ser Ser Ile Arg
2585 2590 2595
Asn Phe Asp Gln Ala Met Asn Arg Ala Gln Ser Gln Ile Asn Thr
2600 2605 2610
Ala Lys Ser Asp Ala Asp Gln Val Ile Gly Thr Glu Phe Ala Thr
2615 2620 2625
Pro Gln Gln Val Asn Ser Ala Leu Ser Lys Val Gln Ala Ala Gln
2630 2635 2640
Asn Lys Ile Asn Glu Ala Lys Ala Leu Leu Gln Asn Lys Ala Asp
2645 2650 2655
Asn Ser Gln Leu Val Arg Ala Lys Glu Gln Leu Gln Gln Ser Ile
2660 2665 2670
Gln Pro Ala Ala Ser Thr Asp Gly Met Thr Gln Asp Ser Thr Arg
2675 2680 2685
Asn Tyr Lys Asn Lys Arg Gln Ala Ala Glu Gln Ala Ile Gln His
2690 2695 2700
Ala Asn Ser Val Ile Asn Asn Gly Asp Ala Thr Ser Gln Gln Ile
2705 2710 2715
Asn Asp Ala Lys Asn Thr Val Glu Gln Ala Gln Arg Asp Tyr Val
2720 2725 2730
Glu Ala Lys Ser Asn Leu Arg Ala Asp Lys Ser Gln Leu Gln Ser
2735 2740 2745
Ala Tyr Asp Thr Leu Asn Arg Asp Val Leu Thr Asn Asp Lys Lys
2750 2725 2760
Pro Ala Ser Val Arg Arg Tyr Asn Glu Ala Ile Ser Asn Ile Arg
2765 2770 2775
Lys Glu Leu Asp Thr Ala Lys Ala Asp Ala Ser Ser Thr Leu Arg
2780 2785 2790
Asn Thr Asn Pro Ser Val Glu Gln Val Arg Asp Ala Leu Asn Lys
2795 2800 2805
Ile Asn Thr Val Gln Pro Lys Val Asn Gln Ala Ile Ala Leu Leu
2810 2815 2820
Gln Pro Lys Glu Asn Asn Ser Glu Leu Val Gln Ala Lys Lys Arg
2825 2830 2835
Leu Gln Asp Ala Val Asn Asp Ile Pro Gln Thr Gln Gly Met Thr
2840 2845 2850
Gln Gln Thr Ile Asn Asn Tyr Asn Asp Lys Gln Arg Glu Ala Glu
2855 2860 2865
Arg Ala Leu Thr Ser Ala Gln Arg Val Ile Asp Asn Gly Asp Ala
2870 2875 2880
Thr Thr Gln Glu Ile Thr Ser Glu Lys Ser Lys Val Glu Gln Ala
2885 2890 2895
Met Gln Ala Leu Thr Asn Ala Lys Ser Asn Leu Arg Ala Asp Lys
2900 2905 2910
Asn Glu Leu Gln Thr Ala Tyr Asn Lys Leu Ile Glu Asn Val Ser
2915 2920 2925
Thr Asn Gly Lys Lys Pro Ala Ser Ile Arg Gln Tyr Glu Thr Ala
2930 2935 2940
Lys Ala Arg Ile Gln Asn Gln Ile Asn Asp Ala Lys Asn Glu Ala
2945 2950 2955
Glu Arg Ile Leu Gly Asn Asp Asn Pro Gln Val Ser Gln Val Thr
2960 2965 2970
Gln Ala Leu Asn Lys Ile Lys Ala Ile Gln Pro Lys Leu Thr Glu
2975 2980 2985
Ala Ile Asn Met Leu Gln Asn Lys Glu Asn Asn Thr Glu Leu Val
2990 2995 3000
Asn Ala Lys Asn Arg Leu Glu Asn Ala Val Asn Asp Thr Asp Pro
3005 3010 3015
Thr His Gly Met Thr Gln Glu Thr Ile Asn Asn Tyr Asn Ala Lys
3020 3025 3030
Lys Arg Glu Ala Gln Asn Glu Ile Gln Lys Ala Asn Met Ile Ile
3035 3040 3045
Asn Asn Gly Asp Ala Thr Ala Gln Asp Ile Ser Ser Glu Lys Ser
3050 3055 3060
Lys Val Glu Gln Val Leu Gln Ala Leu Gln Asn Ala Lys Asn Asp
3065 3070 3075
Leu Arg Ala Asp Lys Arg Glu Leu Gln Thr Ala Tyr Asn Lys Leu
3080 3085 3090
Ile Gln Asn Val Asn Thr Asn Gly Lys Lys Pro Ser Ser Ile Gln
3095 3100 3105
Asn Tyr Lys Ser Ala Arg Arg Asn Ile Glu Asn Gln Tyr Asn Thr
3110 3115 3120
Ala Lys Asn Glu Ala His Asn Val Leu Glu Asn Thr Asn Pro Thr
3125 3130 3135
Val Asn Ala Val Glu Asp Ala Leu Arg Lys Ile Asn Ala Ile Gln
3140 3145 3150
Pro Glu Val Thr Lys Ala Ile Asn Ile Leu Gln Asp Lys Glu Asp
3155 3160 3165
Asn Ser Glu Leu Val Arg Ala Lys Glu Lys Leu Asp Gln Ala Ile
3170 3175 3180
Asn Ser Gln Pro Ser Leu Asn Gly Met Thr Gln Glu Ser Ile Asn
3185 3190 3195
Asn Tyr Thr Thr Lys Arg Arg Glu Ala Gln Asn Ile Ala Ser Ser
3200 3205 3210
Ala Asp Thr Ile Ile Asn Asn Gly Asp Ala Ser Ile Glu Gln Ile
3215 3220 3225
Thr Glu Asn Lys Ile Arg Val Glu Glu Ala Thr Asn Ala Leu Asn
3230 3235 3240
Glu Ala Lys Gln His Leu Thr Ala Asp Thr Thr Ser Leu Lys Thr
3245 3250 3255
Glu Val Arg Lys Leu Ser Arg Arg Gly Asp Thr Asn Asn Lys Lys
3260 3265 3270
Pro Ser Ser Val Ser Ala Tyr Asn Asn Thr Ile His Ser Leu Gln
3275 3280 3285
Ser Glu Ile Thr Gln Thr Glu Asn Arg Ala Asn Thr Ile Ile Asn
3290 3295 3300
Lys Pro Ile Arg Ser Val Glu Glu Val Asn Asn Ala Leu His Glu
3305 3310 3315
Val Asn Gln Leu Asn Gln Arg Leu Thr Asp Thr Ile Asn Leu Leu
3320 3325 3330
Gln Pro Leu Ala Asn Lys Glu Ser Leu Lys Glu Ala Arg Asn Arg
3335 3340 3345
Leu Glu Ser Lys Ile Asn Glu Thr Val Gln Thr Asp Gly Met Thr
3350 3355 3360
Gln Gln Ser Val Glu Asn Tyr Lys Gln Ala Lys Ile Lys Ala Gln
3365 3370 3375
Asn Glu Ser Ser Ile Ala Gln Thr Leu Ile Asn Asn Gly Asp Ala
3380 3385 3390
Ser Asp Gln Glu Val Ser Thr Glu Ile Glu Lys Leu Asn Gln Lys
3395 3400 3405
Leu Ser Glu Leu Thr Asn Ser Ile Asn His Leu Thr Val Asn Lys
3410 3415 3420
Glu Pro Leu Glu Thr Ala Lys Asn Gln Leu Gln Ala Asn Ile Asp
3425 3430 3435
Gln Lys Pro Ser Thr Asp Gly Met Thr Gln Gln Ser Val Gln Ser
3440 3445 3450
Tyr Glu Arg Lys Leu Gln Glu Ala Lys Asp Lys Ile Asn Ser Ile
3455 3460 3465
Asn Asn Val Leu Ala Asn Asn Pro Asp Val Asn Ala Ile Arg Thr
3470 3475 3480
Asn Lys Val Glu Thr Glu Gln Ile Asn Asn Glu Leu Thr Gln Ala
3485 3490 3495
Lys Gln Gly Leu Thr Val Asp Lys Gln Pro Leu Ile Asn Ala Lys
3500 3505 3510
Thr Ala Leu Gln Gln Ser Leu Asp Asn Gln Pro Ser Thr Thr Gly
3515 3520 3525
Met Thr Glu Ala Thr Ile Gln Asn Tyr Asn Ala Lys Arg Gln Lys
3530 3535 3540
Ala Glu Gln Val Ile Gln Asn Ala Asn Lys Ile Ile Glu Asn Ala
3545 3550 3555
Gln Pro Ser Val Gln Gln Val Ser Asp Glu Lys Ser Lys Val Glu
3560 3565 3570
Gln Ala Leu Ser Glu Leu Asn Asn Ala Lys Ser Ala Leu Arg Ala
3575 3580 3585
Asp Lys Gln Glu Leu Gln Gln Ala Tyr Asn Gln Leu Ile Gln Pro
3590 3595 3600
Thr Asp Leu Asn Asn Lys Lys Pro Ala Ser Ile Thr Ala Tyr Asn
3605 3610 3615
Gln Arg Tyr Gln Gln Phe Ser Asn Glu Leu Asn Ser Thr Lys Thr
3620 3625 3630
Asn Thr Asp Arg Ile Leu Lys Glu Gln Asn Pro Ser Val Ala Asp
3635 3640 3645
Val Asn Asn Ala Leu Asn Lys Val Arg Glu Val Gln Gln Lys Leu
3650 3655 3660
Asn Glu Ala Arg Ala Leu Leu Gln Asn Lys Glu Asp Asn Ser Ala
3665 3670 3675
Leu Val Arg Ala Lys Glu Gln Leu Gln Gln Ala Val Asp Gln Val
3680 3685 3690
Pro Ser Thr Glu Gly Met Thr Gln Gln Thr Lys Asp Asp Tyr Asn
3695 3700 3705
Ser Lys Gln Gln Ala Ala Gln Gln Glu Ile Ser Lys Ala Gln Gln
3710 3715 3720
Val Ile Asp Asn Gly Asp Ala Thr Thr Gln Gln Ile Ser Asn Ala
3725 3730 3735
Lys Thr Asn Val Glu Arg Ala Leu Glu Ala Leu Asn Asn Ala Lys
3740 3745 3750
Thr Gly Leu Arg Ala Asp Lys Glu Glu Leu Gln Asn Ala Tyr Asn
3755 3760 3765
Gln Leu Thr Gln Asn Ile Asp Thr Ser Gly Lys Thr Pro Ala Ser
3770 3775 3780
Ile Arg Lys Tyr Asn Glu Ala Lys Ser Arg Ile Gln Thr Gln Ile
3785 3790 3795
Asp Ser Ala Lys Asn Glu Ala Asn Ser Ile Leu Thr Asn Asp Asn
3800 3805 3810
Pro Gln Val Ser Gln Val Thr Ala Ala Leu Asn Lys Ile Lys Ala
3815 3820 3825
Val Gln Pro Glu Leu Asp Lys Ala Ile Ala Met Leu Lys Asn Lys
3830 3835 3840
Glu Asn Asn Asn Ala Leu Val Gln Ala Lys Gln Gln Leu Gln Gln
3845 3850 3855
Ile Val Asn Glu Val Asp Pro Thr Gln Gly Met Thr Thr Asp Thr
3860 3865 3870
Ala Asn Asn Tyr Lys Ser Lys Lys Arg Glu Ala Glu Asp Glu Ile
3875 3880 3885
Gln Lys Ala Gln Gln Ile Ile Asn Asn Gly Asp Ala Thr Glu Gln
3890 3895 3900
Gln Ile Thr Asn Glu Thr Asn Arg Val Asn Gln Ala Ile Asn Ala
3905 3910 3915
Ile Asn Lys Ala Lys Asn Asp Leu Arg Ala Asp Lys Ser Gln Leu
3920 3925 3930
Glu Asn Ala Tyr Asn Gln Leu Ile Gln Asn Val Asp Thr Asn Gly
3935 3940 3945
Lys Lys Pro Ala Ser Ile Gln Gln Tyr Gln Ala Ala Arg Gln Ala
3950 3955 3960
Ile Glu Thr Gln Tyr Asn Asn Ala Lys Ser Glu Ala His Gln Ile
3965 3970 3975
Leu Glu Asn Ser Asn Pro Ser Val Asn Glu Val Ala Gln Ala Leu
3980 3985 3990
Gln Lys Val Glu Ala Val Gln Leu Lys Val Asn Asp Ala Ile His
3995 4000 4005
Ile Leu Gln Asn Lys Asp Asn Asn Ser Ala Leu Val Thr Ala Lys
4010 4015 4020
Asn Gln Leu Gln Gln Ser Val Asn Asp Gln Pro Leu Thr Thr Gly
4025 4030 4035
Met Thr Gln Asp Ser Ile Asn Asn Tyr Glu Ala Lys Arg Asn Glu
4040 4045 4050
Ala Gln Ser Ala Ile Arg Asn Ala Glu Ala Val Ile Asn Asn Gly
4055 4060 4065
Asp Ala Thr Ala Lys Gln Ile Ser Asp Glu Lys Ser Lys Val Glu
4070 4075 4080
Gln Ala Leu Ala His Leu Asn Asp Ala Lys Gln Gln Leu Thr Ala
4085 4090 4095
Asp Thr Thr Glu Leu Gln Thr Ala Val Gln Gln Leu Asn Arg Arg
4100 4105 4110
Gly Asp Thr Asn Asn Lys Lys Pro Arg Ser Ile Asn Ala Tyr Asn
4115 4120 4125
Lys Ala Ile Gln Ser Leu Glu Thr Gln Ile Thr Ser Ala Lys Asp
4130 4135 4140
Asn Ala Asn Ala Val Ile Gln Lys Pro Ile Arg Thr Val Gln Glu
4145 4150 4155
Val Asn Asn Ala Leu Gln Gln Val Asn Gln Leu Asn Gln Gln Leu
4160 4165 4170
Thr Glu Ala Ile Asn Gln Leu Gln Pro Leu Ser Asn Asn Asp Ala
4175 4180 4185
Leu Lys Ala Ala Lys Leu Asn Leu Glu Asn Lys Ile Asn Gln Thr
4190 4195 4200
Val Gln Thr Asp Gly Met Thr Gln Gln Ser Ile Glu Ala Tyr Gln
4205 4210 4215
Asn Ala Lys Arg Val Ala Gln Asn Glu Ser Asn Thr Ala Leu Ala
4220 4225 4230
Leu Ile Asn Asn Gly Asp Ala Asp Glu Gln Gln Ile Thr Thr Glu
4235 4240 4245
Thr Asp Arg Val Asn Gln Gln Thr Thr Asn Leu Thr Gln Ala Ile
4250 4255 4260
Asn Gly Leu Thr Val Asn Lys Glu Pro Leu Glu Thr Ala Lys Thr
4265 4270 4275
Ala Leu Gln Asn Asn Ile Asp Gln Val Pro Ser Thr Asp Gly Met
4280 4285 4290
Thr Gln Gln Ser Val Ala Asn Tyr Asn Gln Lys Leu Gln Ile Ala
4295 4300 4305
Lys Asn Glu Ile Asn Thr Ile Asn Asn Val Leu Ala Asn Asn Pro
4310 4315 4320
Asp Val Asn Ala Ile Lys Thr Asn Lys Ala Glu Ala Glu Arg Ile
4325 4330 4335
Ser Asn Asp Leu Thr Gln Ala Lys Asn Asn Leu Gln Val Asp Thr
4340 4345 4350
Gln Pro Leu Glu Lys Ile Lys Arg Gln Leu Gln Asp Glu Ile Asp
4355 4360 4365
Gln Gly Thr Asn Thr Asp Gly Met Thr Gln Asp Ser Val Asp Asn
4370 4375 4380
Tyr Asn Asp Ser Leu Ser Ala Ala Ile Ile Glu Lys Gly Lys Val
4385 4390 4395
Asn Lys Leu Leu Lys Arg Asn Pro Thr Val Glu Gln Val Lys Glu
4400 4405 4410
Ser Val Ala Asn Ala Gln Gln Val Ile Gln Asp Leu Gln Asn Ala
4415 4420 4425
Arg Thr Ser Leu Val Pro Asp Lys Thr Gln Leu Gln Glu Ala Lys
4430 4435 4440
Asn Arg Leu Glu Asn Ser Ile Asn Gln Gln Thr Asp Thr Asp Gly
4445 4450 4455
Met Thr Gln Asp Ser Leu Asn Asn Tyr Asn Asp Lys Leu Ala Lys
4460 4465 4470
Ala Arg Gln Asn Leu Glu Lys Ile Ser Lys Val Leu Gly Gly Gln
4475 4480 4485
Pro Thr Val Ala Glu Ile Arg Gln Asn Thr Asp Glu Ala Asn Ala
4490 4495 4500
His Lys Gln Ala Leu Asp Thr Ala Arg Ser Gln Leu Thr Leu Asn
4505 4510 4515
Arg Glu Pro Tyr Ile Asn His Ile Asn Asn Glu Ser His Leu Asn
4520 4525 4530
Asn Ala Gln Lys Asp Asn Phe Lys Ala Gln Val Asn Ser Ala Pro
4535 4540 4545
Asn His Asn Thr Leu Glu Thr Ile Lys Asn Lys Ala Asp Thr Leu
4550 4555 4560
Asn Gln Ser Met Thr Ala Leu Ser Glu Ser Ile Ala Asp Tyr Glu
4565 4570 4575
Asn Gln Lys Gln Gln Glu Asn Tyr Leu Asp Ala Ser Asn Asn Lys
4580 4585 4590
Arg Gln Asp Tyr Asp Asn Ala Val Asn Ala Ala Lys Gly Ile Leu
4595 4600 4605
Asn Gln Thr Gln Ser Pro Thr Met Ser Ala Asp Val Ile Asp Gln
4610 4615 4620
Lys Ala Glu Asp Val Lys Arg Thr Lys Thr Ala Leu Asp Gly Asn
4625 4630 4635
Gln Arg Leu Glu Val Ala Lys Gln Gln Ala Leu Asn His Leu Asn
4640 4645 4650
Thr Leu Asn Asp Leu Asn Asp Ala Gln Arg Gln Thr Leu Thr Asp
4655 4660 4665
Thr Ile Asn His Ser Pro Asn Ile Asn Ser Val Asn Gln Ala Lys
4670 4675 4680
Glu Lys Ala Asn Thr Val Asn Thr Ala Met Thr Gln Leu Lys Gln
4685 4690 4695
Thr Ile Ala Asn Tyr Asp Asp Glu Leu His Asp Gly Asn Tyr Ile
4700 4705 4710
Asn Ala Asp Lys Asp Lys Lys Asp Ala Tyr Asn Asn Ala Val Asn
4715 4720 4725
Asn Ala Lys Gln Leu Ile Asn Gln Ser Asp Ala Asn Gln Ala Gln
4730 4735 4740
Leu Asp Pro Ala Glu Ile Asn Lys Val Thr Gln Arg Val Asn Thr
4745 4750 4755
Thr Lys Asn Asp Leu Asn Gly Asn Asp Lys Leu Ala Glu Ala Lys
4760 4765 4770
Arg Asp Ala Asn Thr Thr Ile Asp Gly Leu Thr Tyr Leu Asn Glu
4775 4780 4785
Ala Gln Arg Asn Lys Ala Lys Glu Asn Val Gly Lys Ala Ser Thr
4790 4795 4800
Lys Thr Asn Ile Thr Ser Gln Leu Gln Asp Tyr Asn Gln Leu Asn
4805 4810 4815
Ile Ala Met Gln Ala Leu Arg Asn Ser Val Asn Asp Val Asn Asn
4820 4825 4830
Val Lys Ala Asn Ser Asn Tyr Ile Asn Glu Asp Asn Gly Pro Lys
4835 4840 4845
Glu Ala Tyr Asn Gln Ala Val Thr His Ala Gln Thr Leu Ile Asn
4850 4855 4860
Ala Gln Ser Asn Pro Glu Met Ser Arg Asp Val Val Asn Gln Lys
4865 4870 4875
Thr Gln Ala Val Asn Thr Ala His Gln Asn Leu His Gly Gln Gln
4880 4885 4890
Lys Leu Glu Gln Ala Gln Ser Ser Ala Asn Thr Glu Ile Gly Asn
4895 4900 4905
Leu Pro Asn Leu Thr Asn Thr Gln Lys Ala Lys Glu Lys Glu Leu
4910 4915 4920
Val Asn Ser Lys Gln Thr Arg Thr Glu Val Gln Glu Gln Leu Asn
4925 4930 4935
Gln Ala Lys Ser Leu Asp Ser Ser Met Gly Thr Leu Lys Ser Leu
4940 4945 4950
Val Ala Lys Gln Pro Thr Val Gln Lys Thr Ser Val Tyr Ile Asn
4955 4960 4965
Glu Asp Gln Pro Glu Gln Ser Ala Tyr Asn Asp Ser Ile Thr Met
4970 4975 4980
Gly Gln Thr Ile Ile Asn Lys Thr Ala Asp Pro Val Leu Asp Lys
4985 4990 4995
Thr Leu Val Asp Asn Ala Ile Ser Ash Ile SerThr Lys Glu Asn
5000 5005 5010
Ala Leu His Gly Glu Gln Lys Leu Thr Thr Ala Lys Thr Glu Ala
5015 5020 5025
Ile Asn Ala Leu Asn Thr Leu Ala Asp Leu Asn Thr Pro Gln Lys
5030 5035 5040
Glu Ala Ile Lys Thr Ala Ile Asn Thr Ala His Thr Arg Thr Asp
5045 5050 5055
Val Thr Ala Glu Gln Ser Lys Ala Asn Gln Ile Asn Ser Ala Met
5060 5065 5070
His Thr Leu Arg Gln Asn Ile Ser Asp Asn Glu Ser Val Thr Asn
5075 5080 5085
Glu Ser Asn Tyr Ile Asn Ala Glu Pro Glu Lys Gln His Ala Phe
5090 5095 5100
Thr Glu Ala Leu Asn Asn Ala Lys Glu Ile Val Asn Glu Gln Gln
5105 5110 5115
Ala Thr Leu Asp Ala Asn Ser Ile Asn Gln Lys Ala Gln Ala Ile
5120 5125 5130
Leu Thr Thr Lys Asn Ala Leu Asp Gly Glu Glu Gln Leu Arg Arg
5135 5140 5145
Ala Lys Glu Asn Ala Asp Gln Glu Ile Asn Thr Leu Asn Gln Leu
5150 5155 5160
Thr Asp Ala Gln Arg Asn Ser Glu Lys Gly Leu Val Asn Ser Ser
5165 5170 5175
Gln Thr Arg Thr Glu Val Ala Ser Gln Leu Ala Lys Ala Lys Glu
5180 5185 5190
Leu Asn Lys Val Met Glu Gln Leu Asn His Leu Ile Asn Gly Lys
5195 5200 5205
Asn Gln Met Ile Asn Ser Ser Lys Phe Ile Asn Glu Asp Ala Asn
5210 5215 5220
Gln Gln Gln Ala Tyr Ser Asn Ala Ile Ala Ser Ala Glu Ala Leu
5225 5230 5235
Lys Asn Lys Ser Gln Asn Pro Glu Leu Asp Lys Val Thr Ile Glu
5240 5245 5250
Gln Ala Ile Asn Asn Ile Asn Ser Ala Ile Asn Asn Leu Asn Gly
5255 5260 5265
Glu Ala Lys Leu Thr Lys Ala Lys Glu Asp Ala Val Ala Ser Ile
5270 5275 5280
Asn Asn Leu Ser Gly Leu Thr Asn Glu Gln Lys Thr Lys Glu Asn
5285 5290 5295
Gln Ala Val Asn Gly Ala Gln Thr Arg Asp Gln Val Ala Asn Lys
5300 5305 5310
Leu Arg Asp Ala Glu Ala Leu Asp Gln Ser Met Gln Thr Leu Arg
5315 5320 5325
Asp Leu Val Asn Asn Gln Asn Ala Ile His Ser Thr Ser Asn Tyr
5330 5335 5340
Phe Asn Glu Asp Ser Thr Gln Lys Asn Thr Tyr Asp Asn Ala Ile
5345 5350 5355
Asp Asn Gly Ser Thr Tyr Ile Thr Gly Gln His Asn Pro Glu Leu
5360 5365 5370
Asn Lys Ser Thr Ile Asp Gln Thr Ile Ser Arg Ile Asn Thr Ala
5375 5380 5385
Lys Asn Asp Leu His Gly Val Glu Lys Leu Gln Arg Asp Lys Gly
5390 5395 5400
Thr Ala Asn Gln Glu Ile Gly Gln Leu Gly Tyr Leu Asn Asp Pro
5405 5410 5415
Gln Lys Ser Gly Glu Glu Ser Leu Val Asn Gly Ser Asn Thr Arg
5420 5425 5430
Ser Glu Val Glu Glu His Leu Asn Glu Ala Lys Ser Leu Asn Asn
5435 5440 5445
Ala Met Lys Gln Leu Arg Asp Lys Val Ala Glu Lys Thr Asn Val
5450 5455 5460
Lys Gln 5er Ser Asp Tyr Ile Asn Asp Ser Thr Glu His Gln Arg
5465 5470 5475
Gly Tyr Asp Gln Ala Leu Gln Glu Ala Glu Asn Ile Ile Asn Glu
5480 5485 5490
Ile Gly Asn Pro Thr Leu Asn Lys Ser Glu Ile Glu Gln Lys Leu
5495 5500 5505
Gln Gln Leu Thr Asp Ala Gln Asn Ala Leu Gln Gly Ser His Leu
5510 5515 5520
Leu Glu Glu Ala Lys Asn Asn Ala Ile Thr Gly Ile Asn Lys Leu
5525 5530 5535
Thr Ala Leu Asn Asp Ala Gln Arg Gln Lys Ala Ile Glu Asn Val
5540 5545 5550
Gln Ala Gln Gln Thr Ile Pro Ala Val Asn Gln Gln Leu Thr Leu
5555 5560 5565
Asp Arg Glu Ile Asn Thr Ala Met Gln Ala Leu Arg Asp Lys Val
5570 5575 5580
Gly Gln Gln Asn Asn Val His Gln Gln Ser Asn Tyr Phe Asn Glu
5585 5590 5595
Asp Glu Gln Pro Lys His Asn Tyr Asp Asn Ser Val Gln Ala Gly
5600 5605 5610
Gln Thr Ile Ile Asp Lys Leu Gln Asp Pro Ile Met Asn Lys Asn
5615 5620 5625
Glu Ile Glu Gln Ala Ile Asn Gln Ile Asn Thr Thr Gln Thr Ala
5630 5635 5640
Leu Ser Gly Glu Asn Lys Leu His Thr Asp Gln Glu Ser Thr Asn
5645 5650 5655
Arg Gln Ile Glu Gly Leu Ser Ser Leu Asn Thr Ala Gln Ile Asn
5660 5665 5670
Ala Glu Lys Asp Leu Val Asn Gln Ala Lys Thr Arg Thr Asp Val
5675 5680 5685
Ala Gln Lys Leu Ala Ala Ala Lys Glu Ile Asn Ser Ala Met Ser
5690 5695 5700
Asn Leu Arg Asp Gly Ile Gln Asn Lys Glu Asp Ile Lys Arg Ser
5705 5710 5715
Ser Ala Tyr Ile Asn Ala Asp Pro Thr Lys Val Thr Ala Tyr Asp
5720 5725 5730
Gln Ala Leu Gln Asn Ala Glu Asn Ile Ile Asn Ala Thr Pro Asn
5735 5740 5745
Val Glu Leu Asn Lys Ala Thr Ile Glu Gln Ala Leu Ser Arg Val
5750 5755 5760
Gln Gln Ala Gln Gln Asp Leu Asp Gly Val Gln Gln Leu Ala Asn
5765 5770 5775
Ala Lys Gln Gln Ala Thr Gln Thr Val Asn Gly Leu Asn Ser Leu
5780 5785 5790
Asn Asp Gly Gln Lys Arg Glu Leu Asn Leu Leu Ile Asn Ser Ala
5795 5800 5805
Asn Thr Arg Thr Lys Val Gln Glu Glu Leu Asn Lys Ala Thr Glu
5810 5815 5820
Leu Asn His Ala Met Glu Ala Leu Arg Asn Ser Val Gln Asn Val
5825 5830 5835
Asp Gln Val Lys Gln Ser Ser Asn Tyr Val Asn Glu Asp Gln Pro
5840 5845 5850
Glu Gln His Asn Tyr Asp Asn Ala Val Asn Glu Ala Gln Ala Thr
5855 5860 5865
Ile Asn Asn Asn Ala Gln Pro Val Leu Asp Lys Leu Ala Ile Glu
5870 5875 5880
Arg Leu Thr Gln Thr Val Asn Thr Thr Lys Asp Ala Leu His Gly
5885 5890 5895
Ala Gln Lys Leu Thr Gln Asp Gln Gln Ala Ala Glu Thr ely Ile
5900 5905 5910
Arg Gly Leu Thr Ser Leu Asn Glu Pro Gln Lys Asn Ala Glu Val
5915 5920 5925
Ala Lys Val Thr Ala Ala Thr Thr Arg Asp Glu Val Arg Asn Ile
5930 5935 5940
Arg Gln Glu Ala Thr Thr Leu Asp Thr Ala Met Leu Gly Leu Arg
5945 5950 5955
Lys Ser Ile Lys Asp Lys Asn Asp Thr Lys Asn Ser Ser Lys Tyr
5960 5965 5970
Ile Asn Glu Asp His Asp Gln Gln Gln Ala Tyr Asp Asn Ala Val
5975 5980 5985
Asn Asn Ala Gln Gln Val Ile Asp Glu Thr Gln Ala Thr Leu Ser
5990 5995 6000
Ser Asp Thr Ile Asn Gln Leu Ala Asn Ala Val Thr Gln Ala Lys
6005 6010 6015
Ser Asn Leu His Gly Asp Thr Lys Leu Gln His Asp Lys Asp Ser
6020 6025 6030
Ala Lys Gln Thr Ile Ala Gln Leu Gln Asn Leu Asn Ser Ala Gln
6035 6040 6045
Lys His Met Glu Asp Ser Leu Ile Asp Asn Glu Ser Thr Arg Thr
6050 6055 6060
Gln Val Gln His Asp Leu Thr Glu Ala Gln Ala Leu Asp Gly Leu
6065 6070 6075
Met Gly Ala Leu Lys Glu Ser Ile Lys Asp Tyr Thr Asn Ile Val
6080 6085 6090
Ser Asn Gly Asn Tyr Ile Asn Ala Glu Pro Ser Lys Lys Gln Ala
6095 6100 6105
Tyr Asp Ala Ala Val Gln Asn Ala Gln Asn Ile Ile Asn Gly Thr
6110 6115 6120
Asn Gln Pro Thr Ile Asn Lys Gly Asn Val Thr Thr Ala Thr Gln
6125 6130 6135
Thr Val Lys Asn Thr Lys Asp Ala Leu Asp Gly Asp His Arg Leu
6140 6145 6150
Glu Glu Ala Lys Asn Asn Ala Asn Gln Thr Ile Arg Asn Leu Ser
6155 6160 6165
Asn Leu Asn Asn Ala Gln Lys Asp Ala Glu Lys Asn Leu Val Asn
6170 6175 6180
Ser Ala Ser Thr Leu Glu Gln Val Gln Gln Asn Leu Gln Thr Ala
6185 6190 6195
Gln Gln Leu Asp Asn Ala Met Gly Glu Leu Arg Gln Ser Ile Ala
6200 6205 6210
Lys Lys Asp Gln Val Lys Ala Asp Ser Lys Tyr Leu Asn Glu Asp
6215 6220 6225
Pro Gln Ile Lys Gln Asn Tyr Asp Asp Ala Val Gln Arg Val Glu
6230 6235 6240
Thr Ile Ile Asn Glu Thr Gln Asn Pro Glu Leu Leu Lys Ala Asn
6245 6250 6255
Ile Asp Gln Ala Thr Gln Ser Val Gln Asn Ala Glu Gln Ala Leu
6260 6265 6270
His Gly Ala Glu Lys Leu Asn Gln Asp Lys Gln Thr Ser Ser Thr
6275 6280 6285
Glu Leu Asp Gly Leu Thr Asp Leu Thr Asp Ala Gln Arg Glu Lys
6290 6295 6300
Leu Arg Glu Gln Ile Asn Thr Ser Asn Ser Arg Asp Asp Ile Lys
6305 6310 6315
Gln Lys Ile Glu Gln Ala Lys Ala Leu Asn Asp Ala Met Lys Lys
6320 6325 6330
Leu Lys Glu Gln Val Ala Gln Lys Asp Gly Val His Ala Asn Ser
6335 6340 6345
Asp Tyr Thr Asn Glu Asp Ser Ala Gln Lys Asp Ala Tyr Asn Asn
6350 6355 6360
Ala Leu Lys Gln Ala Glu Asp Ile Ile Asn Asn Ser Ser Asn Pro
6365 6370 6375
Asn Leu Asn Ala Gln Asp Ile Thr Asn Ala Leu Asn Asn Ile Lys
6380 6385 6390
Gln Ala Gln Asp Asn Leu His Gly Ala Gln Lys Leu Gln Gln Asp
6395 6400 6405
Lys Asn Thr Thr Asn Gln Ala Ile Gly Asn Leu Asn His Leu Asn
6410 6415 6420
Gln Pro Gln Lys Asp Ala Leu Ile Gln Ala Ile Asn Gly Ala Thr
6425 6430 6435
Ser Arg Asp Gln Val Ala Glu Lys Leu Lys Glu Ala Glu Ala Leu
6440 6445 6450
Asp Glu Ala Met Lys Gln Leu Glu Asp Gln Val Asn Gln Asp Asp
6455 6460 6465
Gln Ile Ser Asn Ser Ser Pro Phe Ile Asn Glu Asp Ser Asp Lys
6470 6475 6480
Gln Lys Thr Tyr Asn Asp Lys Ile Gln Ala Ala Lys Glu Ile Ile
6485 6490 6495
Asn Gln Thr Ser Asn Pro Thr Leu Asp Lys Gln Lys Ile Ala Asp
6500 6505 6510
Thr Leu Gln Asn Ile Lys Asp Ala Val Asn Asn Leu His Gly Asp
6515 6520 6525
Gln Lys Leu Ala Gln Ser Lys Gln Asp Ala Asn Asn Gln Leu Asn
6530 6535 6540
His Leu Asp Asp Leu Thr Glu Glu Gln Lys Asn His Phe Lys Pro
6545 6550 6555
Leu Ile Asn Asn Ala Asp Thr Arg Asp Glu Val Asn Lys Gln Leu
6560 6565 6570
Glu Ile Ala Lys Gln Leu Asn Gly Asp Met Ser Thr Leu His Lys
6575 6580 6585
Val Ile Asn Asp Lys Asp Gln Ile Gln His Leu Ser Asn Tyr Ile
6590 6595 6600
Asn Ala Asp Asn Asp Lys Lys Gln Asn Tyr Asp Asn Ala Ile Lys
6605 6610 6615
Glu Ala Glu Asp Leu Ile His Asn His Pro Asp Thr Leu Asp His
6620 6625 6630
Lys Ala Leu Gln Asp Leu Leu Asn Lys Ile Asp Gln Ala His Asn
6635 6640 6645
Glu Leu Asn Gly Glu Ser Arg Phe Lys Gln Ala Leu Asp Asn Ala
6650 6655 6660
Leu Asn Asp Ile Asp Ser Leu Asn Ser Leu Asn Val Pro Gln Arg
6665 6670 6675
Gln Thr Val Lys Asp Asn Ile Asn His Val Thr Thr Leu Glu Ser
6680 6685 6690
Leu Ala Gln Glu Leu Gln Lys Ala Lys Glu Leu Asn Asp Ala Met
6695 6700 6705
Lys Ala Met Arg Asp Ser Ile Met Asn Gln Glu Gln Ile Arg Lys
6710 6715 6720
Asn Ser Asn Tyr Thr Asn Glu Asp Leu Ala Gln Gln Asn Ala Tyr
6725 6730 6735
Asn His Ala Val Asp Lys Ile Asn Asn Ile Ile Gly Glu Asp Asn
6740 6745 6750
Ala Thr Met Asp Pro Gln Ile Ile Lys Gln Ala Thr Gln Asp Ile
6755 6760 6765
Asn Thr Ala Ile Asn Gly Leu Asn Gly Asp Gln Lys Leu Gln Asp
6770 6775 6780
Ala Lys Thr Asp Ala Lys Gln Gln Ile Thr Asn Phe Thr Gly Leu
6785 6790 6795
Thr Glu Pro Gln Lys Gln Ala Leu Glu Asn Ile Ile Asn Gln Gln
6800 6805 6810
Thr Ser Arg Ala Asn Val Ala Lys Gln Leu Ser His Ala Lys Phe
6815 6820 6825
Leu Asn Gly Lys Met Glu Glu Leu Lys Val Ala Val Ala Lys Ala
6830 6835 6840
Ser Leu Val Arg Gln Asn Ser Asn Tyr Ile Asn Glu Asp Val Ser
6845 6850 6855
Glu Lys Glu Ala Tyr Glu Gln Ala Ile Ala Lys Gly Gln Glu Ile
6860 6865 6870
Ile Asn Ser Glu Asn Asn Pro Thr Ile Ser Ser Thr Asp Ile Asn
6875 6880 6885
Arg Thr Ile Gln Glu Ile Asn Asp Ala Glu Gln Asn Leu His Gly
6890 6895 6900
Asp Asn Lys Leu Arg Gln Ala Gln Glu Ile Ala Lys Asn Glu Ile
6905 6910 6915
Gln Asn Leu Asp Gly Leu Asn Ser Ala Gln Ile Thr Lys Leu Ile
6920 6925 6930
Gln Asp Ile Gly Arg Thr Thr Thr Lys Pro Ala Val Thr Gln Lys
6935 6940 6945
Leu Glu Glu Ala Lys Ala Ile Asn Gln Ala Met Gln Gln Leu Lys
6950 6955 6960
Gln Ser Ile Ala Asp Lys Asp Ala Thr Leu Asn Ser Ser Asn Tyr
6965 6970 6975
Leu Asn Glu Asp Ser Glu Lys Lys Leu Ala Tyr Asp Asn Ala Val
6980 6985 6990
Ser Gln Ala Glu Gln Leu Ile Asn Gln Leu Asn Asp Pro Thr Met
6995 7000 7005
Asp Ile Ser Asn Ile Gln Ala Ile Thr Gln Lys Val Ile Gln Ala
7010 7015 7020
Lys Asp Ser Leu His Gly Ala Asn Lys Leu Ala Gln Asn Gln Ala
7025 7030 7035
Asp Ser Asn Leu Ile Ile Asn Gln Ser Thr Asn Leu Asn Asp Lys
7040 7045 7050
Gln Lys Gln Ala Leu Asn Asp Leu Ile Asn His Ala Gln Thr Lys
7055 7060 7065
Gln Gln Val Ala Glu Ile Ile Ala Gln Ala Asn Lys Leu Asn Asn
7070 7075 7080
Glu Met Gly Thr Leu Lys Thr Leu Val Glu Glu Gln Ser Asn Val
7085 7090 7095
His Gln Gln Ser Lys Tyr Ile Asn Glu Asp Pro Gln Val Gln Asn
7100 7105 7110
Ile Tyr Asn Asp Ser Ile Gln Lys Gly Arg Glu Ile Leu Asn Gly
7115 7120 7125
Thr Thr Asp Asp Val Leu Asn Asn Asn Lys Ile Ala Asp Ala Ile
7130 7135 7140
Gln Asn Ile His Leu Thr Lys Asn Asp Leu His Gly Asp Gln Lys
7145 7150 7155
Leu Gln Lys Ala Gln Gln Asp Ala Thr Asn Glu Leu Asn Tyr Leu
7160 7165 7170
Thr Asn Leu Asn Asn Ser Gln Arg Gln Ser Glu His Asp Glu Ile
7175 7180 7185
Asn Ser Ala Pro Ser Arg Thr Glu Val Ser Asn Asp Leu Asn His
7190 7195 7200
Ala Lys Ala Leu Asn Glu Ala Met Arg Gln Leu Glu Asn Glu Val
7205 7210 7215
Ala Leu Glu Asn Ser Val Lys Lys Leu Ser Asp Phe Ile Asn Glu
7220 7225 7230
Asp Glu Ala Ala Gln Asn Glu Tyr Ser Asn Ala Leu Gln Lys Ala
7235 7240 7245
Lys Asp Ile Ile Asn Gly Val Pro Ser Ser Thr Leu Asp Lys Ala
7250 7255 7260
Thr Ile Glu Asp Ala Leu Leu Glu Leu Gln Asn Ala Arg Glu Ser
7265 7270 7275
Leu His Gly Glu Gln Lys Leu Gln Glu Ala Lys Asn Gln Ala Val
7280 7285 7290
Ala Glu Ile Asp Asn Leu Gln Ala Leu Asn Pro Gly Gln Val Leu
7295 7300 7305
Ala Glu Lys Thr Leu Val Asn Gln Ala Ser Thr Lys Pro Glu Val
7310 7315 7320
Gln Glu Ala Leu Gln Lys Ala Lys Glu Leu Asn Glu Ala Met Lys
7325 7330 7335
Ala Leu Lys Thr Glu Ile Asn Lys Lys Glu Gln Ile Lys Ala Asp
7340 7345 7350
Ser Arg Tyr Val Asn Ala Asp Ser Gly Leu Gln Ala Asn Tyr Asn
7355 7360 7365
Ser Ala Leu Asn Tyr Gly Ser Gln Ile Ile Ala Thr Thr Gln Pro
7370 7375 7380
Pro Glu Leu Asn Lys Asp Val Ile Asn Arg Ala Thr Gln Thr Ile
7385 7390 7395
Lys Thr Ala Glu Asn Asn Leu Asn Gly Gln Ser Lys Leu Ala Glu
7400 7405 7410
Ala Lys Ser Asp Gly Asn Gln Ser Ile Glu His Leu Gln Gly Leu
7415 7420 7425
Thr Gln Ser Gln Lys Asp Lys Gln His Asp Leu Ile Asn Gln Ala
7430 7435 7440
Gln Thr Lys Gln Gln Val Asp Asp Ile Val Asn Asn Ser Lys Gln
7445 7450 7455
Leu Asp Asn Ser Met Asn Gln Leu Gln Gln Ile Val Asn Asn Asp
7460 7465 7470
Asn Thr Val Lys Gln Asn Ser Asp Phe Ile Asn Glu Asp Ser Ser
7475 7480 7485
Gln Gln Asp Ala Tyr Asn His Ala Ile Gln Ala Ala Lys Asp Leu
7490 7495 7500
Ile Thr Ala His Pro Thr Ile Met Asp Lys Asn Gln Ile Asp Gln
7505 7510 7515
Ala Ile Glu Asn Ile Lys Gln Ala Leu Asn Asp Leu His Gly Ser
7520 7525 7530
Asn Lys Leu Ser Glu Asp Lys Lys Glu Ala Ser Glu Gln Leu Gln
7535 7540 7545
Asn Leu Asn Ser Leu Thr Asn Gly Gln Lys Asp Thr Ile Leu Asn
7550 7555 7560
His Ile Phe Ser Ala Pro Thr Arg Ser Gln Val Gly Glu Lys Ile
7565 7570 7575
Ala Ser Ala Lys Gln Leu Asn Asn Thr Met Lys Ala Leu Arg Asp
7580 7585 7590
Ser Ile Ala Asp Asn Asn Glu Ile Leu Gln Ser Ser Lys Tyr Phe
7595 7600 7605
Asn Glu Asp Ser Glu Gln Gln Asn Ala Tyr Asn Gln Ala Val Asn
7610 7615 7620
Lys Ala Lys Asn Ile Ile Asn Asp Gln Pro Thr Pro Val Met Ala
7625 7630 7635
Asn Asp Glu Ile Gln Ser Val Leu Asn Glu Val Lys Gln Thr Lys
7640 7645 7650
Asp Asn Leu His Gly Asp Gln Lys Leu Ala Asn Asp Lys Thr Asp
7655 7660 7665
Ala Gln Ala Thr Leu Asn Ala Leu Asn Tyr Leu Asn Gln Ala Gln
7670 7675 7680
Arg Gly Asn Leu Glu Thr Lys Val Gln Asn Ser Asn Ser Arg Pro
7685 7690 7695
Glu Val Gln Lys Val Val Gln Leu Ala Asn Gln Leu Asn Asp Ala
7700 7705 7710
Met Lys Lys Leu Asp Asp Ala Leu Thr Gly Asn Asp Ala Ile Lys
7715 7720 7725
Gln Thr Ser Asn Tyr Ile Asn Glu Asp Thr Ser Gln Gln Val Asn
7730 7735 7740
Phe Asp Glu Tyr Thr Asp Arg Gly Lys Asn Ile Val Ala Glu Gln
7745 7750 7755
Thr Asn Pro Asn Met Ser Pro Thr Asn Ile Asn Thr Ile Ala Asp
7760 7765 7770
Lys Ile Thr Glu Ala Lys Asn Asp Leu His Gly Val Gln Lys Leu
7775 7780 7785
Glu Gln Ala Gln Gln Gln Ser Ile Asn Thr Ile Asn Gln Met Thr
7790 7795 7800
Gly Leu Asn Gln Ala Gln Lys Glu Gln Leu Asn Gln Glu Ile Gln
7805 7810 7815
Gln Thr Gln Thr Arg Ser Glu Val His Gln Val Ile Lys Lys Ala
7820 7825 7830
Gln Ala Leu Asn Asp Ser Met AsnThr Leu Arg Gln Ser Ile Thr
7835 7840 7845
Asp Glu Asn Glu Val Lys Gln Thr Ser Asn Tyr Ile Asn Glu Thr
7850 7855 7860
Val Gly Asn Gln Thr Ala Tyr Asn Asn Ala Val Asp Arg Val Lys
7865 7870 7875
Gln Ile Ile Asn Gln Thr Ser Asn Pro Thr Met Asn Pro Leu Glu
7880 7885 7890
Val Glu Arg Ala Thr Ser Asn Val Lys Thr Ser Lys Asp Ala Leu
7895 7900 7905
His Gly Glu Arg Glu Leu Asn Asp Asn Lys Asn Ser Lys Thr Phe
7910 7915 7920
Ala Val Asn His Leu Asp Asn Leu Asn Gln Ala Gln Lys Glu Ala
7925 7930 7935
Leu Thr His Glu Ile Glu Gln Ala Thr Ile Val Ser Gln Val Asn
7940 7945 7950
Asn Ile Tyr Asn Lys Ala Lys Ala Leu Asn Asn Asp Met Lys Lys
7955 7960 7965
Leu Lys Asp Ile Val Ala Gln Gln Asp Asn Val Arg Gln Ser Asn
7970 7975 7980
Asn Tyr Ile Asn Glu Asp Ser Thr Pro Gln Asn Met Tyr Asn Asp
7985 7990 7995
Thr Ile Asn His Ala Gln Ser Ile Ile Asp Gln Val Ala Asn Pro
8000 8005 8010
Thr Met Ser His Asp Glu Ile Glu Asn AlaIleAsn Asn Ile Lys
8015 8020 8025
His Ala Ile Asn Ala Leu Asp Gly Glu His Lys Leu Gln Gln Ala
8030 8035 8040
Lys Glu Asn Ala Asn Leu Leu Ile Asn Ser Leu Asn Asp Leu Asn
8045 8050 8055
Ala Pro Gln Arg Asp Ala Ile Asn Arg Leu Val Asn Glu Ala Gln
8060 8065 8070
Thr Arg Glu Lys Val Ala Glu Gln Leu Gln Ser Ala Gln Ala Leu
8075 8080 8085
Asn Asp Ala Met Lys His Leu Arg Asn Ser Ile Gln Asn Gln Ser
8090 8095 8100
Ser Val Arg Gln Glu Ser Lys Tyr Ile Asn Ala Ser Asp Ala Lys
8105 8110 8115
Lys Glu Gln Tyr Asn His Ala Val Arg Glu Val Glu Asn Ile Ile
8120 8125 8130
Asn Glu Gln His Pro Thr Leu Asp Lys Glu Ile Ile Lys Gln Leu
8135 8140 8145
Thr Asp Ala Val Asn Gln Ala Asn Asn Asp Leu Asn Gly Val Glu
8150 8155 8160
Leu Leu Asp Ala Asp Lys Gln Asn Ala His Gln Ser Ile Pro Thr
8165 8170 8175
Leu Met His Leu Asn Gln Ala Gln Gln Asn Ala Leu Asn Glu Lys
8180 8185 8190
Ile Asn Asn Ala Val Thr Arg Ala Glu Val Ala Ala Ile Ile Gly
8195 8200 8205
Gln Ala Lys Ile Leu Asp His Ala Met Glu Asn Leu Glu Glu Ser
8210 8215 8220
Ile Lys Asp Lys Glu Gln Val Lys Gln Ser Ser Asn Tyr Ile Asn
8225 8230 8235
Glu Asp Pro Asp Val Gln Glu Thr Tyr Asn Asn Ala Val Asp His
8240 8245 8250
Val Thr Glu Ile Leu Asn Gln Thr Val Asn Pro Thr Leu Ser Ile
8255 8260 8265
Glu Asp Ile Glu His Ala Ile Asn Glu Val Asn Gln Ala Lys Lys
8270 8275 8280
Gln Leu Arg Gly Lys Gln Lys Leu Tyr Gln Thr Ile Asp Leu Ala
8285 8290 8295
Asp Lys Glu Leu Ser Lys Leu Asp Asp Leu Thr Ser Gln Gln Ser
8300 8305 8310
Ser Ser Ile Ser Asn Gln Ile Tyr Thr Ala Lys Thr Arg Thr Glu
8315 8320 8325
Val Ala Gln Ala Ile Glu Lys Ala Lys Ser Leu Asn His Ala Met
8330 8335 8340
Lys Ala Leu Asn Lys Val Tyr Lys Asn Thr Asp Lys Val Leu Asp
8345 8350 8355
Ser Ser Arg Phe Ile Asn Glu Asp Gln Pro Glu Lys Glu Ala Tyr
8360 8365 8370
Gln Gln Ala Ile Asn His Val Asp Ser Ile Ile His Arg Gln Thr
8375 8380 8385
Asn Pro Glu Met Asp Pro Thr Val Ile Asn Ser Ile Thr His Glu
8390 8395 8400
Leu Glu Thr Ala Gln Asn Asn Leu His Gly Asp Gln Lys Leu Ala
8405 8410 8415
His Ala Gln Gln Asp Ala Ala Asn Val Ile Asn Gly Leu Ile His
8420 8425 8430
Leu Asn Val Ala Gln Arg Glu Val Met Ile Asn Ala Asn Thr Asn
8435 8440 8445
Ala Thr Thr Arg Glu Lys Val Ala Lys Asn Leu Asp Asn Ala Gln
8450 8455 8460
Ala Leu Asp Lys Ala Met Glu Thr Leu Gln Gln Val Val Ala His
8465 8470 8475
Lys Asn Asn Ile Leu Asn Asp Ser Lys Tyr Leu Asn Glu Asp Ser
8480 8485 8490
Lys Tyr Gln Gln Gln Tyr Asp Arg Val Val Ala Asp Ala Glu Gln
8495 8500 8505
Leu Leu Asn Gln Thr Thr Asn Pro Thr Leu Glu Pro Tyr Lys Ile
8510 8515 8520
Asp Ile Val Lys Asp Asn Val Leu Ala Asn Glu Lys Ile Leu Phe
8525 8530 8535
Gly Ala Glu Lys Leu Ser Tyr Asp Lys Ser Asn Ala Asn Asp Glu
8540 8545 8550
Ile Lys His Met Asn Tyr Leu Asn Asn Ala Gln Lys Gln Ser Ile
8555 8560 8565
Lys Asp Met Ile Ser His Ala Ala Leu Arg Thr Glu Val Lys Gln
8570 8575 8580
Leu Leu Gln Gln Ala Lys Thr Leu Asp Glu Ala Met Lys Ser Leu
8585 8590 8595
Glu Asp Lys Thr Gln Val Val Ile Thr Asp Thr Thr Leu Ser Asn
8600 8605 8610
Tyr Thr Glu Ala Ser Glu Asp Lys Lys Glu Lys Val Asp Gln Thr
8615 8620 8625
Val Ser His Ala Gln Ala Ile Ile Asp Lys Ile Asn Gly Ser Asn
8630 8635 8640
Val Ser Leu Asp Gln Val Arg Gln Ala Leu Glu Gln Leu Thr Gln
8645 8650 8655
Ala Ser Glu Asn Leu Asp Gly Asp Gln Arg Val Glu Glu Ala Lys
8660 8665 8670
Val His Ala Asn Gln Thr Ile Asp Gln Leu Thr His Leu Asn Ser
8675 8680 8685
Leu Gln Gln Gln Thr Ala Lys Glu Ser Val Lys Asn Ala Thr Lys
8690 8695 8700
Leu Glu Glu Ile Ala Thr Ala Ser Asn Asp Ala Leu Ala Leu Asn
8705 8710 8715
Lys Val Met Gly Lys Leu Glu Gln Phe Ile Asn His Ala Asp Ser
8720 8725 8730
Val Glu Asn Ser Asp Asn Tyr Arg Gln Ala Asp Asp Asp Lys Ile
8735 8740 8745
Ile Ala Tyr Asp Asp Ala Leu Glu His Gly Gln Asp Ile Gln Lys
8750 8755 8760
Ser Asn Ala Thr Gln Asn Glu Ala Lys Gln Ala Leu Gln Gln Leu
8765 8770 8775
Ile Asn Ala Glu Thr Ser Leu Asn Gly Phe Glu Arg Leu Asn His
8780 8785 8790
Ala Arg Pro Arg Ala Leu Glu Tyr Ile Lys Ser Leu Glu Lys Ile
8795 8800 8805
Asn Asn Ala Gln Lys Ser Ala Leu Glu Asp Lys Val Thr Gln Ser
8810 8815 8820
His Asp Leu Leu Glu Leu Glu His Leu Val Asn Glu Gly Thr Asn
8825 8830 8835
Leu Asn Asp Ile Met Gly Glu Leu Ala Asn Ala Ile Val Asn Asn
8840 8845 8850
Tyr Ala Pro Thr Lys Ala Ser Ile Asn Tyr Ile Asn Ala Asp Asn
8855 8860 8865
Leu Arg Lys Asp Asn Phe Thr Gln Ala Ile Asn Asn Ala Arg Asp
8870 8875 8880
Ala Leu Asn Lys Thr Gln Gly Gln Asn Leu Asp Phe Asn Ala Ile
8885 8890 8895
Asp Thr Phe Lys Asp Asp Ile Phe Lys Thr Lys Asp Ala Leu Asn
8900 8905 8910
Gly Ile Glu Arg Leu Thr Ala Ala Lys Ser Lys Ala Glu Lys Leu
8915 8920 8925
Ile Asp Ser Leu Lys Phe Ile Asn Lys Ala Gln Phe Thr His Ala
8930 8935 8940
Asn Asp Glu Ile Met Asn Thr Asn Ser Ile Ala Gln Leu Ser Arg
8945 8950 8955
Ile Val Asn Gln Ala Phe Asp Leu Asn Asp Ala Met Lys Ser Leu
8960 8965 8970
Arg Asp Glu Leu Asn Asn Lys Ala Phe Pro Val Gln Ala Ser Ser
8975 8980 8985
Asn Tyr Ile Asn Ser Asp Glu Asp Leu Lys Gln Gln Phe Asp His
8990 8995 9000
Ala Leu Ser Asn Ala Arg Lys Val Leu Ala Lys Glu Asn Gly Lys
9005 9010 9015
Asn Leu Asp Glu Ile Gln Ile Glu Gly Leu Lys Gln Val Ile Glu
9020 9025 9030
Asp Thr Lys Asp Ala Leu Asn Gly Ile Gln Arg Leu Ser Lys Ala
9035 9040 9045
Lys Ala Lys Ala Ile Gln Tyr Val Gln Ser Leu Ser Tyr Ile Asn
9050 9055 9060
Asp Ala Gln Arg His Ile Ala Glu Asn Asn Ile His Asn Ser Asp
9065 9070 9075
Asp Leu Ser Ser Leu Ala Asn Thr Leu Ser Lys Ala Ser Asp Leu
9080 9085 9090
Asp Asn Ala Met Lys Asp Leu Arg Asp Thr Leu Glu Ser Asn Ser
9095 9100 9105
Thr Ser Val Pro Asn Ser Val Asn Tyr Ile Asn Ala Asp Lys Asn
9110 9115 9120
Phe Gln Ile Glu Phe Asp Glu Ala Leu Gln Gln Ala Ser Ala Thr
9125 9130 9135
Ser Ser Lys Thr Ser Glu Asn Pro Ala Thr Ile Glu Glu Val Leu
9140 9145 9150
Gly Leu Ser Gln Ala Ile Tyr Asp Thr Lys Asn Ala Leu Asn Gly
9155 9160 9165
Glu Gln Arg Leu Ala Thr Glu Lys Ser Lys Asp Leu Lys Leu Ile
9170 9175 9180
Lys Gly Leu Lys Asp Leu Asn Lys Ala Gln Leu Glu Asp Val Thr
9185 9190 9195
Asn Lys Val Asn Ser Ala Asn Thr Leu Thr Glu Leu Ser Gln Leu
9200 9205 9210
Thr Gln Ser Thr Leu Lys Leu Asn Asp Lys Met Lys Leu Leu Arg
9215 9220 9225
Asp Lys Leu Lys Thr Leu Val Asn Pro Val Lys Ala Ser Leu Asn
9230 9235 9240
Tyr Arg Asn Ala Asp Tyr Asn Leu Lys Arg Gln Phe Asn Lys Ala
9245 9250 9255
Leu Lys Glu Ala Lys Gly Ile Leu Asn Lys Asn Ser Gly Pro Asn
9260 9265 9270
Val Asn Ile Asn Asp Ile Gln His Leu Leu Thr Gln Ile Asp Asn
9275 9280 9285
Ala Lys Asp Gln Leu Asn Gly Glu Arg Arg Leu Lys Glu His Gln
9290 9295 9300
Gln Lys Ser Glu Val Phe Ile Ile Lys Glu Leu Asp Ile Leu Asn
9305 9310 9315
Asn Ala Gln Lys Ala Ala Ile Ile Asn Gln Ile Arg Ala Ser Lys
9320 9325 9330
Asp Ile Lys Ile Ile Asn Gln Ile Val Asp Asn Ala Ile Glu Leu
9335 9340 9345
Asn Asp Ala Met Gln Gly Leu Lys Glu His Val Ala Gln Leu Thr
9350 9355 9360
Ala Thr Thr Lys Asp Asn Ile Glu Tyr Leu Asn Ala Asp Glu Asp
9365 9370 9375
Leu Lys Leu Gln Tyr Asp Tyr Ala Ile Asn Leu Ala Asn Asn Val
9380 9385 9390
Leu Asp Lys Glu Asn Gly Thr Asn Lys Asp Ala Asn Ile Ile Ile
9395 9400 9405
Gly Met Ile Gln Asn Met Asp Asp Ala Arg Ala Leu Leu Asn Gly
9410 9415 9420
Ile Glu Arg Leu Lys Asp Ala Gln Thr Lys Ala His Asn Asp Ile
9425 9430 9435
Lys Asp Thr Leu Lys Arg Gln Leu Asp Glu Ile Glu His Ala Asn
9440 9445 9450
Ala Thr Ser Asn Ser Lys Ala Gln Ala Lys Gln Met Val Asn Glu
9455 9460 9465
Glu Ala Arg Lys Ala Phe Ser Asn Ile Asn His Ala Thr Ser Asn
9470 9475 9480
Asp Leu Val Asn Gln Ala Lys Asp Glu Gly Gln Ser Ala Ile Glu
9485 9490 9495
His Ile His Ala Asp Glu Leu Pro Lys Ala Lys Leu Asp Ala Asn
9500 9505 9510
Gln Met Ile Asp Gln Lys Val Glu Asp Ile Asn His Leu Ile Ser
9515 9520 9525
Gln Asn Pro Asn Leu Ser His Asp Glu Lys Asn Lys Leu Ile Ser
9530 9535 9540
Gln Ile Asn Lys Leu Val Asn Gly Ile Lys Asp Glu Ile Gln Gln
9545 9550 9555
Ala Ile Asn Lys Gln Gln Ile Glu Asn Ala Thr Thr Lys Leu Asp
9560 9565 9570
Glu Val Ile Glu Thr Thr Lys Lys Leu Ile Ile Ala Lys Ala Glu
9575 9580 9585
Ala Lys Gln Val Ile Lys Glu Leu Ser Gln Lys Lys Arg Asp Ala
9590 9595 9600
Ile Asn Asn Asn Thr Asp Leu Thr Pro Ser Gln Lys Ala His Ala
9605 9610 9615
Leu Ala Asp Ile Asp Lys Thr Glu Lys Asp Ala Leu Gln His Ile
9620 9625 9630
Glu Asn Ser Asn Ser Ile Asp Asp Ile Asn Asn Asn Lys Lys His
9635 9640 9645
Ala Phe Asn Thr Leu Ala His Ile Ile Ile Trp Asp Thr Asp Gln
9650 9655 9660
Gln Pro Leu Val Phe Glu Leu Pro Glu Leu Ser Leu Gln Asn Ala
9665 9670 9675
Leu Val Thr Ser Glu Val Val Val His Arg Asp Glu Thr Ile Ser
9680 9685 9690
Leu Glu Ser Ile Ile Gly Ala Met Thr Leu Thr Asp Glu Leu Lys
9695 9700 9705
Val Asn Ile Val Ser Leu Pro Asn Thr Asp Lys Val Ala Asp His
9710 9715 9720
Leu Thr Ala Lys Val Lys Val Ile Leu Ala Asp Gly Ser Tyr Val
9725 9730 9735
Thr Val Asn Val Pro Val Lys Val Val Glu Lys Glu Leu Gln Ile
9740 9745 9750
Ala Lys Lys Asp Ala Ile Lys Thr Ile Asp Val Leu Val Lys Gln
9755 9760 9765
Lys Ile Lys Asp Ile Asp Ser Asn Asn Glu Leu Thr Ser Thr Gln
9770 9775 9780
Arg Glu Asp Ala Lys Ala Glu Ile Glu Arg Leu Lys Lys Gln Ala
9785 9790 9795
Ile Asp Lys Val Asn His Ser Lys Ser Ile Lys Asp Ile Glu Thr
9800 9805 9810
Val Lys Arg Thr Asp Phe Glu Glu Ile Asp Gln Phe Asp Pro Lys
9815 9820 9825
Arg Phe Thr Leu Asn Lys Ala Lys Lys Asp Ile Ile Thr Asp Val
9830 9835 9840
Asn Thr Gln Ile Gln Asn Gly Phe Lys Glu Ile Glu Thr Ile Lys
9845 9850 9855
Gly Leu Thr Ser Asn Glu Lys Thr Gln Phe Asp Lys Gln Leu Thr
9860 9865 9870
Glu Leu Gln Lys Glu Phe Leu Glu Lys Val Glu His Ala His Asn
9875 9880 9885
Leu Val Glu Leu Asn Gln Leu Gln Gln Glu Phe Asn Asn Arg Tyr
9890 9895 9900
Lys His Ile Leu Asn Gln Ala His Leu Leu Gly Glu Lys His Ile
9905 9910 9915
Ala Glu His Lys Leu Gly Tyr Val Val Val Asn Lys Thr Gln Gln
9920 9925 9930
Ile Leu Asn Asn Gln Ser Ala Ser Tyr Phe Ile Lys Gln Trp Ala
9935 9940 9945
Leu Asp Arg Ile Lys Gln Ile Gln Leu Glu Thr Met Asn Ser Ile
9950 9955 9960
Arg Gly Ala His Thr Val Gln Asp Val His Lys Ala Leu Leu Gln
9965 9970 9975
Gly Ile Glu Gln Ile Leu Lys Val Asn Val Ser Ile Ile Asn Gln
9980 9985 9990
Ser Phe Asn Asp Ser Leu His Asn Phe Asn Tyr Leu His Ser Lys
9995 10000 10005
Phe Asp Ala Arg Leu Arg Glu Lys Asp Val Ala Asn His Ile Val
10010 10015 10020
Gln Thr Glu Thr Phe Lys Glu Val Leu Lys Gly Thr Gly Val Glu
10025 10030 10035
Pro Gly Lys Ile Asn Lys Glu Thr Gln Gln Pro Lys Leu His Lys
10040 10045 10050
Asn Asp Asn Asp Ser Leu Phe Lys His Leu Val Asp Asn Phe Gly
10055 10060 10065
Lys Thr Val Gly Val Ile Thr Leu Thr Gly Leu Leu Ser Ser Phe
10070 10075 10080
Trp Leu Val Leu Ala Lys Arg Arg Lys Lys Glu Glu Glu Glu Lys
10085 10090 10095
Gln Ser Ile Lys Asn His His Lys Asp Ile Arg Leu Ser Asp Thr
10100 10105 10110
Asp Lys Ile Asp Pro Ile Val Ile Thr Lys Arg Lys Ile Asp Lys
10115 10120 10125
Glu Glu Gln Ile Gln Asn Asp Asp Lys His Ser Ile Pro Val Ala
10130 10135 10140
Lys His Lys Lys Ser Lys Glu Lys Gln Leu Ser Glu Glu Asp Ile
10145 10150 10155
His Ser Ile Pro Val Val Lys Arg Lys Gln Asn Ser Asp Asn Lys
10160 10165 10170
Asp Thr Lys Gln Lys Lys Val Thr Ser Lys Lys Lys Lys Thr Pro
10175 10180 10185
Gln Ser Thr Lys Lys Val Val Lys Thr Lys Lys Arg Ser Lys Lys
10190 10195 10200
<210>33
<211>1014
<212>DNA
<213>表皮葡萄球菌
<400>33
ttgcgaaaag acgtgataga agtggttaat aaagttgaag attactactt taaaagttat 60
ccaattcaat acaatccaat aattgaatat tttaaccaaa ttaaaaataa aaaagtaatt 120
gtgtcattaa aaatatataa ggtttataaa aaaattgtgg aaaatattca tgatactgaa 180
agtcaatgga tatattctcc tgaacatgca ttacacccaa tagaatttat agaatcattt 240
tgtaaacata taaagggaaa gtatgctgga acaccaattg aattagaatt atggcaaaaa 300
gcaggaatag caactatttt tggtttcatt aataaaaaaa ctaaagaaag aaaatatcaa 360
gaaatctttt gggtggtggc tcgtaaaaat ggtaagtcaa ctatatctag tggaatagcg 420
ttatatttgc tcggtgctga tggtgaaggt ggcccagaag tatacacagt ggctaccaaa 480
aaagatcaag caaaaatagt atggaacgat gctaaaaaga tggtgaataa atcgccgtta 540
ttaaaactcg atttcgtaac taaagtagct gagatattaa caccttttaa tgatggacaa 600
ttaattcccc ttggtcgaga tagtgatact acagatgggt taaatgtaca tggtgctatt 660
atggatgaag tgcatgcttg gaaaacaatg caaatgtacg atgtggtttt tgacggaata 720
tctgcacgtg ataatccttt aattctagca ataactactg cgggaacaat aagaaactct 780
gtgtatgata taaaatatga agaatcagaa aatataatca atgggttatg ggaagatgaa 840
ggatataaaa atgaacgatt tttacctttg atatatgaat tagattcacg agaagaatgg 900
atagatgaaa gttgttggct aaaagccaat ccaggattag gttcaataaa gaaaatagat 960
gctatcaaaa ctaaagtaaa tagagctaag aagaatgctt tatttagagc aacc 1014
<210>34
<211>930
<212>DNA
<213>表皮葡萄球菌
<400>34
gtgaaaaaaa ttctcgcttt agcaatagca tttttaatta tccttgccgc atgtgggaat 60
cacagtaacc atgaacatca ctcacatgaa ggaaaattaa aagttgtaac tacaaactct 120
attctctatg acatggttaa acgtgtcggt ggaaataagg tcgatgttca tagcatcgtt 180
ccagtaggac aagatccaca tgaatatgag gttaaaccta aagatattaa agcattaaca 240
gatgctgacg ttgtatttta taatggttta aacctagaaa ctggaaatgg ttggtttgaa 300
aaagcacttg accaagcagg aaaatcaaca aaagataaaa atgtgatagc agcatcaaat 360
aatgttaaac caatatactt aaatggtgag gaaggtaaca aaaacaaaca agatccacat 420
gcatggttaa gtttagagaa tggaattaaa tacgtaaaaa caatacaaaa atcactagaa 480
catcatgata aaaaagataa gtctacatat gaaaaacaag ggaatgcata tatatcaaaa 540
ttagaagaac ttaataaaga tagtaaaaat aaatttgatg acatacccaa aaatcaacgt 600
gccatgatga caagtgaagg tgcatttaaa tattttgctc aacaattcga tgttaaacca 660
ggttatattt gggagataaa cacagaaaaa caaggtacac ctggtcaaat gaaacaagcc 720
attaaatttg ttaaagataa tcatttaaaa catttattag tcgaaacaag cgtagataaa 780
aaagctatgc aaagtttatc agaagaaact aagaaagata tttatggtga agtatttacc 840
gactctatag gtaaggcagg tactaaaggt gactcatact ataaaatgat gaaatctaat 900
attgatacaa tacatggtag tatgaaataa 930
<210>35
<211>1131
<212>DNA
<213>表皮葡萄球菌
<400>35
ttggaggtag ataatatgaa aattgggatt cctaaagaaa taaagaataa tgagaatcga 60
gtggggttat ccccaagtgg tgtacatgca cttgtagacc aaggacatga agttttagta 120
gaaacaaatg ctggtctagg atcttacttt gaagatggtg attatcaaga agccggtgcc 180
aaaattgttg atgagcagtc aaaagcttgg gatgttgata tggtcatcaa agttaaagaa 240
ccacttgaat cggaatacaa attctttaaa gaagagttaa tcttatttac ttatttacac 300
cttgcgaatg aacagaaatt aactcaggca cttgtggaca acaaggttat atctattgcc 360
tatgaaactg tacaattacc agacggttct ttaccgttat taacaccaat gagtgaagtg 420
gctggtagaa tgtctacaca agtgggagct gaatttttac aaagatttaa tggaggtatg 480
ggtatcttac taggtggcat acctggagta cctaaaggca aagtcactat cattggtggt 540
ggtcaagcag gtacaaatgc agctaagata gctttaggat tgggagctga agtgacaata 600
ctagatgtta atcctaaacg tttagaagaa ttagaggact tatttgatgg cagagtaaga 660
acaattatgt ctaatccatt aaatatagaa atgtatgtga aagaaagcga tttagtgatt 720
ggagcagtcc ttattccagg tgctaaagct ccaaacttag tgactgaaga tatgataaaa 780
gaaatgaaag atggatcagt gattgtagat attgcgatag atcaaggtgg aatttttgaa 840
acaactgata agattactac tcatgataat ccgacttaca ctaaacatgg tgtcgtgcat 900
tatgctgtag ctaatatgcc aggtgccgtt ccacgtacat ctacaattgg attgaacaat 960
gcaacattac cttatgcgca attattggct aataaaggtt atcgtgaagc atttaaagta 1020
aatcatccat tatctctagg tctgaataca tttaatggac atgtgactaa taagaatgta 1080
gctgatacat ttaattttga atacacttca attgaagatg cattgaaata a 1131
<210>36
<211>1203
<212>DNA
<213>表皮葡萄球菌
<400>36
atggaagcga tcgatacatg tccaaacaaa tattcaacta taaggagagt tttaataatg 60
aataaaaaaa cgcaaatgat acatggggga catacgacag acaactatac tggagcagtg 120
acaacaccta tttatcaaac aagtacttat ttacaagatg atattggtga tttaagacaa 180
gggtacgaat attcacgtac tgcaaatcct acacgtgcgt ctcttgaaag tgttattgct 240
aatttagaac atggtaagca tggttttgct tttggttcag gaatggcagc aattagtgca 300
gttatcatgt tattagataa aggagatcac ttagttctta attctgatgt ttatggtggc 360
acatatcgtg cattaactaa agtatttact cgctttggta tagacgtaga ttttgttgat 420
acaactaaaa ttgaaaacat tgaacaatat attaaacctg aaactaaaat gttatatgta 480
gaaacacctt caaatccatt attgcgtgtg actgatatta aagcatcagc aaaaattgca 540
aaaaaatatg atttgatatc tgtagtcgat aatacattta tgacacctta ctaccaaaac 600
cctttagact ttggtattga tatcgtattg cattcggcta ctaaatatat tggaggccat 660
agtgatgttg tagctggtct tgttgctact gctgatgatg atttagcaga acgtctaggc 720
tttatttcaa attctacagg tggtgtactt ggacctcaag atagctattt attaatcaga 780
ggtattaaaa cgctaggtct aagaatggag caaataaacc gaaacgttga aggtattgtg 840
caaatgttac aaaagcaccc taaagttcaa caagtattcc atcctagtat taaggaacat 900
atgaactata ctatccatca aaatcaagca actgggcata caggggtagt atcttttgaa 960
gttaaagata cagaagcggc taaacaagtg attcacgcaa caaactactt tacactggca 1020
gagagtttag gggcagttga aagtctaatt tctgtaccgg cacttatgac gcatgcgtcc 1080
atcccatcag atgtaagagc caaggaaggt attacggatg gtctcattcg tttatctatt 1140
ggtattgaag acacagaaga cttagttaat gatttagaac aagccttaaa tactttgaga 1200
taa 1203
<210>37
<211>633
<212>DNA
<213>表皮葡萄球菌
<400>37
ttggaactac aattagccat tgatttatta aataaagaag aagcagcaaa attagctcaa 60
aaagttgaag aatatgtaga tattgttgaa attggtacgc caattgtaat taatgaaggg 120
ttacctgcag ttcaacattt aaatgaaaat attaataatg ctaaagtatt agctgacttg 180
aaaattatgg atgcagcaga ttacgaagtg agccaagcag taaaatatgg tgcagatatt 240
gttacaattt taggtgttgc tgaagatgct tcaattaaag cagcagttga agaagcgcat 300
aaacatggaa aagcattgct tgttgatatg atagcagtgc aaaacttaga acaacgtgct 360
aaagaactag atgagatggg tgcagactat atcgcagttc atacaggtta cgacttacaa 420
gctgaaggaa aatctccatt agacagcttg cgtacagtta aatctgttat caaaaactct 480
aaggttgcag tagcaggtgg tattaaacca gatactatca aagatattgt tgctgaagat 540
ccagatttag ttattgttgg tggcggtatt gcgaatgctg acgatcctgt agaagcagca 600
aaacaatgta gagcagctat tgaaggtaaa taa 633
<210>38
<211>714
<212>DNA
<213>表皮葡萄球菌
<400>38
atgacaaaat taaatgttaa agtgtttgcg gatggtgcag atattgaaga aatgaaatca 60
gcatataaga atcaactcgt tgatggtttt acaacgaatc caagcttgat ggctaaagcg 120
ggtgtaactg attataaagc ttttgcagag gaagtggtta gtgaaatacc agacgcttca 180
atttcttttg aggtgtttgc tgacgattta cctactatgg aaaaagaagc tgagatttta 240
aaacaatatg gtgataatgt atttgtaaaa attcctattg ttacaacaac tggtgagtct 300
acactaccat taattaaacg tttatcatcg aaacaggtaa ggttgaatgt cacggctgtc 360
tatactatag agcaagtaaa agcaattact gacgctgtaa ctgaaggtgt gccaacatat 420
gtgtcagtat ttgcaggacg cattgcagat actggggttg atccacttcctttgatgaaa 480
gaatcagtta aggtaactca tagtaaagaa ggcgttcaat tattatgggc aagttgtcgt 540
gaagtatata atgtaatcca agctgatgaa attggagctg atattattac ttgcccagct 600
gatgttgtaa aaaaggttaa taacaattta ggccgggata taggagaact ttcagtagat 660
acagtcaaag gttttgccaa agacattcaa agttccggtt tgtcaatttt ataa 714
<210>39
<211>795
<212>DNA
<213>表皮葡萄球菌
<400>39
gtgaatatat tgaaaatcca aatacttcaa ttcaatgtag aacgtggaaa tgttgataaa 60
aatatgcaaa atatcaaaac taagtttaat caatacttag ataaagatac cagtgtcgtc 120
gtgcttccag aaatgtggaa taacggttat gcattagaag aattagaaca aaaagctgat 180
aaaaatctta aagacagctc tctctttata aaagacttag cacatacatt taatgtagat 240
atcattgcag gttcagtatc aaatataaga gaaaaccata tatataatac tgcttttgca 300
attaataaaa acaaagaatt gattaatgaa tatgacaaag tacatctcgt gccaatgtta 360
cgtgagccag actttttatg tggtggaaat gtagtccctg aaccttttta tttatctgat 420
caaacacttg tgacgcaaat catttgttat gacttacgat ttccagagat attgcgctat 480
ccagctagaa aaggtgctaa aattgctttt tatgtagcac agtggcctag ctcaagacta 540
gatcattggt tatcattact aaaagcgaga gcaatcgaaa atgatatttt tattgtagct 600
tgtaatagtt gtggtgatga tggtcacacc aattatgctg gaaattcaat tgtcattaat 660
cctaatggtg aaattttagg ccatttagat gataaagaag gtgtactaac aacacatatc 720
gatgtagact tagtagatca acaaagagaa tatattccag ttttcagaaa tctaaaacca 780
catctttata aatag 795
<210>40
<211>888
<212>DNA
<213>表皮葡萄球菌
<400>40
atgtctaaaa tagtaggatc agatcgagtt aaaagaggaa tggctgaaat gcaaaaaggc 60
ggtgtcatta tggacgtcgt taatgcagaa caagctaaaa ttgctgaaga agccggagct 120
gttgccgtaa tggcattaga gcgtgtacca tcagatattc gtgctgctgg cggtgttgca 180
cgtatggcga atcctaaaat agttgaagaa gttatgaatg ccgtatcaat tccggttatg 240
gctaaagcca gaattggtca tattacagaa gctagagttt tagaatcgat gggtgttgac 300
tatatagatg agtctgaagt attaacgcct gcagacgaag aatatcattt aagaaaagat 360
caatttacag ttccttttgt gtgtggctgt cgtaacttag gtgaagcagc acgacgcatt 420
ggtgaaggtg cggcgatgtt gcgtacgaaa ggtgaacctg gtactggtaa tattgttgaa 480
gctgtccgtc atatgagacg tgttaattct gaagttagcc gcttaacagt tatgaatgat 540
gatgaaatta tgacatttgc aaaagatttg ggtgcacctt atgaagtatt aaaacaaatt 600
aaagataatg gacgtcttcc tgtagttaat tttgcagctg gtggtgttgc tacgcctcag 660
gatgcagcac taatgatgga attaggtgca gatggtgtat ttgttggttc aggtatattt 720
aaatctgaag atcctgaaaa atttgctaaa gctatcgttc aagctacaac acattatcaa 780
gattatgagt taatcggaaa attggctagt gagctaggta cggctatgaa aggtctagat 840
attaatcaaa tttcactaga agaaagaatg caagagcgtg gttggtaa 888
<210>41
<211>1746
<212>DNA
<213>表皮葡萄球菌
<400>41
atggaggatg ctgtggtgga gatggatgct gttaaatact taaataaatt gaatttagat 60
aacattgagt taacaaaata tttgtttttt actggtaaag gcggcgtagg taaaacgacg 120
atatcaagtt ttattgcttt aaacttagca gagaatggaa agaaagtagc tttagtaagt 180
actgatccag ctagtaattt acaagatgta tttcaaatgg aattatctaa taaattaact 240
aaatatcaac ctatacctaa tctctctata gccaattttg acccgattgt tgctgcagac 300
gattataaag cacaatctat agaaccttat gagggtattc taccagaaga tgtgctttct 360
gaaatgaaag aacagttaag tggttcatgt acagttgaag tagcagcatt taatgaattt 420
acaaattttt tatccgataa aactttagaa caagaatttg atttcattat atttgataca 480
gctcccacag gtcacacctt gagaatgctt gaattacctt ctgcatggac agattattta 540
aatacaacga gtaatgacgc ttcttgctta ggtcaattat caggtttaaa tgaaaataga 600
gttaaatata attcagcact tgaaaaacta cgtaaccaag atgatacgac catgatgtta 660
gttgcgagac ctactcactc ttctatatat gaaattcaaa gagcgcaaca agaattacaa 720
caactgtcaa tttctaaatt caaagtaatc attaacaact atatagaaga aagtcacggt 780
ttaatttcga gtcagatgaa atcagaacaa gataaaaaca ttaatcattt tactgaatgg 840
ttaaataaca atcatgctta ttacgttcca tataaaaatc agaaagaaga aggtatagaa 900
agtttaacta atctattaaa tgatgataac ttaattgaaa atgatgactt tattgttgaa 960
gatcatccgc aattcaataa attaatcgat gaaattgaaa atagtaaagt tcaatattta 1020
tttacaatgg gaaaaggtgg cgttggtaaa acgacagtag caacgcaatt agctacaacg 1080
ttatctaata aaggatatcg tgttctttta gcaactactg accctactaa agaaattaat 1140
gttgaaacta caagtaattt aaatactgct tatattgatg aagaacaagc attagaaaag 1200
tataaaaaag aagtactagc cacagtgaat gatgatacac cacaagacga tattgattat 1260
attatggaag atttaaaatc accttgtaca gaagaaatag catttttcaa agcctttagt 1320
gacattatgg agaatcaaga cgacatggat tacgtcattg tagatacagc tcctacaggc 1380
cataccttgc tgttacttga ttctagtgaa aatcatcata gagaattaaa gaaaaaatca 1440
actcaaacta ccagtaatgt tgaaacatta ttacccaaaa ttcaaaataa aaatttaaca 1500
cagatgataa ttgtaacatt agcagaaaaa acaccttatt tagaatctaa acgtttagta 1560
gaagatttaa atagagctaa tataggccat aattggtggg ttgttaatca atcgttagtt 1620
acgctaaatc aacgtgatga cctttttagt aacaaaaaag aagatgaatc attttggata 1680
aacaagatta aaaatgaaag tcttgataat tactttgtca taccttatcg agtattagaa 1740
tattga 1746
<210>42
<211>1011
<212>DNA
<213>表皮葡萄球菌
<400>42
atggcaatta aagtagcaat taatggtttt ggtagaattg gtcgtttagc attcagaaga 60
attcaagatg tagaaggtct tgaagtagtt gcagttaacg acttaacaga tgacgatatg 120
ttagctcatt tattaaaata cgatactatg caaggtcgtt tcactggaga agttgaagtt 180
atcgaaggtg gattccgtgt gaacggtaaa gaaattaaat cattcgatga accagatgct 240
ggtaaattac catggggcga tttagatatc gacgtagtat tagaatgtac tggtttctat 300
actgataaag aaaaagcaca agctcacatc gatgcaggtg ctaaaaaagt attaatctca 360
gctccagcta aaggtgatgt aaaaacaatc gtattcaaca ctaaccatga tacattagat 420
ggttcagaaa cagttgtttc aggtgcttct tgtactacta actcattagc accagttgca 480
aaagttttaa gtgacgaatt cggtttagtt gaaggtttca tgactacaat tcacgcttac 540
actggtgacc aaaatacaca agacgcacct cacagaaaag gtgacaaacg tcgtgcacgt 600
gcagcagctg aaaatattat ccctaactca acaggtgctg ctaaagctat cggtaaagtt 660
attccagaaa tcgatggtaa attagacggt ggagcacaac gtgttccagt tgctactggt 720
tctttaactg aattaactgt agtattagac aaacaagatg taactgttga ccaagttaac 780
agtgctatga aacaagcttc tgacgaatca ttcggttaca ctgaagacga aatcgtatct 840
tctgatattg ttggtatgac ttacggttca ttatttgatg cgactcaaac tcgtgttatg 900
actgttggag atcgtcaatt agttaaagtt gcagcttggt acgacaatga aatgtcttac 960
actgctcaat tagtacgtac attagctcac ttagctgaac tttctaaata a 1011
<210>43
<211>1305
<212>DNA
<213>表皮葡萄球菌
<400>43
atgccaatta ttacagatgt ttacgctcgc gaagtcttag actcacgtgg taacccaaca 60
gttgaagttg aagtattaac tgaaagcggt gctttcggac gtgcattagt accttctggt 120
gcttctactg gtgaacatga agcagttgaa ttacgtgatg gagataaatc acgttattta 180
ggtaaaggtg tgactaaagc ggtagaaaat gttaacgaaa tgatcgcacc agaaatcgtt 240
gaaggtgaat tttcagtttt agatcaagta tctattgata aaatgatgat tcaattagac 300
ggtacacaca acaaaggtaa attaggtgca aatgccattt taggtgtttc tattgccgta 360
gctcgtgcag ctgctgactt attaggtcaa ccattatata aatatttagg tggatttaat 420
ggtaaacaat tgccagtacc tatgatgaat attgttaatg gtggttctca ctcagatgca 480
ccaattgctt tccaagagtt catgatttta cctgtaggtg ctgagtcatt caaagaatca 540
ttacgttggg gtgcagaaat cttccataac cttaaatcaa tcttaagtga acgtggttta 600
gaaactgcag taggtgatga aggtggtttc gctcctagat ttgaaggcac tgaagacgct 660
gtagaaacta ttattaaagc tatcgaaaaa gcaggataca aaccaggtga agatgtattc 720
ttaggatttg actgtgcttc ttctgaattc tatgaaaatg gtgtttatga ttacactaaa 780
ttcgaaggtg aacacggtgc taaacgtagt gcagcagagc aagttgacta cttagaagaa 840
ttaattggta aatatccaat catcactatt gaagatggta tggatgaaaa cgattgggaa 900
ggttggaaac aattaactga tcgtatcggt gataaagttc aattagttgg tgatgattta 960
ttcgtaacta acactgaaat tttatctaaa ggtatcgaac aaggtattgg taactcaatc 1020
ttaatcaaag taaaccaaat cggtacatta actgaaacat tcgatgctat tgaaatggct 1080
caaaaagctg gatatactgc ggttgtatct caccgttctg gtgaaactga agatactaca 1140
attgctgata tcgcagttgc tacaaatgca ggccaaatta aaacaggttc attatctaga 1200
actgaccgta ttgctaaata caatcaatta ttacgtattg aagatgaatt atacgaaaca 1260
gctaaatttg aaggaattaa atctttctac aatttagata aataa 1305
<210>44
<211>1407
<212>DNA
<213>表皮葡萄球菌
<400>44
atggtagttg gagatttccc aattgaaaca gatactattg taataggagc aggtccaggt 60
ggatatgtcg cagccattcg cgcggctcaa ttaggacaaa aggtaacaat cgttgagaaa 120
ggtaatttag gtggtgtatg cttaaacgtt ggttgtatac cttcaaaagc attactacat 180
gcttctcatc gctttgttga agcgcaaaat tcagaaaact taggggtaat tgctgaaagc 240
gtttcgttaa actatcaaaa agttcaagaa ttcaagactt ctgtagttaa taaattaact 300
ggcggtgttg aaggactttt aaaaggtaac aaagtagaga ttgttagagg tgaagcttat 360
ttcgttgata acaatagttt acgtgtcatg gacgaaaaga gtgctcaaac ttacaatttc 420
aaacatgcga ttatagctac aggttcaaga ccaattgaaa ttccaaattt tgaatttggt 480
aaacgtgtta tcgattcaac aggagcttta aatctacaag aagtacctaa caaactagtt 540
gtagttggtg gcggatatat cggttctgaa ttaggtactg cttttgcaaa ctttggctct 600
gaagttacta tccttgaagg tgcaaaagat attttaggcg gatttgaaaa gcaaatgaca 660
caacctgtta aaaaaggtat gaaagaaaaa ggtatcgaaa tcgttactga agcaatggca 720
aaatctgcag aagaaactga aaatggtgtc aaagtaactt atgaggcaaa aggtgaggaa 780
caaactatcg aagctgatta tgtattagtt acagttggcc gtcgccctaa tactgatgaa 840
ttaggattag aagaacttgg tctgaaattt gctgatcgtg gattactaga agtggacaaa 900
caaagtcgta cttctattga aaatatcttt gcgattggag atattgtacc tggattacca 960
ttagctcaca aagctagtta tgaaggtaaa gttgctgctg aagcgataga tggtcaagcc 1020
gcagaggtag actatattgg tatgccagca gtttgcttta cagaaccaga attagcacaa 1080
gttggttata ctgaagctca agcaaaagaa gaaggtttat caattaaagc ttctaaattc 1140
ccttatgcag ctaatggacg agctttatca ttagatgata caaatggttt tgttaagtta 1200
attacactta aagaagatga tacgcttatt ggagcacaag ttgtaggtac tggcgcatct 1260
gatattatct ctgaattagg tttagctatt gagtcaggta tgaatgctga agatatcgca 1320
ttaactgtac atgcacaccc aactttaggt gaaatgacaa tggaagctgc tgaaaaagca 1380
attggttatc caattcatac tatgtaa 1407
<210>45
<211>840
<212>DNA
<213>表皮葡萄球菌
<400>45
atggacttag caactaaata ttttaatcaa atcaactggc gttatgtcga tcattcaagt 60
ggtttagagc ccatgcaatc ttttgcgttt gatgacactt tttccgaaag cgttggtaaa 120
gatttatctt gtaatgtagt acgaacgtgg atacatcaac acaccgtgat tttgggcatt 180
catgattcgc gtttaccatt tttaagtgat ggtattcgtt ttcttacaga tgaacaagga 240
tataatgcaa ttgttaggaa ttctggtggc ttgggtgtcg tattagatca aggaatttta 300
aacatatctt tgatttttaa aggacaaacc gaaacgacta ttgatgaagc ctttacagtg 360
atgtatttat tgattaataa aatgtttgag gatgaagatg ttagtatcga tactaaagaa 420
attgagcaat cgtattgccc aggaaaattt gatttaagta ttaatgataa gaaatttgcc 480
gggatttcgc agcgacgagt acgtggtggt atcgcagtgc aaatatactt atgtattgaa 540
ggttctggct cagaacgggc attaatgatg caacagtttt atcaacgtgc gcttaaaggg 600
gagactacta aatttcacta tccagacata gatccctcat gtatggcatc tttagaaacc 660
cttttaaata gagaaattaa agtgcaagat gttatgtttt tattattata tgcactaaaa 720
gatttagggg caaacttaaa tatggatcct attacagaag acgagtggac acgttacgaa 780
gggtattatg ataagatgtt agaacgcaat gcgaaaatga atgaaaaatt agatttttag 840
<210>46
<211>933
<212>DNA
<213>表皮葡萄球菌
<400>46
atggcacaaa aacctgtaga ttatgttaca caaattattg ggaatacacc tgtagtcaaa 60
ttaagaaacg ttgttgatga tgatgcagct gatatttatg ttaagttaga atatcaaaat 120
ccaggtggtt cggtaaaaga tcgtatcgct ttagcgatga ttgaaaaagc tgagcgtgaa 180
gggaaaatta aacctggtga tacaatcgtt gagcctacga gtggtaacac tggtataggt 240
ctagcatttg tatgtgctgc caaggggtac aaagcagttt ttacaatgcc tgaaacaatg 300
agccaagagc gccgtaactt attaaaagct tatggtgctg aactagtatt aacaccagga 360
tctgaagcta tgaaaggtgc aataaaaaaa gctaaagaat taaaagaaga gcacggctat 420
tttgaaccac aacaattcga aaatccagca aatcctgaaa ttcatgaact tacaactgga 480
ccagaattag ttgaacaatt tgaaggtcga caaattgatg catttttagc tggtgtagga 540
actggtggta cgttatctgg tgttggtaaa gtattgaaga aagaatatcc aaatgtggaa 600
atagtagcta ttgaacctga agcttctcca gtattaagcg gtggtgaacc aggccctcat 660
aaattacaag gattgggagc aggtttcgta cctgatactt taaatacaga agtttatgac 720
agcatcatca aagtaggtaa tgatactgct atggatatgg cacgtcgtgt tgctagagaa 780
gaaggtatat tagcaggtat ttcatctggt gctgcaatat atgctgctat tcaaaaagca 840
aaagaattag gtaaaggtaa aacagttgta acagtattac caagtaatgg ggaacgttac 900
ttatcaacac cattatattc atttgataat taa 933
<210>47
<211>1428
<212>DNA
<213>表皮葡萄球菌
<400>47
atgcattttg aaacagtaat cggacttgaa gttcatgttg agttaaaaac ggactcaaaa 60
atgttctctc catcacccgc acattttgga gctgaaccaa attcaaatac aaatgttatc 120
gacttagctt atccaggtgt attaccagta gttaatagac gtgcagtaga ttgggcaatg 180
agagcttcaa tggcattaaa tatggatatt gctacaaatt caaaatttga tcgtaaaaac 240
tatttctatc cagataatcc aaaagcatat caaatttctc agtttgatca acctattgga 300
gaaaatggct atattgatat tgaagttgat ggagaaacaa aacgtatcgg tattacacgt 360
cttcatatgg aagaagatgc aggtaaatca acacataaag atggttattc tctagtagac 420
ttaaaccgtc aaggtacgcc attaattgaa attgtatctg aacccgatat tcgttcacct 480
aaagaagcat atgcttatct agaaaaacta cgttcaatca ttcaatatac aggtgtatct 540
gattgtaaaa tggaagaggg atccctacgt tgtgatgcta atatttcact tcgtccatat 600
ggtcaaaagg aatttggtac aaaaactgaa ttgaaaaacc ttaactcatt taactacgtt 660
aaaaaaggtt tagaatatga agagaaacgt caagaagaag aattattaaa tggtggagag 720
attggtcaag aaacacgtcg atttgatgaa tctactggta aaacaatttt aatgcgtgtg 780
aaagaaggtt cagatgatta tagatatttc cctgaaccag atattgtacc attatatgta 840
gatgaagatt ggaaagcacg tgtaagagaa acaattccag aattgccaga tgaacgtaaa 900
gctaaatacg taaatgatct tggactacca gaatatgatg cgcatgtatt aacattaact 960
aaagaaatgt ctgatttctt tgaaggcgca attgaccatg gtgcagatgt taaacttact 1020
tccaactggt taatgggagg tgttaacgag tatcttaata aaaatcaagt tgaattaaaa 1080
gatacgcaac taacacctga aaatttagct ggtatgatta aattaataga agacggaaca 1140
atgagtagta aaatcgctaa aaaagttttt ccagaactag cagaaaatgg tggagatgct 1200
aaacaaatta tggaagataa aggtttagta caaatttctg atgaagcaac actacttaaa 1260
tttgtaacag atgcattaga taataatcca caatcaatag aagattataa aaatggtaaa 1320
ggtaaagcta tgggattctt agtgggccaa attatgaaag cttctaaagg tcaagctaac 1380
ccacaaaaag ttaatagcct attaaaacaa gaattagata accgttaa 1428
<210>48
<211>1095
<212>DNA
<213>表皮葡萄球菌
<400>48
atgttaaaac gtgcaaatga aaatgaagag gcttggaata atatgcttaa aaattatagt 60
gaagcctatc cggaattagc tgaagaattt aaattagcaa tgagtggtaa gttaccaaat 120
aattacgctg atgccttacc agaatatgat ttaaatcaca gtggtgcttc tagagctgat 180
tcaggagaaa taattcaaaa attaagcgag tttgtacctt cattctttgg tggatcagca 240
gacttagcag gttcaaataa atctaacgtt aaagaagcta aagattataa taaagatact 300
ccagaaggta aaaacgtatg gtttggtgta cgtgaatttg caatgggagc agcaataaac 360
ggcatggcag cacatggtgg acttcatcca tatgcagcaa cattctttgt attcagtgat 420
tacctaaaac cagctttacg attatcatca atcatgggac tcaattcaac gttcatcttt 480
actcatgatt caattgctgt aggtgaagat ggccctacac acgaacctat tgaacaatta 540
gcaggtcttc gtgctattcc taacatgaat gttattcgtc cagctgatgg taatgaaaca 600
cgtgtagctt gggaagttgc acttgaatca gaacaaacac caacatcatt agtgttaact 660
cgtcaaaatt taccaacttt ggatgttgat aaacaaacag ttgaaaatgg tgtgagaaaa 720
ggtgcatata ttgtttttga aacagaacaa caacttgaat atttattatt ggcatctgga 780
tcagaagtta atttagctgt agaagccgca aaagaattag agcaacaagg taaaggtgta 840
cgagttattt ctatgccaaa ctggtacgca tttgaacaac aatcttctga atataaagaa 900
tcaattttac cttctgatgt tactaaacgt atagctatcg aaatggcatc accacttggt 960
tggcataaat atgttggaat tgaaggtaaa gtcattggta taaatagttt tggcgctagt 1020
gctcctggag atttagtagt tgaaaagtat ggattcacta aagaaaatat tttaaaacaa 1080
gtccgttcat tataa 1095
<210>49
<211>1005
<212>DNA
<213>表皮葡萄球菌
<400>49
gtggaatcag tgagaggttt aaaaatttta agtgtaattg gcttattgtt tgttttaatt 60
gcaactgcag catgtggaaa taatagttca agtaactcaa gtaaagagtc atcaaaagat 120
ggagttgaaa tcaagcacga agaaggtact acgaaagtac ctaaacaccc taaacgtgtt 180
gttgttcttg agtattcatt tgttgatgcg ttagttgctt tagatgttaa acctgttggg 240
atagcggatg ataacaaaaa aaatcgtatt attaaaccat taagagataa aattggaaaa 300
tacacttctg taggaacacg taagccacct aacttagaag aaatcagtaa acttaaacca 360
gatttaatta ttgctgataa taatagacac aaaggtattt ataaagactt aaataaaatt 420
gctcctacga ttgaactgaa aagtttcgat ggagattata atgaaaatat tgatgctttt 480
aaaacaattt caaaagcttt aggtaaagaa gaagaaggta aaaaacgctt agaagaacac 540
gataagaaaa ttgaagaata taaaaaagaa ataactatgg ataaaaatca aaaggtattg 600
cctgcagtag ctgctaaatc aggtttgctt gctcatccaa gcaactctta tgttggtcaa 660
ttcctaagtc aactaggttt taaagaagca ttaagtgatg atgttactaa aggtttaagt 720
aagtatctta aaggacctta cttacaaatg aacactgaaa ctttatctca agtgaatcct 780
gagcgtatgt tcataatgac aaacaaagca agttctaacg aaccttcact aaaagaacta 840
gaaaaagatc ctgtatggaa gaaattaaac gctgtgaaaa atcaacgtgt tgatatttta 900
gaccgtgact tatgggcaag atcacgtggt ttaatttctt cagaagaaat ggcaaaagaa 960
cttgttgaat tatctaagac agatagtaaa aaagataata agtaa 1005
<210>50
<211>1236
<212>DNA
<213>表皮葡萄球菌
<400>50
atgagagata aatttgaaat aacttttatt aagaatagga gagatttaat aatggcaaaa 60
gaaaaatttg atcgctcaaa agaacatgcc aatattggta ctatcggtca cgttgaccat 120
ggtaaaacaa ctttaacagc tgctatcgca actgtattag ctaaaaatgg tgacactgtt 180
gcacaatcat acgatatgat tgacaacgct ccagaagaaa aagaacgtgg tattacaatc 240
aatactgcac atatcgaata ccaaactgac aaacgtcact atgctcacgt tgactgccca 300
ggacacgctg actatgttaa aaacatgatc actggtgcag ctcaaatgga cggcggtatc 360
ttagttgtat ctgctgctga cggtccaatg ccacaaactc gtgaacacat cttattatca 420
cgtaacgttg gtgtaccagc attagttgta ttcttaaaca aagttgacat ggtagacgac 480
gaagaattat tagaattagt tgaaatggaa gttcgtgact tattaagcga atatgacttc 540
ccaggtgacg atgtacctgt aatcgctggt tctgcattaa aagcattaga aggcgatgct 600
gaatacgaac aaaaaatctt agacttaatg caagcagttg atgattacat tccaactcca 660
gaacgtgatt ctgacaaacc attcatgatg ccagttgagg acgtattctc aatcactggt 720
cgtggtactg ttgctacagg ccgtgttgaa cgtggtcaaa tcaaagttgg tgaagaagtt 780
gaaatcatcg gtatgcacga aacttctaaa acaactgtta ctggtgtaga aatgttccgt 840
aaattattag actacgctga agctggtgac aacatcggtg ctttattacg tggtgttgca 900
cgtgaagacg tacaacgtgg tcaagtatta gctgctcctg gttctattac accacacaca 960
aaattcaaag ctgaagtata cgtattatct aaagatgaag gtggacgtca cactccattc 1020
ttcactaact atcgcccaca attctatttc cgtactactg acgtaactgg tgttgtaaac 1080
ttaccagaag gtacagaaat ggttatgcct ggcgacaacg ttgaaatgac agttgaatta 1140
atcgctccaa tcgctatcga agacggaact cgtttctcaa ttcgtgaagg tggacgtact 1200
gttggatcag gcgttgtaac tgaaatcttt gaataa 1236
<210>51
<211>1287
<212>DNA
<213>表皮葡萄球菌
<400>51
atgatgagtt ttgaaaaatc tattaaagca atggagcaag ctgagaaatt aatgcctggc 60
ggtgttaaca gtcccgtaag agcatttaaa tcagtagaca caccagctat ttttatggat 120
catggtgaag gatctaaaat atatgatatt gatggaaatg aatacattga ttatgtgcta 180
agttggggcc cattaattct gggacataaa aatcaacaag ttatatccaa attacatgaa 240
gcagtagata aaggtacaag cttcggcgct tcaacacttc aagaaaataa acttgctgaa 300
cttgtgattg accgtgtacc ttcaattgaa aaagtaagaa tggtttcctc aggaactgaa 360
gctactttag acacacttcg tttagctagg ggttatacag gacgtaataa aattataaaa 420
tttgaagggt gttatcatgg acacagtgat tctttattga ttaaagcagg atcaggtgtt 480
gcaacactag gtttacctga ttcaccaggc gtccctgaag gtattgctaa aaacactatc 540
acggtgccat ataatgattt agattcactt aaattagcgt tcgaaaaata tggcgatgat 600
attgctggtg ttattgttga accggttgct ggaaatatgg gtgtagtgcc tccagtgaat 660
ggatttctac aaggtttaag agatattact aatgaatatg gagcattact tatatttgat 720
gaagtgatga ctggtttccg tgtaggttat aattgtgcgc aaggatactt tggtgtaaca 780
cctgatttaa cttgcttagg aaaagtgata ggtggaggtt tacccgttgg agcttttggt 840
ggtaaaaaag aaattatgga ttacattgct cctgttggga ctatttatca agctggcaca 900
ctttcaggta atcctttagc aatgactagt ggttatgaaa cattgagtca acttactcct 960
gaatcttatg agtattttaa ttctctagga gatatacttg aaaaaggatt aaaagaggta 1020
tttgctaagt ataatgttcc aatcacagta aatcgcgctg gttcaatgat tggttacttc 1080
ttaaatgagg ggcctgtaac aaattttgag gaagcaaata aaagtgattt aaaattattt 1140
agtaatatgt atagagaaat ggctaaggaa ggtgtttaca taccaccttc acaatttgaa 1200
ggaacatttt tatcaactgc acatactaaa gatgatattg agaaaactat ccaagcattt 1260
gataatgcat taagtcgtat tgtgtga 1287
<210>52
<211>861
<212>DNA
<213>表皮葡萄球菌
<400>52
atgcctttag tttcaatgaa agaaatgtta atcgatgcga aagaaaacgg ttatgcggtt 60
ggtcaataca atcttaataa cctcgaattt acacaagcta ttttagaagc gtctcaagaa 120
gagaatgcgc cagttatttt aggtgtttct gaaggggcag ctcgttatat gagtggtttt 180
tatacagttg tgaaaatggt agaaggttta atgcatgact taaacatcac aatcccagta 240
gcaattcatt tagaccacgg ttcaagcttt gaaaaatgta aagaagcaat tgatgctgga 300
ttcacatctg taatgattga tgcatctcat agtccttttg aagaaaatgt tgaaatcact 360
tctaaagtag ttgagtatgc tcatgataga ggcgtttctg tagaagctga attaggtaca 420
gttggtggac aagaagacga cgtagttgct gatggcgtta tctatgcaga ccctaaagaa 480
tgtcaagaat tagtagaaaa aactggaatt gatactttag ctccagcatt aggttctgta 540
catggaccat ataaaggtga acctaaatta ggatttaaag agatggaaga aattggtgct 600
tcaactggat tacctttagt attacacggt ggtacaggta ttccaactaa agatattcaa 660
aaagctattc cttatggtac tgctaaaatt aacgtgaata ctgaaaatca aattgcgtct 720
gctaaagcag ttcgtgaagt attaaacaac gacaaagatg tgtatgatcc acgtaaatat 780
ttaggaccag cacgtgaagc aattaaagag acagttaaag gtaaaattag agaattcggt 840
acttctaatc gcgctaaata a 861
<210>53
<211>1407
<212>DNA
<213>表皮葡萄球菌
<400>53
atgacacaac aaattggagt agtgggttta gcagtaatgg ggaaaaacct agcttggaat 60
attgaatcac gtggttatag tgtttctgtt tataaccgat caagacaaaa aactgatgaa 120
atggttaaag aatcgcctgg aagagaaatt tacccaacat actcattaga agaatttgta 180
gaatctttag agaaacctcg taagatttta ttaatggtaa aagctggacc tgcaacagat 240
gccactatag atggtttatt acctttatta gacgatgatg atattttaat tgatggtggt 300
aatactaatt accaagatac gattcgtcga aataaagctt tagctgaaag tagtattaac 360
tttattggta tgggagtttc tggtggagaa atcggcgcac tcacgggccc ttctttaatg 420
ccaggtggtc aaaaagatgc ttataacaaa gtcagcgata tcttggacgc aattgctgct 480
aaggcacaag atggtgcttc atgtgtaact tacattggcc ctaatggtgc aggacattat 540
gttaagatgg tacacaatgg tatcgaatat gcagatatgc aattaattgc tgaaagttat 600
gcaatgatga aagatttatt aggcatgtca cataaagaaa tttctcaaac ttttaaagaa 660
tggaatgctg gagaacttga aagttattta atagaaatta caggtgatat tttcaataaa 720
ttagatgatg acaatgaagc acttgtagaa aaaatattag atactgcagg tcaaaaaggc 780
acaggtaaat ggacttcaat taacgcacta gaattaggtg ttcctttaac aatcattaca 840
gaatctgtat ttgcgagatt catctcatca attaaagaag aacgtgttac tgcttctaaa 900
tctttaaaag gacctaaagc acattttgaa ggcgataaaa aaacattctt agaaaaaata 960
cgtaaggcac tttatatgag taaaatatgc tcatatgcac aaggtttcgc tcaaatgaga 1020
aaagccagtg aagataatga gtggaatttg aaattaggcg aattagcaat gatttggcgt 1080
gaaggttgta ttattcgtgc acaattccta caaaaaatta aagatgccta cgataataat 1140
gaaaacttac aaaacttatt attagaccct tacttcaaaa acattgttat ggaatatcaa 1200
gatgcactac gtgaagtagt agctactagc gtgtacaatg gcgtgccaac acctggtttt 1260
tcagcaagta taaattatta tgatagttat cgctcagagg atttacctgc aaacttaatt 1320
caagcacaac gtgattactt tggcgcacat acttatgaac gtaaagaccg tgaaggtatt 1380
ttccatacac aatgggtaga agaataa 1407
<210>54
<211>789
<212>DNA
<213>表皮葡萄球菌
<400>54
atgaaaagac ttttactttg cattgttgca cttgtttttg ttttagcagc ctgtggcaac 60
aattcatcta acaataaaga taatcaatca agcagtaaag acaaggatac gttaagagtt 120
ggtacggaag gtacatatgc gccctttact taccataata aaaaagatca attaacaggt 180
tatgatattg atgtgattaa agcagttgca aaagaagaaa atcttaaact taagtttaat 240
gaaacgtcat gggattcaat gtttgcagga ttagatgctg gtcgttttga tgttattgca 300
aatcaagtgg gtgtgaataa agatagagag aaaaaatata aattctctga accttacaca 360
tattcaagtg ctgtacttgt tgttcgtgaa aatgaaaaag atattacatc attcaatgat 420
gtaaaaggta aaaagttagc acaaacgttt acgtctaatt atggtcaatt ggctaaagat 480
aagggtgcgg acattactaa ggtagatgga tttaatcaat caatggactt actattatct 540
aaacgtgtag atggtacatt taacgacagt ttatcttact tagattacag aaaacaaaag 600
cctaatgcta aaattaaagc aatcaaagga catgcagaac aaaataaatc agcatttgca 660
ttctctaaga aggttgatga aaaaacgatt gagaaattta ataaaggcct agaaaaaatt 720
agagataatg gtgaattagc taaaattggt aagaaatggt ttggtcaaga tgtttctaaa 780
cctgaataa 789
<210>55
<211>933
<212>DNA
<213>表皮葡萄球菌
<400>55
gtgtatatga ctaaatatgt gttgaaacga ttgtgttata tgtttgtgtc gttatttatt 60
gttataacaa ttacattttt cttaatgaaa ttaatgccag gatctccgtt taatgacaca 120
aaacttaatg cgcaacaaaa agaaatatta aatgaaaagt acggtttgaa tgatccagta 180
gcattacaat atgttaatta tttgaaaaat gtagtaacag gtgattttgg caactcattt 240
caatatcata atatgccagt gtgggattta gttaaaccac gattgatacc ttcaatggag 300
atgggaataa cagctatggt tattggtgtt gttttaggtt tagtattagg tgttgctgct 360
gctactaaac aaaatacatg ggtagactat acaacaacaa ttatctctgt tatcgcagta 420
tcagtgccgt catttgtctt agcagtttta ttgcagtatg tatttgcagt taagttagaa 480
tggtttccag ttgcaggatg ggaaggtttt tctacagcta ttttaccttc tctagcacta 540
tcagctacag ttttagcaac tgttgcaaga tatattagag ctgaaatgat tgaagtactc 600
agttcagatt acatactttt agctcgagct aaaggaaatt ctactttaaa agtgctcttt 660
ggacatgcat tacgaaatgc attaattcct attattacaa tcattgtacc tatgttagca 720
ggtatattaa caggaacatt aacaattgaa aatatctttg gtgttccagg attaggtgat 780
caatttgttc gttctataac tacaaatgat ttttcagtca tcatggctac aacgatatta 840
ttcagtactt tatttattgt ttcgatcttt attgtagaca ttttatatgg tgttatcgat 900
ccaagaattc gtgtacaagg gggcaagaaa taa 933
<210>56
<211>1545
<212>DNA
<213>表皮葡萄球菌
<400>56
gtgaatgaag agcaaagaaa ggctggaacg ataaatattc tagcagaacg tgatcgtaaa 60
gctgagaaag attatagtaa atactttgaa caagtgtatc agccacctag cttaaaagaa 120
gctaaaaaaa gaggaaaaca agaagttcaa tataacagag attttcatat agatgaaaaa 180
tacaaaggta tgggtaaagg tcgcactttt ttaattaaaa catatggatg tcaaatgaat 240
gcacatgaca ctgaagttat ggcaggaata ttaaatgcat taggatatag tgctacttcg 300
gatattaatg aagcggatgt gattttaatt aatacatgcg ccattagaga aaatgctgaa 360
aataaagtct ttagtgaaat aggaaattta aaacatttaa aaaaagaacg cccagattgt 420
ttaattgggg tgtgtggttg catgtctcaa gaagaatcag tcgtaaataa aatattaaaa 480
tcttatcaaa atgtagatat ggtttttggg acacacaaca ttcatcattt acctgagatt 540
ttagaagagg catatttatc taaagcgatg gtagttgaag tatggtctaa agagggagac 600
atcatcgaaa atttacctaa agtgcgtgac ggtcacatta aagcttgggt taatattatg 660
tatggttgcg ataagttttg tacttattgt attgttccat ttactagagg aaaagaacgt 720
agtcgtcgtc cagaggacat cattgatgag gttagagaat tagcaagaga aggttatcaa 780
gaaattacct tattaggtca aaatgtaaat tcatatggta aagatatcga aggtctggat 840
tatgaattag gtgacttatt ggaagatatt tctaaaattg atatacctcg tgttcgtttt 900
acaacaagtc atccttggga ctttacagat cgaatgattg aagttatagc taaaggtggg 960
aacatagtac cgcatatcca tttaccggta caatcaggta ataaccaagt attaaagata 1020
atggggcgta aatatacaag agagagttat cttgatttag tttcaagaat aaaggaagct 1080
atccctaacg tagctctaac tactgatatc atagtaggtt atcctaatga aactgtagaa 1140
caatttgaag aaacattatc attatatgat gacgttcaat ttgagcatgc atacacatat 1200
ttatattcac aaagagatgg aacaccagca gctaaaatga aggataacgt acctttagaa 1260
gtgaaaaaag aacgtttgca aaggcttaat aagaaggttg gaatatattc tcaacaagca 1320
atgagtcagt atgaaggtaa gattgttacg gtattatgtg aaggttctag taaaaaagat 1380
gagaatgttc tagcaggcta tactgataaa aataaacttg tgaattttaa aggaccaaga 1440
gagagcattg gtaaactcgt tgatgtcaaa attgacgagg caaaacaata ttctttaaat 1500
ggaacattta tacaagaaca tcaacgttca atggtgacac aataa 1545
<210>57
<211>1185
<212>DNA
<213>表皮葡萄球菌
<400>57
atgtcacgca tagtattagc tgaagcatat cgaacaccta taggcgtgtt tggtggtgta 60
tttaaggata tacctgccta tgaactaggt gcaacagtta ttcgtcaaat tttagaacat 120
agtcaaatag atcctaatga aatcaatgaa gttattctag gaaacgtatt acaggcaggt 180
caaggacaaa atcctgctcg tattgctgcg attcatggtg gtgtgccaga agcggtacct 240
tcttttactg taaataaagt ttgcggttct ggattaaaag cgattcaact tgcctatcaa 300
tctattgtag cgggagataa tgagattgtt atcgctggag gcatggaaag tatgtctcaa 360
tctccaatgc ttcttaaaaa tagtcgtttc ggttttaaaa tgggaaatca aactttagaa 420
gatagtatga tagctgatgg tttaactgat aagtttaatg attaccatat gggtatcaca 480
gccgaaaatc tagttgaaca gtatcagatt agtcgtaaag aacaagatca atttgcattc 540
gattctcaac aaaaagcatc acgtgcacaa caagctggtg tatttgatgc tgaaattgta 600
cctgtagagg taccacaacg taaaggcgac cccctaatta tttctcaaga tgaaggcatt 660
agacctcaaa cgacaattga taagttagca caactccgtc cagcatttaa aaaagatgga 720
tcagtaactg ctggtaatgc atccggtatc aatgacggtg ctgctgctat gctcgttatg 780
acggaggaca aagcgaaagc attgggctta caacctatag ctgtattaga tagttttggt 840
gcgagtggtg tggcgccttc aattatgggt attggtccag ttgaagcgat acataaagct 900
ttaaaacgtt ctaataaagt gataaatgat gttgatattt ttgaattaaa cgaagctttt 960
gcagcgcaat caattgctgt aaaccgtgag ttgcaattac cgcaagataa agtcaatgtt 1020
aatggtggtg cgattgcact aggacatccg ataggggctt cgggtgcgcg tactttagtt 1080
tcattattac atcaattaag tgatgctaag ccaacaggtg tggcatcttt atgtatcggt 1140
ggcggtcaag gtatcgctac ggttgtatct aaatatgaag tttaa 1185
<210>58
<211>879
<212>DNA
<213>表皮葡萄球菌
<400>58
atggcaattt cagcaaaact tgttaaagaa ttacgtgaaa aaactggcgc aggaatgatg 60
gattgtaaaa aagcgctaac tgaaactgat ggtgacatcg ataaagcgat tgactactta 120
cgtgaaaaag gtattgcaaa agcagctaaa aaagctgacc gtatcgcagc agaaggactt 180
gtacacgttg aagtaaaaga taatgaagct gcaatcgttg agattaattc agaaacagac 240
ttcgtagcac gtaacgaagg tttccaagaa ttagttaaag aaattgctaa ccatatttta 300
gatagcaagg tagaaacagt agacgctttg atggaatcta aattatctag cggtaaaact 360
gttgatgaaa gaatgaaaga agctatctca acaattggtg aaaaattaag tatccgtcgt 420
ttctctatca gaacaaaaac tgataatgat gcatttggtg catatttaca catgggtgga 480
cgtattggtg tgttaactgt agtggaaggt actactgatg aagaagctgc taaagacgta 540
gcaatgcaca ttgcggcaat caaccctaag tatgtttctt ctgaacaagt aagcgaagaa 600
gaaatcaatc atgaaagaga agtattaaaa caacaagcat taaacgaagg taaaccagag 660
aaaatcgttg aaaaaatggt tgaaggtcgt ttacgtaaat atttacaaga aatttgtgct 720
gtagatcaaa acttcgttaa aaatccagac gaaactgttg aagctttctt aaaagctaaa 780
ggtggtaaac ttactgattt cgttcgttat gaagttggag aaggtatgga aaaacgtgaa 840
gaaaactttg ctgaagaagt taaaggacaa atgaaataa 879
<210>59
<211>933
<212>DNA
<213>表皮葡萄球菌
<400>59
atgactgaag tagattttga tgtagcaata atcggtgcag gtcctgccgg tatgacagca 60
gcagtatatg catctcgtgc caatttaaaa actgtcatga ttgaacgcgg tatgccaggc 120
ggtcaaatgg caaacactga agaagtagag aattttccag gatttgagat gatcacaggt 180
cctgacttat ctactaaaat gtttgaacat gctaaaaaat ttggtgcgga ataccaatat 240
ggcgatatta aatctgttga agataaaggc gactataaag ttatcaattt agggaataaa 300
gagataacag cacatgcagt tattatctca actggagcag agtataaaaa gattggcgtt 360
cctggtgaac aagaattagg aggacgtgga gtaagttatt gtgcggtttg tgatggagca 420
ttctttaaaa ataaacgtct tttcgtaatt ggcggcggag attcagcggt agaagaaggt 480
actttcttaa ctaaatttgc agataaagta acgattgttc accgtagaga tgaattacgt 540
gcacaaaaca tcttgcaaga acgtgccttc aaaaatgata aagttgactt tatttggagt 600
catacactta aaacaattaa tgaaaaagat ggtaaagttg gttcagttac acttgaatca 660
actaaagatg gtgctgaaca gacttatgat gccgacggtg tattcattta tattggaatg 720
aaaccactca cagcaccatt taaaaatctt ggtattacaa atgacgcggg atacattgtc 780
acacaagatg acatgagtac taaagtacga ggtatttttg ctgcaggtga cgttcgtgat 840
aaagggttac gtcaaattgt tactgctaca ggagacggta gtattgcggc tcaaagtgca 900
gctgattata ttacagaatt aaaagataat taa 933
<210>60
<211>1398
<212>DNA
<213>表皮葡萄球菌
<400>60
atgactcaaa agtatagata tcctactttt ttagaatcta tttctactat tttagttatg 60
gttgtcgttg tagtaattgg ttttgttttc tttaatgtcc cgatacaaat attattatta 120
atttcttcag cttatgcagc attgattgca catagagtgg gattaaaatg gaaggattta 180
gaagagggga ttactcatcg attgagcacg gcgatgccag ctatctttat tattttagct 240
gttggaatca ttgtaggaag ttggatgtat tctggaacag ttccagcgtt aatttactat 300
ggacttaaat ttttaaaccc aagttattta ttagtatctg catttataat cagtgcaatg 360
acttcaatcg ctacaggaac ggcttgggga tcggcatcta cagcaggcat tgcactcata 420
tcaattgcta atcaattagg tgtgccagca ggtatggctg ctggtgccat tattgcaggg 480
gcggtttttg gtgataaaat gtctccatta tctgatacta caaatttggc agctcttgta 540
actaaagtta atatttttgc tcacattaaa tcgatgatgt ggacaacaat ccctgcttct 600
ataataggat tggctatatg gtttattgtt ggattacaat ataagggaga cgcaaataca 660
caacaaattc aaaatctatt aaaagaatta acaacaattt ataacttgaa tttttgggta 720
tggatcccac ttattatcat agttttatgt ttaatattta gaatctctac agtaccgtca 780
atgcttatct ctagtatcag tgctttagtt attggaacat tcgatcatca atttaatatg 840
aaagatggtt ttaaagcttc ttttgatgga tttaatcata caatgctaca ccagtctcat 900
atttcagata atgctaagac gttgattgag cagggtggta tgatgagtat gactcaaatc 960
attgtaacta tattttgtgg ttatgctttt gctggtattg ttgaaaaggc aggttgttta 1020
gacgtaattt tagagacaat agctaaaggc gtaaagtcag ttggaacact aatattaata 1080
actgtagttt gtagtattat gctagtattt gcagctggag ttgcttcaat agttattatt 1140
atggtaggcg tacttatgaa agatatgttc gaaaagatga atgtctcaaa gtcagtgtta 1200
tctcgtacac ttgaagattc aagtacaatg gtattgccac tcattccatg gggcacatct 1260
ggtatatatt atgcacacca acttaatgtt tcagttgatc agttctttat atgggcaatc 1320
ccatgttact tatgtgcatt cattgcaata atttatggct ttacaggtat aggaattaaa 1380
aaaataagta gaaaataa 1398
<210>61
<211>708
<212>DNA
<213>表皮葡萄球菌
<400>61
atgaaaaaaa cagttatcgc ttctacatta gcagtatctt taggaattgc aggttacggt 60
ttatcaggac atgaagcaca cgcttcagaa actacaaacg ttgataaagc acacttagta 120
gatttagcac aacataatcc tgaagaatta aatgctaaac cagttcaagc tggtgcttac 180
gatattcatt tcgtagacaa tggataccaa tacaacttca cttcaaatgg ttctgaatgg 240
tcatggagct acgctgtagc tggttcagat gctgattaca cagaatcatc atcaaaccaa 300
gaagtaagtg caaatacaca atctagtaac acaaatgtac aagctgtttc agctccaact 360
tcttcagaaa gtcgtagcta cagcacatca actacttcat actcagcacc aagccataac 420
tacagctctc acagtagttc agtaagatta tcaaatggta atactgctgg ttctgtaggt 480
tcatatgctg ctgctcaaat ggctgcacgt actggtgtat ctgcttcaac atgggaacac 540
atcattgcta gagaatcaaa tggtcaatta catgcacgta atgcttcagg tgctgctgga 600
ttattccaaa ctatgccagg ttggggttca actggttcag taaatgatca aatcaatgcc 660
gcttataaag catataaagc acaaggttta tctgcttggg gtatgtaa 708
<210>62
<211>891
<212>DNA
<213>表皮葡萄球菌
<400>62
atgaataaag aacaattaga aaaaatgact catggtaaag gattcattgc tgcattagac 60
caaagtggtg gtagtacacc taaagcactt aaagaatatg gtgtgaatga agaccaatac 120
agtaatgaag acgaaatgtt ccaacttgtt cacgatatgc gtacacgtgt tgtaacttca 180
ccttcatttt cacctgataa aattttaggt gcgattttat tcgaacaaac tatggatcgc 240
gaagttgaag gtaaatacac tggagactat ttagcggaca aaggcgttgt tcctttctta 300
aaagtcgaca aaggtcttgc tgaagagaaa aatggcgtac aattaatgaa acctattgat 360
gatttagatg aaactttaga tcgtgcaaat gaacgtcata tcttcggtac taaaatgcgt 420
tctaacatcc ttgaacttaa tgaacaagga atcaaagatg ttgttgaaca acaatttgaa 480
ttcgctaaaa aaatcatcgc taaaggttta gtacctatta tcgaaccaga agttaatatt 540
aatgctaaag ataaatctga aattgagaaa gttttaaaag ctgaaatcaa aaaaggttta 600
gattcattaa acgatgatca attagttatg ttaaaattaa ctattcctac tgaagctaac 660
ttatataaag atttagctga ccaccctaat gttgtacgtg tagtagtatt atcaggtggt 720
tacagccgag atgaagctaa caaattgtta aaagataacg atgaattaat tgcaagcttc 780
tcacgtgcat tagcaagtga cttacgtgct agccaatcac aagaagaatt cgataaagca 840
ttaggcgatg ctgtagattc aatctatgat gcgtcagtaa ataaaaacta a 891
<210>63
<211>792
<212>DNA
<213>表皮葡萄球菌
<400>63
ttgaaagaga gatttattaa gaaaactcat tatttagact atcaatttga tgagcctact 60
gatattaagt taggtttcac tactcgagaa aatgggttaagtccttatcc taatcatagt 120
tttaatatgg cgagatatat cagtgacagt gcacatcata ttacacatca tcaagatatc 180
ttagcgaatc ttattggtta tccaagagat gaatgggttt ttcctataca aacacatgat 240
agtcgtatcg ttgaagttac aagtgaacat aaaggaacaa atattgatga actaactgat 300
gatttacatg gcatagatgg aatgtatact tttgattctc acattcttct tactatgtgt 360
tatgcggatt gcgtacctgt atatttttat agtgaaccac atggatatat aggattagca 420
catgcaggtt ggcgaggaac atatggtcaa atagtaaaag acatgctaaa aaaagtggat 480
tttgattatg aagacttaaa gattgtaatt ggtccagcaa cttcaaattc ttatgaaatc 540
aatgatgata taaaaaataa gtttgaggaa ttaaccattg attcaacttt atatattgag 600
accagaggta aaaatcaaca tggtattgat ttgaaaaacg ctaacgcact tcttctagaa 660
gaagctggag ttccatcaaa aaacatatac gttacggaat atgcaacttc agaaaactta 720
gatttattct tttcatatcg tgttgaaaaa ggacagacgg gacgtatgtt agcatttatt 780
ggacggaagt aa 792
<210>64
<211>30612
<212>DNA
<213>表皮葡萄球菌
<400>64
atgaagagca aaccgaaatt aaacggtcgg aacatctgct cttttttatt gagcaaatgt 60
atgagttatt cattgtcaaa attatcaaca ttaaaaacgt ataattttca aatcacatca 120
aacaacaaag aaaaaacatc aagaatagga gtggcaatag ctttgaataa tcgtgataaa 180
ttacaaaaat ttagtattcg aaaatacgca attggaacat tttctactgt gattgcaaca 240
cttgtgttca tgggtatcaa tacaaaccat gcaagtgccg acgagttgaa tcaaaatcaa 300
aagttaatta aacaattaaa tcaaacagat gatgatgatt cgaatacgca tagtcaagaa 360
atcgaaaata acaaacaaaa ttctagtggg cagactgaat cattacgttc atcaactagt 420
caaaatcaag caaatgcacg actgtcggat caattcaaag acactaatga aacatcgcaa 480
caattaccta caaatgtttc ggatgatagt atcaatcaat cgcatagtga agcaaatatg 540
aataacgaac cattgaaagt tgataatagt actatgcaag cacatagtaa aatagtaagc 600
gatagcgatg ggaatgcttc tgaaaataaa catcataaac taacagaaaa tgtacttgca 660
gaaagccgag caagtaaaaa tgacaaagag aaagagaatc tacaagagaa agataaatcg 720
cagcaagtac atccaccatt agataaaaat gcattacaag ctttttttga cgcatcatat 780
cacaattaca gaatgattga tagagatcgt gcggatgcaa cagaatatca aaaagtcaaa 840
tctacttttg actacgtcaa tgacttacta ggtaataatc aaaatattcc ttcagaacag 900
cttgtttcgg catatcaaca attagagaaa gcattagaac ttgcacgtac gttatcacaa 960
cgatctacta cagaaaaacg tggtagaaga agtacgagaa gtgttgttga gaatcgttca 1020
tcaagaagcg attacttaga tgctagaact gaatattatg tttcaaaaga cgatgatgat 1080
tctggtttcc ctcctggtac tttcttccat gcttcaaata gaagatggcc ttataattta 1140
ccaagatcta ggaacatctt acgtgcttct gatgtacaag gtaatgctta tatcactaca 1200
aaacgactta aagatggata tcaatgggat attttattta atagtaatca taaagggcat 1260
gaatatatgt actattggtt tggacttcca agtgatcaaa caccaactgg tccagtaact 1320
ttcactatta tcaaccgtga tggttcaagt acatctactg gtggcgttgg atttggatca 1380
ggtgcaccac tacctcaatt ttggagatca gcaggtgcta ttaattctag cgtagcgaat 1440
gattttaaac atggctccgc tacaaattat gcattttatg atggtgttaa taatttttct 1500
gactttgcta gagggggaga attatacttc gacagagaag gcgctacaca aactaataaa 1560
tattatggcg atgaaaactt cgcattgcta aatagtgaga aaccagatca aataagagga 1620
ttagatacaa tatatagttt taaaggtagt ggtgatgtaa gttatcgtat ttcatttaaa 1680
actcaaggag ctccaactgc aagattgtat tatgctgctg gcgcgcgttc tggtgaatat 1740
agacaagcaa cgaactataa ccaactctat gtcgaacctt ataagaatta tcgaaatcga 1800
gtacagtcaa atgtccaagt taaaaatcgt acacttcatt taaaaagaac aatcagacaa 1860
ttcgatccta cattacagag aactactgat gttcctattt tggatagtga cggttccgga 1920
agtattgatt cggtatacga cccattaagt tatgtaaaga atgtgactgg tacagtccta 1980
ggtatttatc catcttatct tccgtataat caggaaagat ggcagggagc taatgcaatg 2040
aatgcctatc aaattgaaga acttttttca caagaaaatc ttcaaaatgc agcacgttca 2100
ggtcgtccaa ttcaatttct tgtaggtttt gatgttgaag atagccatca taaccctgaa 2160
actcttttac cagtaaattt atatgtaaaa cctgagttaa aacatacaat tgagttatat 2220
cacgataatg aaaaacaaaa tagaaaggaa ttttcagtatcgaaacgagc gggccatggt 2280
gttttccaaa taatgagtgg aacgcttcat aacactgtag gatcaggaat attaccttat 2340
caacaagaga ttcgtatcaa acttactagt aatgaaccaa ttaaagatag tgaatggtct 2400
attacaggat atcctaacac gcttacatta caaaacgctg tgggtagaac aaataatgct 2460
actgaaaaaa acttagctct tgttggtcat attgatccag gaaattattt catcactgtt 2520
aagtttggtg ataaagtaga acaatttgaa attagatcaa aaccaactcc accaagaatc 2580
attacaactg ctaatgaatt acgtggaaat cctaaccaca agcctgaaat aagagtaaca 2640
gatataccaa atgatactac tgctaaaatc aaacttgtga tgggcggaac cgatggtgat 2700
catgatccag aaataaatcc atatactgtc cctgaaaact acacagtagt tgcagaagca 2760
taccatgata atgatccaag taaaaatggg gtcttaacat tccgttcatc agactacctt 2820
aaagatctac cattaagcgg tgaattaaag gcaattgttt attacaatca atatgtacaa 2880
tcaaacttta gtaatagcgt tccgtttagt agcgatacaa caccacctac aattaatgaa 2940
ccagcaggac tagttcataa gtattacagg ggagatcatg tagaaattac tcttccagtc 3000
actgataata ctggcggttc aggtttaaga gatgtaaacg tcaatttacc tcaaggttgg 3060
acaaaaacct ttacaatcaa tcctaataat aatactgagg gtacgcttaa gttaattggt 3120
aatataccta gtaatgaagc atataatacg acatatcatt tcaatattac tgcaaccgat 3180
aattctggaa atacaacaaa tccagctaaa acctttattt taaatgttgg taagttggct 3240
gatgatttaa atccagtcgg attatctaga gatcaactac aattagtgac agacccttct 3300
tcattatcta attccgaacg agaagaggta aaaagaaaaa taagtgaagc aaatgctaat 3360
ataagatcat atttattaca aaataaccca atactcgctg gagtaaacgg cgatgttaca 3420
ttttattata gagatggttc tgtagatgtt attgatgctg aaaatgtaat cacatatgag 3480
cccgaaagaa aatccatttt cagtgaaaat ggtaatacaa ataaaaaaga agcagtaatc 3540
actattgcta gaggacaaaa ctataccatt ggtccaaact taagaaaata tttctcatta 3600
agtaatggtt cggatttacc taatagagat ttcacctcta tatcagctat tggatcttta 3660
ccttcatcga gtgaaattag tcgactcaat gttggaaatt ataactatag agttaatgct 3720
aaaaatgctt atcataagac tcaacaagaa cttaatttaa aacttaaaat agtagaggtt 3780
aatgcaccta ctggtaataa tcgtgtatat agagttagta cttataattt aactaatgat 3840
gaaatcaata aaatcaaaca agcatttaaa gcagctaatt ctggacttaa tttaaacgat 3900
aacgatatca ctgtttcgaa taactttgac catagaaatg ttagtagtgt gacagtaact 3960
atacgtaagg gcgatttgat aaaagagttt tcatcaaatc tcaataatat gaatttctta 4020
cgttgggtta atataaggga tgattatacc atttcgtgga cttctagtaa gattcaaggt 4080
agaaatacag atggtggatt agaatggtca ccagatcata aatcacttat ttataaatat 4140
gatgcaacat taggtagaca aataaatact aatgacgtgt taactttact tcaagcaaca 4200
gctaaaaact caaatttacg ttcaaatatc aatagtaatg aaaaacagtt agcagaacga 4260
gggtctaatg ggtattctaa atctataatt agagatgatg gcgagaaatc ttatttactt 4320
aactcaaatc ctattcaagt attagactta gtagaaccag ataatggtta cggtggacgt 4380
caagtcagtc attctaacgt tatatataat gaaaaaaatt cttctatcgt aaatggtcaa 4440
gttccagaag ctaatggggc atccgctttt aatattgata aagttgttaa agctaatgcg 4500
gcaaataatg gtattatggg tgttatctat aaggcacaat tatacttagc accatacagt 4560
ccaaaaggtt acattgaaaa attaggccaa aatttaagca ataccaataa cgtgattaat 4620
gtttattttg tgccttctga taaagtaaat cctagtataa ctgtaggtaa ttacgaccat 4680
catacggtat attctggtga aacatttaaa aatactatca atgtaaatga taattatgga 4740
ttaaatacag tagcttctac aagtgatagt gcaattacta tgaccagaaa caacaacgag 4800
ttagtaggtc aggctcctaa tgttactaat agcacaaata aaattgtaaa agttaaagcc 4860
acagataaaa gtggaaatga aagtattgtt tctttcacag taaatataaa accattaaac 4920
gagaaatata gaataacaac ttcatcaagt aatcaaacac cagtgagaat tagtaatatt 4980
caaaacaatg ctaacctttc aattgaagat caaaatagag taaaatcttc actcagcatg 5040
actaaaattt taggtacaag aaattatgtc aatgagtcaa ataatgacgt tcgtagtcaa 5100
gttgtaagta aagtaaatag aagtgggaac aatgctacag ttaatgttac aactacattt 5160
tctgatggta caactaatac aataaccgtt ccagttaaac atgtgttatt agaagttgta 5220
cctactacta gaacaacagt aagaggacaa caatttccaa ccggcaaagg aacttcccca 5280
aatgatttct ttagtttaag aacgggaggt ccagttgatg cgagaatagt ttgggttaat 5340
aatcagggac ccgatataaa tagtaatcaa attggtagag atttaacatt acacgctgaa 5400
atattctttg atggtgaaac aacaccaatt agaaaagata cgacttacaa acttagtcaa 5460
tctattccaa agcaaatata tgaaacaact atcaatggtc gatttaattc atcaggtgat 5520
gcatatccag gaaattttgt tcaagcagta aatcaatatt ggccagaaca tatggacttc 5580
agatgggccc aaggatcagg cacaccaagt tctcgtaatg caggttcatt tactaaaaca 5640
gttacggtag tttatcaaaa cggccaaact gaaaacgtta atgtactatt caaagtcaaa 5700
ccaaataaac ctgttattga tagtaatagt gtgatttcaa aaggacaatt aaatggtcaa 5760
caaattttag ttcgaaatgt tccacaaaat gcacaagtca ctctatatca atcaaatgga 5820
actgttattc ctaatacaaa tacaactata gattctaatg gtatagctac tgtaacaatt 5880
caaggcactc taccaaccgg aaatattact gctaaaacct caatgacaaa taatgtaacg 5940
tacactaaac aaaatagtag tggaattgct tcaaatacaa ctgaagatat aagtgttttt 6000
tcagaaaaca gtgatcaagt aaatgttacc gctggcatgc aagctaaaaa tgatggtatt 6060
aaaataatta aaggtacaaa ctataatttt aatgacttca atagtttcat aagtaatata 6120
ccagcccatt ctactcttac atggaacgag gagcctaata gttggaaaaa caacatcggt 6180
actacaacaa aaactgttac agttactcta cctaatcatc aaggtacgag aactgtagat 6240
attccaataa caatctatcc aacagttaca gctaagaatc cagtaagaga tcaaaaagga 6300
cgaaacttaa ccaatggtac tgacgtttat aattatatta tttttgaaaa taataaccgt 6360
cttggaggaa cagcttcttg gaaagacaat cgtcaacctg ataaaaacat agccggtgta 6420
caaaatttaa ttgcacttgt taattatcct ggcatatcta caccattaga agttcctgtt 6480
aaagtgtggg tatataattt tgatttcact caacctatct acaaaattca agtaggagat 6540
acattcccta aaggaacatg ggcaggctat tacaaacatc ttgaaaatgg agagggatta 6600
ccaatagatg gttggaaatt ttattggaac cagcaaagta caggaactac tagtgatcaa 6660
tggcaatcat tagcatatac tagaactcct tttgttaaaa ctggtactta tgatgtcgtt 6720
aatcctagca actggggtgt ttggcaaaca tcacaatcag ctaaatttat agttacaaat 6780
gctaaaccta atcaaccaac cataactcag tctaaaactg gtgatgtaac agtaacacct 6840
ggtgctgtgc gtaatatact aataagtggg acaaatgatt atatccaagc atctgcagat 6900
aagattgtta ttaataaaaa tggaaataaa ttaactacat ttgttaagaa taatgatggt 6960
cgttggactg ttgaaactgg gtcacctgac ataaatggta tcggaccaac aaataacgga 7020
actgctatat ctttaagtcg attagcagtt agacctgggg attcaataga agcaatagcg 7080
actgaaggtt ccggagaaac tataagtact tcagcaacta gtgaaattta tattgtcaaa 7140
gctccacaac ctgaacaagt agcaactcat acttatgata atggaacatt cgatatatta 7200
cctgacaatt cacgtaattc tttaaatcca actgaacgtg tcgaaattaa ttacactgaa 7260
aaattaaatg gcaatgaaac acaaaaatca ttcactatta ctaaaaataa caacggcaaa 7320
tggacgataa ataataaacc aaattatgtc gagttcaatc aggataatgg taaagttgta 7380
ttttcggcca atacaattaa acctaattct caaattacaa taactcctaa agcaggtcag 7440
ggtaacactg aaaacacaaa tcctactgta attcaagcac ctgcgcaaca tactttaaca 7500
atcaatgaaa ttgttaaaga acagggtcaa aatgtgacta atgatgatat taataatgcg 7560
gttcaagtgc caaataaaaa tagagttgcg attaaacaag gaaacgctct tccaacaaat 7620
ttagctggtg gtagtacatc acatattcca gtagttattt attacagtga tggaagttct 7680
gaagaagcta ctgagactgt tagaactaaa gttaataaaa ccgaattaat caatgctcgt 7740
cgtcgactag atgaagaaat tagtaaagag aacaaaacac catcaagtat cagaaacttt 7800
gatcaagcta tgaatcgtgc tcaatcacaa attaatacag ctaaaagtga tgctgaccaa 7860
gttataggca cagaatttgc aacacctcaa caagtaaatt cagctttatc taaagttcaa 7920
gcggcacaaa ataaaataaa tgaagctaaa gcattattac aaaacaaggc tgataatagt 7980
caacttgtga gagcaaaaga acaattacaa caatcgattc aaccagccgc ttcaactgat 8040
ggtatgactc aagatagcac aaggaactac aaaaataaac gccaagcagc tgaacaagca 8100
atacaacatg caaatagcgt tataaataat ggagatgcaa catcccaaca aattaatgat 8160
gctaaaaaca cagttgaaca ggcacagaga gattatgttg aagctaaaag caacttacgt 8220
gctgataagt cacagttaca aagcgcttat gatacgttaa atagagatgt tttaacaaat 8280
gataaaaagc cagcatctgt aagacgctat aatgaagcca tttcaaatat tagaaaagaa 8340
ttagatacag ctaaagcgga tgcaagtagt actttgcgaa acaccaatcc ttccgttgaa 8400
caagttagag acgctttaaa taaaataaat actgttcaac ctaaagtgaa tcaagcaatt 8460
gctttacttc aaccaaaaga aaataattca gaacttgtac aagctaaaaa acgtttacaa 8520
gacgctgtaa atgacatacc tcaaacacaa ggtatgacac aacaaacaat taataattat 8580
aatgacaaac aacgtgaagc tgaaagagca cttacatctg cacaaagagt gattgataat 8640
ggggatgcta caactcaaga aattacttct gaaaaatcta aagtagagca agcaatgcaa 8700
gctttaacta atgctaaaag taatctgaga gctgataaga atgagttaca gactgcatat 8760
aacaaattaa ttgagaacgt atctaccaat ggtaaaaaac cggcgagtat acgtcaatac 8820
gaaacagcca aagccagaat acaaaatcaa attaatgatg ctaaaaatga agcggagcga 8880
attttaggta atgataatcc acaagtatca caagtaactc aagcattgaa caaaatcaaa 8940
gctattcaac caaaattaac agaagctatc aacatgcttc aaaacaaaga aaataataca 9000
gaattagtca atgctaaaaa cagacttgaa aatgcagtaa atgatacaga tccaacacac 9060
ggtatgactc aagaaacaat taataattac aacgctaaaa agcgagaagc tcaaaatgaa 9120
atacaaaaag cgaacatgat tattaataat ggagatgcta ctgctcaaga tatttcttct 9180
gaaaaatcta aagtagagca agtattacaa gcattacaaa atgctaagaa tgacttaaga 9240
gctgataaaa gagaattaca gactgcatac aataaactta tacaaaatgt taataccaat 9300
ggtaaaaaac catctagtat tcaaaactat aagtctgcaa gacgaaatat cgaaaaccaa 9360
tataataccg ctaaaaatga agcacataat gttcttgaaa atacaaaccc tactgtaaat 9420
gcagtagaag atgctttacg taagataaat gcaattcaac cagaggttac aaaagctatt 9480
aatatacttc aagataaaga agataatagc gaacttgtta gagcaaaaga aaaattagat 9540
caagcgatta atagtcaacc atcactaaat ggtatgactc aagaatctat taataattac 9600
acaacaaaac gtagagaagc acaaaatata gcaagttctg ctgacactat tattaataat 9660
ggggatgcat ctattgaaca aataacagaa aataaaattc gagttgaaga ggcaactaat 9720
gcacttaacg aagcaaaaca acatttaacg gcagatacaa cttctttaaa aactgaagta 9780
cggaaattaa gtaggagagg cgacacaaac aacaaaaagc ctagcagtgt tagtgcttat 9840
aacaatacta ttcattcgct acaatctgaa attacacaga ctgaaaatag agcaaatact 9900
atcatcaata agcctattcg ttctgttgaa gaagtaaata atgcattgca tgaagtaaac 9960
caattgaacc aacgcttaac agatacaatt aacttattac aacctttagc gaataaagaa 10020
agcttaaaag aagctcgtaa tcgacttgaa agtaaaatta atgaaaccgt tcaaacagac 10080
ggtatgactc aacaatctgt tgagaattat aagcaagcta aaataaaagc tcaaaatgaa 10140
tctagtattg cacaaactct tattaataat ggtgatgcat ctgatcaaga agtttctaca 10200
gaaatagaaa aattaaatca aaagctgtct gaattaacaa attcaatcaa tcacttaaca 10260
gttaataaag aacctttaga aactgccaaa aatcagttac aagcaaatat tgaccaaaaa 10320
cctagcactg atggtatgac gcaacaatct gtacaaagct atgaacgtaa actacaagaa 10380
gccaaagata aaataaactc aattaataat gtcttagcta acaatccaga tgttaatgct 10440
atcagaacaa acaaagttga gacggaacaa atcaataatg aattaacaca ggcgaaacaa 10500
ggtcttactg ttgataaaca accattgatt aatgcaaaaa ctgctttgca acaaagtcta 10560
gataatcaac caagtactac tggtatgact gaagcaacaa ttcaaaatta taacgctaaa 10620
cgtcaaaaag cagagcaagt tatacaaaat gcaaataaaa ttattgaaaa cgctcaacct 10680
agtgtacaac aagtgtctga tgagaaatct aaggtagagc aagcactcag tgaattgaac 10740
aacgccaaat cagcgcttag agctgataaa caagaattac agcaagcata taatcagttg 10800
attcaaccaa cggatttaaa taataagaaa ccagcttcta tcactgcgta caatcaaaga 10860
tatcaacaat ttagtaacga attgaacagc actaaaacaa atacagatcg cattttaaaa 10920
gagcaaaatc caagtgtagc tgatgtcaac aatgcactaa ataaagtaag agaagtacaa 10980
caaaaattaa acgaagccag agcactttta caaaataaag aagataatag tgcactagtt 11040
cgagccaaag aacaacttca acaggcagtt gaccaagtcc cttcaacaga aggtatgacg 11100
caacaaacta aagatgatta caattcaaaa caacaagctg ctcaacaaga aatatcaaaa 11160
gcacaacaag ttatcgataa tggcgatgcg actacacaac aaatttctaa cgccaaaaca 11220
aatgttgaac gcgctttaga agcattaaat aatgcaaaaa ctggtttaag agcagataaa 11280
gaggaacttc aaaatgcata taatcaatta actcaaaata ttgatacgag cggtaaaacg 11340
cctgcaagta tcaggaaata caatgaagct aagtcacgta ttcaaactca aattgattca 11400
gctaaaaatg aagcaaacag tattttaaca aatgacaatc ctcaagtatc acaagtgact 11460
gctgcgttaa acaaaataaa agctgttcaa cctgaattag ataaagcgat agcaatgctt 11520
aaaaataaag agaataataa tgcattggtt caagcgaaac aacaacttca acaaattgtt 11580
aatgaagtag atccaacaca aggcatgaca acagatactg ctaataacta taaatcaaaa 11640
aaacgtgaag ctgaagatga aatacaaaaa gctcaacaaa tcattaacaa tggcgatgcc 11700
actgagcaac aaattactaa cgaaacaaat agagtaaatc aagcgattaa tgcaataaac 11760
aaagccaaaa acgatttacg tgctgataag tctcaattgg aaaatgctta taaccaatta 11820
atacaaaatg ttgatacaaa tggtaaaaaa cctgctagta ttcaacaata ccaagctgct 11880
cgacaagcta ttgagacgca atacaataac gctaaatcag aagcacatca aattcttgaa 11940
aatagtaacc cttcagttaa tgaagtagca caagcattac aaaaagttga agctgtacaa 12000
cttaaagtta atgacgcgat tcatatactt caaaataaag ataataatag tgcacttgtc 12060
acagctaaaa atcaacttca gcaatcagtt aatgatcaac cattaacaac aggtatgact 12120
caagattcta ttaataacta tgaagctaag agaaatgagg ctcaaagtgc tatcagaaat 12180
gcagaagctg tcatcaacaa tggcgatgca actgcaaaac aaatttcaga cgagaaatct 12240
aaagttgaac aagcactagc acatttgaat gatgctaaac agcaattaac tgcagatact 12300
actgaattac aaacagcagt tcaacaatta aacagaagag gcgatacaaa taataaaaag 12360
ccaagaagta tcaatgcata taataaagca attcaatcat tagaaacaca aattacttct 12420
gctaaagata atgccaacgc tgtgatacaa aaacctatac gtactgttca agaggtaaat 12480
aatgcattac aacaagtaaa tcagttgaat caacaattaa ctgaagcaat taatcaactt 12540
caaccgctat caaataatga tgcattaaaa gctgcaaaat taaatttaga aaataaaatt 12600
aatcaaactg tacaaactga tggtatgaca caacaatcta tagaggctta tcaaaacgct 12660
aaacgcgtag cccaaaatga atctaacact gctttagcat taattaataa cggcgatgcc 12720
gatgaacaac aaattacaac tgaaacagac cgagtcaatc agcaaactac aaacttaact 12780
caagcaatta acgggttaac agttaataaa gaaccattag aaaccgctaa aacagcgtta 12840
caaaataaca tcgaccaggt acctagtaca gatggtatga ctcagcaatc tgttgcaaat 12900
tataatcaaa aactacaaat agctaaaaac gaaattaaca caattaataa cgttttagcg 12960
aacaatccag atgttaatgc aatcaaaacg aataaagcag aagcggaacg aatcagtaac 13020
gatttaacac aagctaagaa taacttacaa gttgatactc aacctttaga aaaaataaaa 13080
agacaacttc aagatgaaat tgatcaaggt actaacacag atggaatgac tcaagattca 13140
gtggataatt acaatgatag cttaagtgca gcaattatag aaaaaggcaa agtaaataaa 13200
ttacttaaac gtaatccgac agtagaacaa gttaaagaga gcgttgctaa tgcacaacaa 13260
gtcatacaag atttacaaaa tgctcgaact tcacttgttc cagacaaaac tcaacttcaa 13320
gaagctaaaa atagattaga aaacagtatt aaccaacaaa cagatactga cggcatgact 13380
caagattcgc ttaacaatta taatgataaa ttagcaaaag ctagacaaaa ccttgaaaaa 13440
atatctaaag ttttaggtgg tcaacctact gtagctgaaa ttagacaaaa tacagatgaa 13500
gcaaatgcac ataaacaagc attagacact gcacgttctc aacttacatt aaatagagag 13560
ccatatatca atcatattaa taatgaaagt catttaaata acgcgcaaaa agataatttt 13620
aaagctcaag ttaactcagc acctaatcat aatactttag aaacgattaa aaataaggct 13680
gatactttaa atcaatctat gacagcatta agtgaaagta ttgcagatta cgaaaatcaa 13740
aaacaacaag aaaattattt agatgcatct aacaataaac gtcaagacta tgacaatgca 13800
gtcaatgcgg ctaaaggtat tttaaaccaa actcaaagtc cgacaatgag tgctgatgtg 13860
attgatcaaa aagctgaaga tgttaaacgt acgaaaactg cgttagatgg aaatcaaaga 13920
ttagaagttg ctaaacaaca agcacttaat catttaaata ccttaaatga tttaaacgat 13980
gctcagcgac aaactttaac tgatactata aatcactctc caaacatcaa ttcagtgaat 14040
caagctaaag aaaaagctaa tactgttaac acagcaatga ctcaactgaa acaaactatt 14100
gctaactatg acgatgaatt gcatgacggc aattacatta atgcagataa agacaaaaaa 14160
gatgcttata ataacgctgt taacaatgct aaacaactga ttaatcaatc tgatgctaat 14220
caagcacaac ttgatccagc tgaaattaat aaagttacac aaagagtcaa tacgactaaa 14280
aatgatctaa atggtaatga caaattggct gaagctaaaa gagatgctaa tacaaccatt 14340
gatggtttaa cttatctaaa tgaagctcaa cgtaacaaag ctaaagaaaa tgtaggcaaa 14400
gcttctacaa aaacaaatat tacgagtcag ttacaagatt acaatcaatt gaatattgct 14460
atgcaagcat tacgtaacag tgtgaacgac gttaacaatg ttaaagcaaa tagcaattat 14520
ataaatgaag ataatggtcc aaaagaagct tacaatcaag ccgttactca tgctcaaaca 14580
ttgataaatg cacaatctaa ccctgaaatg agccgtgacg tagtaaatca aaaaacacaa 14640
gcagtaaata ctgcccatca gaatttacat ggacaacaaa agttagaaca agcacaaagt 14700
agtgctaata cagaaatcgg taacttacca aacttaacta atactcaaaa agctaaagaa 14760
aaggaactgg taaatagtaa acaaactcgt acggaagtac aagaacaact taaccaagct 14820
aagtcactag atagttctat gggcacgtta aaatcattag ttgctaaaca acctacagta 14880
caaaaaacaa gtgtttatat taacgaagat caacctgagc aatctgccta caatgattcc 14940
attacaatgg gacaaactat aattaataaa acagctgatc cagtacttga taaaacttta 15000
gttgataacg caatcagtaa catttcaact aaagagaatg cactgcatgg tgaacaaaaa 15060
ttaacaactg ctaaaacgga agcaattaat gcacttaata cattagctga tttaaacaca 15120
cctcagaaag aggctattaa aacagctatt aacactgctc atacaagaac tgatgtaact 15180
gcagagcaaa gtaaggctaa tcaaataaat agtgcaatgc acacgttgag acaaaacatt 15240
tctgacaacg aatcagtaac aaacgaaagt aattatatta acgctgaacc cgaaaaacaa 15300
catgccttta ctgaggctct aaataatgct aaagaaatag ttaatgaaca acaagccact 15360
cttgatgcca attcaattaa ccaaaaagca caagcgattc ttactactaa aaatgcttta 15420
gatggtgaag aacaattacg tcgtgctaaa gaaaatgccg atcaagaaat caatacgtta 15480
aatcaattga ctgatgcgca aagaaatagt gaaaaaggtt tagtcaacag ttctcaaact 15540
agaacagaag ttgcttctca attagcaaaa gctaaagaac taaataaggt gatggaacaa 15600
ctgaatcacc ttatcaatgg taaaaaccaa atgataaata gcagtaaatt tatcaatgaa 15660
gatgcgaacc aacaacaagc atattcaaat gcgattgcaa gtgcagaagc gcttaaaaac 15720
aaatcacaaa accctgaatt agataaagta acaattgaac aagcaattaa taatattaat 15780
tctgcaatta acaatctaaa cggtgaagct aaactgacta aagctaaaga agatgctgtt 15840
gcttcaataa acaacctaag cggattaaca aacgagcaaa aaacaaaaga aaatcaagcc 15900
gttaatggcg ctcaaactag agaccaagtt gctaataaat tacgtgatgc tgaagcatta 15960
gatcaatcaa tgcaaacatt acgtgactta gttaacaatc aaaatgcaat acattcaaca 16020
agtaattatt ttaacgagga ttcaactcaa aagaatactt atgataatgc aattgataat 16080
ggctcgacat atataactgg tcaacacaat ccagaattaa ataaatctac tattgatcaa 16140
acgattagcc gaattaacac agctaaaaat gatttacatg gtgtagaaaa gttacaaaga 16200
gataagggaa ctgctaatca agaaattgga caattaggtt atttaaatga ccctcaaaaa 16260
tctggtgagg aatccttagt caacggttca aatacacgtt ctgaagtaga agagcatctt 16320
aatgaagcta aatcattaaa taatgcaatg aaacaattaa gagataaagt agctgaaaag 16380
actaatgtca aacaaagtag cgattacatt aatgattcaa ctgaacatca acgtgggtat 16440
gatcaagcac ttcaagaagc agaaaatatt attaatgaaa tcggtaatcc aacattaaat 16500
aaatcggaaa ttgaacaaaa gttacaacaa ttgactgacg ctcaaaatgc gttacaaggt 16560
tcacatctat tagaagaagc taaaaataat gcgattactg gaatcaataa acttacagca 16620
ttaaatgatg cacaacgtca aaaagcaatt gaaaatgttc aagcacagca gacaatccca 16680
gcagttaatc aacaattaac tttggataga gaaataaata ctgcaatgca agctttacga 16740
gataaagtag gccaacaaaa taacgttcac caacaaagta attatttcaa tgaagatgaa 16800
caaccaaaac ataactatga taattctgta caagccggtc aaactattat tgataaactt 16860
caagatccaa tcatgaacaa aaatgaaatt gagcaggcta ttaatcaaat caatacgact 16920
caaacagcgt taagtggaga aaataaatta cacactgacc aagaaagcac aaatagacaa 16980
atagaaggtt tatctagttt gaacacagct caaatcaacg ccgaaaaaga tttagtcaat 17040
caagctaaaa caagaacaga tgttgctcaa aagttagctg cagctaaaga aataaattct 17100
gctatgagta atttaagaga tggcattcaa aataaagagg acatcaaacg tagcagtgca 17160
tatatcaacg cagatccgac taaagttaca gcttacgatc aagcactaca gaacgcagaa 17220
aatatcatca atgccacacc aaacgtagag cttaataaag ctacaattga acaagcgcta 17280
tcacgcgttc aacaagcaca acaagatctt gatggtgttc aacaattagc taatgctaaa 17340
caacaagcta cacaaactgt caatgggtta aatagcttaa atgacggtca aaagcgtgaa 17400
ttaaatctat taattaattc agctaatacc cgtacaaaag tacaagaaga attaaacaaa 17460
gcaactgaat tgaaccatgc gatggaagct ttaagaaaca gtgttcaaaa cgttgatcaa 17520
gtaaaacaaa gtagcaatta tgtcaatgaa gatcaacctg aacagcacaa ttatgataat 17580
gctgtcaatg aagctcaagc tacaatcaac aacaatgctc aacctgttct agacaaatta 17640
gctatagaac gtttaactca aactgttaac actacaaaag atgcattaca tggtgctcaa 17700
aaactgacac aagaccaaca agctgctgaa actggaatac gtggtttaac gagtctcaat 17760
gaacctcaga aaaatgctga agtagctaaa gtaactgcag caacaacacg tgatgaagtg 17820
agaaatattc gtcaagaagc aacaacatta gatactgcaa tgcttggttt acgtaaaagc 17880
attaaagata aaaacgatac taaaaatagt agtaaatata ttaatgagga tcatgaccaa 17940
caacaagctt atgacaatgc tgtaaataat gctcaacaag ttatcgatga aactcaagca 18000
acgttaagct cagatacaat caatcaattg gcaaatgccg taactcaagc taaatctaat 18060
cttcatggag atactaaact acaacacgat aaagatagtg ctaaacaaac gattgctcaa 18120
ttacagaatt tgaattcagc tcaaaaacat atggaagatt ctttaattga taatgaatct 18180
acacgtacgc aagtccaaca cgatttaaca gaagctcaag ctttagatgg tttaatgggt 18240
gccttaaaag aaagtattaa agattatact aatattgttt caaacggtaa ttacatcaat 18300
gcggaaccat ctaagaaaca agcatatgat gcagctgtac aaaatgctca aaatataata 18360
aatggaacga atcaaccaac aattaataaa ggtaatgtca ctacagcaac acaaaccgtg 18420
aaaaatacta aagatgcctt agacggtgat catagattag aggaagctaa aaataatgcc 18480
aatcaaacaa tcagaaatct atctaatttg aacaatgccc aaaaagatgc agagaaaaat 18540
ctagttaata gcgcatcaac attagaacaa gttcaacaaa acttacaaac cgctcaacaa 18600
ttagataatg ctatgggtga gttacgacaa agtattgcta aaaaagatca agtgaaagca 18660
gatagtaaat atctaaatga agatcctcaa attaagcaaa actatgatga tgcagttcaa 18720
cgtgttgaaa ctattattaa cgaaactcaa aaccctgaat tacttaaagc aaacattgac 18780
caagcaactc aatccgttca aaatgcagaa caagctttac atggtgctga aaaattaaat 18840
caagacaaac aaacgtcttc gacagaacta gatggattaa cagatttaac agatgcacaa 18900
cgtgaaaaac tcagagaaca aattaacact tctaatagta gagatgatat taagcaaaaa 18960
attgagcaag caaaagcact aaatgacgca atgaaaaaac ttaaagaaca agttgcgcaa 19020
aaagatggtg ttcatgctaa cagtgattat acaaatgaag attctgcaca aaaagatgcg 19080
tataataatg cacttaaaca agcggaagac attattaata acagctcaaa tcctaactta 19140
aatgcacaag acattactaa tgctttaaat aatattaaac aagcacaaga taaccttcat 19200
ggagctcaaa aattacagca agacaaaaat acaactaatc aagccattgg taacttaaat 19260
catcttaatc aacctcaaaa agatgcgctt atacaagcta ttaatggagc tacatctagg 19320
gaccaagttg cagaaaaact taaagaggcc gaagcgcttg atgaagctat gaaacaactt 19380
gaagatcaag tgaatcaaga tgatcaaatt tcaaatagca gcccattcat aaatgaagac 19440
tcagacaaac aaaaaactta taatgataaa atccaagctg caaaagaaat aattaatcaa 19500
acatctaatc caaccttaga taaacaaaaa attgctgata cacttcaaaa tattaaagat 19560
gcagtgaata atttacatgg tgatcaaaaa ttagctcaat ctaaacaaga tgctaataat 19620
caattaaatc atttagatga cttaaccgaa gaacaaaaaa accattttaa accgttaatt 19680
aataatgctg atactcgaga tgaggtaaat aaacaactag agattgctaa acaattaaat 19740
ggtgatatga gtacacttca taaagtcata aatgataaag atcaaattca acatttaagc 19800
aattacatta atgctgataa tgataaaaaa caaaattatg ataatgctat taaagaagct 19860
gaggatttaa ttcataatca tccagataca ttagatcata aagcattaca agatttatta 19920
aacaagatag accaagcgca taacgaatta aatggagaat ccagatttaa acaggcttta 19980
gacaatgctt taaacgacat agatagctta aacagtctca atgttccaca acgccaaact 20040
gttaaggata acatcaacca tgtgacaact ctagaaagtt tagctcaaga attgcagaaa 20100
gcaaaagagc ttaatgatgc tatgaaagca atgagagata gcattatgaa tcaagagcaa 20160
attcgtaaaa atagcaatta tactaatgaa gacttagctc aacaaaatgc ctataatcat 20220
gcagtagata aaataaataa cattattggt gaagacaatg cgacgatgga tcctcaaata 20280
atcaaacaag caactcaaga tataaataca gctataaatg gattaaatgg agatcaaaaa 20340
cttcaagatg caaagacaga tgctaaacaa caaattacta actttactgg tttaactgaa 20400
ccacaaaaac aagcattgga aaacatcatt aaccaacaaa caagcagagc aaatgttgct 20460
aaacagttaa gtcatgctaa attcttaaat ggaaaaatgg aagaattaaa agttgcagta 20520
gccaaagcgt cattagtaag acaaaatagt aactatatta atgaagatgt ctctgaaaaa 20580
gaagcatatg aacaagctat cgcaaaaggt caggaaataa ttaattcaga aaataatcca 20640
acaataagta gtactgatat caatcgtacc attcaagaaa ttaatgatgc tgaacaaaat 20700
cttcatggtg ataataaatt aagacaagca caggaaattg caaagaatga aatacaaaat 20760
ctagacggat taaattcagc tcaaataaca aaattaatcc aagatatagg cagaacaaca 20820
actaaacctg cagtaactca gaaactagaa gaagcaaaag caataaacca agctatgcaa 20880
caacttaaac aaagtatagc cgataaggat gctactctaa attctagtaa ctatctcaat 20940
gaagattctg agaaaaagtt agcgtacgat aatgctgtaa gccaagctga acaactcata 21000
aatcaactta acgacccaac tatggatata agtaatattc aagctattac tcaaaaggtc 21060
attcaagcaa aagattcatt gcacggtgcg aataaacttg cacaaaatca agcagattca 21120
aatttaataa taaatcaatc aacaaattta aatgataaac aaaagcaagc attaaatgac 21180
ttaattaatc atgctcaaac taaacagcaa gtggcagaaa taattgcaca agctaataag 21240
ttaaataacg aaatgggcac actaaaaaca ctcgtagaag aacagtcaaa cgttcatcaa 21300
caaagtaaat atattaatga agatccgcaa gttcaaaata tttataatga ctccattcaa 21360
aaaggtcgag aaatattaaa cggcactaca gatgatgttt taaacaacaa taaaatagca 21420
gatgccattc aaaacattca tttaactaaa aacgatttac atggtgatca aaaattacaa 21480
aaagcacaac aagatgcaac caatgaatta aactatttaa caaatctaaa caattctcaa 21540
agacaaagcg agcatgatga gattaactct gctccttcaa gaactgaagt ttctaatgat 21600
ttaaatcatg ctaaagcact taatgaagct atgcgtcaac ttgagaatga agttgctctt 21660
gaaaacagtg ttaaaaaatt aagcgacttt atcaatgaag atgaagcggc acaaaatgaa 21720
tatagtaatg cacttcaaaa agctaaagac attatcaacg gcgttccaag tagcacttta 21780
gataaagcta caattgaaga tgctttatta gaattgcaaa atgctagaga aagtttacat 21840
ggtgagcaaa aacttcaaga ggctaaaaat caagctgttg ctgaaattga taatttacaa 21900
gcattaaatc ctggacaggt tcttgctgaa aaaacattag ttaaccaagc atcaaccaaa 21960
ccagaagttc aagaagcctt acaaaaagca aaagaactta atgaagctat gaaagcactg 22020
aaaactgaaa taaataaaaa agaacaaatc aaggctgata gtagatatgt aaatgctgac 22080
agtggtcttc aagcaaatta caattctgcg ttaaattatg gttctcaaat tattgcaact 22140
acccaaccac cagagcttaa taaagatgta ataaatagag caactcaaac gattaaaact 22200
gctgaaaata atttaaatgg gcaatctaaa ttagcagagg ctaagtcaga cggaaatcaa 22260
agcatcgaac atttgcaagg attaacacaa tcacaaaaag ataaacaaca tgatttaatt 22320
aatcaagctc aaactaaaca acaggtagat gatatcgtaa ataactctaa acaattagat 22380
aactctatga atcaactaca acaaattgtt aacaatgaca atacagtaaa acaaaatagt 22440
gatttcatta atgaagattc cagccaacag gatgcttata atcatgcaat tcaagcagca 22500
aaagatttga taactgctca tcctactatc atggataaaa atcaaataga tcaagctatt 22560
gaaaatatca aacaagcact taatgattta cacggtagta ataaactatc agaagataaa 22620
aaagaagctt cagaacaact acaaaacctt aatagcttga cgaacgggca aaaagatacg 22680
attttaaatc atattttcag tgcaccaaca agaagccaag taggagaaaa aattgcaagt 22740
gctaaacaat taaataatac aatgaaagca cttagagatt ctattgctga taataatgaa 22800
attttacaaa gtagtaagta cttcaatgaa gattctgaac aacaaaatgc ttataatcaa 22860
gccgtaaata aagctaaaaa tataattaat gatcaaccaa caccagtaat ggcaaatgat 22920
gagattcaaa gtgtcctaaa tgaagttaaa caaactaaag ataatttaca tggtgatcaa 22980
aaacttgcta acgacaagac agatgcccaa gcaacattaa atgcgttaaa ttacttaaat 23040
caagcgcaaa gaggtaatct tgaaactaaa gttcaaaact ctaattctag accagaagta 23100
caaaaagtag ttcaattagc aaatcaactt aatgatgcga tgaaaaaatt agatgatgct 23160
ttaactggta atgacgcaat aaaacaaacg agtaattata ttaatgaaga tacttctcaa 23220
caagttaact ttgatgagta tacagataga ggtaaaaaca tagttgctga acaaacaaat 23280
ccaaatatgt ctccaactaa tattaacact attgctgata aaattactga agctaaaaat 23340
gatttacatg gcgtacaaaa actagaacaa gctcaacaac agtccatcaa tactattaat 23400
caaatgactg gtctaaacca agctcaaaaa gaacaattaa atcaagaaat tcaacaaact 23460
caaacccgtt ctgaagtaca tcaagtaatt aaaaaagcac aagctttaaa tgattcaatg 23520
aatactttac gtcaaagtat cactgatgag aatgaagtta aacaaacaag taactacatc 23580
aatgaaactg ttggtaatca aactgcatat aacaatgccg ttgatcgtgt aaaacaaata 23640
atcaatcaaa catctaatcc aactatgaat cctttagagg tggaacgtgc aacatcaaat 23700
gtaaaaactt ctaaagatgc acttcatggt gaacgtgaat tgaatgacaa taaaaattca 23760
aaaacttttg cagtcaatca cttagataac ctcaatcaag ctcaaaaaga agcattaact 23820
catgaaattg aacaagcaac tatagtttca caagtaaata atatctataa caaagcgaaa 23880
gctttaaata atgatatgaa aaaacttaaa gatatcgttg ctcaacaaga taatgtgaga 23940
caatcaaaca attatataaa cgaggatagt acacctcaaa atatgtacaa cgatacaatt 24000
aatcatgcac aatcaatcat tgatcaagta gcaaacccta cgatgtctca tgacgaaata 24060
gagaatgcaa tcaataacat aaagcatgcc atcaatgcac tcgatggaga acataaatta 24120
caacaagcaa aagaaaatgc aaacttattg attaatagtt taaacgattt aaatgcacca 24180
caaagagatg ccataaatag attggttaat gaagctcaaa caagagaaaa agtagctgaa 24240
caacttcaaa gtgctcaagc tctaaatgat gctatgaagc atttaagaaa cagcattcaa 24300
aatcaatcat ccgtaagaca agagagcaaa tatattaatg caagtgatgc taaaaaagag 24360
caatataatc acgcagttag agaagtcgaa aatattatca atgaacaaca tccaacattg 24420
gataaagaaa taattaagca actaacggat gctgtaaatc aagcgaataa tgacttaaat 24480
ggcgttgaat tattagatgc tgataagcaa aacgcacatc aatcgatacc tacattgatg 24540
cacttaaatc aagcacaaca aaacgcatta aatgaaaaaa ttaataacgc agttaccaga 24600
gctgaagttg cggctattat tggccaagca aaaatactcg atcatgctat ggagaattta 24660
gaagaaagta tcaaagataa agagcaagtc aaacagtcaa gtaactatat taatgaagac 24720
cctgatgttc aagaaacata caataacgcc gttgatcatg tgacagaaat acttaatcaa 24780
acagtaaatc caactttatc tattgaagat atagagcatg ctatcaacga agttaatcaa 24840
gcgaaaaaac aactcagagg taaacaaaaa ctttatcaaa ctatcgattt agctgataaa 24900
gaattaagta aattggatga tttaacatca caacaaagca gttcaatatc taatcaaata 24960
tatactgcta aaacgagaac agaagttgcc caagcaattg aaaaagcaaa atcattaaat 25020
catgcaatga aagcacttaa caaagtatat aaaaatacag ataaagtgtt agatagtagt 25080
cgattcatta acgaagatca acccgaaaaa gaggcgtatc aacaagctat aaatcacgtt 25140
gattcaatca ttcatagaca aacaaatcct gaaatggatc caacagtaat caatagcata 25200
actcatgaac tcgaaacagc tcaaaataac ttacatggtg atcagaaact tgctcatgca 25260
caacaagatg ccgctaatgt aattaatggt ctaattcatc ttaatgttgc tcaacgcgag 25320
gtaatgataa atgcgaatac aaatgctaca acacgcgaaa aagttgcaaa gaacttagat 25380
aatgctcaag ctcttgataa agctatggaa acactacaac aagtagttgc tcataaaaat 25440
aatatattga acgatagtaa atatttaaat gaagattcaa aatatcaaca acaatacgat 25500
cgagttgttg ctgacgccga acaactactt aatcagacaa caaatccaac attagaacct 25560
tataaaatcg atattgttaa ggataatgtc ctagctaacg aaaaaatact atttggcgca 25620
gaaaaactat catatgacaa atcaaatgca aatgatgaaa ttaaacatat gaattatctt 25680
aataatgcac aaaagcaatc tataaaagat atgatttctc acgcagcatt aagaactgaa 25740
gttaaacaac ttctgcaaca agctaaaacc cttgatgaag ctatgaaatc acttgaagat 25800
aaaactcaag tagtgattac agatactact ttgtctaatt acactgaagc ttcagaggat 25860
aaaaaggaaa aagtagacca aactgtatca catgctcaag caatcattga taaaataaat 25920
ggctcaaatg taagtttaga tcaagtacga caagcactag aacaattaac tcaagcatca 25980
gaaaacctcg atggtgatca gcgagttgaa gaagctaaag ttcatgctaa tcaaacaatt 26040
gaccaattaa cacatcttaa ttcattacaa caacaaactg cgaaagaaag tgttaaaaac 26100
gcaacaaaac tagaagaaat cgctactgct agtaacgatg ctctggcatt aaacaaagta 26160
atgggtaaat tagaacaatt cattaatcat gctgattctg ttgaaaatag tgataattat 26220
agacaagccg acgacgacaa aattatcgct tatgatgatg cactagaaca tggacaagat 26280
atacaaaaat ctaatgcaac ccaaaatgaa gcaaaacaag cgttacaaca attaataaat 26340
gcagaaacat cgttaaatgg tttcgaaaga ttaaatcatg ctagaccacg agctttagaa 26400
tatattaaat cactagaaaa aataaacaat gctcaaaagt ctgctttaga ggataaagta 26460
acgcaatcgc atgatttatt agaattagaa catcttgtca acgagggcac aaacctcaat 26520
gacattatgg gtgaattagc taacgcaatc gttaataact atgctccaac caaagcaagt 26580
ataaattata ttaacgccga taacctacgc aaagataact ttactcaagc tatcaacaat 26640
gcacgtgatg cactcaacaa aactcaaggt cagaacttag atttcaatgc aattgataca 26700
tttaaagatg atatattcaa aactaaagat gcacttaacg gtattgaacg tttaacagct 26760
gcaaaatcaa aagcagaaaa actaattgat agtttaaaat ttattaataa agctcaattc 26820
acacatgcaa atgatgaaat tatgaatact aattctattg cacaattgtc tagaatcgtg 26880
aatcaagcat ttgatttaaa tgatgcaatg aaatctttaa gagatgaact taataataaa 26940
gcttttcctg tccaagcaag ctcaaattat ataaattcag atgaagattt aaaacaacaa 27000
tttgaccatg ctttaagtaa tgctcgaaaa gtacttgcaa aagaaaatgg taaaaattta 27060
gatgaaatac aaattgaggg actcaaacaa gtgattgagg atactaaaga tgctttaaat 27120
ggtatccaac gtttatcaaa agctaaagct aaagcaattc aatacgtaca atctttatct 27180
tatatcaatg atgcacagcg tcatattgct gaaaataata ttcacaactc tgatgattta 27240
tcatctttag caaatacatt atctaaagct agtgatttag ataatgcaat gaaagactta 27300
cgagatactc tagaaagtaa ttcaacttct gttccaaata gtgtgaatta tattaatgct 27360
gataagaatt ttcaaattga atttgatgag gcgctacaac aagcaagtgc aacaagttct 27420
aaaacttcag aaaatccagc aacgattgaa gaagtattag gtcttagtca agccatttac 27480
gatacaaaaa atgcattgaa tggtgaacaa cgacttgcaa ctgagaagag caaagatcta 27540
aaattaataa aaggattaaa agatttaaat aaagcacaac ttgaagatgt cacaaacaag 27600
gtaaattcag caaatacttt aacagagtta tctcagctca ctcaatcaac gttaaaatta 27660
aacgataaaa tgaaattatt gagagataag cttaaaacct tagtaaatcc tgttaaagca 27720
agtttaaatt atagaaacgc tgattataat ttaaaacgtc aatttaacaa agctttaaaa 27780
gaagctaaag gcatattaaa taaaaatagc ggtccaaatg tcaatatcaa tgacattcaa 27840
catcttttaa cacaaataga taatgctaaa gaccaattaa atggtgaacg acgtctaaaa 27900
gaacatcaac aaaaatctga agtatttatt attaaagaat tagatatact taataatgct 27960
caaaaagctg caataattaa tcagattaga gcgtctaaag acattaaaat aattaatcaa 28020
atcgttgata atgcaataga attaaatgat gctatgcaag gtttaaaaga acatgtagct 28080
caattaacag caactacaaa agacaacatt gaatatttaa atgctgatga agaccttaaa 28140
ttacaatatg attacgctat caacttagcg aataatgttc ttgacaaaga aaacggtaca 28200
aataaagacg ctaatatcat aattggaatg attcaaaaca tggatgatgc tagagcactt 28260
ctaaatggaa ttgaaagact taaagatgct caaacaaaag cacataatga cattaaagat 28320
acgctcaaac gtcaacttga tgaaattgaa cacgctaatg caacatcaaa ttctaaggct 28380
caagcaaaac aaatggtaaa tgaggaagct agaaaagcgt tttctaatat taatcacgca 28440
acatcaaatg atttagttaa tcaagcaaaa gatgaagggc aatctgcaat tgaacacata 28500
catgcagatg aattacctaa agcgaaacta gatgctaatc aaatgattga ccaaaaagtt 28560
gaagatataa atcacttaat tagtcaaaat ccaaacttat cacatgatga aaaaaataaa 28620
ctaatatctc aaattaataa gttagtaaat ggaattaagg atgaaattca acaagctata 28680
aacaaacaac aaatagaaaa tgctacaaca aaactagatg aagtcattga aactactaaa 28740
aaattaatta tcgccaaagc tgaagctaaa caagtgataa aagagttatc acaaaagaaa 28800
cgagatgcaa taaataacaa cactgattta acaccttctc aaaaggcaca tgctttagca 28860
gatattgata aaacagaaaa agatgcactt caacatatcg aaaattctaa ttcaattgat 28920
gatatcaata acaataaaaa gcatgcattt aatactttag ctcatatcat tatttgggat 28980
actgatcagc aaccattagt ttttgaacta cctgaattga gccttcaaaa tgctttagta 29040
acaagtgagg tggttgttca cagagatgaa actatttcat tagaatctat aattggagct 29100
atgactttaa ctgatgaact taaagtcaat attgtttcat taccgaacac tgataaagta 29160
gctgatcacc taaccgctaa agttaaggtt attttagctg atggctcata tgtcactgta 29220
aatgttccag tcaaagttgt agaaaaagaa ttacaaatag ctaaaaagga tgctataaaa 29280
acaattgatg ttctggtaaa acaaaaaatc aaagatatag attctaataa cgaattaacg 29340
tctactcaac gtgaagatgc aaaagctgaa attgaaagat tgaaaaagca agccatcgat 29400
aaagtgaatc attcaaaatc gattaaagat attgaaacag taaaacgaac tgattttgaa 29460
gaaatagatc agtttgatcc taaacgcttt acgctaaata aagctaaaaa ggatatcatt 29520
actgatgtta atactcaaat ccaaaatggt ttcaaagaaa ttgaaacaat aaaaggttta 29580
acttctaatg aaaaaactca gtttgataaa caattaactg aactacaaaa agaattttta 29640
gaaaaagtcg agcatgctca taatttagta gaattaaatc aattacaaca agagtttaat 29700
aatagatata aacatatttt aaaccaagca catttactag gtgaaaaaca tatagcagaa 29760
cataaattag gatatgttgt agtaaacaaa actcagcaaa tactaaataa tcaatctgct 29820
tcttacttta taaaacaatg ggcacttgat agaattaaac aaattcaact agaaacgatg 29880
aattcaattc gtggtgcgca taccgtacaa gatgtacaca aagcattatt acaaggtata 29940
gagcaaatct tgaaagtaaa tgtaagtatt ataaatcaat ctttcaacga ttccttgcat 30000
aactttaatt atcttcattc aaaatttgat gctagattaa gagaaaagga tgttgcaaac 30060
catatcgtac aaactgaaac attcaaagaa gttctaaaag gaacgggtgt tgaaccaggt 30120
aaaatcaaca aagaaacaca gcaaccaaaa cttcataaga atgataatga tagcctattc 30180
aaacatttag ttgataattt cggcaaaact gtaggtgtta ttacattaac tggtttactt 30240
tctagtttct ggttagtttt ggctaaaaga cgtaaaaaag aagaagaaga aaaacaatcg 30300
ataaaaaatc atcacaaaga tattcgtctt tcagatactg ataaaataga tccaattgta 30360
ataactaagc gtaaaataga taaagaagaa caaattcaaa acgatgacaa acattcaatt 30420
ccagttgcta aacataagaa atctaaagaa aagcaattga gtgaagagga tattcattca 30480
atccccgtcg ttaagcgtaa acaaaacagt gataacaaag atacaaaaca gaagaaagtt 30540
acttctaaaa agaagaaaac gcctcaatca actaaaaaag ttgtaaaaac caaaaagcgt 30600
tctaaaaagt aa 30612
Claims (48)
1.一种免疫原性组合物,其包含具有选自一或多个SEQ ID NO:1到SEQ ID NO:32、其生物等效物或其片段的氨基酸序列的多肽。
2.根据权利要求1所述的免疫原性组合物,其中所述多肽可与受表皮葡萄球菌(Staphylococus epidermidis)感染的兔的血清中的抗体免疫反应。
3.根据权利要求1或2所述的免疫原性组合物,其中所述多肽与一或多种兔血清蛋白结合。
4.根据权利要求1至3中任一或多项权利要求所述的免疫原性组合物,其另外包含医药学上可接受的载剂。
5.根据权利要求1至4中任一或多项权利要求所述的免疫原性组合物,其另外包含一或多种佐剂。
6.根据权利要求1至5中任一或多项权利要求所述的免疫原性组合物,其中所述多肽是从表皮葡萄球菌获得。
7.根据权利要求1至6中任一或多项权利要求所述的免疫原性组合物,其中所述多肽另外包含异源氨基酸。
8.根据权利要求1至7中任一或多项权利要求所述的免疫原性组合物,其中所述多肽为融合多肽。
9.根据权利要求1至8中任一或多项权利要求所述的免疫原性组合物,其中所述多肽为重组多肽。
10.根据权利要求1至9中任一或多项权利要求所述的免疫原性组合物,其中所述多肽是从表皮葡萄球菌分离。
11.根据权利要求1至10中任一或多项权利要求所述的免疫原性组合物,其中所述多肽包含表皮葡萄球菌的中和表位。
12.根据权利要求1至11中任一或多项权利要求所述的免疫原性组合物,其中所述多肽为脂蛋白。
13.根据权利要求1至12中任一或多项权利要求所述的免疫原性组合物,所述组合物另外包含表皮葡萄球菌多糖抗原。
14.根据权利要求1至13中任一或多项权利要求所述的免疫原性组合物,所述组合物另外包含金黄葡萄球菌(Staphylococcus aureus)多糖或多肽抗原。
15.根据权利要求1至14中任一或多项权利要求所述的免疫原性组合物,其中所述多肽包含选自由SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO:11、SEQ ID NO:12、SEQID NO:14、SEQ ID NO:18、SEQ ID NO:19、SEQ ID NO:20、SEQ ID NO:23、SEQID NO:26、SEQ ID NO:27和SEQ ID NO:30、其生物等效物或其片段组成的群组的表皮葡萄球菌多肽序列。
16.根据权利要求1至15中任一或多项权利要求所述的免疫原性组合物,其中所述多肽是由聚核苷酸编码,所述聚核苷酸包含与选自SEQ ID NO:33到SEQ ID NO:64中一者或其简并变异体或其片段的核苷酸序列具有至少约95%同一性的核苷酸序列。
17.根据权利要求1至16中任一或多项权利要求所述的免疫原性组合物,其中所述聚核苷酸是得自表皮葡萄球菌。
18.根据权利要求1至17中任一或多项权利要求所述的免疫原性组合物,其中所述表皮葡萄球菌聚核苷酸序列是选自由SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:43、SEQ ID NO:44、SEQ ID NO:46、SEQ ID NO:50、SEQ ID NO:51、SEQ ID NO:52、SEQ ID NO:55、SEQ ID NO:58、SEQ ID NO:59和SEQ ID NO:62或其简并变异体或其片段组成的群组。
19.根据权利要求1至18中任一或多项权利要求所述的免疫原性组合物,其中所述聚核苷酸另外包含异源核苷酸。
20.一种免疫原性组合物,其包含具有选自SEQ ID NO:33到SEQ ID NO:64中一者、其简并变异体或其片段的核苷酸序列的聚核苷酸,且所述聚核苷酸是包含于表达载体中。
21.根据权利要求20所述的免疫原性组合物,其中所述表皮葡萄球菌聚核苷酸序列是选自由SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:43、SEQ ID NO:44、SEQ IDNO:46、SEQ ID NO:50、SEQ ID NO:51、SEQ ID NO:52、SEQ ID NO:55、SEQ IDNO:58、SEQ ID NO:59和SEQ ID NO:62或其简并变异体或其片段组成的群组。
22.根据权利要求20或21所述的免疫原性组合物,其中所述载体为质粒DNA。
23.根据权利要求20至22中任一或多项权利要求所述的免疫原性组合物,其中所述聚核苷酸为重组聚核苷酸。
24.根据权利要求20至23中任一或多项权利要求所述的免疫原性组合物,其中所述聚核苷酸是从表皮葡萄球菌获得。
25.根据权利要求24所述的免疫原性组合物,其中所述聚核苷酸包含异源核苷酸。
26.根据权利要求20至23中任一或多项权利要求所述的免疫原性组合物,其中所述聚核苷酸操作地连接到一个或多个基因表达调控元件。
27.根据权利要求24所述的免疫原性组合物,其中所述聚核苷酸引导表皮葡萄球菌的中和表位的表达。
28.根据权利要求20至23中任一或多项权利要求所述的免疫原性组合物,其另外包含转染促进剂。
29.根据权利要求28所述的免疫原性组合物,其中所述转染促进剂为布比卡因(bupivicaine)。
30.一种诱导对抗表皮葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:具有选自一或多个SEQ ID NO:1到SEQ ID NO:32或其生物等效物或其片段的氨基酸序列的多肽,和医药学上可接受的载剂。
31.根据权利要求30所述的方法,其中所述多肽另外包含异源氨基酸。
32.根据权利要求31所述的方法,其中所述多肽为融合多肽。
33.根据权利要求30所述的方法,其另外包含佐剂。
34.根据权利要求30或31所述的方法,其中所述多肽为重组多肽。
35.一种诱导对抗表皮葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:具有选自一或多个SEQ ID NO:33到SEQ ID NO:64、其简并变异体或其片段的核苷酸序列的聚核苷酸,和医药学上可接受的载剂。
36.根据权利要求35所述的方法,其另外包含载体。
37.根据权利要求35所述的方法,其中所述载体为质粒DNA。
38.根据权利要求35所述的方法,其中所述聚核苷酸为重组聚核苷酸。
39.根据权利要求35所述的方法,其中所述聚核苷酸另外包含异源核苷酸。
40.根据权利要求35所述的方法,其中所述聚核苷酸操作地连接到一个或多个基因表达调控元件。
41.根据权利要求35所述的方法,其另外包含佐剂。
42.根据权利要求35所述的方法,其中所述组合物另外包含转染促进剂。
43.根据权利要求42所述的方法,其中所述转染促进剂为布比卡因。
44.一种诱导对抗金黄葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:选自由SEQ ID NO:8、SEQ ID NO:10、SEQ ID NO:11、SEQ ID NO:12、SEQ ID NO:14、SEQ ID NO:18、SEQ ID NO:19、SEQ ID NO:20、SEQ ID NO:23、SEQ ID NO:26、SEQ ID NO:27和SEQ ID NO:30、其生物等效物或其片段组成的群组的表皮葡萄球菌多肽序列。
45.一种诱导对抗金黄葡萄球菌的免疫反应的方法,其包含向哺乳动物投与免疫原性量的组合物,所述组合物包含:选自由SEQ ID NO:40、SEQ ID NO:42、SEQ ID NO:43、SEQ ID NO:44、SEQ ID NO:46、SEQ ID NO:50、SEQ ID NO:51、SEQ ID NO:52、SEQ ID NO:55、SEQ ID NO:58、SEQ ID NO:59和SEQ ID NO:62或其简并变异体或其片段组成的群组的表皮葡萄球菌聚核苷酸序列。
46.一种用于检测和/或鉴别生物样本中的表皮葡萄球菌的方法,其包含:
(a)在允许杂交的条件下,使所述样本与聚核苷酸的寡核苷酸探针接触,所述聚核苷酸包含选自SEQ ID NO:33到SEQ ID NO:64中一者或其简并变异体或其片段的核苷酸序列;和
(b)检测所述样本中杂交复合物的存在,其中杂交复合物表明所述样本中存在表皮葡萄球菌。
47.一种用于检测和/或鉴别生物样本中抗表皮葡萄球菌的抗体的方法,其包含:
(a)在允许免疫复合物形成的条件下,使所述样本与多肽接触,所述多肽包含选自SEQ ID NO:1到SEQ ID NO:32中一者或其生物等效物或其片段的氨基酸序列;和
(b)检测所述样本中免疫复合物的存在,其中免疫复合物表明所述样本中存在表皮葡萄球菌。
48.一种根据权利要求1至29中任一或多项权利要求所述的组合物,其是用于诱导对抗表皮葡萄球菌的免疫反应的方法中。
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Cited By (4)
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CN102647999A (zh) * | 2009-04-14 | 2012-08-22 | 诺华有限公司 | 用于免疫接种以抵御金黄色葡萄球菌的组合物 |
CN104736165A (zh) * | 2012-08-31 | 2015-06-24 | 诺华股份有限公司 | 用于针对金黄色葡萄球菌的免疫的稳定化的蛋白质 |
CN112521464A (zh) * | 2014-03-26 | 2021-03-19 | 葛兰素史密丝克莱恩生物有限公司 | 突变型葡萄球菌抗原 |
CN109843910A (zh) * | 2016-10-21 | 2019-06-04 | 索克普拉科学与工程公司 | 对抗葡萄球菌感染的疫苗构建体及其用途 |
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WO2007001423A2 (en) | 2007-01-04 |
IL182546A0 (en) | 2008-12-29 |
US8445000B2 (en) | 2013-05-21 |
JP2008517918A (ja) | 2008-05-29 |
EP2340848A2 (en) | 2011-07-06 |
KR20070068455A (ko) | 2007-06-29 |
TW200619228A (en) | 2006-06-16 |
EP2298341A2 (en) | 2011-03-23 |
CA2583121A1 (en) | 2007-01-04 |
US20150196629A1 (en) | 2015-07-16 |
EP2213298A2 (en) | 2010-08-04 |
ZA200703274B (en) | 2008-06-25 |
AU2005333603A1 (en) | 2007-01-04 |
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