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19 pages, 5378 KiB  
Article
First Report on Choanephora cucurbitarum Causing Choanephora Rot in Chenopodium Plants and Its Sensitivity to Fungicide
by Hui Yin, Miao Tian, Yufei Peng, Nan Qin, Hong Lü, Lu Ren and Xiaojun Zhao
J. Fungi 2023, 9(9), 881; https://doi.org/10.3390/jof9090881 - 28 Aug 2023
Cited by 4 | Viewed by 1606
Abstract
Choanephora rot of Chenopodium plants (CRC) was observed at the flowering stages in seven plantations of Shanxi Province, China. CRC had caused leaf, stem, and panicle neck rot of C. quinoa, panicle neck and stem rot of C. formosanum, and stem [...] Read more.
Choanephora rot of Chenopodium plants (CRC) was observed at the flowering stages in seven plantations of Shanxi Province, China. CRC had caused leaf, stem, and panicle neck rot of C. quinoa, panicle neck and stem rot of C. formosanum, and stem rot of C. album. Typical symptoms included water-soaked, rapid soft rotting, and abundant sporulation on the whole panicle necks, stems, and leaves. Based on morphological characteristics, phylogenetic analyses, and pathogenicity tests, the pathogens were identified as Choanephoraceae cucurbitarum. Sporangiola and sporangiospore of C. cucurbitarum germinated at 30 °C and were able to germinate by two h post-inoculation (hpi). The germination rates of sporangiola and sporangiospore significantly increased at 3 to 4 hpi, and the germination rates ranged from 91.53 to 97.67%. The temperature had a significant effect on the pathogenicity of C. cucurbitarum the optimum pathogenic temperatures for stems of C. quinoa, C. formosanum and C. album were 30 °C after one day post-inoculation. Choanephoraceae cucurbitarum could infect white and red quinoa panicle necks between 20 and 30 °C, and the average lesion lengths were 0.21 to 3.62 cm. Among the five tested fungicides (boscalid, dimethomorph, isopyrazam, propiconazole, and tebuconazole), isopyrazam showed higher sensitivity to sporangiola germination of C. cucurbitarum, with an EC50 value of 0.6550 μg/mL. Isopyrazam and tebuconazole strongly inhibited the sporangiospore germination of C. cucurbitarum, which showed EC50 values of 0.4406 and 0.3857 μg/mL. To our knowledge, the present study found for the first time that C. cucurbitarum is a pathogen causing panicle neck of C. formosanum and stem rot of C. formosanum and C. album, while CRC first appeared in the quinoa panicle necks, and gradually expanded to stems and leaves. Full article
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Figure 1
<p>Symptoms of Choanephora rot on panicle necks, stems, and leaves of <span class="html-italic">Chenopodium quinoa</span> (<b>A</b>) panicle necks and stems of <span class="html-italic">C. formosanum</span> (<b>B</b>) and stems of <span class="html-italic">C. album</span> (<b>C</b>).</p>
Full article ">Figure 2
<p>Morphological characteristics of <span class="html-italic">Choanephora cucurbitarum</span> from <span class="html-italic">Chenopodium</span> plants. (<b>A</b>) Colony on PDA for 2 days, (<b>B</b>) sporangiophores bearing sporangiola, (<b>C</b>–<b>G</b>) sporangiophores with apically dilated and bearing secondary vesicles, (<b>H</b>,<b>I</b>) sporangiola readily detached at maturity, (<b>J</b>–<b>L</b>) secondary vesicles with a head of sporangiola, (<b>M</b>) mature sporangiola with mulberry-like head, (<b>N</b>) sporangiola with longitudinal striation, (<b>O</b>) sporangiophores bearing sporangia, (<b>P</b>,<b>Q</b>) pale yellow to yellow sporangium, (<b>R</b>) sporangiophore bearing mature sporangium, (<b>S</b>,<b>T</b>) dehiscent sporangium, (<b>U</b>) sporangiospores from sporangia, and (<b>V</b>) sporangiospores with appendages.</p>
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<p>Phylogenetic tree of <span class="html-italic">Choanephora cucurbitarum</span> isolates (LMJM-2, LMJM-3, LMJM-5, LMJM-7, and LMJM-9) from <span class="html-italic">Chenopodium</span> plants and their related isolates based on LSU and ITS sequences using the maximum likelihood (ML) method. Ex-type strains were indicated with (T) in the end of the taxa labels, and our strains are in bold.</p>
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<p>Germination of the sporangiola (<b>A</b>) and sporangiospores (<b>B</b>) of <span class="html-italic">Choanephora cucurbitarum</span> at 2, 3, and 4 h (<b>C</b>).</p>
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<p>Symptoms on <span class="html-italic">Chenopodium quinoa</span> (<b>A</b>), <span class="html-italic">C. formosanum</span> (<b>B</b>), and <span class="html-italic">C. album</span> (<b>C</b>) induced by inoculation of representative isolates (LMJM-2, LMJM-3, LMJM-5, LMJM-7, and LMJM-9) of <span class="html-italic">Choanephora cucurbitarum</span>.</p>
Full article ">Figure 6
<p>Effect of temperature on pathogenicity of the representative isolates of <span class="html-italic">Choanephora cucurbitarum</span>. (<b>A</b>) Pathogenicity on stems of <span class="html-italic">C. quinoa</span>, <span class="html-italic">C. formosanum</span>, and <span class="html-italic">C. album</span> at different temperatures, (<b>B</b>) lesions lengths on panicle necks of white and red quinoa that were inoculated with <span class="html-italic">Choanephora cucurbitarum</span> and incubated at different temperatures. Data were analyzed with SPSS statistics 19.0 by one-way ANOVA, and means were compared using Tukey’s test at a significance level of <span class="html-italic">p</span> = 0.05. Different letters indicate significant differences (<span class="html-italic">p</span> = 0.05).</p>
Full article ">Figure 7
<p>Effects of five fungicides on germination of sporangiola and sporangiospores of isolate LMJM-2. (<b>A</b>) Inhibition activities of five fungicides on germination of sporangiola and sporangiospores, (<b>B</b>) morphology of germ tubes of sporangiola and sporangiospores treated with five fungicides at EC<sub>50</sub>. Different letters indicate significant differences (<span class="html-italic">p</span> = 0.05).</p>
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12 pages, 1921 KiB  
Article
Two New Species of Backusella (Mucorales, Mucoromycota) from Soil in an Upland Forest in Northeastern Brazil with an Identification Key of Backusella from the Americas
by Catarina Letícia Ferreira de Lima, Joana D’arc Alves Leitão Lundgren, Thuong Thuong Thi Nguyen, Thalline Rafhaella Leite Cordeiro, Diogo Xavier Lima, Luciana Melo Sartori Gurgel, Diogo Paes da Costa, Hyang Burm Lee and André Luiz Cabral Monteiro de Azevedo Santiago
J. Fungi 2022, 8(10), 1038; https://doi.org/10.3390/jof8101038 - 30 Sep 2022
Cited by 3 | Viewed by 2069
Abstract
During a survey of Mucorales from a forest located in Pernambuco state, Brazil, two new Backusella species were discovered and described based on morphological and molecular data (internal transcribed spacer and large subunit ribosomal DNA sequences). Both species were characterized as unbranched sporangiophores [...] Read more.
During a survey of Mucorales from a forest located in Pernambuco state, Brazil, two new Backusella species were discovered and described based on morphological and molecular data (internal transcribed spacer and large subunit ribosomal DNA sequences). Both species were characterized as unbranched sporangiophores and sporangia with columellae of varied shapes forming. Multispored sporangiola were frequent, whereas unispored sporangiola were rare. URM 8395 forms sporangiophores that may support hyaline, slightly curved or circinate pedicels with multispored sporangiola at their apical portion, and abundant giant cells and chlamydospores. Columellae of sporangia are hyaline, conical (majority), or ellipsoidal with a truncate base, globose to subglobose or subglobose to conical, and, rarely, with slight medial constriction. URM 8427 does not form sporangiola from pedicels, giant cells are not observed, and columellae of sporangia are globose to subglobose, cylindrical with a truncate base, some with a slight constriction, applanate, obovoid, ellipsoidal, or, rarely, conical. Some columellae may have one side more swollen than the other and some are arranged obliquely on the sporangiophores. Sterile sporangia may or may not be formed on short sporophores. The detailed description and illustration of both novel species as well as an identification key for Backusella from the Americas are provided. Full article
(This article belongs to the Special Issue Diversity of Undiscovered Fungal Taxa and Novel Antifungal Agents)
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<p>Phylogenetic tree of <span class="html-italic">Backusella</span> based on maximum likelihood analysis of a combined DNA dataset of internal transcribed spacer and large subunit sequences. Bootstrap values for Bayesian posterior probabilities over 0.90 and maximum likelihood higher than 70% are placed above the branches. Bootstrap values lower than 0.90 and 70% are marked with “*”. The bar indicates the number of substitutions per position. <span class="html-italic">Mucor indicus</span> CBS 226.29 was used as an outgroup. The newly generated sequences of <span class="html-italic">B</span>. <span class="html-italic">obliqua</span> URM 8427 and <span class="html-italic">B. brasiliensis</span> URM 8395 are indicated in blue. Ex-type, ex-epitype, ex-lectotype, and ex-neotype strains are marked with T, ET, LT, and NT, respectively.</p>
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<p><span class="html-italic">Backusella brasiliensis</span> (URM 8395): (<b>A</b>) sporangiophore with sporangium; (<b>B</b>) pedicellate sporangiola arising from the sporangiophore; (<b>C</b>) sporangiophore branch with sporangium; (<b>D</b>) short-branched sporophore bearing only sporangiola; (<b>E</b>,<b>F</b>) sporangiophore with columella; (<b>G</b>) terminal chlamydospores; (<b>H</b>) giant cell; and (<b>I</b>) sporangiospores. Scale bars = 25 μm.</p>
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<p><span class="html-italic">Backusella obliqua</span> (URM 8427): (<b>A</b>) sporangiophore with sporangium; (<b>B</b>) branched sporangiophore with sporangia; (<b>C</b>) branched sporangiophore with sporangium and columella; (<b>D</b><b>–G</b>) sporangiophore with columella; (<b>H</b>) short-branched sporophore bearing uni- and multispored sporangiola; (<b>I</b>) short-branched sporophore bearing only multispored sporangiola and columella; and (<b>J</b>) sporangiospores. Scale bars: (<b>A</b>,<b>D</b>–<b>G</b>,<b>J</b>) = 25 μm; (<b>B</b>,<b>C</b>) = 200 μm; (<b>H</b>,<b>I</b>) = 50 μm.</p>
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23 pages, 1809 KiB  
Review
Updates on the Taxonomy of Mucorales with an Emphasis on Clinically Important Taxa
by Grit Walther, Lysett Wagner and Oliver Kurzai
J. Fungi 2019, 5(4), 106; https://doi.org/10.3390/jof5040106 - 14 Nov 2019
Cited by 128 | Viewed by 15048
Abstract
Fungi of the order Mucorales colonize all kinds of wet, organic materials and represent a permanent part of the human environment. They are economically important as fermenting agents of soybean products and producers of enzymes, but also as plant parasites and spoilage organisms. [...] Read more.
Fungi of the order Mucorales colonize all kinds of wet, organic materials and represent a permanent part of the human environment. They are economically important as fermenting agents of soybean products and producers of enzymes, but also as plant parasites and spoilage organisms. Several taxa cause life-threatening infections, predominantly in patients with impaired immunity. The order Mucorales has now been assigned to the phylum Mucoromycota and is comprised of 261 species in 55 genera. Of these accepted species, 38 have been reported to cause infections in humans, as a clinical entity known as mucormycosis. Due to molecular phylogenetic studies, the taxonomy of the order has changed widely during the last years. Characteristics such as homothallism, the shape of the suspensors, or the formation of sporangiola are shown to be not taxonomically relevant. Several genera including Absidia, Backusella, Circinella, Mucor, and Rhizomucor have been amended and their revisions are summarized in this review. Medically important species that have been affected by recent changes include Lichtheimia corymbifera, Mucor circinelloides, and Rhizopus microsporus. The species concept of Rhizopus arrhizus (syn. R. oryzae) is still a matter of debate. Currently, species identification of the Mucorales is best performed by sequencing of the internal transcribed spacer (ITS) region. Ecologically, the Mucorales represent a diverse group but for the majority of taxa, the ecological role and the geographic distribution remain unknown. Understanding the biology of these opportunistic fungal pathogens is a prerequisite for the prevention of infections, and, consequently, studies on the ecology of the Mucorales are urgently needed. Full article
(This article belongs to the Special Issue Mucorales and Mucormycosis)
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<p>Morphology of the Mucorales. (<b>a</b>) Zygospore with equal suspensors of <span class="html-italic">Mucor endophyticus</span> CBS 385.95; (<b>b</b>) azygospore of <span class="html-italic">Mucor bainieri</span> CBS 293.63; (<b>c</b>) zygospores with unequal suspensors of <span class="html-italic">Mucor multiplex</span> (syn. <span class="html-italic">Zygorhynchus multiplex</span>) CBS 110662; (<b>d</b>) top view on a young mycelium with transitorily recurved sporangiophores; (<b>e</b>) recurved sporangiophore and (<b>f</b>) columella of <span class="html-italic">Backusella recurva</span> CBS 318.52; (<b>g</b>) sporangium with circumscissile zone of dehiscence and (<b>h</b>) discharged sporangium of <span class="html-italic">Pilaira anomla</span> CBS 699.71; (<b>i</b>) sporangiola-bearing complex sporophore of <span class="html-italic">Thamnidium elegans</span> CBS 341.55; (<b>j</b>) circinate sporangiophore branches with columellae and detached sporangiospores of <span class="html-italic">Circinella umbellata</span>; (<b>k</b>) hyphae of <span class="html-italic">Rhizopus microsporus</span> in human lung tissue. Scale bars = 50 µm except of d = 500 µm.</p>
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<p>Classification of zygomycete fungi including the Mucorales based on Spatafora et al. [<a href="#B12-jof-05-00106" class="html-bibr">12</a>]. Bold printed taxa contain pathogenic species.</p>
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<p>Morphology of the opportunistic members of the Mucorales. (<b>a</b>) Sporangiophore with sporangium and indistinct apophysis and (<b>b</b>) with columella and detached sporangiospores of <span class="html-italic">Rhizopus arrhizus</span> JMRC:NRZ:1217; (<b>c</b>) sympodially branched sporangiophore of <span class="html-italic">Mucor circinelloides</span> NRZ-2019-468; (<b>d</b>) sympodially branched sporangiophore of <span class="html-italic">Mucor ramosissimus</span> CBS 135.65; (<b>e</b>) sporangiophore with columellae and detached sporangiospores of <span class="html-italic">Lichtheimia ramosa</span> NRZ-2019-435; (<b>f</b>) sporangiophore with columellae and detached sporangiospores of <span class="html-italic">Rhizomucor pusillus</span> JMRC:NRZ:0496; (<b>g</b>,<b>k</b>) sporangiophores of <span class="html-italic">Apophysomyces variabilis</span>; (<b>h</b>) sporophore with sporangiola and columella at the place of the former sporangium of <span class="html-italic">Thamnostylum lucknowense</span> JMRC:SF:00845; (<b>i</b>) sporophore of <span class="html-italic">Saksenaea</span> sp.; (<b>j</b>) sporophore with merosporangia of <span class="html-italic">Syncephalastrum racemosum</span> CBS 302.65; (<b>l</b>) young sporangiophore of <span class="html-italic">Actinomucor elegans</span> CBS 111556; (<b>m</b>) sporophores with single-spored sporangiola of <span class="html-italic">Cunninghamella bertholletiae.</span> Scale bars = 50 µm.</p>
Full article ">
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