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10 pages, 1381 KiB  
Case Report
Mogamulizumab and Concomitant Hypofractionated Low-Dose Total Skin Electron Beam Therapy (2 × 4 Gy) in Cutaneous T-Cell Lymphoma: Proof of Principle, Report of Two Cases
by Mathias Oymanns, Michael Daum-Marzian and Chalid Assaf
Curr. Oncol. 2024, 31(9), 5412-5421; https://doi.org/10.3390/curroncol31090400 - 13 Sep 2024
Viewed by 234
Abstract
Patients with advanced-stage mycosis fungoides (MF IIB–IVB) and Sézary syndrome (SS) have poor prognoses, with survival ranging from 4.7 to 1.4 years depending on the disease stage. There is a need for therapeutic approaches that lead to long-lasting responses and improved quality of [...] Read more.
Patients with advanced-stage mycosis fungoides (MF IIB–IVB) and Sézary syndrome (SS) have poor prognoses, with survival ranging from 4.7 to 1.4 years depending on the disease stage. There is a need for therapeutic approaches that lead to long-lasting responses and improved quality of life and survival. Mogamulizumab, a humanized antibody against the CCR4 molecule, and low-dose total skin electron beam therapy (TSEBT) are two known established treatments for MF and SS as a monotherapy. However, little is known about the potential additive effect on the combination of both treatments. We report here for the first time the concurrent use of low-dose hypofractionated TSEBT (2 × 4 Gy) with mogamulizumab. Based on two relapsed/refractory and advanced-stage CTCL patients, we show that this combination may be well tolerated in advanced-stage MF or SS and may potentially lead to an additive treatment effect on response times, particularly in the skin and blood within two weeks. We propose that this combination may be a treatment option for patients with SS. Further research is needed to understand the efficacy and tolerability profile of this therapeutic combination and to determine if there is an additive effect of the combination on the response rates when compared with the monotherapy. Full article
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<p>Case 1: Concurrent mogamulizumab and TSEBT regimen. IV, intravenous; TSEBT, total skin electron beam therapy.</p>
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<p>Patient with Sézary syndrome—case 1—(<b>a</b>) before and (<b>b</b>) after 2 administrations of mogamulizumab and concurrent TSEBT at 2 Gy. TSEBT, total skin electron beam therapy.</p>
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<p>Case 2: Concurrent mogamulizumab and TSEBT regimen. IV, intravenous; TSEBT, total skin electron beam therapy.</p>
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<p>Patient 2 with Sézary syndrome (<b>a</b>) before and (<b>b</b>) after 11 administrations of mogamulizumab and 2 concurrent administrations of TSEBT at 4 Gy weekly.</p>
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10 pages, 1172 KiB  
Review
Clinical and Histologic Variants of CD8+ Cutaneous T-Cell Lymphomas
by Madisen A. Swallow, Goran Micevic, Amanda Zhou, Kacie R. Carlson, Francine M. Foss and Michael Girardi
Cancers 2024, 16(17), 3087; https://doi.org/10.3390/cancers16173087 - 5 Sep 2024
Viewed by 353
Abstract
Although the vast majority of CTCL subtypes are of the CD4+ T-helper cell differentiation phenotype, there is a spectrum of CD8+ variants that manifest wide-ranging clinical, histologic, and phenotypic features that inform the classification of the disease. CD8, like CD4, and cytotoxic molecules [...] Read more.
Although the vast majority of CTCL subtypes are of the CD4+ T-helper cell differentiation phenotype, there is a spectrum of CD8+ variants that manifest wide-ranging clinical, histologic, and phenotypic features that inform the classification of the disease. CD8, like CD4, and cytotoxic molecules (including TIA and granzyme) are readily detectable via IHC staining of tissue and, when expressed on the phenotypically abnormal T-cell population, can help distinguish specific CTCL subtypes. Nonetheless, given that the histopathologic differential for CD8+ lymphoproliferative disorders and lymphomas may range from very indolent lymphomatoid papulosis (LyP) to aggressive entities like CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma (AECTCL), CD8 and/or cytotoxic molecule expression alone is insufficient for diagnosis and is not in itself an indicator of prognosis. We present a review of CTCL subtypes that can demonstrate CD8 positivity: CD8+ mycosis fungoides (MF), LyP type D, subcutaneous panniculitis-like T-cell lymphoma (SPTCL), primary cutaneous gamma/delta T-cell lymphoma (PCGDTL), CD8+ AECTCL, and acral CD8+ T-cell lymphoproliferative disorder (acral CD8+ TCLPD). These diseases may have different clinical manifestations and distinctive treatment algorithms. Due to the rare nature of these diseases, it is imperative to integrate clinical, histologic, and immunohistochemical findings to determine an accurate diagnosis and an appropriate treatment plan. Full article
(This article belongs to the Special Issue Cutaneous Lymphoma)
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<p>The cutaneous T-cell lymphoma entities divided into typically CD4-positive and CD8-positive lymphomas.</p>
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<p>When constructing a diagnostic decision tree for CD8+ T-cell lymphoma, it is crucial to consider the key distinguishing features, particularly immunohistochemistry (IHC) differences and clinical decision points. The IHC differences, shown in the diamonds, include cytotoxic markers such as granzyme and TIA, as well as CD30 positivity. Clinical decision points, shown in rectangles, are also essential components of the decision-making process. Together, these elements help in accurately differentiating and diagnosing CD8+ T-cell lymphoma.</p>
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14 pages, 1964 KiB  
Review
Clinical and Dermoscopic Patterns of Basal Cell Carcinoma and Its Mimickers in Skin of Color: A Practical Summary
by Emmanouil Karampinis, Konstantina-Eirini Georgopoulou, Elli Kampra, Efterpi Zafiriou, Aimilios Lallas, Elizabeth Lazaridou, Zoe Apalla, Biswanath Behera and Enzo Errichetti
Medicina 2024, 60(9), 1386; https://doi.org/10.3390/medicina60091386 - 24 Aug 2024
Viewed by 421
Abstract
The diagnosis of basal cell carcinoma (BCC) in dark phototypes can be a challenging task due to the lack of relevant clues and its variable presentation. In this regard, there is growing evidence that dermoscopy may benefit the recognition of BCC even for [...] Read more.
The diagnosis of basal cell carcinoma (BCC) in dark phototypes can be a challenging task due to the lack of relevant clues and its variable presentation. In this regard, there is growing evidence that dermoscopy may benefit the recognition of BCC even for skin of color (SoC). The objective of this review is to provide an up-to-date overview on clinical and dermoscopic patterns of BCC in SoC, also comparing such findings with those of the main clinical mimickers reported in the literature. A comprehensive search of the literature through the PubMed electronic database was carried out in order to identify papers describing the clinical and dermoscopic features of BCC in dark phototypes (IV–VI). By finding macroscopic clinical presentations of BCCs in SoC patients and any possible clinical mimickers considered in the retrieved papers, we built a differential diagnosis list and analyzed the dermoscopic findings of such conditions to facilitate the diagnosis of BCC. BCC in darker skin may present as pigmented nodular lesions, pigmented patches or plaques, ulcers, erythematous nodular lesions, erythematous plaques or patches, or scar-like lesions, depending on its subtype and body site. The differential diagnosis for BCC in patients with SoC includes squamous cell carcinoma, melanoma, nevi, adnexal tumors and sebaceous keratosis. Additionally, it differs from that of Caucasians, as it also includes lesions less common in fair skin, such as dermatosis papulosa nigra, melanotrichoblastoma, and pigmented dermatofibrosarcoma protuberans, and excludes conditions like actinic keratosis and keratoacanthoma, which rarely appear in darker skin. The resulting differences also include infectious diseases such as deep cutaneous mycosis and inflammatory dermatoses. The most prevalent differentiating dermoscopic feature for BCC includes blue, black and gray dots, though arborizing vessels still remain the predominant BCC feature, even in dark phototypes. Diagnostic approach to BCC in dark-skinned patients varies due to the prevalence of dermoscopy findings associated with hyperpigmented structures. Clinicians should be aware of such points of differentiation for a proper management of this tumor in SoC. Full article
(This article belongs to the Special Issue Inflammatory Skin Diseases and Comorbidities)
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<p>Presenting macroscopic and dermoscopic presentation of BCC in Indian patient. Image (<b>A</b>) showing a pigmented patch and image (<b>B</b>) indicating the respective dermoscopy image with the presence of structureless black or leaf-like areas in a pink stroma.</p>
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<p>Presenting a sebaceous keratosis on the skin of the ring finger of a dark-skinned individual as a pigmented patch (similar presentation as BCC or acral melanoma) (Image (<b>A</b>)). Image (<b>B</b>) shows the differently tanned finger-like structures, which is dermoscopy characteristic of sebaceous keratosis.</p>
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<p>Presenting dermoscopy images of a nodular lesion-BCC in an Indian patient. Image (<b>A</b>) shows the pigmented structures on the periphery of the lesions with blue-white veil a centrally while in image (<b>B</b>) the arborising vessels are present on a pink-brownish stroma with co-existing white chrysalis structures.</p>
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18 pages, 3193 KiB  
Article
Quantitative MRI of a Cerebral Cryptococcoma Mouse Model for In Vivo Distinction between Different Cryptococcal Molecular Types
by Luigi Musetta, Shannon Helsper, Lara Roosen, Dries Maes, Anca Croitor Sava, Liesbeth Vanherp, Willy Gsell, Greetje Vande Velde, Katrien Lagrou, Wieland Meyer and Uwe Himmelreich
J. Fungi 2024, 10(8), 593; https://doi.org/10.3390/jof10080593 - 22 Aug 2024
Viewed by 379
Abstract
The controversially discussed taxonomy of the Cryptococcus neoformans/Cryptococcus gattii species complex encompasses at least eight major molecular types. Cerebral cryptococcomas are a common manifestation of cryptococcal neurological disease. In this study, we compared neurotypical symptoms and differential neurovirulence induced by one [...] Read more.
The controversially discussed taxonomy of the Cryptococcus neoformans/Cryptococcus gattii species complex encompasses at least eight major molecular types. Cerebral cryptococcomas are a common manifestation of cryptococcal neurological disease. In this study, we compared neurotypical symptoms and differential neurovirulence induced by one representative isolate for each of the eight molecular types studied. We compared single focal lesions caused by the different isolates and evaluated the potential relationships between the fungal burden and properties obtained with quantitative magnetic resonance imaging (qMRI) techniques such as diffusion MRI, T2 relaxometry and magnetic resonance spectroscopy (MRS). We observed an inverse correlation between parametric data and lesion density, and we were able to monitor longitudinally biophysical properties of cryptococcomas induced by different molecular types. Because the MRI/MRS techniques are also clinically available, the same approach could be used to assess image-based biophysical properties that correlate with fungal cell density in lesions in patients to determine personalized treatments. Full article
(This article belongs to the Special Issue Cryptococcus Infections and Pathogenesis)
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<p><b>Neurovirulence evaluation of BALB/cAnNCrl mice infected by stereotactic injection with cryptococcal isolates of the different major molecular types.</b> (<b>A</b>,<b>B</b>): The graphs show a longitudinal assessment of neurotypical symptoms in mice stereotactically infected with various CN (VN I–IV) or CG (VG I–IV) molecular types. Each graph shows the morbidity scoring per mouse group with standard deviation (<span class="html-italic">p</span>-values: *** &lt; 0.001, **** &lt; 0.0001). (<b>C</b>): The isolates were classified on the day of the average time needed for the morbidity score to reach a level of 2. “very high” (≤6 days), “high” (&gt;6 days to ≤10 days), “medium” (&gt;10 days to ≤15 days), “low” (≥16 days), or “non-neurovirulent” due to full recovery. (<b>D</b>): normalized brain fungal burden (Colony forming units divided by brain weight) shows a higher fungal burden in the CN species compared to the CG, Unpaired Welch’s <span class="html-italic">t</span> test (<span class="html-italic">p</span>-value = 0.0059 **).</p>
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<p><b>Longitudinal T<sub>2–</sub>weighted MR images of two representative CN/CG isolates and assessment of cryptococcomas lesion volume induced by isolates of the different major molecular types.</b> (<b>A</b>). Longitudinal T<sub>2</sub>–weighted MR images in the axial orientation of a representative animal infected with the VN I isolate. (<b>B</b>). Longitudinal T<sub>2</sub>–weighted MR images in the axial orientation of a representative animal infected with the VG I isolate. The graphs in (<b>C</b>,<b>D</b>) show the longitudinal evaluation of the lesion volume induced by the different CN (VN I–IV) or CG (VG I–IV) molecular types. Each time point shows the average lesion volume with standard deviation (n = 4).</p>
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<p><b>Cryptococcal lesion volume and density at endpoint induced by different molecular types.</b> (<b>A</b>,<b>B</b>) boxplots show endpoint median lesion volume distribution, standard deviation and statistical differences of CN and CG isolates, respectively (<span class="html-italic">p</span>-values: *** &lt; 0.001). The graphs (<b>C</b>,<b>D</b>) show lesion density (LD), calculated by the logarithm of CFU/lesion volume. One-way ANOVA with Fisher LSD test. (<b>E</b>) Comparison of lesion density (LD) by grouping all CN and all CG isolates. Unpaired Welch’s <span class="html-italic">t</span> test. (<span class="html-italic">p</span>-values: *** &lt; 0.001, **** &lt; 0.0001). VG III is shown for reference in graphs (<b>B</b>,<b>D</b>); however, since it is a non-neurovirulent isolate, it was not included in (<b>E</b>) or any statistical analysis.</p>
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<p><b>Evaluation of T<sub>2</sub> values in the lesion material and in the contralateral hemisphere in a single brain lesion model of cryptococcosis.</b> (<b>A</b>,<b>B</b>) Longitudinal T<sub>2</sub> maps of lesions representing one CN and one CG–relevant molecular type. (<b>C</b>,<b>D</b>) Longitudinal assessment of T<sub>2</sub> values in the lesion and in the contralateral brain as reference for isolates of CN and CG species complexes. (<b>E</b>) Correlation matrix of T<sub>2</sub> values shows predicted mean difference between all isolates and relative statistical difference expressed in <span class="html-italic">p</span>–value in stars. Statistical analysis was performed with mixed effect analysis 2–way ANOVA with Tukey’s multiple comparison. (<span class="html-italic">p</span>–values: * &lt; 0.05, ** &lt; 0.01, *** &lt; 0.001, **** &lt; 0.0001).</p>
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<p><b>Evaluation of ADC values in the lesion material and contralateral hemisphere in a single lesion brain model of cryptococcosis.</b> (<b>A</b>,<b>B</b>) Longitudinal ADC maps of lesions representing one CN and one CG (<b>B</b>) relevant molecular type. (<b>C</b>,<b>D</b>) Longitudinal assessment of ADC values in the lesion and in the contralateral brain for reference for isolates of CN and CG species complexes. (<b>E</b>) Correlation matrix of ADC values shows predicted mean difference between all isolates and relative statistical difference expressed in <span class="html-italic">p</span>–value in stars. Statistical analysis was performed with mixed effect analysis 2–way ANOVA with Tukey’s multiple comparison. (<span class="html-italic">p</span>–values: * &lt; 0.05, ** &lt; 0.01, *** &lt; 0.001, **** &lt; 0.0001).</p>
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<p><b>qMRI analysis (T<sub>2</sub> and ADC values) of the lesions at endpoint induced by isolates of different molecular types and correlation with lesion density (LD).</b> (<b>A</b>). Comparison between average CN, CG, and contralateral brain T<sub>2</sub> values. (<b>B</b>,<b>C</b>). T<sub>2</sub> values of CN and CG at endpoint show statistical differences between isolates. (<b>D</b>). Comparison between ADC values of CN, CG, and contralateral side. Statistical differences were calculated with one–way ANOVA with Welch’s multiple comparison test (<span class="html-italic">p</span>–values: * &lt; 0.05, ** &lt; 0.01, *** &lt; 0.001, **** &lt; 0.0001). VG III is shown for reference but is not included in the statistical analysis. (<b>E</b>,<b>F</b>). ADC values of CN and CG at endpoint with statistical differences between isolates. (<b>G</b>,<b>H</b>). Graphs show Pearson linear correlation (r) of T<sub>2</sub> and ADC values to fungal lesion density (LD). (<b>I</b>). India ink stainings confirm a reduction in cell density within CG compared to CN, supporting the association between the increased capsule size and T<sub>2</sub>/ADC values. (<b>J</b>). Lesion cell structure model that links decreased cell density in CG compared to CN with increased capsule size and T<sub>2</sub>/ADC values as proposed by Vanherp et al. [<a href="#B38-jof-10-00593" class="html-bibr">38</a>].</p>
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6 pages, 1210 KiB  
Case Report
Atypical Presentation of Invasive Aspergillosis during Treatment with Mogamulizumab
by Paolo Pavone, Laura Arletti, Fiorella Ilariucci, Tommaso Albano, Deborah Lusetti, Romina Corsini, Francesco Merli and Sergio Mezzadri
J. Fungi 2024, 10(8), 584; https://doi.org/10.3390/jof10080584 - 17 Aug 2024
Viewed by 519
Abstract
Treatment with CCR-4 antagonists has been shown to be protective against the development of invasive pulmonary aspergillosis in animal models. Herein, we present a case of fatal invasive pulmonary aspergillosis in a patient receiving Mogamulizumab. A 64-year-old man with refractory mycosis fungoides was [...] Read more.
Treatment with CCR-4 antagonists has been shown to be protective against the development of invasive pulmonary aspergillosis in animal models. Herein, we present a case of fatal invasive pulmonary aspergillosis in a patient receiving Mogamulizumab. A 64-year-old man with refractory mycosis fungoides was found to have diffuse bilateral pulmonary nodules during a chest CT in June 2022. Bronchoalveolar lavage (BAL) fungal and bacterial cultures and galactomannan were negative, as well as serum beta-glucan and galactomannan. Histology showed a lymphoid infiltrate with a negative fungal stain, so a presumptive diagnosis of lymphoma infiltration was made, and the patient started the CCR-4 antagonist Mogamulizumab treatment in August 2022. He had no symptoms until November when he presented to the hematology clinic reporting dyspnea. He had neutrophilic leukocytosis (18.610 cells/µL), his c-reactive protein was 27 mg/dL, and his skin lesions from mycosis fungoides were just starting to improve. A CT scan showed large diffuse bilateral severely necrotic cavitated lesions with thick walls and apparently synchronous evolution. Beta-glucan was 31 pg/mL (wako method), while serum galactomannan 3.6. BAL was positive for Aspergillus fumigatus culture and galactomannan. Patient started voriconazole but, despite being in a stable condition, he suddenly died after two days. Discussion: Paradoxically, worsening of the chronic pulmonary aspergillosis has been reported after nivolumab treatment, and immune reconstitution syndromes are usually seen during neutrophil recovery after intensive chemotherapy. Our patient already presented indolent lung lesions from 5 months before and he remained completely asymptomatic until the aspergillosis diagnosis when he quickly passed away. Even if a progression of the lesions was expected in 5 months, this case had an atypical presentation. During the 5-month period, he had no pulmonary symptoms, and his c-reactive protein was negative. Furthermore, in the setting of the natural progression of subacute/chronic aspergillosis, a different radiological picture was expected with a less severe and probably asynchronous evolution. We think that the immune restoration associated with Mogamulizumab (also supported by the concurrent clinical response of the skin lesions) could have been detrimental in this case, exacerbating a catastrophic immune response or alternatively masquerading the clinical progression of aspergillosis. Clinicians should be aware of immune reconstitution syndromes possibly leading to fatal outcomes in immunocompromised patients starting CCR-4 antagonists. Full article
(This article belongs to the Special Issue Diagnosis of Invasive Fungal Diseases)
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<p>CT chest before and after Mogamulizumab treatment. Previously seen nodular lesions are substituted by massively necrotic and cavitated lesions.</p>
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18 pages, 910 KiB  
Review
Microbiota and Recurrent Pregnancy Loss (RPL); More than a Simple Connection
by Jenny Valentina Garmendia, Claudia Valentina De Sanctis, Marián Hajdúch and Juan Bautista De Sanctis
Microorganisms 2024, 12(8), 1641; https://doi.org/10.3390/microorganisms12081641 - 10 Aug 2024
Viewed by 852
Abstract
Recurrent Pregnancy Loss (RPL) affects 1–2% of women, and its triggering factors are unclear. Several studies have shown that the vaginal, endometrial, and gut microbiota may play a role in RPL. A decrease in the quantity of Lactobacillus crispatus in local microbiota has [...] Read more.
Recurrent Pregnancy Loss (RPL) affects 1–2% of women, and its triggering factors are unclear. Several studies have shown that the vaginal, endometrial, and gut microbiota may play a role in RPL. A decrease in the quantity of Lactobacillus crispatus in local microbiota has been associated with an increase in local (vaginal and endometrial) inflammatory response and immune cell activation that leads to pregnancy loss. The inflammatory response may be triggered by gram-negative bacteria, lipopolysaccharides (LPS), viral infections, mycosis, or atypia (tumor growth). Bacterial structures and metabolites produced by microbiota could be involved in immune cell modulation and may be responsible for immune cell activation and molecular mimicry. Gut microbiota metabolic products may increase the amount of circulating pro-inflammatory lymphocytes, which, in turn, will migrate into vaginal or endometrial tissues. Local pro-inflammatory Th1 and Th17 subpopulations and a decrease in local Treg and tolerogenic NK cells are accountable for the increase in pregnancy loss. Local microbiota may modulate the local inflammatory response, increasing pregnancy success. Analyzing local and gut microbiota may be necessary to characterize some RPL patients. Although oral supplementation of probiotics has not been shown to modify vaginal or endometrial microbiota, the metabolites produced by it may benefit patients. Lactobacillus crispatus transplantation into the vagina may enhance the required immune tolerogenic response to achieve a normal pregnancy. The effect of hormone stimulation and progesterone to maintain early pregnancy on microbiota has not been adequately studied, and more research is needed in this area. Well-designed clinical trials are required to ascertain the benefit of microbiota modulation in RPL. Full article
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<p>General overview of the differences between eubiosis and dysbiosis in the vagina. In the vaginal lumen, the expected protective effect of immunoglobulins, complement proteins, antimicrobial peptides, peroxide production, and lactic acid. In dysbiosis, the protective effect is lost, and the inflammatory response is due to bacterial proteins, increasing cell death inflammatory mediators. This increase in inflammatory mediators leads to a decrease in vaginal tolerogenic milieu, which is the response to the reduction of annidation and increase of pregnancy loss.</p>
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9 pages, 2997 KiB  
Case Report
Disseminated Infection with Aspergillus fumigatus in a Scarlet Macaw Parrot (Ara macao)—A Case Report
by Oana Irina Tanase, Geta Pavel, Ozana Maria Hritcu, Mihaela Anca Dascalu, Bianca Elena Bratuleanu, Cristina Mihaela Rimbu and Florentina Daraban Bocaneti
Animals 2024, 14(15), 2282; https://doi.org/10.3390/ani14152282 - 5 Aug 2024
Viewed by 641
Abstract
A 3-year-old male scarlet macaw parrot (Ara macao) was presented to the Exotic Animal Clinic at the Faculty of Veterinary Medicine, Iași University of Life Sciences (Iași, Romania) for its postmortem examination. According to the owner, the parrot had been raised [...] Read more.
A 3-year-old male scarlet macaw parrot (Ara macao) was presented to the Exotic Animal Clinic at the Faculty of Veterinary Medicine, Iași University of Life Sciences (Iași, Romania) for its postmortem examination. According to the owner, the parrot had been raised only in captivity and after 5 days of inappetence, lethargy, and mild respiratory clinical signs, the parrot died. The post mortem examination revealed various-sized granulomas and caseous plaques in the lungs, air sacs, spleen, intestinal serosa, and liver. Microscopically, the granulomas were characterized by a necrotic center and the infiltration of numerous multinucleated giant cells and epithelioid-like cells and by the presence of hyphae typical of Aspergillus spp. Moreover, in the liver tissue, a diffuse inflammation, with numerous fungal hyphae, was noted. The fungal culture and the PCR assay allowed for the isolation and identification of Aspergillus fumigatus from the lung and liver samples. The macroscopical lesions and the histopathological findings, with the fungal isolation and molecular confirmation of Aspergillus fumigatus by nested PCR, provided the basis for the diagnosis of disseminated aspergillosis. To the authors’ best knowledge, this is the first report of disseminated infection caused by Aspergillus fumigatus in a scarlet macaw parrot (Ara macao). Full article
(This article belongs to the Special Issue Wildlife Diseases: Pathology and Diagnostic Investigation)
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<p>Macroscopic findings in parrot aspergillosis: (<b>a</b>) lungs showing fungal granulomas of various sizes (black arrows); (<b>b</b>) disseminated granulomas on spleen and intestinal serosa (yellow arrowheads).</p>
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<p>(<b>a</b>) Lung granuloma consisting of a central mass of necrotic exudate under Masson’s trichrome staining and 20× magnification. Inset shows higher magnification of granulomas, with numerous fungal hyphae under Masson’s trichrome staining and 40× magnification. (<b>b</b>) Fungal hyphae with a characteristic architecture consisting of 45° dichotomous branches in lung granuloma lesion, under PAS staining, 40× magnification. (<b>c</b>) Liver: fungal hyphae (black arrows), hemosiderin granules phagocytosis (black star), and congestion (red arrow) under Masson’s trichrome staining and 100× magnification.</p>
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<p>Cytology from the lung granuloma smears shows: (<b>a</b>) inflammatory cells and multinucleated giant cells (black arrow) under May–Grünwald–Giemsa staining, 40× magnification; (<b>b</b>) fungal hyphae (white arrowheads) under May-Grünwald Giemsa staining and 40× magnification.</p>
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<p>(<b>a</b>) Cultural characteristics of <span class="html-italic">Aspergillus fumigatus</span> colony: dense smoky and gray-green colonies on Sabouraud dextrose agar media; (<b>b</b>) cultural characteristics of <span class="html-italic">Aspergillus fumigatus</span> colony on Mueller–Hinton agar media showing gray-green colony (black arrow); (<b>c</b>) microscopical morphologies of <span class="html-italic">Aspergillus fumigatus</span> revealed by lactophenol cotton blue staining: typical columnar conidia heads (white arrow) showing characteristic form of vesicles under Lactophenol cotton blue staining, and ×20 magnification. (<b>d</b>) Molecular confirmation of genus <span class="html-italic">Aspergillus</span> and <span class="html-italic">Aspergillus fumigatus</span>: line 1: 1.2 kb molecular weight marker; lines 2 and 5 C-negative control; the product of 521 bp was amplified in line 3 (lung) and 4 (liver) samples by ASAP primers; using nested PCR, a product of 310 bp corresponding to <span class="html-italic">Aspergillus fumigatus</span> was obtained in the lung (line 6) and liver (line 7) samples using ASPU/AFI3 primers.</p>
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10 pages, 253 KiB  
Review
Assessing Health-Related Quality of Life in Mycosis Fungoides and Sézary Syndrome: Unmet Needs
by Danielle Brazel, Cecilia Larocca and Michi M. Shinohara
Cancers 2024, 16(15), 2757; https://doi.org/10.3390/cancers16152757 - 3 Aug 2024
Viewed by 603
Abstract
Mycosis fungoides (MF) and Sézary syndrome (SS) can impair multiple dimensions of health-related quality of life (HRQoL). Currently, there is no standardized assessment tool for measuring HRQoL in patients with MF/SS. Here, we describe the existing literature on multiple dimensions of HRQoL in [...] Read more.
Mycosis fungoides (MF) and Sézary syndrome (SS) can impair multiple dimensions of health-related quality of life (HRQoL). Currently, there is no standardized assessment tool for measuring HRQoL in patients with MF/SS. Here, we describe the existing literature on multiple dimensions of HRQoL in MF/SS with a special focus on the gaps in the current knowledge and identify future directions necessary to assess the HRQoL of patients with this disease. Full article
(This article belongs to the Special Issue Cutaneous Lymphoma)
13 pages, 2243 KiB  
Article
The Association of Chronic Pulmonary Aspergillosis and Chronic Pulmonary Histoplasmosis with MDR-TB Patients in Indonesia
by Noni N. Soeroso, Lambok Siahaan, Selfi Khairunnisa, Raden Ajeng Henny Anggriani, Aida Aida, Putri C. Eyanoer, Elvita R. Daulay, Erlina Burhan, Anna Rozaliyani, Ronny Ronny, Robiatul Adawiyah, David W. Denning and Retno Wahyuningsih
J. Fungi 2024, 10(8), 529; https://doi.org/10.3390/jof10080529 - 29 Jul 2024
Viewed by 819
Abstract
In Indonesia, 2.4% of all new tuberculosis patients had multi-drug resistant disease (MDR-TB); an estimated 24,000 incidences. Historical case series of MDR-TB described a high frequency of cavitation and poor prognosis. The diagnosis of chronic pulmonary aspergillosis (CPA) relies on raised levels of [...] Read more.
In Indonesia, 2.4% of all new tuberculosis patients had multi-drug resistant disease (MDR-TB); an estimated 24,000 incidences. Historical case series of MDR-TB described a high frequency of cavitation and poor prognosis. The diagnosis of chronic pulmonary aspergillosis (CPA) relies on raised levels of Aspergillus IgG antibodies, and detectable Histoplasma IgG antibodies are suspicious for chronic pulmonary histoplasmosis (CPH). We investigated whether MDR-TB patients might have concurrent CPH or CPA. This was a cross-sectional study with 50 MDR-TB patients. ELISA was used to detect Histoplasma IgG antibodies and lateral flow assay was used to detect Aspergillus IgG/IgM antibodies. Several other possible disease determinants were assessed by multivariate analysis. Of the 50 MDR-TB patients, 14 (28%) and 16 (32%) had positive Histoplasma or Aspergillus serology; six patients (12%) had dual antibody reactivity. Radiological abnormalities in positive patients included diffuse or local infiltrates, nodules, consolidation, and apical cavities, consistent with CPH and CPA. Patients with detectable fungal antibodies tended to have worse disease, and 4 of 26 (15.3%) died in the first 5 months of dual infection (p = 0.11 compared with no deaths in those with only MDR-TB). The criteria for the diagnosis of CPH and CPA were fulfilled in those with moderately and far advanced disease (13 of 14 or 93%) and 12 of 16 (75%), respectively. Damp housing was the only determinant associated with Histoplasma antibodies (PR 2.01; 95%CI 0.56–7.19), while pets were associated with the Aspergillus antibody (PR 18.024; 95%CI 1.594–203.744). CPA or CPH are probably frequent in MDR-TB patients in Indonesia and may carry a worse prognosis. Full article
(This article belongs to the Special Issue Epidemiology of Invasive Mycosis in the Hospital)
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<p>Chest X-ray examples in cases of chronic pulmonary histoplasmosis and aspergillosis: (<b>a</b>,<b>b</b>) far advanced radiological findings, (<b>c</b>) moderately advanced radiological findings.</p>
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<p>Sampling interval between the diagnosis of MDR-TB and the detection of <span class="html-italic">Aspergillus</span> and <span class="html-italic">Histoplasma</span> antibodies. Those patients who were positive for antibodies could be divided into three clusters, i.e., early (1–7 months), medium (8–14 months) and late-onset (15–21 months) of fungal infection, but sampling was only carried out on one occasion.</p>
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14 pages, 1098 KiB  
Review
Novel Insights into Sporotrichosis and Diabetes
by Mariana de Araujo Oliveira, Sandro Rogério de Almeida and Joilson O. Martins
J. Fungi 2024, 10(8), 527; https://doi.org/10.3390/jof10080527 - 29 Jul 2024
Viewed by 643
Abstract
Sporotrichosis is a type of zoonotic subcutaneous mycosis caused by different species of dimorphic fungus of the genus Sporothrix, and it is the most common form of subcutaneous mycosis in Latin America. Sporotrichosis is generally restricted to cutaneous and lymphatic tissue (i.e., [...] Read more.
Sporotrichosis is a type of zoonotic subcutaneous mycosis caused by different species of dimorphic fungus of the genus Sporothrix, and it is the most common form of subcutaneous mycosis in Latin America. Sporotrichosis is generally restricted to cutaneous and lymphatic tissue (i.e., localized forms), and involvement in the viscera (i.e., disseminated or disseminated cutaneous form) is uncommon, especially in the central nervous system. However, immunosuppression in individuals with diabetes mellitus can lead to the disseminated form of the disease due to a failure to eliminate the pathogen and poor infection treatment outcomes. Possible correlations between patients with diabetes and their greater susceptibility to disseminated cases of sporotrichosis include a decreased cytokine response after stimulation, increased oxidative stress, decreased chemotaxis, phagocytic activity, adhesion and rolling of neutrophils and monocytes/macrophages, and increased macrophage/monocyte and polymorphonuclear cell apoptosis. Therefore, this review highlights novel insights into diabetes and sporotrichosis by investigating how chronic inflammation affects and aggravates the infection, the possible causes of the greater susceptibility of Sporothrix sp. to hematogenous dissemination in immunocompromised patients, and the main alterations that this dissemination can cause. Full article
(This article belongs to the Special Issue Fungal Infections: Immune Defenses and New Therapeutic Strategies)
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<p>Distribution of feline sporotrichosis cases in Brazil, focusing on São Paulo and Rio de Janeiro, in recent years. The map was constructed based on case reports available in the literature showing a scenario of evident fungal infection [<a href="#B8-jof-10-00527" class="html-bibr">8</a>,<a href="#B21-jof-10-00527" class="html-bibr">21</a>,<a href="#B22-jof-10-00527" class="html-bibr">22</a>,<a href="#B32-jof-10-00527" class="html-bibr">32</a>,<a href="#B33-jof-10-00527" class="html-bibr">33</a>,<a href="#B34-jof-10-00527" class="html-bibr">34</a>,<a href="#B35-jof-10-00527" class="html-bibr">35</a>,<a href="#B36-jof-10-00527" class="html-bibr">36</a>,<a href="#B37-jof-10-00527" class="html-bibr">37</a>,<a href="#B38-jof-10-00527" class="html-bibr">38</a>,<a href="#B39-jof-10-00527" class="html-bibr">39</a>,<a href="#B40-jof-10-00527" class="html-bibr">40</a>,<a href="#B41-jof-10-00527" class="html-bibr">41</a>,<a href="#B42-jof-10-00527" class="html-bibr">42</a>,<a href="#B43-jof-10-00527" class="html-bibr">43</a>,<a href="#B44-jof-10-00527" class="html-bibr">44</a>,<a href="#B45-jof-10-00527" class="html-bibr">45</a>,<a href="#B46-jof-10-00527" class="html-bibr">46</a>].</p>
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<p>Innate, cellular, and humoral immune responses play important roles in controlling sporotrichosis. After inoculation, innate immune mechanisms are activated to control infection directly and stimulate a specific immune response involving Th1 and Th17 subsets of T lymphocytes. APCs (antigen-presenting cells) recognize and phagocytose fungi, after which immunogenic peptides are presented to T lymphocytes. TCD4+ lymphocytes, macrophages, CD8<sup>+</sup> cells, and IFN-γ production are important for granuloma formation. After two months of infection, the IL-1β, IL-6, IL-4, and TNF-α levels increase. Macrophage activation occurs primarily via TNF-α, which stimulates macrophages to produce NO (nitric oxide), which is highly cytotoxic to <span class="html-italic">Sporothrix</span> sp.</p>
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<p>Possible explanations for the greater susceptibility to hematogenous dissemination of <span class="html-italic">Sporothrix</span> sp. in individuals with T1DM and T2DM. Individuals with diabetes exhibit immune dysfunction, such as a decreased cytokine response (IL-2, IL-10, IL-6, and IL-22), increased oxidative stress, decreased chemotaxis, phagocytic activity, adhesion and rolling of neutrophils and monocytes/macrophages, and increased macrophage/monocyte and polymorphonuclear cell apoptosis, which allow the fungus to spread via the hematogenous route and reach other organs, such as the heart, kidneys, brain, and bones.</p>
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25 pages, 5763 KiB  
Article
Candida tropicalis PMT2 Is a Dispensable Gene for Viability but Required for Proper Interaction with the Host
by Marco J. Hernández-Chávez, Iván Martínez-Duncker, Diana M. Clavijo-Giraldo, Luz A. López-Ramirez and Héctor M. Mora-Montes
J. Fungi 2024, 10(7), 502; https://doi.org/10.3390/jof10070502 - 20 Jul 2024
Viewed by 862
Abstract
Candidemia is an opportunistic mycosis with high morbidity and mortality rates. Even though Candida albicans is the main causative agent, other Candida species, such as Candida tropicalis, are relevant etiological agents of candidiasis and candidemia. Compared with C. albicans, there is currently [...] Read more.
Candidemia is an opportunistic mycosis with high morbidity and mortality rates. Even though Candida albicans is the main causative agent, other Candida species, such as Candida tropicalis, are relevant etiological agents of candidiasis and candidemia. Compared with C. albicans, there is currently limited information about C. tropicalis’ biological aspects, including those related to the cell wall and the interaction with the host. Currently, it is known that its cell wall contains O-linked mannans, and the contribution of these structures to cell fitness has previously been addressed using cells subjected to chemical treatments or in mutants where O-linked mannans and other wall components are affected. Here, we generated a C. tropicalis pmt2∆ null mutant, which was affected in the first step of the O-linked mannosylation pathway. The null mutant was viable, contrasting with C. albicans where this gene is essential. The phenotypical characterization showed that O-linked mannans were required for filamentation; proper cell wall integrity and organization; biofilm formation; protein secretion; and adhesion to extracellular matrix components, in particular to fibronectin; and type I and type II collagen. When interacting with human innate immune cells, it was found that this cell wall structure is dispensable for cytokine production, but mutant cells were more phagocytosed by monocyte-derived macrophages. Furthermore, the null mutant cells showed virulence attenuation in Galleria mellonella larvae. Thus, O-linked mannans are minor components of the cell wall that are involved in different aspects of C. tropicalis’ biology. Full article
(This article belongs to the Section Fungal Cell Biology, Metabolism and Physiology)
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<p>A guide tree constructed with <span class="html-italic">Candida albicans PMT</span> family members and putative orthologs on <span class="html-italic">Candida tropicalis</span>. The amino acid sequences of <span class="html-italic">C. albicans PMT</span> family members, along with the putative orthologs identified in <span class="html-italic">C. tropicalis</span>, were downloaded from (<a href="http://www.candidagenome.org/" target="_blank">http://www.candidagenome.org/</a>, accessed on 30 April 2024), used in multiple sequence alignments in Clustal Omega (<a href="https://www.ebi.ac.uk/jdispatcher/msa/clustalo" target="_blank">https://www.ebi.ac.uk/jdispatcher/msa/clustalo</a>, accessed on 30 April 2024), and from this, the guide tree was constructed. Labels starting with Ca are <span class="html-italic">C. albicans</span> sequences, whilst those beginning with CTRG are from <span class="html-italic">C. tropicalis</span>.</p>
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<p>Complementation of <span class="html-italic">Candida albicans PMT2</span>/<span class="html-italic">pmt2</span>∆ heterozygous mutant with <span class="html-italic">Candida tropicalis</span> CTRG_05668. In (<b>A</b>), yeasts were incubated in YPD broth added with different concentrations of Congo red, calcofluor white, or hygromycin B and incubated for 24 h at 30 °C, and growth was measured by absorbance at 600 nm. Data are shown as a percentage of fungal growth in culture with no perturbing agent added. Data are means ± SD of three independent experiments performed in duplicates. The curves generated with the heterozygous mutant or the <span class="html-italic">pmt6</span>∆ null mutants were significantly different from those generated with the WT control strain or the heterozygous mutant complemented with CTRG_05668 (<span class="html-italic">p</span> &lt; 0.05 when compared by two-way ANOVA). In (<b>B</b>), colony morphology after 5 days at 30 °C on Spider medium. Scale bars, 1 mm. Strains used are NGY152 (WT), HMY211 (<span class="html-italic">PMT2</span>/<span class="html-italic">pmt2</span>Δ), HMY212 (<span class="html-italic">PMT2</span>/<span class="html-italic">pmt2</span>Δ + CTRG_05668), HMY213 (<span class="html-italic">pmt6</span>Δ), and HMY214 (<span class="html-italic">pmt6</span>Δ + CTRG_05668).</p>
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<p>The <span class="html-italic">Candida tropicalis pmt2</span>∆ null mutant fails to undergo dimorphism. Yeast cells grown in RPMI 1640 supplemented with 2.5% (<span class="html-italic">v</span>/<span class="html-italic">v</span>) fetal calf serum for 3.5 h at 37 °C. Scale bars 10 µm. Strains used are MYA-3404 (WT), HMY218 (<span class="html-italic">pmt2</span>Δ), and HMY220 (<span class="html-italic">pmt2</span>Δ + <span class="html-italic">PMT2</span>).</p>
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<p>Cell wall analysis of <span class="html-italic">Candida tropicalis</span> wild-type, <span class="html-italic">pmt2</span>∆, and reintegrant control strains. In (<b>A</b>), cell walls were acid hydrolyzed and monosaccharides were analyzed by high-performance anion-exchange chromatography with pulsed amperometric detection. In (<b>B</b>), cell walls were alkali-hydrolyzed and used to quantify cell wall protein content with a colorimetric method. In (<b>C</b>), cell walls were trimmed with endoglycosidase H or β-elimination, releasing <span class="html-italic">N</span>-linked or <span class="html-italic">O</span>-linked mannans, respectively. The free glycans were quantified and data were normalized to 10<sup>9</sup> yeasts. In (<b>D</b>), yeasts were incubated with fluorescein isothiocyanate conjugated wheat germ agglutinin or IgG Fc-dectin-1 chimera and anti-Fc IgG-fluorescein isothiocyanate specific lectins to label either chitin or β-1,3-glucan, respectively, and the fluorescence of 300 cells was estimated. Data are shown as mean ± SD of three independent experiments performed in duplicate. * <span class="html-italic">p</span> &lt; 0.05 when compared to WT, or reintegrant control strain. Strains used are MYA-3404 (WT), HMY218 (<span class="html-italic">pmt2</span>Δ), and HMY220 (<span class="html-italic">pmt2</span>Δ + <span class="html-italic">PMT2</span>).</p>
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<p>Susceptibility to Congo red, calcofluor white, and hygromycin B in the <span class="html-italic">Candida tropicalis pmt2</span>∆. Yeasts were incubated in YPD added with different concentrations of Congo red, calcofluor white, or hygromycin B; plates incubated for 24 h at 30 °C; and cell growth was measured by reading absorbance at 600 nm. Results are shown as a percentage of those obtained with control cultures were no perturbing agent was included. The same strain grown in the absence of any perturbing agent corresponds to 100%. Data are means ± SD of three independent experiments performed in duplicates. Strains used are MYA-3404 (WT), HMY218 (<span class="html-italic">pmt2</span>Δ), and HMY220 (<span class="html-italic">pmt2</span>Δ + <span class="html-italic">PMT2</span>).</p>
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<p>Analysis of <span class="html-italic">Candida tropicalis</span> adhesion to extracellular matrix components by ELISA. The extracellular matrix proteins were used to coat 96-well plates, yeasts were added to the plates, nonadherent cells were washed, and adhesion was detected with anti-<span class="html-italic">Candida</span> polyclonal antibodies and peroxidase-conjugated anti-rabbit IgG. Results are means ± SD of three independent experiments performed in duplicate. * <span class="html-italic">p</span> &lt; 0.05 when compared to wild-type (WT) strain. Strains used are MYA-3404 (WT), HMY218 (<span class="html-italic">pmt2</span>Δ), and HMY220 (<span class="html-italic">pmt2</span>Δ + <span class="html-italic">PMT2</span>).</p>
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<p>Cytokine stimulation in human peripheral blood mononuclear cells. In (<b>A</b>), yeast and human cells were co-incubated at 37 °C for 24 h, and the secreted cytokines were quantified by ELISA. * <span class="html-italic">p</span> &lt; 0.05 when compared to wild-type (WT) strain. <sup>†</sup> <span class="html-italic">p</span> &lt; 0.05 when compared to untreated cells. In (B), human cells were preincubated with 200 μg mL−1 laminarin before the interactions with yeasts. HK: heat-killed cells. * <span class="html-italic">p</span> &lt; 0.05 when compared to WT strain. ** <span class="html-italic">p</span> &lt; 0.05 when compared to live yeasts. <sup>†</sup> <span class="html-italic">p</span> &lt; 0.05 when compared to untreated cells. Data are means ± SD obtained with samples from eight donors, assayed in duplicate wells. Strains used are MYA-3404 (WT), HMY218 (<span class="html-italic">pmt2</span>Δ), and HMY220 (<span class="html-italic">pmt2</span>Δ + <span class="html-italic">PMT2</span>).</p>
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<p>Phagocytosis of <span class="html-italic">Candida tropicalis</span> by human monocyte-derived macrophages. In (<b>A</b>), yeasts and human monocyte-derived macrophages were co-incubated at 37 °C for 2 h and 5% (<span class="html-italic">v</span>/<span class="html-italic">v</span>) CO<sub>2</sub> and fungal uptake were analyzed by flow cytometry. Depending on the positivity in the different detection channels, human cells interacting with at least one yeast were classified as in phagocytosis’s early, intermediate, and late stages. In (<b>B</b>), similar experiments as those described in (<b>A</b>) were performed but human cells were preincubated with 200 µg mL<sup>−1</sup> laminarin for 1 h at 37 °C. Here, only cells in the late stage of phagocytosis were plotted. * <span class="html-italic">p</span> &lt; 0.05 when compared to wild-type (WT) cells. <sup>†</sup> <span class="html-italic">p</span> &lt; 0.05 when compared to untreated cells. Results are shown as mean ± SD with samples from eight donors analyzed in duplicate. Strains used are MYA-3404 (WT), HMY218 (<span class="html-italic">pmt2</span>Δ), and HMY220 (<span class="html-italic">pmt2</span>Δ + <span class="html-italic">PMT2</span>).</p>
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<p>The <span class="html-italic">Candida tropicalis pmt2</span>∆ null mutant shows virulence attenuation in <span class="html-italic">Galleria mellonella</span> larvae. Larva groups, containing 30 individuals were inoculated with 2.0 × 10<sup>7</sup> yeasts of the corresponding strain, and mortality was recorded daily. PBS refers to a larva group inoculated only with PBS, the vehicle used to prepare fungal inoculums. Data are shown in Kaplan–Meier plots. Strains used are MYA-3404 (WT), HMY218 (<span class="html-italic">pmt2</span>Δ), and HMY220 (<span class="html-italic">pmt2</span>Δ + <span class="html-italic">PMT2</span>).</p>
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8 pages, 3008 KiB  
Communication
Outbreak of Feline Sporotrichosis with Zoonotic Potential in the Seventh Health District of Maceió-AL
by Ana Paula de Castro Pires, Júllia de Oliveira Siqueira, Maria Rafaela Pereira Gomes, Janaína André da Silva, Alisson Luiz da Costa, João Paulo de Castro Marcondes and Aryanna Kelly Pinheiro Souza
J. Fungi 2024, 10(7), 473; https://doi.org/10.3390/jof10070473 - 10 Jul 2024
Viewed by 720
Abstract
Sporotrichosis is a mycosis with zoonotic potential caused by species of Sporothrix. Once thought rare in northeastern Brazil, the disease has recently been spreading, leading to an emergency health issue. In this paper, we describe an outbreak of feline sporotrichosis in the [...] Read more.
Sporotrichosis is a mycosis with zoonotic potential caused by species of Sporothrix. Once thought rare in northeastern Brazil, the disease has recently been spreading, leading to an emergency health issue. In this paper, we describe an outbreak of feline sporotrichosis in the Seventh Health District of Maceió-AL. We collected samples from 23 domiciled and non-domiciled felines without regard for age, breed, sex, and neutering state. Skin samples were analyzed cytologically under a light microscope and seeded onto Sabouraud dextrose agar at 25 °C for from 15 to 30 days. Fifteen of the twenty-three cats with suspected skin lesions were positive for Sporothrix spp. on either cytological or microbiological evaluation. Most of the infected cats were male, young adults, non-neutered, with free access to external areas, and living in environments with poor sanitation, a high population density, and an accumulation of garbage and organic matter. Three owners were bitten or scratched by infected cats and subsequently developed suspicious cutaneous lesions suggestive of sporotrichosis. The epidemiological features of feline sporotrichosis in the outbreaks of Maceió seemed to share similarities with the data obtained from outbreaks in current hyperendemic areas. Identifying geographical sites of infection and providing compulsory notification of the disease is essential for avoiding an epidemic in Alagoas. Full article
(This article belongs to the Special Issue Fungal Diseases in Animals, 3rd Edition)
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<p>Neighborhood distribution by health districts in Maceió-Alagoas.</p>
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<p>Distribution of the outbreaks of sporotrichosis in Maceió-AL. Within the black lines is the Cidade Universitária neighborhood. The yellow square shows the location of the first outbreak, and the purple rectangle delimits the area of the second outbreak.</p>
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<p>Feline sporotrichosis in the Seventh Health District of Maceió-AL, northeastern Brazil. (<b>A</b>) Cat presenting multiple ulcerative, exudative, and hemorrhagic lesions on the face. (<b>B</b>) Cytologic sample exhibiting intense pyogranulomatous inflammation and intra-histocyte yeast structures (red arrows). Fast panoptic stain, 40×. (<b>C</b>) Yeast formed seven days following inoculation on Sabouraud dextrose agar at 37 °C. Obj. 40×. (<b>D</b>) Tape prep of fungal growth in Sabouraud agar stained with lactophenol cotton blue showing colonies of undifferentiated hyphae in a daisy-petal pattern (blue circles). Obj. 40×.</p>
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8 pages, 778 KiB  
Brief Report
Coccidioidomycosis in Immunocompromised at a Non-Endemic Referral Center in Mexico
by Carla M. Román-Montes, Lisset Seoane-Hernández, Rommel Flores-Miranda, Andrea Carolina Tello-Mercado, Andrea Rangel-Cordero, Rosa Areli Martínez-Gamboa, José Sifuentes-Osornio, Alfredo Ponce-de-León and Fernanda González-Lara
J. Fungi 2024, 10(6), 429; https://doi.org/10.3390/jof10060429 - 18 Jun 2024
Viewed by 755
Abstract
The incidence and distribution of coccidioidomycosis are increasing. Information scarcity is evident in Mexico, particularly in non-endemic zones and specific populations. We compared the treatment and outcomes for patients with isolated pulmonary infections and those with disseminated coccidioidomycosis, including mortality rates within six [...] Read more.
The incidence and distribution of coccidioidomycosis are increasing. Information scarcity is evident in Mexico, particularly in non-endemic zones and specific populations. We compared the treatment and outcomes for patients with isolated pulmonary infections and those with disseminated coccidioidomycosis, including mortality rates within six weeks of diagnosis. Of 31 CM cases, 71% were male and 55% were disseminated. For 42% of patients, there was no evidence of having lived in or visited an endemic region. All patients had at least one comorbidity, and 58% had pharmacologic immunosuppressants. The general mortality rate was 30%; without differences between disseminated and localized disease. In our research, we describe a CM with a high frequency of disseminated disease without specific risk factors and non-significant mortality. Exposure to endemic regions was not found in a considerable number of subjects. We consider diverse reasons for why this may be, such as climate change or migration. Full article
(This article belongs to the Special Issue Dimorphic Fungal Pathogen Coccidioides and Coccidioidomycosis)
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<p>This map of Mexico and the Southwestern United States shows where infections are supposed to have been acquired. It is color-coded to differentiate between known or not known to be endemic regions [<a href="#B14-jof-10-00429" class="html-bibr">14</a>].</p>
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17 pages, 3825 KiB  
Article
The Prognostic Value of Histopathological Features in Early-Stage Mycosis Fungoides: Insights from a Retrospective–Prospective Cohort Study
by Sandra Jerkovic Gulin, Ivana Ilic and Romana Ceovic
Dermatopathology 2024, 11(2), 161-176; https://doi.org/10.3390/dermatopathology11020017 - 14 Jun 2024
Viewed by 758
Abstract
Primary cutaneous lymphomas (PCLs), especially mycosis fungoides (MF), pose significant diagnostic and therapeutic challenges. This study aims to correlate initial histological features with the disease course and survival in MF patients. A retrospective–prospective cohort study was conducted on 83 patients diagnosed with early-stage [...] Read more.
Primary cutaneous lymphomas (PCLs), especially mycosis fungoides (MF), pose significant diagnostic and therapeutic challenges. This study aims to correlate initial histological features with the disease course and survival in MF patients. A retrospective–prospective cohort study was conducted on 83 patients diagnosed with early-stage MF at the Departments of Dermatovenerology and Pathology, UHC Zagreb, from January 2003 to December 2012. The analyzed histopathological parameters included lichenoid dermal lymphocyte infiltrate, Pautrier microabscesses, and lymphocyte atypia. Patients with more than 30 guardian lymphocytes per 100 keratinocytes exhibited worse overall and progression-free survival. Furthermore, those with over 50% atypical lymphocytes demonstrated a faster progression rate. A dense lichenoid dermal infiltrate and a high count of lymphocyte “keepers” significantly increased the mortality risk within five years of diagnosis. This study did not fully confirm the hypothesis regarding the prognostic value of large Pautrier microabscesses but highlighted the importance of dense lichenoid infiltrates. The study identified new potential histopathological prognostic factors in early-stage MF, suggesting the need for larger studies to confirm these findings. The identification of such predictors could enhance the prognostic stratification and guide more tailored therapeutic approaches for MF patients. Full article
(This article belongs to the Section Clinico-Pathological Correlation in Dermatopathology)
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<p>“Haloed” lymphocytes named lymphocyte “keepers” in the basal layer of the epidermis and lichenoid infiltrate in Mycosis fungoides: (<b>a</b>) H&amp;E, magnification ×20; (<b>b</b>) H&amp;E, magnification ×20; (<b>c</b>) cd3, magnification ×10; (<b>d</b>) cd4, magnification ×10.</p>
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<p>Overall survival curve.</p>
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<p>Lichenoid dermal infiltrate—survival.</p>
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<p>Pautrier microabscesses—survival.</p>
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<p>Lymphocyte “keepers”—survival.</p>
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<p>Lichenoid dermal infiltrate—progression.</p>
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<p>Lymphocyte “keepers”—progression.</p>
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<p>Lymphocyte atypia—progression.</p>
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<p>Lymphocyte atypia—progression.</p>
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14 pages, 2313 KiB  
Article
The Clinical Characteristics and Antimicrobial Resistance of Staphylococcus aureus Isolated from Patients with Staphylococcal Scalded Skin Syndrome (SSSS) in Southwestern China
by Yidan Wu, Hengfeng Wu, Man Wu, Wanchen Wei, Yuying Wei, Tiantian Li, Cunwei Cao and Zhijian Yao
Antibiotics 2024, 13(6), 516; https://doi.org/10.3390/antibiotics13060516 - 31 May 2024
Viewed by 895
Abstract
Staphylococcal scalded skin syndrome (SSSS) is a rare, toxin-mediated, desquamating bacterial infectious dermatosis. So far, data from Southwestern China is scarce. This study aimed to investigate the clinical characteristics of SSSS patients in our hospital, the relative proportion of methicillin-resistant Staphylococcus aureus (MRSA) [...] Read more.
Staphylococcal scalded skin syndrome (SSSS) is a rare, toxin-mediated, desquamating bacterial infectious dermatosis. So far, data from Southwestern China is scarce. This study aimed to investigate the clinical characteristics of SSSS patients in our hospital, the relative proportion of methicillin-resistant Staphylococcus aureus (MRSA) in skin and soft tissue secretions, and the drug sensitivity of S. aureus to better assist dermatologists in the diagnosis and treatment of SSSS. We reviewed the demographic characteristics, clinical manifestations, treatment regimens, therapeutic efficacy, laboratory test results, drug sensitivity, and outcome data of 79 SSSS patients from January 2012 to December 2021. Statistical analysis was performed using t tests and chi-square tests. Among the 79 SSSS patients, MRSA was detected in 35 (44.3%) isolates: 34 community-acquired (CA)-MRSA (97.1%) and 1 hospital-acquired (HA)-MRSA. The SSSS incidence increased annually from 2012 to 2014 and then decreased gradually after peaking in 2015. All the isolates were sensitive to vancomycin, tigecycline, linezolid, moxifloxacin, levofloxacin, and ciprofloxacin; were completely resistant to penicillin; and had low sensitivity to clindamycin and erythromycin. Interestingly, the sensitivity of MRSA to tetracycline increased annually after 2015. The resistance rates to common drugs previously used to treat SSSS increased. These findings may accelerate diagnosis and improve empirical antibiotic use, suggesting that clinicians should prescribe drugs according to antimicrobial susceptibility. Full article
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<p>Methicillin-resistant <span class="html-italic">S. aureus</span> (MRSA) and methicillin-susceptible <span class="html-italic">S. aureus</span> (MSSA) infections in SSSS patients from 2012 to 2021.</p>
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<p>Comparison of the efficacy of glucocorticoid use between 2012 and 2021.</p>
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<p>Comparison of the antimicrobial susceptibility of isolates from patients with MSSA infection between 2012–2016 and 2017–2021.</p>
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<p>Comparison of the antimicrobial susceptibility of isolates from patients with MRSA infection between 2012–2016 and 2017–2021.</p>
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<p>Flow chart of the exclusion and inclusion criteria for this study.</p>
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