Iván Martínez-Duncker, Jorge Mayorga-Rodríguez, Manuela Gómez-Gaviria, José A Martínez-Álvarez, Dario A Baruch-Martínez, Luz A López-Ramírez, Héctor M Mora-Montes
{"title":"墨西哥西部一个高流行区申克孢子丝菌临床分离株的表型、免疫学特征和抗真菌敏感性。","authors":"Iván Martínez-Duncker, Jorge Mayorga-Rodríguez, Manuela Gómez-Gaviria, José A Martínez-Álvarez, Dario A Baruch-Martínez, Luz A López-Ramírez, Héctor M Mora-Montes","doi":"10.1093/mmy/myaf073","DOIUrl":null,"url":null,"abstract":"<p><p>Sporothrix schenckii is the most prevalent etiological agent of sporotrichosis in Mexico, a neglected subcutaneous mycosis with hyperendemic foci in mountainous regions. Despite its public health importance, the phenotypic and virulence-related features of clinical isolates circulating in these areas remain poorly characterized. Ten clinical isolates were molecularly identified and assessed for virulence by determining enzymatic activity (proteases, lipases, catalase), biofilm formation, adhesion to extracellular matrix proteins, antifungal susceptibility, and cell wall composition. Host interaction was evaluated through cytokine profiling in human peripheral blood mononuclear cells, and virulence was assessed using the Galleria mellonella invertebrate infection model. All isolates were confirmed as S. schenckii. Compared to a reference strain, a subset of isolates (740, 742, 183, and 1798) displayed reduced adhesion, extracellular enzymatic activity, and catalase production, as well as altered mannose and rhamnose cell wall content. These isolates induced significantly lower TNFα and higher IL-10 levels in PBMCs and were markedly less virulent in G. mellonella, exhibiting lower mortality, cytotoxicity, and immune activation. All isolates were biofilm producers, and some showed reduced susceptibility to itraconazole or fluconazole. This study reveals phenotypic diversity among S. schenckii clinical isolates in a Mexican hyperendemic region and identifies a subgroup with reduced virulence and immune stimulation capacity. These findings enhance our understanding of the host-pathogen dynamics of sporotrichosis and may inform future diagnostic and therapeutic strategies in endemic settings.</p>","PeriodicalId":18586,"journal":{"name":"Medical mycology","volume":" ","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phenotypic immunological profiling and antifungal susceptibility of Sporothrix schenckii clinical isolates from a hyperendemic region in western Mexico.\",\"authors\":\"Iván Martínez-Duncker, Jorge Mayorga-Rodríguez, Manuela Gómez-Gaviria, José A Martínez-Álvarez, Dario A Baruch-Martínez, Luz A López-Ramírez, Héctor M Mora-Montes\",\"doi\":\"10.1093/mmy/myaf073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Sporothrix schenckii is the most prevalent etiological agent of sporotrichosis in Mexico, a neglected subcutaneous mycosis with hyperendemic foci in mountainous regions. Despite its public health importance, the phenotypic and virulence-related features of clinical isolates circulating in these areas remain poorly characterized. Ten clinical isolates were molecularly identified and assessed for virulence by determining enzymatic activity (proteases, lipases, catalase), biofilm formation, adhesion to extracellular matrix proteins, antifungal susceptibility, and cell wall composition. Host interaction was evaluated through cytokine profiling in human peripheral blood mononuclear cells, and virulence was assessed using the Galleria mellonella invertebrate infection model. All isolates were confirmed as S. schenckii. Compared to a reference strain, a subset of isolates (740, 742, 183, and 1798) displayed reduced adhesion, extracellular enzymatic activity, and catalase production, as well as altered mannose and rhamnose cell wall content. These isolates induced significantly lower TNFα and higher IL-10 levels in PBMCs and were markedly less virulent in G. mellonella, exhibiting lower mortality, cytotoxicity, and immune activation. All isolates were biofilm producers, and some showed reduced susceptibility to itraconazole or fluconazole. This study reveals phenotypic diversity among S. schenckii clinical isolates in a Mexican hyperendemic region and identifies a subgroup with reduced virulence and immune stimulation capacity. These findings enhance our understanding of the host-pathogen dynamics of sporotrichosis and may inform future diagnostic and therapeutic strategies in endemic settings.</p>\",\"PeriodicalId\":18586,\"journal\":{\"name\":\"Medical mycology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical mycology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/mmy/myaf073\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical mycology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/mmy/myaf073","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Phenotypic immunological profiling and antifungal susceptibility of Sporothrix schenckii clinical isolates from a hyperendemic region in western Mexico.
Sporothrix schenckii is the most prevalent etiological agent of sporotrichosis in Mexico, a neglected subcutaneous mycosis with hyperendemic foci in mountainous regions. Despite its public health importance, the phenotypic and virulence-related features of clinical isolates circulating in these areas remain poorly characterized. Ten clinical isolates were molecularly identified and assessed for virulence by determining enzymatic activity (proteases, lipases, catalase), biofilm formation, adhesion to extracellular matrix proteins, antifungal susceptibility, and cell wall composition. Host interaction was evaluated through cytokine profiling in human peripheral blood mononuclear cells, and virulence was assessed using the Galleria mellonella invertebrate infection model. All isolates were confirmed as S. schenckii. Compared to a reference strain, a subset of isolates (740, 742, 183, and 1798) displayed reduced adhesion, extracellular enzymatic activity, and catalase production, as well as altered mannose and rhamnose cell wall content. These isolates induced significantly lower TNFα and higher IL-10 levels in PBMCs and were markedly less virulent in G. mellonella, exhibiting lower mortality, cytotoxicity, and immune activation. All isolates were biofilm producers, and some showed reduced susceptibility to itraconazole or fluconazole. This study reveals phenotypic diversity among S. schenckii clinical isolates in a Mexican hyperendemic region and identifies a subgroup with reduced virulence and immune stimulation capacity. These findings enhance our understanding of the host-pathogen dynamics of sporotrichosis and may inform future diagnostic and therapeutic strategies in endemic settings.
期刊介绍:
Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.