Yakun Shao, Jin Shao, Sybren de Hoog, Paul Verweij, Lin Bai, Riina Richardson, Malcolm Richardson, Zhe Wan, Ruoyu Li, Jin Yu, Yinggai Song
{"title":"新出现的抗真菌抗性:来自易感性谱和基因突变分析的见解。","authors":"Yakun Shao, Jin Shao, Sybren de Hoog, Paul Verweij, Lin Bai, Riina Richardson, Malcolm Richardson, Zhe Wan, Ruoyu Li, Jin Yu, Yinggai Song","doi":"10.1080/22221751.2025.2450026","DOIUrl":null,"url":null,"abstract":"<p><p><b>ABSTRACT</b><i>Trichophyton</i> species, the leading cause of dermatophytosis globally, are increasingly resistant to antifungal treatments, concerns about effective management strategies. In light of the absence of established resistance criteria for terbinafine and azoles, coupled with a dearth of research on resistance mechanisms in <i>Trichophyton</i>, antifungal susceptibility and drug resistance gene diversity were analyzed across 64 <i>T. mentagrophytes</i>, 65 <i>T. interdigitale</i>, and 2 <i>T. indotineae</i> isolates collected in China between 1999 and 2024 and 101 published <i>T. indotineae</i> strains. Analyses of the minimum inhibitory concentrations (MICs) of terbinafine, itraconazole, voriconazole, posaconazole, and isavuconazole revealed a concerning increase in <i>T. indotineae</i> with terbinafine resistance, including two novel isolates from China. Compared with <i>T. interdigitale, T. mentagrophytes</i> presented higher terbinafine MICs but similar azole susceptibility. Notably, 27 <i>T. interdigitale</i> isolates were classified as non-wild-type for terbinafine. Genetic diversity was analyzed for the <i>SQLE</i>, <i>CYP51A</i> and <i>CYP51B</i> gene. Specifically, <i>T. indotineae</i> isolates presented SQLE protein changes linked to terbinafine resistance. SQLE diversity was linked to terbinafine sensitivity, whereas alterations in CYP51A were associated with itraconazole sensitivity, with notable statistical significance evident across various protein isoforms. The relationship between protein diversity and drug sensitivity is presented in detail. Together, these findings highlight a growing prevalence of antibiotic resistance among <i>Trichophyton</i> and identify potential target genes for new therapies, underscoring the need for ongoing monitoring and offering directions for novel therapeutics.</p>","PeriodicalId":11602,"journal":{"name":"Emerging Microbes & Infections","volume":" ","pages":"2450026"},"PeriodicalIF":8.4000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11740296/pdf/","citationCount":"0","resultStr":"{\"title\":\"Emerging antifungal resistance in <i>Trichophyton mentagrophytes</i>: insights from susceptibility profiling and genetic mutation analysis.\",\"authors\":\"Yakun Shao, Jin Shao, Sybren de Hoog, Paul Verweij, Lin Bai, Riina Richardson, Malcolm Richardson, Zhe Wan, Ruoyu Li, Jin Yu, Yinggai Song\",\"doi\":\"10.1080/22221751.2025.2450026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>ABSTRACT</b><i>Trichophyton</i> species, the leading cause of dermatophytosis globally, are increasingly resistant to antifungal treatments, concerns about effective management strategies. In light of the absence of established resistance criteria for terbinafine and azoles, coupled with a dearth of research on resistance mechanisms in <i>Trichophyton</i>, antifungal susceptibility and drug resistance gene diversity were analyzed across 64 <i>T. mentagrophytes</i>, 65 <i>T. interdigitale</i>, and 2 <i>T. indotineae</i> isolates collected in China between 1999 and 2024 and 101 published <i>T. indotineae</i> strains. Analyses of the minimum inhibitory concentrations (MICs) of terbinafine, itraconazole, voriconazole, posaconazole, and isavuconazole revealed a concerning increase in <i>T. indotineae</i> with terbinafine resistance, including two novel isolates from China. Compared with <i>T. interdigitale, T. mentagrophytes</i> presented higher terbinafine MICs but similar azole susceptibility. Notably, 27 <i>T. interdigitale</i> isolates were classified as non-wild-type for terbinafine. Genetic diversity was analyzed for the <i>SQLE</i>, <i>CYP51A</i> and <i>CYP51B</i> gene. Specifically, <i>T. indotineae</i> isolates presented SQLE protein changes linked to terbinafine resistance. SQLE diversity was linked to terbinafine sensitivity, whereas alterations in CYP51A were associated with itraconazole sensitivity, with notable statistical significance evident across various protein isoforms. The relationship between protein diversity and drug sensitivity is presented in detail. 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Emerging antifungal resistance in Trichophyton mentagrophytes: insights from susceptibility profiling and genetic mutation analysis.
ABSTRACTTrichophyton species, the leading cause of dermatophytosis globally, are increasingly resistant to antifungal treatments, concerns about effective management strategies. In light of the absence of established resistance criteria for terbinafine and azoles, coupled with a dearth of research on resistance mechanisms in Trichophyton, antifungal susceptibility and drug resistance gene diversity were analyzed across 64 T. mentagrophytes, 65 T. interdigitale, and 2 T. indotineae isolates collected in China between 1999 and 2024 and 101 published T. indotineae strains. Analyses of the minimum inhibitory concentrations (MICs) of terbinafine, itraconazole, voriconazole, posaconazole, and isavuconazole revealed a concerning increase in T. indotineae with terbinafine resistance, including two novel isolates from China. Compared with T. interdigitale, T. mentagrophytes presented higher terbinafine MICs but similar azole susceptibility. Notably, 27 T. interdigitale isolates were classified as non-wild-type for terbinafine. Genetic diversity was analyzed for the SQLE, CYP51A and CYP51B gene. Specifically, T. indotineae isolates presented SQLE protein changes linked to terbinafine resistance. SQLE diversity was linked to terbinafine sensitivity, whereas alterations in CYP51A were associated with itraconazole sensitivity, with notable statistical significance evident across various protein isoforms. The relationship between protein diversity and drug sensitivity is presented in detail. Together, these findings highlight a growing prevalence of antibiotic resistance among Trichophyton and identify potential target genes for new therapies, underscoring the need for ongoing monitoring and offering directions for novel therapeutics.
期刊介绍:
Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses.
The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries.
This journal addresses topics of critical biological and clinical importance, including but not limited to:
- Epidemic surveillance
- Clinical manifestations
- Diagnosis and management
- Cellular and molecular pathogenesis
- Innate and acquired immune responses between emerging microbes and their hosts
- Drug discovery
- Vaccine development research
Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.