Azole resistance in Aspergillus flavus and associated fitness cost.

IF 4.1 2区 医学 Q1 DERMATOLOGY Mycoses Pub Date : 2024-07-01 DOI:10.1111/myc.13766
Elie Djenontin, Anne Debourgogne, Bita Mousavi, Laurence Delhaes, Muriel Cornet, Isabel Valsecchi, Makiath Adebo, Jacques Guillot, Françoise Botterel, Eric Dannaoui
{"title":"Azole resistance in Aspergillus flavus and associated fitness cost.","authors":"Elie Djenontin, Anne Debourgogne, Bita Mousavi, Laurence Delhaes, Muriel Cornet, Isabel Valsecchi, Makiath Adebo, Jacques Guillot, Françoise Botterel, Eric Dannaoui","doi":"10.1111/myc.13766","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The resistance of Aspergillus flavus to the azole antifungal drugs is an emerging problem. Mutations in the molecular targets of the azole antifungals - CYP 51 A, B and C - are possible mechanisms of resistance, but data to confirm this hypothesis are scarce. In addition, the behaviour of resistant strains in vitro and in vivo is not yet understood.</p><p><strong>Objectives: </strong>This study had 3 objectives. The first was to compare the sequences of CYP51 A, B and C in resistant and susceptible strains of A. flavus. The second was to look for the existence of a fitness cost associated with resistance. The third was to evaluate the activity of voriconazole and posaconazole on resistant strains in the Galleria mellonella model.</p><p><strong>Methods: </strong>The CYP51 A, B and C sequences of seven resistant strains with those of four susceptible strains are compared. Fitness costs were assessed by growing the strains in RPMI medium and testing their virulence in G. mellonella larvae. In addition, G. mellonella larvae infected with strains of A. flavus were treated with voriconazole and posaconazole.</p><p><strong>Results: </strong>In the CYP51A sequences, we found the A91T, C708T and A1296T nucleotide substitutions only in the resistant strains. The resistant strains showed a fitness cost with reduced in vitro growth and reduced virulence in G. mellonella. In vivo resistance to posaconazole is confirmed in a strain with the highest MIC for this antifungal agent.</p><p><strong>Conclusions: </strong>These results allow to conclude that some substitutions in CYP51 genes, in particular CYP51A, contribute to resistance to azole drugs in A. flavus. The study of the relationship between drug dosage and treatment duration with resistance and the reduction of fitness costs in resistant strains is a major perspective of this study. This work could help to establish recommendations for the treatment of infections with resistant strains of A. flavus.</p>","PeriodicalId":18797,"journal":{"name":"Mycoses","volume":"67 7","pages":"e13766"},"PeriodicalIF":4.1000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mycoses","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/myc.13766","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The resistance of Aspergillus flavus to the azole antifungal drugs is an emerging problem. Mutations in the molecular targets of the azole antifungals - CYP 51 A, B and C - are possible mechanisms of resistance, but data to confirm this hypothesis are scarce. In addition, the behaviour of resistant strains in vitro and in vivo is not yet understood.

Objectives: This study had 3 objectives. The first was to compare the sequences of CYP51 A, B and C in resistant and susceptible strains of A. flavus. The second was to look for the existence of a fitness cost associated with resistance. The third was to evaluate the activity of voriconazole and posaconazole on resistant strains in the Galleria mellonella model.

Methods: The CYP51 A, B and C sequences of seven resistant strains with those of four susceptible strains are compared. Fitness costs were assessed by growing the strains in RPMI medium and testing their virulence in G. mellonella larvae. In addition, G. mellonella larvae infected with strains of A. flavus were treated with voriconazole and posaconazole.

Results: In the CYP51A sequences, we found the A91T, C708T and A1296T nucleotide substitutions only in the resistant strains. The resistant strains showed a fitness cost with reduced in vitro growth and reduced virulence in G. mellonella. In vivo resistance to posaconazole is confirmed in a strain with the highest MIC for this antifungal agent.

Conclusions: These results allow to conclude that some substitutions in CYP51 genes, in particular CYP51A, contribute to resistance to azole drugs in A. flavus. The study of the relationship between drug dosage and treatment duration with resistance and the reduction of fitness costs in resistant strains is a major perspective of this study. This work could help to establish recommendations for the treatment of infections with resistant strains of A. flavus.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
黄曲霉的唑类抗药性及相关的适应成本。
背景:黄曲霉对唑类抗真菌药物的耐药性是一个新出现的问题。唑类抗真菌药物的分子靶标(CYP 51 A、B 和 C)发生突变可能是产生耐药性的机制,但证实这一假设的数据很少。此外,耐药菌株在体外和体内的表现也尚不清楚:本研究有三个目标。目的:本研究有三个目的,首先是比较黄曲霉抗性菌株和易感菌株中 CYP51 A、B 和 C 的序列。第二是寻找与抗性相关的适应成本。第三是评估伏立康唑和泊沙康唑在Galleria mellonella模型中对抗性菌株的活性:方法:比较了七株抗性菌株与四株易感菌株的 CYP51 A、B 和 C 序列。通过在 RPMI 培养基中培养这些菌株并测试其对 G. mellonella 幼虫的毒力,对其健康成本进行了评估。此外,还用伏立康唑和泊沙康唑处理了感染黄曲霉菌株的 G. mellonella 幼虫:结果:在 CYP51A 序列中,我们只在抗性菌株中发现了 A91T、C708T 和 A1296T 核苷酸置换。耐药菌株的体外生长能力和对 G. mellonella 的毒力都有所下降,因此需要付出一定的代价。体内对泊沙康唑的耐药性在一株对该抗真菌剂具有最高 MIC 值的菌株中得到了证实:这些结果可以得出结论,CYP51 基因中的某些替代基因,特别是 CYP51A,会导致黄曲霉对唑类药物产生耐药性。研究药物剂量和治疗时间与耐药性之间的关系以及降低耐药菌株的健康成本是本研究的一个重要视角。这项工作有助于制定治疗黄曲霉抗药性菌株感染的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Mycoses
Mycoses 医学-皮肤病学
CiteScore
10.00
自引率
8.20%
发文量
143
审稿时长
6-12 weeks
期刊介绍: The journal Mycoses provides an international forum for original papers in English on the pathogenesis, diagnosis, therapy, prophylaxis, and epidemiology of fungal infectious diseases in humans as well as on the biology of pathogenic fungi. Medical mycology as part of medical microbiology is advancing rapidly. Effective therapeutic strategies are already available in chemotherapy and are being further developed. Their application requires reliable laboratory diagnostic techniques, which, in turn, result from mycological basic research. Opportunistic mycoses vary greatly in their clinical and pathological symptoms, because the underlying disease of a patient at risk decisively determines their symptomatology and progress. The journal Mycoses is therefore of interest to scientists in fundamental mycological research, mycological laboratory diagnosticians and clinicians interested in fungal infections.
期刊最新文献
High-Resolution Melting Assay to Detect the Mutations That Cause the Y132F and G458S Substitutions at the ERG11 Gene Involved in Azole Resistance in Candida parapsilosis. First Reported Cases of Terbinafine-Resistant Trichophyton indotineae Isolates in Israel: Epidemiology, Clinical Characteristics and Response to Treatment. Multicentre Study of Candida parapsilosis Blood Isolates in Türkiye Highlights an Increasing Rate of Fluconazole Resistance and Emergence of Echinocandin and Multidrug Resistance. The In Vitro Activity of Rezafungin Against Uncommon Species of Candida. Detecting Echinocandin Resistance in C. glabrata Using Commercial Methods: Are CLSI or EUCAST Breakpoints Suitable for Categorical Classification?
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1