金黄色念珠菌ERG3突变引起的获得性两性霉素B耐药。

IF 4.5 2区 医学 Q2 MICROBIOLOGY
Lauryn Massic, Laura A Doorley, Sarah J Jones, Irene Richardson, Danielle Denise Siao, Lauren Siao, Philip Dykema, Chi Hua, Emily Schneider, Christina A Cuomo, P David Rogers, Stephanie Van Hooser, Josie E Parker, Steven L Kelly, David Hess, Jeffrey M Rybak, Mark Pandori
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引用次数: 0

摘要

耳念珠菌(原耳念珠菌)于2009年首次发现,是一种新兴的多重耐药真菌,可引起侵袭性感染,粗死亡率为30%至60%。目前,30-50%的金黄色葡萄球菌分离株对两性霉素B具有内在耐药性。在本研究中,我们利用全基因组测序、大规模表型筛选、全面的甾醇谱分析和CRISPR基因型逆转表征了一例获得性两性霉素B耐药的临床病例。本研究获得的数据证明,导致ERG3移码的缺失显著有助于观察到的抗性表型,而ERG4的无义突变可能更适度地促进抗性。该分离物的特性还揭示了适应度成本与麦角甾醇生产的减少和其他晚期甾醇的替代有关。本文报道了金黄色葡萄球菌ERG3移码突变对两性霉素B耐药的临床病例描述,标志着对这种真菌病原体抗真菌耐药性的理解取得了进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acquired amphotericin B resistance attributed to a mutated ERG3 in Candidozyma auris.

First identified in 2009, Candidozyma auris (formerly Candida auris) is an emerging multidrug-resistant fungus that can cause invasive infections with a crude mortality rate ranging from 30 to 60%. Currently, 30-50% of C. auris isolates are intrinsically resistant to amphotericin B. In this study, we characterized a clinical case of acquired amphotericin B resistance using whole-genome sequencing, a large-scale phenotypic screen, comprehensive sterol profiling, and genotypic reversion using CRISPR. Data obtained in this study provide evidence that a deletion resulting in a frameshift in ERG3 significantly contributes to the observed resistant phenotype, and a nonsense mutation in ERG4 may more modestly contribute to resistance. Characterization of this isolate also revealed that a fitness cost is associated with the abrogation of ergosterol production and its replacement with other late-stage sterols. This article presents a clinical case description of amphotericin B resistance from a frameshift mutation in ERG3 in C. auris and marks an advancement in the understanding of antifungal resistance in this fungal pathogen.

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来源期刊
CiteScore
10.00
自引率
8.20%
发文量
762
审稿时长
3 months
期刊介绍: Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.
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