首页> 外文期刊>Clinical microbiology and infection: European Society of Clinical Microbiology and Infectious Diseases >Discontinuation of echinocandin and azole treatments led to the disappearance of an FKS alteration but not azole resistance during clonal Candida glabrata persistent candidaemia
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Discontinuation of echinocandin and azole treatments led to the disappearance of an FKS alteration but not azole resistance during clonal Candida glabrata persistent candidaemia

机译:棘皮菌素和唑类药物治疗的中止导致克隆性光滑念珠菌持续性念珠菌血症期间FKS改变的消失,但不引起唑耐药性的消失

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摘要

To give an indication of a fitness cost conferred by FKS mutation-associated echinocandin resistance in Candida glabrata during human infection. Six C. glabrata clinical strains sequentially isolated from blood and a hepatic abscess in a solid organ transplant recipient were analysed. The patient had received long-term azole and echinocandin therapy for invasive aspergillosis and persistent candidaemia. Minimal inhibitory concentrations were determined by the European Committee on Antimicrobial Susceptibility Testing (EUCAST) broth microdilution method. Molecular mechanisms of antifungal resistance were determined by sequencing hot spots of the FKS. Strain relatedness was determined using a microsatellite-based typing method. Typing analysis revealed an identical microsatellite pattern for all isolates, supporting a close relation. The first C. glabrata isolate showed wild-type phenotype (i.e. susceptibility to echinocandins and low level of azole resistance). After voriconazole therapy, the C. glabrata quickly acquired pan-azole resistance. Later, echinocandin treatment led to the emergence of a FKS2 S663P alteration and echinocandin resistance. After disruption of both azole and echinocandin therapy in favour of liposomal amphotericin B, C. glabrata isolates regained full susceptibility to echinocandin and lost the FKS2 S663P alteration while nonetheless maintaining their pan-azole resistance. Our clinical report supports the potential existence of a fitness cost conferred by FKS mutation in C. glabrata, as disruption of treatment led to a rapid disappearance of the resistant clone. This suggests that a more restricted use and/or a discontinuous administration of echinocandins may limit the spread of clinical resistance to this class. (C) 2016 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
机译:为了说明在人类感染过程中,光滑念珠菌与FKS突变相关的棘皮菌素抗性所赋予的健身成本。分析了从实体器官移植受者的血液和肝脓肿中依次分离出的六种光滑念珠菌临床菌株。该患者接受了长期的唑类和棘皮菌素治疗侵入性曲霉病和持续念珠菌血症。最小抑菌浓度由欧洲抗菌药物敏感性试验委员会(EUCAST)肉汤微量稀释方法确定。通过对FKS热点进行测序来确定抗真菌抗性的分子机制。应变相关性是使用基于微卫星的分型方法确定的。打字分析显示所有分离物的微卫星图案相同,支持密切的关系。第一个光滑念珠菌分离物表现出野生型表型(即对棘手oc蛋白的易感性和对唑的抗性水平低)。伏立康唑治疗后,光滑念珠菌迅速获得泛唑耐药性。后来,棘皮菌素治疗导致出现FKS2 S663P改变和棘皮菌素抗性。在破坏唑和echinocandin的治疗后,使用脂质体两性霉素B分离后,光滑念珠菌分离株完全恢复对echinocandin的敏感性,并失去了FKS2 S663P的改变,但仍保持了对泛唑的抗性。我们的临床报告支持在光滑小球藻中由FKS突变赋予健身成本的潜在存在,因为治疗中断会导致抗性克隆的快速消失。这表明棘手and素的更严格的使用和/或不连续的给药可能限制了对该类药物的临床耐药性扩散。 (C)2016欧洲临床微生物学和传染病学会。由Elsevier Ltd.出版。保留所有权利。

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