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从实体器官移植受者毛霉病病例调查中获得的临床和环境毛霉科分离株的遗传多样性。

Genetic diversity of clinical and environmental Mucorales isolates obtained from an investigation of mucormycosis cases among solid organ transplant recipients.

机构信息

University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

出版信息

Microb Genom. 2020 Dec;6(12). doi: 10.1099/mgen.0.000473. Epub 2020 Nov 27.

Abstract

Mucormycoses are invasive infections by species and other Mucorales. Over 10 months, four solid organ transplant (SOT) recipients at our centre developed mucormycosis due to (=2), (=1) or (=1), at a median 31.5 days (range: 13-34) post-admission. We performed whole genome sequencing (WGS) on 72 Mucorales isolates (45 . , 19 . , six . , two species) from these patients, from five patients with community-acquired mucormycosis, and from hospital and regional environments. Isolates were compared by core protein phylogeny and global genomic features, including genome size, guanine-cytosine percentages, shared protein families and paralogue expansions. Patient isolates fell into six core phylogenetic lineages (clades). Phylogenetic and genomic similarities of isolates recovered 7 months apart from two SOT recipients in adjoining hospitals suggested a potential common source exposure. However, isolates from other patients and environmental sites had unique genomes. Many isolates that were indistinguishable by core phylogeny were distinct by one or more global genomic comparisons. Certain clades were recovered throughout the study period, whereas others were found at particular time points. In conclusion, mucormycosis cases could not be genetically linked to a definitive environmental source. Comprehensive genomic analyses eliminated false associations between Mucorales isolates that would have been assigned using core phylogenetic or less extensive genomic comparisons. The genomic diversity of Mucorales mandates that multiple isolates from individual patients and environmental sites undergo WGS during epidemiological investigations. However, exhaustive surveillance of fungal populations in a hospital and surrounding community is probably infeasible.

摘要

毛霉病是由接合菌纲和其他毛霉目真菌引起的侵袭性感染。在过去的 10 个月中,我们中心的 4 名实体器官移植(SOT)受者在入院后 31.5 天(范围:13-34 天)中位数内因 (=2)、 (=1)或 (=1)发展为毛霉病。我们对来自这些患者的 72 株毛霉目真菌(45 株. ,19 株. ,6 株. ,2 株 种)、5 例社区获得性毛霉病患者和医院及地区环境中的 72 株毛霉目真菌进行了全基因组测序(WGS)。通过核心蛋白系统发育和包括基因组大小、鸟嘌呤-胞嘧啶百分比、共享蛋白质家族和旁系扩张在内的全基因组特征对分离株进行了比较。患者分离株分为 6 个核心系统发育谱系(进化枝)。从 2 名毗邻医院的 SOT 受者身上相隔 7 个月分离到的 分离株的系统发育和基因组相似性表明存在潜在的共同来源暴露。然而,来自其他患者和环境地点的分离株具有独特的基因组。许多通过核心系统发育无法区分的分离株在一个或多个全基因组比较中存在差异。某些进化枝在整个研究期间都有发现,而其他进化枝则在特定时间点出现。总之,毛霉病病例无法通过遗传与明确的环境来源联系起来。综合基因组分析消除了通过核心系统发育或较少全面基因组比较进行鉴定时,毛霉目真菌分离株之间可能存在的错误关联。毛霉目真菌的基因组多样性要求对个体患者和环境地点的多个分离株进行 WGS,以进行流行病学调查。然而,对医院和周围社区中的真菌种群进行详尽的监测可能是不可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ecf/8116672/93bf7b29b231/mgen-6-473-g001.jpg

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