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超越患者接触范围:短读长与长读长测序相结合揭示了2018年至2021年德国一家医院中基因组相关的产碳青霉烯酶肠杆菌科细菌的持续出现及质粒移动性

Beyond patient contact: combined short- and long read sequencing reveals continuous occurrence of genomically related carbapenemase-producing Enterobacterales and plasmid mobility in a hospital, Germany, 2018 to 2021.

作者信息

Leder Nora Helke, Cristofolini Monika, Ehrenberg Sandra, Lohde Mara, Brandt Christian, Pletz Mathias W, Kipp Frank, Stein Claudia

机构信息

Institute for Infectious Diseases and Infection Control, Jena University Hospital, Jena, Germany.

Hygiene and Infection Control, BG Hospital Bergmannstrost Halle, Halle, Germany.

出版信息

Euro Surveill. 2025 Jun;30(23). doi: 10.2807/1560-7917.ES.2025.30.23.2400590.

Abstract

BACKGROUNDCarbapenemase-producing Enterobacterales (CPE) frequently cause nosocomial outbreaks. To investigate these, tracing focused on patients with related CPE strains and spatiotemporal contact (e.g. contact with each other in a room or on a ward during overlapping periods) has limitations. Moreover, as widely available molecular typing methods cannot detect plasmid-related transmissions, carbapenemase gene transfer across enteric bacteria through plasmids in hospitals remains poorly understood.AIMBecause whole-genome sequencing (WGS), particularly long-read sequencing, can offer insights into bacterial relationships both at core-genome and plasmid levels, we tested its utility, using VIM-CPE as example, to investigate plasmid and CPE spread in a hospital beyond outbreaks.METHODSWe included inpatient episodes from 2018 to 2021 involving bearing CPE isolates. Short- and long-read WGS data were combined with patient movement information to identify genomically related hospital-acquired VIM-CPE and putative transmission routes.RESULTSAmong 43 included inpatient episodes, 27 isolates were hospital-acquired, with 23 genomically related based on core-genome or plasmid analyses. For 14 of these 23 isolates, patient movement data supported suspected transmission events. Plasmid and core-genome level analyses revealed that most transmission events did not temporally concur, occurring over up to 33 months. Thus, conventional infection tracing methods focusing on concurrent spatiotemporal contact missed a substantial proportion of transmission events.CONCLUSIONWith our findings, we advocate for broader epidemiological investigations of temporal connections if genomic data suggest relatedness. We emphasise considering plasmid transfer alongside analyses of core-genome relatedness of bacteria beyond patient contact events to study CPE and resistance spread, and guide infection control strategies.

摘要

背景

产碳青霉烯酶肠杆菌科细菌(CPE)经常引发医院感染暴发。为调查这些感染暴发,聚焦于携带相关CPE菌株的患者以及时空接触(例如在重叠时间段内在同一房间或病房内相互接触)的追踪方法存在局限性。此外,由于广泛使用的分子分型方法无法检测与质粒相关的传播,医院内通过质粒在肠道细菌间进行的碳青霉烯酶基因转移仍知之甚少。

目的

由于全基因组测序(WGS),尤其是长读长测序,能够在核心基因组和质粒水平上深入了解细菌之间的关系,我们以VIM-CPE为例,测试了其在调查医院内超出感染暴发范围的质粒和CPE传播情况方面的效用。

方法

我们纳入了2018年至2021年涉及携带CPE分离株的住院病例。将短读长和长读长WGS数据与患者移动信息相结合,以识别基因组相关的医院获得性VIM-CPE及推定的传播途径。

结果

在纳入的43例住院病例中,27株分离株为医院获得性,根据核心基因组或质粒分析,其中23株在基因组上相关。对于这23株分离株中的14株,患者移动数据支持了疑似传播事件。质粒和核心基因组水平分析显示,大多数传播事件在时间上并不一致,发生时间跨度长达33个月。因此,专注于同时空接触的传统感染追踪方法遗漏了很大一部分传播事件。

结论

基于我们的研究结果,我们主张如果基因组数据表明存在相关性,应进行更广泛的关于时间联系的流行病学调查。我们强调,除了分析患者接触事件之外细菌的核心基因组相关性,还应考虑质粒转移,以研究CPE和耐药性传播,并指导感染控制策略。

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