综合分析患者网络和质粒基因组,调查同时携带 blaIMP 和 mcr-9 基因的产碳青霉烯酶肠杆菌的区域性多菌种爆发。

IF 5 2区 医学 Q2 IMMUNOLOGY
Yu Wan, Ashleigh C Myall, Adhiratha Boonyasiri, Frances Bolt, Alice Ledda, Siddharth Mookerjee, Andrea Y Weiße, Maria Getino, Jane F Turton, Hala Abbas, Ruta Prakapaite, Akshay Sabnis, Alireza Abdolrasouli, Kenny Malpartida-Cardenas, Luca Miglietta, Hugo Donaldson, Mark Gilchrist, Katie L Hopkins, Matthew J Ellington, Jonathan A Otter, Gerald Larrouy-Maumus, Andrew M Edwards, Jesus Rodriguez-Manzano, Xavier Didelot, Mauricio Barahona, Alison H Holmes, Elita Jauneikaite, Frances Davies
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引用次数: 0

摘要

背景:产碳青霉烯酶肠杆菌(CPE)对多类抗生素具有耐药性,在医疗保健领域具有挑战性。本研究描述了2016年至2019年期间伦敦地区网络中不同肠杆菌属物种中亚胺培南酶(IMP)编码CPE的出现情况:我们利用电子健康记录对患者路径进行了网络分析,以确定IMP编码CPE阳性患者之间的接触。将编码 IMP 的 CPE 分离物基因组与患者接触者重叠,以暗示潜在的传播事件:对 84 个肠杆菌属分离物进行基因组分析后发现,这些分离物种类繁多(主要是克雷伯菌属、肠杆菌属和大肠埃希菌);86% 的分离物(84 个中有 72 个)含有携带 blaIMP 的 IncHI2 质粒和耐秋水仙碱基因 mcr-9(72 个中有 68 个)。通过对IncHI2质粒进行系统发育分析,发现了3个品系,这3个品系与患者的接触和在4家医院和不同医疗专科之间的流动有显著关联,而这在最初的调查中被漏掉了:综合患者网络和质粒分析,我们发现了一场由质粒介导的种间 blaIMPCPE 疫情爆发,但在标准调查中仍未发现。通过DNA测序和多模态数据整合,本文提出的疫情调查方法为实时识别导致病原体传播的关键因素提供了一个框架。质粒水平的疫情分析表明,耐药性传播的范围可能比猜测的更广,因此可以采取更多干预措施来阻止医院网络内的传播。摘要这是一项利用综合途径网络和基因组学方法,对2016年至2019年期间伦敦地区医院网络内的患者中出现的产亚胺培南酶碳青霉烯酶的肠杆菌进行的调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated Analysis of Patient Networks and Plasmid Genomes to Investigate a Regional, Multispecies Outbreak of Carbapenemase-Producing Enterobacterales Carrying Both blaIMP and mcr-9 Genes.

Background: Carbapenemase-producing Enterobacterales (CPE) are challenging in healthcare, with resistance to multiple classes of antibiotics. This study describes the emergence of imipenemase (IMP)-encoding CPE among diverse Enterobacterales species between 2016 and 2019 across a London regional network.

Methods: We performed a network analysis of patient pathways, using electronic health records, to identify contacts between IMP-encoding CPE-positive patients. Genomes of IMP-encoding CPE isolates were overlaid with patient contacts to imply potential transmission events.

Results: Genomic analysis of 84 Enterobacterales isolates revealed diverse species (predominantly Klebsiella spp, Enterobacter spp, and Escherichia coli); 86% (72 of 84) harbored an IncHI2 plasmid carrying blaIMP and colistin resistance gene mcr-9 (68 of 72). Phylogenetic analysis of IncHI2 plasmids identified 3 lineages showing significant association with patient contacts and movements between 4 hospital sites and across medical specialties, which was missed in initial investigations.

Conclusions: Combined, our patient network and plasmid analyses demonstrate an interspecies, plasmid-mediated outbreak of blaIMPCPE, which remained unidentified during standard investigations. With DNA sequencing and multimodal data incorporation, the outbreak investigation approach proposed here provides a framework for real-time identification of key factors causing pathogen spread. Plasmid-level outbreak analysis reveals that resistance spread may be wider than suspected, allowing more interventions to stop transmission within hospital networks.SummaryThis was an investigation, using integrated pathway networks and genomics methods, of the emergence of imipenemase-encoding carbapenemase-producing Enterobacterales among diverse Enterobacterales species between 2016 and 2019 in patients across a London regional hospital network, which was missed on routine investigations.

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来源期刊
Journal of Infectious Diseases
Journal of Infectious Diseases 医学-传染病学
CiteScore
13.50
自引率
3.10%
发文量
449
审稿时长
2-4 weeks
期刊介绍: Published continuously since 1904, The Journal of Infectious Diseases (JID) is the premier global journal for original research on infectious diseases. The editors welcome Major Articles and Brief Reports describing research results on microbiology, immunology, epidemiology, and related disciplines, on the pathogenesis, diagnosis, and treatment of infectious diseases; on the microbes that cause them; and on disorders of host immune responses. JID is an official publication of the Infectious Diseases Society of America.
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