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携带blaNDM - 7并参与医院内传播的肺炎克雷伯菌ST278分离株的分子进化

Molecular Evolution of a Klebsiella pneumoniae ST278 Isolate Harboring blaNDM-7 and Involved in Nosocomial Transmission.

作者信息

Lynch Tarah, Chen Liang, Peirano Gisele, Gregson Dan B, Church Deirdre L, Conly John, Kreiswirth Barry N, Pitout Johann D

机构信息

Division of Microbiology, Calgary Laboratory Services Department of Pathology and Laboratory Medicine Snyder Institute for Chronic Diseases, Cummings School of Medicine, University of Calgary, Canada.

Public Health Research Institute Tuberculosis Center, Rutgers University, Newark, New Jersey.

出版信息

J Infect Dis. 2016 Sep 1;214(5):798-806. doi: 10.1093/infdis/jiw240. Epub 2016 Jun 9.

Abstract

During 2013, ST278 Klebsiella pneumoniae with blaNDM-7 was isolated from the urine (KpN01) and rectum (KpN02) of a patient in Calgary, Canada. The same strain (KpN04) was subsequently isolated from another patient in the same unit. Interestingly, a carbapenem-susceptible K. pneumoniae ST278 (KpN06) was obtained 1 month later from the blood of the second patient. Next-generation sequencing (NGS) revealed that the loss of carbapenem-resistance in KpN06 was due to a 5-kb deletion on the blaNDM-7-harboring IncX3 plasmid. In addition, an IncFIB plasmid in KpN06 had a 27-kb deletion that removed genes encoding for heavy metal resistance. Phylogenetic analysis showed that the K. pneumoniae ST278 from patient 2 was likely a descendant of KpN02 and that KpN06 was a close progenitor of an environmental ST278. It is unclear whether KpN06 lost the blaNDM-7 gene in vivo. This study detailed the remarkable plasticity and speed of evolutionary changes in multidrug-resistant K. pneumoniae, demonstrating the highly recombinant nature of this species. It also highlights the ability of NGS to clarify molecular microevolutionary events within antibiotic-resistant organisms.

摘要

2013年期间,在加拿大卡尔加里,一株携带blaNDM - 7的ST278肺炎克雷伯菌从一名患者的尿液(KpN01)和直肠(KpN02)中分离得到。随后,同一菌株(KpN04)又从同一科室的另一名患者中分离出来。有趣的是,1个月后从第二名患者的血液中分离出一株对碳青霉烯类敏感的肺炎克雷伯菌ST278(KpN06)。新一代测序(NGS)显示,KpN06中碳青霉烯类耐药性的丧失是由于携带blaNDM - 7的IncX3质粒上发生了5 kb的缺失。此外,KpN06中的一个IncFIB质粒有一个27 kb的缺失,该缺失去除了编码重金属抗性的基因。系统发育分析表明,患者2的肺炎克雷伯菌ST278可能是KpN02的后代,而KpN06是一株环境ST278的近亲祖先。目前尚不清楚KpN06是否在体内丢失了blaNDM - 7基因。本研究详细阐述了多重耐药肺炎克雷伯菌进化变化的显著可塑性和速度,证明了该菌种具有高度的重组性。它还突出了NGS在阐明抗生素耐药菌内分子微进化事件方面的能力。

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