人类感染产志贺毒素大肠杆菌O91血清群的毒力因子分布、耐药基因及系统发育相关性

IF 4.5 3区 医学 Q1 MICROBIOLOGY
Magdalena Nüesch-Inderbinen , Marc J.A. Stevens , Nicole Cernela , Andrea Müller , Michael Biggel , Roger Stephan
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引用次数: 6

摘要

属于O91血清群的产志贺毒素大肠杆菌(STEC)是欧洲与人类疾病相关的最常见的非o157 STEC血清群之一。本研究旨在分析2003-2019年在瑞士收集的48株产志在大肠杆菌O91临床分离株的毒力因子、耐药基因和系统发育相关性。利用短读测序技术对分离株进行全基因组测序,并对一部分分离株进行长读测序。O91:H10 (n = 6)、O91:H14 (n = 40)和O91:H21 (n = 2)。多位点序列分型结果表明,O91:H10分离株均属于序列型(ST)641,而O91:H14分离株分别属于ST33、ST9700或不可分型。两个O91:H21分离株均属于ST442。志贺毒素基因stx1a是最常见的志贺毒素基因亚型,其次是stx2b、stx2d和stx2a。所有分离株均为lee阴性,携带1或2拷贝IrgA粘附素基因iha。在长读序列分离物的一个子集中,鉴定出了携带iha和其他基因(如hes、lesP或agn43)的粘附和自聚集致病性岛位点(LAA-PAI)模块。产志贺毒素大肠杆菌O91:H14大部分携带枯草酶细胞毒素基因subA、大肠杆菌素基因(cba、cea、cib和cma)或微霉素基因(mcmA、mchB、mchC和mchF)。通过肠外致病性大肠杆菌(expc)中的一种或多种毒力因子,包括hlyF、iucC/iutA、kpsE和traT,进一步将STEC O91:H14与STEC O91:H10/H21区分开来。hlyF基因在一种新的镶嵌质粒上被鉴定出来,这种质粒与以前在产志贺毒素大肠杆菌中描述的hlyF+质粒无关。核心基因组系统发育分析显示,STEC O91:H10和STEC O91:H21具有克隆保守性,而STEC O91:H14具有克隆多样性。在三个STEC O91:H14分离株中,鉴定出许多耐药基因,包括介导对氨基糖苷类(aadA、aadA2、aadA9、aadA23、aph(3”)-Ib和aph(6)-Id)、氯霉素(cmlA)、磺胺类(sul2和sul3)和甲氧苄啶(drfA12)耐药的基因。我们的数据有助于理解STEC O91血清组的遗传多样性和不同水平的毒力潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distribution of virulence factors, antimicrobial resistance genes and phylogenetic relatedness among Shiga toxin-producing Escherichia coli serogroup O91 from human infections

Shiga toxin-producing Escherichia coli (STEC) belonging to the serogroup O91 are among the most common non-O157 STEC serogroups associated with human illness in Europe. This study aimed to analyse the virulence factors, antimicrobial resistance genes and phylogenetic relatedness among 48 clinical STEC O91 isolates collected during 2003–2019 in Switzerland. The isolates were subjected to whole genome sequencing using short-read sequencing technologies and a subset of isolates additionally to long-read sequencing. They belonged to O91:H10 (n = 6), O91:H14 (n = 40), and O91:H21 (n = 2). Multilocus sequence typing showed that the O91:H10 isolates all belonged to sequence type (ST)641, while the O91:H14 isolates were assigned to ST33, ST9700, or were non-typeable. Both O91:H21 isolates belonged to ST442. Shiga toxin gene stx1a was the most common Shiga toxin gene subtype among the isolates, followed by stx2b, stx2d and stx2a. All isolates were LEE-negative and carried one or two copies of the IrgA adhesin gene iha. In a subset of long-read sequenced isolates, modules of the Locus of Adhesion and Autoaggregation pathogenicity island (LAA-PAI) carrying iha and other genes such as hes, lesP or agn43 were identified. A large proportion of STEC O91:H14 carried the subtilase cytotoxin gene subA, colicin genes (cba, cea, cib and cma) or microcin genes (mcmA, mchB, mchC and mchF). STEC O91:H14 were further distinguished from STEC O91:H10/H21 by one or more virulence factors found in extraintestinal pathogenic E. coli (ExPEC), including hlyF, iucC/iutA, kpsE and traT. The hlyF gene was identified on a novel mosaic plasmid that was unrelated to hlyF+ plasmids described previously in STEC. Core genome phylogenetic analysis revealed that STEC O91:H10 and STEC O91:H21 were clonally conserved, whereas STEC O91:H14 were clonally diverse. Among three STEC O91:H14 isolates, a number of resistance genes were identified, including genes that mediate resistance to aminoglycosides (aadA, aadA2, aadA9, aadA23, aph(3'')-Ib and aph(6)-Id), chloramphenicol (cmlA), sulphonamides (sul2 and sul3), and trimethoprim (drfA12). Our data contribute to understanding the genetic diversity and differing levels of virulence potential within the STEC O91 serogroup.

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来源期刊
CiteScore
9.70
自引率
0.00%
发文量
18
审稿时长
45 days
期刊介绍: Pathogen genome sequencing projects have provided a wealth of data that need to be set in context to pathogenicity and the outcome of infections. In addition, the interplay between a pathogen and its host cell has become increasingly important to understand and interfere with diseases caused by microbial pathogens. IJMM meets these needs by focussing on genome and proteome analyses, studies dealing with the molecular mechanisms of pathogenicity and the evolution of pathogenic agents, the interactions between pathogens and host cells ("cellular microbiology"), and molecular epidemiology. To help the reader keeping up with the rapidly evolving new findings in the field of medical microbiology, IJMM publishes original articles, case studies and topical, state-of-the-art mini-reviews in a well balanced fashion. All articles are strictly peer-reviewed. Important topics are reinforced by 2 special issues per year dedicated to a particular theme. Finally, at irregular intervals, current opinions on recent or future developments in medical microbiology are presented in an editorial section.
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