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大肠杆菌 ST1193:紧随大肠杆菌 ST131 之后。

Escherichia coli ST1193: Following in the Footsteps of E. coli ST131.

机构信息

Alberta Precision Laboratories, Calgary, Alberta, Canada.

Cummings School of Medicine, University of Calgarygrid.22072.35, Calgary, Alberta, Canada.

出版信息

Antimicrob Agents Chemother. 2022 Jul 19;66(7):e0051122. doi: 10.1128/aac.00511-22. Epub 2022 Jun 6.

Abstract

Escherichia coli ST1193 is an emerging global multidrug (MDR) high-risk clone and an important cause of community-onset urinary and bloodstream infections. ST1193 is imitating E. coli ST131, the most successful MDR clone of all time. Both clones emerged in the early 1990s by acquiring quinolone resistance-determining region (QRDR) mutations, IncF plasmids, virulence factors, and type 1 pilus () recombination. They are the only MDR clones that are dominant among unselected E. coli populations. ST131 is the most frequent clone and ST1193 the second most frequent clone among fluoroquinolone/cephalosporin-resistant E. coli isolates. Both clones have played pivotal roles in the global spread of MDR E. coli. ST1193 originated from ST clonal complex 14 (STc14), is lactose nonfermenting, belongs to phylogenetic group B2, and contains the O type O75. Global ST1193 prevalence has been increasing since 2012, even replacing ST131 in certain regions. genes are rapidly expanding among ST1193 isolates, a scenario that occurred with ST131 during the 2000s. A validated PCR will enable global surveys to determine the extent of ST1193 among One Health E. coli isolates. The rapid emergence of ST1193 is concerning and is adding to the public health burden of MDR E. coli clones. Basic mechanistic, evolutionary, surveillance, and clinical studies are urgently required to investigate the success of ST1193. Such information will aid with management and prevention strategies. The medical community can ill afford to ignore the spread of another global successful MDR high-risk E. coli clone, especially one that is following in the footsteps of E. coli ST131.

摘要

大肠杆菌 ST1193 是一种新兴的全球多药耐药(MDR)高风险克隆体,也是导致社区获得性尿路感染和血流感染的重要原因。ST1193 正在模仿有史以来最成功的 MDR 克隆体大肠杆菌 ST131。这两个克隆体都在 20 世纪 90 年代初通过获得喹诺酮类药物耐药决定区(QRDR)突变、IncF 质粒、毒力因子和 I 型菌毛()重组而出现。它们是唯一在未选择的大肠杆菌群体中占主导地位的 MDR 克隆体。在氟喹诺酮/头孢菌素耐药性大肠杆菌分离株中,ST131 是最常见的克隆体,ST1193 是第二常见的克隆体。这两个克隆体都在 MDR 大肠杆菌的全球传播中发挥了关键作用。ST1193 源自 ST 克隆复合体 14(STc14),不发酵乳糖,属于 B2 进化群,并且含有 O 型 O75。自 2012 年以来,全球 ST1193 的流行率一直在增加,甚至在某些地区取代了 ST131。ST1193 分离株中的 基因正在迅速扩张,这种情况在 21 世纪初的 ST131 中也发生过。一种经过验证的 PCR 将使全球调查能够确定 ST1193 在“One Health”大肠杆菌分离株中的程度。ST1193 的快速出现令人担忧,这增加了 MDR 大肠杆菌克隆体的公共卫生负担。迫切需要进行基础机制、进化、监测和临床研究,以调查 ST1193 的成功原因。这些信息将有助于管理和预防策略。医学界不能忽视另一个全球成功的 MDR 高风险大肠杆菌克隆体的传播,尤其是一个紧随大肠杆菌 ST131 脚步的克隆体。

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