Suppr超能文献

来自肠炎沙门氏菌韦斯特汉普顿血清型和森夫滕贝格血清型的新型质粒编码的水解头孢他啶的CTX-M-53超广谱β-内酰胺酶。

Novel plasmid-encoded ceftazidime-hydrolyzing CTX-M-53 extended-spectrum beta-lactamase from Salmonella enterica serotypes Westhampton and Senftenberg.

作者信息

Doublet Benoît, Granier Sophie A, Robin Frédéric, Bonnet Richard, Fabre Laëtitia, Brisabois Anne, Cloeckaert Axel, Weill François-Xavier

机构信息

Centre National de Référence des Salmonella, Laboratoire des Bactéries Pathogènes Entériques, Institut Pasteur, 28 rue du Docteur Roux, 75724 Paris Cedex 15, France.

出版信息

Antimicrob Agents Chemother. 2009 May;53(5):1944-51. doi: 10.1128/AAC.01581-08. Epub 2009 Mar 9.

Abstract

We describe the characterization of a novel CTX-M beta-lactamase from Salmonella enterica. Four S. enterica isolates (three of serotype Westhampton and one of serotype Senftenberg) resistant to extended-spectrum cephalosporins (cefotaxime and ceftazidime) were recovered in 2004 from living cockles in three supermarkets located in distant geographic areas in France, which got their supplies from the same fishery. The isolates were found to produce a novel extended-spectrum beta-lactamase (ESBL) belonging to the CTX-M-1 phylogenetic group and named CTX-M-53. The CTX-M-53 beta-lactamase harbored the substitution Asp240Gly, like the CTX-M-15 enzyme, which is specifically implicated in a higher catalytic efficiency against ceftazidime. The bla(CTX-M-53) gene was located on a mobilizable 11-kb plasmid, pWES-1. The complete sequence of pWES-1 revealed the presence of a novel insertion sequence, ISSen2, and an IS26 element upstream and downstream of the bla(CTX-M-53) gene, respectively; however, transposition assays of the bla(CTX-M-53) gene were unsuccessful. IS26 elements may have contributed to the acquisition of the bla(CTX-M-53) gene. Interestingly, the mobilization module of the pWES-1 plasmid was similar to that of quinolone resistance plasmids (carrying the qnrS2 gene) from aquatic sources. Although belonging to two serotypes differentiated on the basis of the O-antigen structure (E1 or E4 groups), the isolates were found to be genetically indistinguishable by pulsed-field gel electrophoresis. Multilocus sequence typing showed that the isolates of serotype Westhampton had a sequence type, ST14, common among isolates of serotype Senftenberg. This is the first characterization of the CTX-M-53 ESBL, which represents an additional ceftazidime-hydrolyzing CTX-M enzyme.

摘要

我们描述了一种来自肠炎沙门氏菌的新型CTX-Mβ-内酰胺酶的特性。2004年,在法国三个地理位置相距遥远且均从同一渔场进货的超市中,从活蚶中分离出4株对广谱头孢菌素(头孢噻肟和头孢他啶)耐药的肠炎沙门氏菌菌株(3株为韦斯特汉普顿血清型,1株为森夫滕贝格血清型)。这些分离株被发现产生了一种属于CTX-M-1系统发育群的新型超广谱β-内酰胺酶(ESBL),命名为CTX-M-53。CTX-M-53β-内酰胺酶与CTX-M-15酶一样,具有Asp240Gly替换,这与对头孢他啶更高的催化效率特别相关。bla(CTX-M-53)基因位于一个可移动的11kb质粒pWES-1上。pWES-1的完整序列显示分别在bla(CTX-M-53)基因的上游和下游存在一个新型插入序列ISSen2和一个IS26元件;然而,bla(CTX-M-53)基因的转座试验未成功。IS26元件可能促成了bla(CTX-M-53)基因的获得。有趣的是,pWES-1质粒的移动模块与来自水生来源的喹诺酮耐药质粒(携带qnrS2基因)的移动模块相似。尽管这些分离株基于O抗原结构分为两个不同的血清型(E1或E4组),但通过脉冲场凝胶电泳发现它们在基因上无法区分。多位点序列分型显示,韦斯特汉普顿血清型的分离株具有一种在森夫滕贝格血清型分离株中常见的序列类型ST14。这是对CTX-M-53 ESBL的首次特性描述,它代表了另一种水解头孢他啶的CTX-M酶。

相似文献

引用本文的文献

6
In vitro activity of azithromycin against nontyphoidal Salmonella enterica.阿奇霉素对非伤寒沙门氏菌的体外活性。
Antimicrob Agents Chemother. 2010 Aug;54(8):3498-501. doi: 10.1128/AAC.01678-09. Epub 2010 May 24.

本文引用的文献

10
CTX-M: changing the face of ESBLs in Europe.CTX-M:改变欧洲超广谱β-内酰胺酶的面貌。
J Antimicrob Chemother. 2007 Feb;59(2):165-74. doi: 10.1093/jac/dkl483. Epub 2006 Dec 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验