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爱尔兰都柏林一家三级护理医院肺炎克雷伯菌分离株中质粒介导的AmpCβ-内酰胺酶的检测及分子特征分析

Detection and molecular characterisation of plasmidic AmpC beta-lactamases in Klebsiella pneumoniae isolates from a tertiary-care hospital in Dublin, Ireland.

作者信息

Roche C, Boo T W, Walsh F, Crowley B

机构信息

Department of Microbiology, Central Pathology Laboratory, St James's Hospital, and Department of Clinical Microbiology, University of Dublin, Trinity College, Dublin, Ireland.

出版信息

Clin Microbiol Infect. 2008 Jun;14(6):616-8. doi: 10.1111/j.1469-0691.2008.01998.x. Epub 2008 Apr 5.

Abstract

This study determined the types of AmpC enzymes produced by Klebsiella pneumoniae isolates resistant to third-generation cephalosporins and the clonality of these isolates. The presence of AmpC enzymes was identified by cephalosporin-cloxacillin synergy tests. Genes encoding AmpC enzymes were characterised by PCR and sequencing. Pulsed-field gel electrophoresis (PFGE) was used to type the isolates. Fifteen K. pneumoniae isolates were positive for bla(AmpC), 13 were positive for bla(ACC-1) and two were positive for bla(DHA-1). Production of the DHA-1 enzyme was inducible. The ampR gene was identified upstream of the bla(DHA-1) gene. PFGE demonstrated the polyclonal origin of the isolates carrying bla(ACC-1).

摘要

本研究确定了对第三代头孢菌素耐药的肺炎克雷伯菌分离株所产生的AmpC酶类型以及这些分离株的克隆性。通过头孢菌素-氯唑西林协同试验鉴定AmpC酶的存在。采用聚合酶链反应(PCR)和测序对编码AmpC酶的基因进行特征分析。运用脉冲场凝胶电泳(PFGE)对分离株进行分型。15株肺炎克雷伯菌分离株bla(AmpC)呈阳性,13株bla(ACC-1)呈阳性,2株bla(DHA-1)呈阳性。DHA-1酶的产生是可诱导的。在bla(DHA-1)基因上游鉴定出ampR基因。PFGE显示携带bla(ACC-1)的分离株起源于多克隆。

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