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铜绿假单胞菌临床分离株中1类整合子-35启动子区域点突变导致IMP-5碳青霉烯酶的高水平表达。

High-level expression of IMP-5 carbapenemase owing to point mutation in the -35 promoter region of class 1 integron among Pseudomonas aeruginosa clinical isolates.

作者信息

Brízio Ana, Conceição Teresa, Pimentel Madalena, Da Silva Gabriela, Duarte Aida

机构信息

Laboratory of Microbiology, Faculty of Pharmacy, Lisboa, Portugal.

出版信息

Int J Antimicrob Agents. 2006 Jan;27(1):27-31. doi: 10.1016/j.ijantimicag.2005.08.023. Epub 2005 Dec 15.

Abstract

Eight strains of Pseudomonas aeruginosa producing IMP-5 carbapenemases were collected from three Portuguese hospitals. All isolates were epidemiologically unrelated. The bla(IMP-5) gene was inserted into a class 1 integron previously reported in Acinetobacter baumannii 65FFC. Expression of the the bla(IMP-5) gene in P. aeruginosa has been shown to be driven by the P(1) promoter [TTGATA] in which the cytosine was replaced by thymine, which caused an increase in transcription of bla(IMP-5) that was confirmed by site-directed mutagenesis. The minimum inhibitory concentrations (MICs) of imipenem for Escherichia coli pGMLA-1 (the recombinant from A. baumannii 65FFC) and E. coli pATG-2 (the recombinant from P. aeruginosa isolates) were 0.5 mg/L and >32 mg/L, respectively. This study reports the spread of a class 1 integron In76 with a new point mutation in the P(1) promoter sequence leading to overproduction of IMP-5.

摘要

从葡萄牙的三家医院收集了八株产IMP-5碳青霉烯酶的铜绿假单胞菌菌株。所有分离株在流行病学上均无关联。bla(IMP-5)基因插入到先前在鲍曼不动杆菌65FFC中报道的1类整合子中。已证明铜绿假单胞菌中bla(IMP-5)基因的表达由P(1)启动子[TTGATA]驱动,其中胞嘧啶被胸腺嘧啶取代,这导致bla(IMP-5)转录增加,定点诱变证实了这一点。亚胺培南对大肠杆菌pGMLA-1(来自鲍曼不动杆菌65FFC的重组体)和大肠杆菌pATG-2(来自铜绿假单胞菌分离株的重组体)的最低抑菌浓度(MIC)分别为0.5 mg/L和>32 mg/L。本研究报告了1类整合子In76的传播,其P(1)启动子序列有一个新的点突变,导致IMP-5过量产生。

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