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PA2491(mexS)基因的突变促进了铜绿假单胞菌临床菌株中依赖MexT的mexEF-oprN表达及多药耐药性。

Mutations in PA2491 (mexS) promote MexT-dependent mexEF-oprN expression and multidrug resistance in a clinical strain of Pseudomonas aeruginosa.

作者信息

Sobel Mara L, Neshat Shadi, Poole Keith

机构信息

Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada K7L 3N6.

出版信息

J Bacteriol. 2005 Feb;187(4):1246-53. doi: 10.1128/JB.187.4.1246-1253.2005.

Abstract

Disruption of the PA2491 gene in a mini-Tn5-tet insertion mutant of a clinical isolate of Pseudomonas aeruginosa increased expression of the mexEF-oprN multidrug efflux genes and decreased production of outer membrane protein OprD, concomitant with enhanced resistance to chloramphenicol, quinolones, and imipenem, which was reminiscent of previously described nfxC mutants. PA2491 encodes a probable oxidoreductase previously shown to be positively regulated by the MexT positive regulator of mexEF-oprN expression (T. Kohler, S. F. Epp, L. K. Curty, and J. C. Pechere, J. Bacteriol. 181:6300-6305, 1999). Spontaneous multidrug-resistant mutants of the P. aeruginosa clinical isolate hyperexpressing mexEF-oprN and showing reduced production of OprD were readily selected in vitro, and all of them were shown to carry mutations in PA2491, highlighting the probable significance of such mutations as determinants of MexEF-OprN-mediated multidrug resistance in vivo.

摘要

在铜绿假单胞菌临床分离株的mini-Tn5-tet插入突变体中,PA2491基因的破坏增加了mexEF-oprN多药外排基因的表达,并降低了外膜蛋白OprD的产生,同时增强了对氯霉素、喹诺酮类和亚胺培南的耐药性,这让人联想到先前描述的nfxC突变体。PA2491编码一种可能的氧化还原酶,先前已证明该酶受mexEF-oprN表达的MexT正调控因子的正调控(T. Kohler、S. F. Epp、L. K. Curty和J. C. Pechere,《细菌学杂志》181:6300 - 6305,1999年)。在体外很容易筛选出高表达mexEF-oprN并显示OprD产生减少的铜绿假单胞菌临床分离株的自发多药耐药突变体,并且所有这些突变体都显示在PA2491中携带突变,突出了此类突变作为体内MexEF - OprN介导的多药耐药性决定因素的可能重要性。

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