NalC型多重耐药铜绿假单胞菌中MexAB-OprM的过表达:编码PA3720-PA3719阻遏物的nalC基因的鉴定与表征

MexAB-OprM hyperexpression in NalC-type multidrug-resistant Pseudomonas aeruginosa: identification and characterization of the nalC gene encoding a repressor of PA3720-PA3719.

作者信息

Cao Lily, Srikumar Ramakrishnan, Poole Keith

机构信息

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

出版信息

Mol Microbiol. 2004 Sep;53(5):1423-36. doi: 10.1111/j.1365-2958.2004.04210.x.

Abstract

MexAB-OprM is a multidrug efflux system that contributes to intrinsic and acquired multidrug resistance in Pseudomonas aeruginosa, the latter as a result of mutational hyperexpression of the mexAB-oprM operon. While efflux gene hyperexpression typically results from mutations in the linked mexR repressor gene, it also occurs independently of mexR mutations in so-called nalC mutants that demonstrate more modest mexAB-oprM expression and, thus, more modest multidrug resistance than do mexR strains. Using a transposon insertion mutagenesis approach, nalC mutant strains were selected and the disrupted gene, PA3721, identified. Amplification and sequencing of this gene from previously isolated spontaneous nalC mutants revealed the presence of mutations in all instances and as such, PA3721 has been renamed nalC. PA3721 (nalC) encodes a probable repressor of the TetR/AcrR family and occurs upstream of an apparent two-gene operon, PA3720-PA3719, whose expression was negatively regulated by PA3721. Thus, PA3720-PA3719 was hyperexpressed in transposon insertion and spontaneous nalC mutants. The loss of PA3719 but not of PA3720 expression in a spontaneous nalC mutant reduced MexAB-OprM expression to wild-type levels and compromised multidrug resistance, an indication that hyperexpression of PA3719 only was necessary for the nalC phenotype. Introduction of PA3719 into wild-type P. aeruginosa on a multicopy plasmid was, in fact, sufficient to promote elevated MexAB-OprM expression and multidrug resistance characteristic of a nalC strain. Thus, the nalC (PA3721) mutation serves only to enhance PA3720-PA3719 expression, with expression of PA3719 (encodes a 53 amino acid protein of predicted pI 10.4) directly or indirectly impacting MexAB-OprM expression. Intriguingly, nalC strains produce markedly elevated levels of stable MexR protein suggesting that PA3720-PA3719 hyperexpression somehow modulates MexR repressor activity. The deduced products of PA3720-PA3719 show no homology to sequences presently in the GenBank databases, however, and as such provide no clues as to how this might occur.

摘要

MexAB - OprM是一种多药外排系统,它导致铜绿假单胞菌产生固有和获得性多药耐药性,后者是由于mexAB - oprM操纵子的突变性高表达所致。虽然外排基因的高表达通常是由相连的mexR阻遏基因的突变引起的,但在所谓的nalC突变体中,它也独立于mexR突变而发生,这些突变体表现出比mexR菌株更适度的mexAB - oprM表达,因此多药耐药性也更适度。使用转座子插入诱变方法,筛选出nalC突变体菌株,并鉴定出被破坏的基因PA3721。对先前分离的自发nalC突变体中该基因的扩增和测序显示,所有情况下均存在突变,因此,PA3721已重新命名为nalC。PA3721(nalC)编码一种可能属于TetR/AcrR家族的阻遏蛋白,位于一个明显的双基因操纵子PA3720 - PA3719的上游,其表达受PA3721负调控。因此,PA3720 - PA3719在转座子插入突变体和自发nalC突变体中高表达。在一个自发nalC突变体中,PA3719表达缺失但PA3720表达未缺失,这使MexAB - OprM表达降低至野生型水平,并损害了多药耐药性,这表明仅PA's719的高表达是nalC表型所必需的。实际上,将PA3719通过多拷贝质粒导入野生型铜绿假单胞菌中,足以促进MexAB - OprM表达升高以及产生nalC菌株特有的多药耐药性。因此,nalC(PA3721)突变仅起到增强PA3720 - PA3719表达的作用,PA3719(编码一种预测pI为10.4的53个氨基酸的蛋白质)的表达直接或间接影响MexAB - OprM的表达。有趣的是,nalC菌株产生的稳定MexR蛋白水平明显升高,这表明PA3720 - PA3719的高表达以某种方式调节MexR阻遏蛋白的活性。然而,PA3720 - PA3719的推导产物与目前GenBank数据库中的序列没有同源性,因此无法提供关于这可能如何发生的线索。

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