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流行氟喹诺酮耐药鼠伤寒沙门氏菌血清型 Typhimurium 分离株中 ramRA 基因座天然突变对侵袭性的影响。

Effects of natural mutations in the ramRA locus on invasiveness of epidemic fluoroquinolone-resistant Salmonella enterica serovar Typhimurium isolates.

机构信息

INRA, UMR1282 Infectiologie et Santé Publique, Nouzilly, France.

出版信息

J Infect Dis. 2013 Mar 1;207(5):794-802. doi: 10.1093/infdis/jis755. Epub 2012 Dec 10.

Abstract

BACKGROUND

Fluoroquinolone (FQ) resistance is increasing worldwide among Salmonella species. Among the mechanisms involved, increased efflux via the tripartite AcrAB-TolC efflux system is mainly modulated through control of expression via the ramRA regulatory locus gene products. Interestingly, in some reference strains these have also been experimentally shown to regulate cell invasion-related genes of the type III secretion system 1 (T3SS-1). In this study, we investigated whether natural mutations occurring in this locus in FQ-resistant S. enterica serovar Typhimurium epidemic clones resulted in the same effects.

METHODS

Quantitative reverse transcription polymerase chain reaction and cell invasion assays were used to study 3 clinical FQ-resistant S. Typhimurium isolates representative of the DT104 and DT204 epidemic clones. For comparison, 3 control reference quinolone-susceptible strains were included.

RESULTS

As previously shown, the investigated mutations altering RamR or its DNA-binding site increased expression of efflux genes dependently on ramA. However, the decreased expression of T3SS-1 genes previously reported was not always observed and seemed to be dependent on the genetic background of the FQ-resistant isolate. Indeed, a ramA-dependent decreased invasion of intestinal epithelial cells was only observed for a particular clinical ramR mutant.

CONCLUSIONS

ramRA mutations occurring in clinical FQ-resistant S. Typhimurium isolates may negatively modulate their invasiveness but this is strain-dependent.

摘要

背景

氟喹诺酮(FQ)耐药性在全球范围内的沙门氏菌属中不断增加。在涉及的机制中,通过三部分的AcrAB-TolC 外排系统增加外排主要通过 ramRA 调节基因产物调节表达来调节。有趣的是,在一些参考菌株中,这些基因也已被实验证明可调节 III 型分泌系统 1(T3SS-1)的细胞入侵相关基因。在这项研究中,我们调查了在 FQ 耐药性肠炎沙门氏菌流行克隆中该基因座发生的自然突变是否会产生相同的效果。

方法

使用定量逆转录聚合酶链反应和细胞入侵测定法研究了 3 种临床 FQ 耐药肠炎沙门氏菌分离株,这些分离株代表 DT104 和 DT204 流行克隆。为了比较,还包括了 3 种对照的耐喹诺酮敏感菌株。

结果

如前所述,改变 RamR 或其 DNA 结合位点的研究突变增加了外排基因的表达,这与 ramA 有关。但是,先前报道的 T3SS-1 基因表达降低并不总是观察到,似乎取决于 FQ 耐药分离株的遗传背景。实际上,仅在特定的临床 ramR 突变体中观察到 ramA 依赖性肠上皮细胞侵袭性降低。

结论

在临床 FQ 耐药肠炎沙门氏菌分离株中发生的 ramRA 突变可能会负调节其侵袭性,但这取决于菌株。

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