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CpxRA双组分系统可抑制产肠毒素性大肠杆菌不耐热毒素的基因表达。

The CpxRA two-component system represses gene expression of the heat-labile toxin of enterotoxigenic .

作者信息

Rodríguez-Valverde Diana, León-Montes Nancy, Siqueiros-Cendón Tania, Rivera-Gutiérrez Sandra, Ares Miguel A, De la Cruz Miguel A

机构信息

Unidad de Investigación Médica en Enfermedades Infecciosas y Parasitarias, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.

Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Mexico City, Mexico.

出版信息

J Med Microbiol. 2023 Apr;72(4). doi: 10.1099/jmm.0.001682.

Abstract

Enterotoxigenic (ETEC) strains produce at least one of two types of enterotoxins: the heat-labile (LT) and heat-stable (ST) toxins, which are responsible for the watery secretory diarrhoea that is a hallmark of the human ETEC infection. One regulatory system that controls the transcription of virulence genes in pathogenic bacteria is the CpxRA two-component system (TCS). We reported that the bicistronic operon, which encodes for the A and B subunits of LT, was repressed for the CpxRA TCS by direct binding of CpxR-P from -12 to +6 bp with respect to the transcription start site of . Moreover, the Cpx-response activation down-regulated the transcription of genes, and this negative effect was CpxRA-dependent. Our data show that CpxRA TCS is a negative regulator of the LT, one of the main virulence determinants of ETEC.

摘要

产肠毒素大肠杆菌(ETEC)菌株产生两种肠毒素中的至少一种:不耐热(LT)毒素和耐热(ST)毒素,它们是导致水样分泌性腹泻的原因,而水样分泌性腹泻是人类ETEC感染的一个标志。一种控制致病细菌毒力基因转录的调节系统是CpxRA双组分系统(TCS)。我们报道,编码LT A和B亚基的双顺反子操纵子,被CpxR-P从相对于转录起始位点的-12至+6 bp处直接结合而被CpxRA TCS抑制。此外,Cpx反应激活下调了基因的转录,并且这种负面影响是CpxRA依赖性的。我们的数据表明,CpxRA TCS是LT的负调节因子,LT是ETEC的主要毒力决定因素之一。

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