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Virulence Gene Regulation by CvfA, a Putative RNase: the CvfA-Enolase Complex in Streptococcus pyogenes Links Nutritional Stress, Growth-Phase Control, and Virulence Gene Expression

机译:CvfA,推定的核糖核酸酶的毒力基因调控:化脓性链球菌中的CvfA-烯醇酶复合物链接营养压力,生长阶段控制和毒力基因表达。

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Streptococcus pyogenes, a multiple-auxotrophic human pathogen, regulates virulence gene expression according to nutritional availability during various stages in the infection process or in different infection sites. We discovered that CvfA influenced the expression of virulence genes according to growth phase and nutritional status. The influence of CvfA in C medium, rich in peptides and poor in carbohydrates, was most pronounced at the stationary phase. Under these conditions, up to 30% of the transcriptome exhibited altered expression; the levels of expression of multiple virulence genes were altered, including the genes encoding streptokinase, CAMP factor, streptolysin O, M protein (more abundant in the CvfA? mutant), SpeB, mitogenic factor, and streptolysin S (less abundant). The increase of carbohydrates or peptides in media restored the levels of expression of the virulence genes in the CvfA? mutant to wild-type levels (emm, ska, and cfa by carbohydrates; speB by peptides). Even though the regulation of gene expression dependent on nutritional stress is commonly linked to the stringent response, the levels of ppGpp were not altered by deletion of cvfA. Instead, CvfA interacted with enolase, implying that CvfA, a putative RNase, controls the transcript decay rates of virulence factors or their regulators according to nutritional status. The virulence of CvfA? mutants was highly attenuated in murine models, indicating that CvfA-mediated gene regulation is necessary for the pathogenesis of S. pyogenes. Taken together, the CvfA-enolase complex in S. pyogenes is involved in the regulation of virulence gene expression by controlling RNA degradation according to nutritional stress.
机译:化脓性链球菌是一种多营养型人类病原体,在感染过程的各个阶段或不同感染部位,根据营养状况调节毒力基因的表达。我们发现CvfA根据生长阶段和营养状况影响了毒力基因的表达。 CvfA在富含肽而碳水化合物含量低的C培养基中的影响在固定期最为明显。在这些条件下,多达30%的转录组表现出改变的表达。多种毒力基因的表达水平发生了改变,包括编码链激酶,CAMP因子,链球菌溶血素O,M蛋白(在CvfA ?突变体中含量更高),SpeB,有丝分裂因子和链球菌溶血素S的基因(数量较少)。培养基中碳水化合物或肽的增加将CvfA ?突变体中毒力基因的表达水平恢复为野生型水平( emm ska cfa (碳水化合物); speB (肽)。尽管依赖于营养应激的基因表达调控通常与严格的应答有关,但是 cvfA 的缺失并没有改变ppGpp的水平。取而代之的是,CvfA与烯醇酶相互作用,这表明CvfA(一种假定的RNase)可以根据营养状况控制毒力因子或其调节剂的转录物衰变速率。在鼠模型中,CvfA ?突变体的毒力被高度减弱,表明CvfA介导的基因调控对于 S的发病机理是必需的。化脓。总之, S中的CvfA-烯醇酶复合物。化脓通过根据营养应激控制RNA降解来参与毒力基因表达的调控。

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