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首页> 外文期刊>Molecular Microbiology >Co-regulation of Salmonella enterica genes required for virulence and resistance to antimicrobial peptides by SlyA and PhoP/PhoQ
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Co-regulation of Salmonella enterica genes required for virulence and resistance to antimicrobial peptides by SlyA and PhoP/PhoQ

机译:SlyA和PhoP / PhoQ对毒力和对抗菌肽耐药的沙门氏菌肠基因的共调控

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摘要

Analysis of the transcriptome of slyA mutant Salmonella enterica serovar Typhimurium revealed that many SlyA-dependent genes, including pagC, pagD, ugtL, mig-14, virK, phoN, pgtE, pipB2, sopD2, pagJ and pagK, are also controlled by the PhoP/PhoQ regulatory system. Many SlyA- and PhoP/PhoQ-co-regulated genes have functions associated with the bacterial envelope, and some have been directly implicated in virulence and resistance to antimicrobial peptides. Purified His-tagged SlyA binds to the pagC and mig-14 promoters in regions homologous to a previously proposed 'SlyA-box'. The pagC promoter lacks a consensus PhoP binding site and does not bind PhoP in vitro, suggesting that the effect of PhoP on pagC transcription is indirect. Stimulation of pagC expression by PhoP requires SlyA. Levels of SlyA protein and mRNA are not significantly changed under low-magnesium PhoP-inducing conditions in which pagC expression is profoundly elevated, however, indicating that the PhoP/PhoQ system does not activate pagC expression by altering SlyA protein concentration. Models are proposed in which PhoP may control SlyA activity via a soluble ligand or SlyA may function as an anti-repressor to allow PhoP activation. The absence of almost all SlyA-activated genes from the Escherichia coli K12 genome suggests that the functional linkage between the SlyA and PhoP/PhoQ regulatory systems arose as Salmonella evolved its distinctive pathogenic lifestyle.
机译:对slyA突变型肠炎沙门氏菌血清鼠伤寒沙门氏菌的转录组进行分析后发现,许多SlyA依赖性基因,包括pagC,pagD,ugtL,mig-14,virK,phoN,pgtE,pipB2,sopD2,pagJ和pagK也受到控制。 / PhoQ监管系统。许多SlyA和PhoP / PhoQ共同调控的基因具有与细菌包膜相关的功能,并且其中一些直接与毒力和对抗菌肽的抗性有关。纯化的带有His标签的SlyA在与先前提出的“ SlyA-box”同源的区域中与pagC和mig-14启动子结合。 pagC启动子缺乏共有的PhoP结合位点,并且在体外不结合PhoP,这表明PhoP对pagC转录的影响是间接的。 PhoP刺激pagC表达需要SlyA。在低镁PhoP诱导条件下(其中pagC表达显着升高),SlyA蛋白和mRNA的水平没有明显改变,但是,这表明PhoP / PhoQ系统不会通过改变SlyA蛋白浓度来激活pagC表达。提出了其中PhoP可通过可溶性配体控制SlyA活性或SlyA可充当抗阻遏物以允许PhoP激活的模型。大肠杆菌K12基因组几乎没有所有SlyA激活基因,这表明随着沙门氏菌发展其独特的致病性生活方式,SlyA和PhoP / PhoQ调节系统之间的功能联系开始出现。

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