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首页> 外文期刊>Journal of bacteriology >The Salmonella typhimurium katF (rpoS) gene: cloning, nucleotide sequence, and regulation of spvR and spvABCD virulence plasmid genes.
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The Salmonella typhimurium katF (rpoS) gene: cloning, nucleotide sequence, and regulation of spvR and spvABCD virulence plasmid genes.

机译:鼠伤寒沙门氏菌katF(rpoS)基因:spvR和spvABCD毒力质粒基因的克隆,核苷酸序列和调控。

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The spv region of Salmonella virulence plasmids is essential for the development of a systemic infection in mice. Transcriptional activation of the spvABCD operon occurs during stationary growth phase and is mediated by the regulatory gene product SpvR. We have previously shown that expression of a spvRAB'-cat fusion in Escherichia coli was dependent on the katF (rpoS) locus which encodes an alternative sigma factor (sigma S). The katF gene from Salmonella typhimurium has been cloned, sequenced, and used to construct Salmonella katF mutants by allelic replacement. Using these mutants, we demonstrated by mRNA and gene fusion analyses that sigma S, in conjunction with SpvR, controls the transcription of the regulatory gene spvR. In a second series of experiments, we sought to clarify the relationship between sigma S and SpvR in the control of spvABCD transcription. It was shown that expression of a transcriptional spvAB'-lacZ fusion could be restored in E. coli and Salmonella katF mutants when spvR was expressed in trans from an exogenous promoter. Moreover, identical spvA mRNA startpoints were detected in katF+ and katF strains. These results indicate that the reduction of spvABCD transcription in katF mutants is mainly due to decreased expression of spvR. Finally, mouse inoculation studies with S. typhimurium katF mutants of both wild-type and virulence plasmid-cured strains suggest that katF contributes to Salmonella virulence via the regulation of chromosomal genes in addition to that of spv genes.
机译:沙门氏菌毒力质粒的spv区对于小鼠全身感染的发生至关重要。 spvABCD操纵子的转录激活发生在静止生长期,并由调控基因产物SpvR介导。先前我们已经表明,spvRAB'-cat融合蛋白在大肠杆菌中的表达依赖于编码替代sigma因子(sigma S)的katF(rpoS)基因座。来自鼠伤寒沙门氏菌的katF基因已被克隆,测序并用于通过等位基因置换构建沙门氏菌katF突变体。使用这些突变体,我们通过mRNA和基因融合分析证明了Sigma S与SpvR一起控制调节基因spvR的转录。在第二系列实验中,我们试图阐明在控制spvABCD转录中sigma S和SpvR之间的关系。结果表明,当spvR从外源启动子反式表达时,转录的spvAB'-lacZ融合蛋白的表达可以在大肠杆菌和沙门氏菌katF突变体中恢复。此外,在katF +和katF菌株中检测到相同的spvA mRNA起点。这些结果表明,katF突变体中spvABCD转录的减少主要是由于spvR表达的降低。最后,用鼠伤寒沙门氏菌katF突变体的野生型和毒力质粒治疗菌株进行的小鼠接种研究表明,除了spv基因外,katF还通过调节染色体基因来促进沙门氏菌的毒力。

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