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肠炎沙门氏菌std菌毛操纵子受DNA腺嘌呤甲基化、SeqA和HdfR的调控。

Regulation of the Salmonella enterica std fimbrial operon by DNA adenine methylation, SeqA, and HdfR.

作者信息

Jakomin Marcello, Chessa Daniela, Bäumler Andreas J, Casadesús Josep

机构信息

Departamento de Genética, Facultad de Biología, Universidad de Sevilla, Apartado 1095, E-41080 Sevilla, Spain.

出版信息

J Bacteriol. 2008 Nov;190(22):7406-13. doi: 10.1128/JB.01136-08. Epub 2008 Sep 19.

DOI:10.1128/JB.01136-08
PMID:18805972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2576648/
Abstract

DNA adenine methylase (dam) mutants of Salmonella enterica serovar Typhimurium grown under laboratory conditions express the std fimbrial operon, which is tightly repressed in the wild type. Here, we show that uncontrolled production of Std fimbriae in S. enterica serovar Typhimurium dam mutants contributes to attenuation in mice, as indicated by the observation that an stdA dam strain is more competitive than a dam strain upon oral infection. Dam methylation appears to regulate std transcription, rather than std mRNA stability or turnover. A genetic screen for std regulators showed that the GATC-binding protein SeqA directly or indirectly represses std expression, while the poorly characterized yifA gene product serves as an std activator. YifA encodes a putative LysR-like protein and has been renamed HdfR, like its Escherichia coli homolog. Activation of std expression by HdfR is observed only in dam and seqA backgrounds. These data suggest that HdfR directly or indirectly activates std transcription. Since SeqA is unable to bind nonmethylated DNA, it is possible that std operon derepression in dam and seqA mutants may result from unconstrained HdfR-mediated activation of std transcription. Derepression of std in dam and seqA mutants of S. enterica occurs in only a fraction of the bacterial population, suggesting the occurrence of either bistable expression or phase variation.

摘要

在实验室条件下培养的鼠伤寒沙门氏菌血清型鼠伤寒亚种的DNA腺嘌呤甲基化酶(dam)突变体表达std菌毛操纵子,而该操纵子在野生型中受到严格抑制。在此,我们表明,鼠伤寒沙门氏菌血清型鼠伤寒亚种dam突变体中Std菌毛的不受控制产生导致小鼠体内的毒力减弱,这一点可通过以下观察结果表明:在口服感染时,stdA dam菌株比dam菌株更具竞争力。Dam甲基化似乎调节std转录,而非std mRNA的稳定性或周转。对std调节因子的遗传筛选表明,GATC结合蛋白SeqA直接或间接抑制std表达,而特征不明的yifA基因产物作为std激活剂。YifA编码一种假定的类LysR蛋白,与其大肠杆菌同源物一样,已更名为HdfR。仅在dam和seqA背景中观察到HdfR对std表达的激活。这些数据表明HdfR直接或间接激活std转录。由于SeqA无法结合非甲基化DNA,dam和seqA突变体中std操纵子的去抑制可能是由于HdfR介导的std转录激活不受限制所致。肠炎沙门氏菌dam和seqA突变体中std的去抑制仅发生在一部分细菌群体中,这表明存在双稳态表达或相变。

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