首页> 美国卫生研究院文献>Journal of Bacteriology >Role of Salmonella enterica Serovar Typhimurium Two-Component System PreA/PreB in Modulating PmrA-Regulated Gene Transcription
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Role of Salmonella enterica Serovar Typhimurium Two-Component System PreA/PreB in Modulating PmrA-Regulated Gene Transcription

机译:沙门氏菌血清型鼠伤寒沙门氏菌两组分系统PreA / PreB在调节PmrA调控的基因转录中的作用。

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摘要

The PmrA/PmrB two-component system encoded by the pmrCAB operon regulates the modification of Salmonella enterica serovar Typhimurium lipopolysaccharide leading to polymyxin B resistance. PmrA and PhoP are the only known activators of pmrCAB. A transposon mutagenesis screen for additional regulators of a pmrC::MudJ fusion led to the identification of a two-component system, termed PreA/PreB (pmrCAB regulators A and B), that controls the transcription of the pmrCAB operon in response to unknown signals. The initial observations indicated that insertions in, or a deletion of, the preB sensor, but not the preA response regulator, caused upregulation of pmrCAB. Interestingly, the expression of pmrCAB was not upregulated in a preAB mutant grown in LB broth, implicating PreA in the increased expression of pmrCAB in the preB strain. This was confirmed by overexpression of preA+ in preAB or preB backgrounds, which resulted in significant upregulation or further upregulation of pmrCAB. No such effect was observed in any tested preB+ backgrounds. Additionally, an ectopic construct expressing a preA[D51A] allele also failed to upregulate pmrC in any of the pre backgrounds tested, which implies that there is a need for phosphorylation in the activation of the target genes. The observed upregulation of pmrCAB occurred independently of the response regulators PmrA and PhoP. Although a preB mutation led to increased transcription of pmrCAB, this did not result in a measurable effect on polymyxin B resistance. Our genetic data support a model of regulation whereby, in response to unknown signals, the PreB sensor activates PreA, which in turn indirectly upregulates pmrCAB transcription.
机译:由pmrCAB操纵子编码的PmrA / PmrB两组分系统调节肠炎沙门氏菌血清鼠伤寒沙门氏菌脂多糖的修饰,导致多粘菌素B耐药。 PmrA和PhoP是pmrCAB的唯一已知激活剂。通过转座子诱变筛选pmrC :: MudJ融合蛋白的其他调节子,可以鉴定出一个称为PreA / PreB的两组分系统(pmrCAB调节子A和B),该系统可响应未知信号控制pmrCAB操纵子的转录。 。最初的观察表明,在preB传感器中插入或删除,但未在preA反应调节器中引起pmrCAB上调。有趣的是,在LB肉汤中生长的preAB突变体中pmrCAB的表达没有上调,这暗示PreA参与了preB菌株中pmrCAB表达的增加。在preAB或 preB 背景中preA + 的过表达证实了这一点,这导致 pmrCAB 的显着上调或进一步上调。在任何测试过的 preB + 背景中均未观察到这种效果。另外,表达 preA [D51A]等位基因的异位构建体在任何测试的 pre 背景中也未能上调 pmrC 。在靶基因的激活中需要磷酸化。观察到的 pmrCAB 上调独立于应答调节因子PmrA和PhoP。尽管 preB 突变导致 pmrCAB 的转录增加,但这对多粘菌素B耐药性没有可测量的影响。我们的遗传数据支持一种调节模型,其中PreB传感器响应未知信号激活PreA,从而间接上调 pmrCAB 转录。

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