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噬菌体休克蛋白操纵子成员PspA在rpoE突变型肠炎沙门氏菌鼠伤寒血清型中的补偿作用。

Compensatory role of PspA, a member of the phage shock protein operon, in rpoE mutant Salmonella enterica serovar Typhimurium.

作者信息

Becker Lynne A, Bang Iel-Soo, Crouch Marie-Laure, Fang Ferric C

机构信息

Departments of Laboratory Medicine and Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.

出版信息

Mol Microbiol. 2005 May;56(4):1004-16. doi: 10.1111/j.1365-2958.2005.04604.x.

Abstract

Sigma(E) is an alternative sigma factor that responds to and ameliorates extracytoplasmic stress. In Salmonella enterica serovar Typhimurium (S. Typhimurium), sigma(E) is required for oxidative stress resistance, stationary-phase survival and virulence in mice. Microarray analysis of stationary-phase gene expression in rpoE mutant bacteria revealed a dramatic increase in expression of pspA, a member of the phage shock protein (psp) operon. The psp operon can be induced by filamentous bacteriophages or by perturbations of protein secretion, and is believed to facilitate the maintenance of proton motive force (PMF). We hypothesized that increased pspA expression may represent a compensatory response to the loss of sigma(E) function. Increased pspA expression was confirmed in rpoE mutant Salmonella and also observed in a mutant lacking the F(1)F(0) ATPase. Alternatively, expression of pspA could be induced by exposure to CCCP, a protonophore that disrupts PMF. An rpoE pspA double mutant strain was found to have a stationary-phase survival defect more pronounced than that of isogenic strains harbouring single mutations. The double mutant strains were also more susceptible to killing by CCCP or by a bactericidal/permeability-increasing protein (BPI)-derived anti-microbial peptide. Using fluorescence ratio imaging, differences were observed in the Deltapsi of wild-type and rpoE or pspA mutant bacteria. These findings suggest that pspA expression in S. Typhimurium is induced by alterations in PMF and a functional sigma(E) regulon is essential for the maintenance of PMF.

摘要

σE是一种可应对并缓解胞外应激的替代σ因子。在鼠伤寒沙门氏菌中,σE对于抵抗氧化应激、在稳定期存活以及在小鼠体内的毒力而言是必需的。对rpoE突变细菌稳定期基因表达进行的微阵列分析显示,噬菌体休克蛋白(psp)操纵子成员pspA的表达显著增加。psp操纵子可由丝状噬菌体或蛋白质分泌的扰动诱导,并且被认为有助于维持质子动力势(PMF)。我们推测,pspA表达增加可能代表对σE功能丧失的一种补偿反应。在rpoE突变沙门氏菌中证实了pspA表达增加,并且在缺乏F1F0 ATP酶的突变体中也观察到了这一现象。此外,暴露于CCCP(一种破坏PMF的质子载体)可诱导pspA的表达。发现一种rpoE pspA双突变菌株在稳定期的存活缺陷比携带单突变的同基因菌株更为明显。双突变菌株对CCCP或杀菌/通透性增加蛋白(BPI)衍生的抗菌肽杀伤也更敏感。使用荧光比率成像,观察到野生型与rpoE或pspA突变细菌的Δψ存在差异。这些发现表明,鼠伤寒沙门氏菌中pspA的表达由PMF的改变诱导,并且一个功能性的σE调节子对于维持PMF至关重要。

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