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σE调控基因在大肠杆菌尿路致病性中的作用。

Role of sigma E-regulated genes in Escherichia coli uropathogenesis.

作者信息

Redford Peter, Welch Rodney A

机构信息

Dept. of Medical Microbiology & Immunology, Rm. 481 MSB, 1300 University Ave., Madison, WI 53706-1532, USA.

出版信息

Infect Immun. 2006 Jul;74(7):4030-8. doi: 10.1128/IAI.01984-05.

Abstract

The sigma E regulon encodes proteins for maintenance and repair of the Escherichia coli cell envelope. Previously, we observed that an antirepressor of sigma E, DegS, is essential for uropathogenic E. coli virulence. Here we use a mouse urinary tract infection model to assay the virulence of mutants of E. coli genes described as sigma E dependent. Deletion mutants of candidate genes were made in the uropathogenic E. coli strain CFT073. Swiss Webster female mice were inoculated with a mixture of mutant and wild-type strains. Bladder and kidney homogenates were cultured 2 days after infection, and CFU of the wild type and mutant were compared. Eleven mutants were assayed, and two, CFT073 degP and CFT073 skp, showed significantly diminished survival compared to wild type. DegP is a chaperone and degradase active in the periplasm. Skp is also a periplasmic chaperone. The virulence of the skp deletion mutant could not be restored by complementation with skp. The virulence of the degP deletion mutant, in contrast, could be restored. However, complementation with a degP allele encoding a serine-to-alanine (S210A) mutation at the protease active site fails to restore virulence. Unlike degP mutants in other bacteria, the E. coli degP mutant is tolerant of oxidative stress. It disappears abruptly from bladder and kidney cultures between 6 and 12 hours after inoculation. A mutant of degQ, a close homolog of degP, was not attenuated in mice. This is the first report that the DegP degradase is an E. coli virulence factor in an animal infection model.

摘要

σE 调控子编码用于大肠杆菌细胞包膜维持和修复的蛋白质。此前,我们观察到σE 的抗阻遏物DegS 对尿路致病性大肠杆菌的毒力至关重要。在此,我们使用小鼠尿路感染模型来测定被描述为依赖σE 的大肠杆菌基因突变体的毒力。在尿路致病性大肠杆菌菌株CFT073 中构建了候选基因的缺失突变体。将突变体和野生型菌株的混合物接种到瑞士 Webster 雌性小鼠体内。感染2 天后培养膀胱和肾脏匀浆,并比较野生型和突变体的菌落形成单位(CFU)。对11 个突变体进行了测定,其中两个,即CFT073 degP 和CFT073 skp,与野生型相比,存活能力显著降低。DegP 是一种在周质中具有活性的伴侣蛋白和降解酶。Skp 也是一种周质伴侣蛋白。skp 缺失突变体的毒力不能通过skp 互补来恢复。相比之下,degP 缺失突变体的毒力可以恢复。然而,用在蛋白酶活性位点编码丝氨酸到丙氨酸(S210A)突变的degP 等位基因进行互补不能恢复毒力。与其他细菌中的degP 突变体不同,大肠杆菌degP 突变体对氧化应激具有耐受性。它在接种后6 至12 小时之间从膀胱和肾脏培养物中突然消失。degQ 是degP 的紧密同源物,其突变体在小鼠中没有减弱毒力。这是关于DegP 降解酶在动物感染模型中是大肠杆菌毒力因子这一情况的首次报道。

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