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本文引用的文献

1
Periplasmic peptidyl prolyl cis-trans isomerases are not essential for viability, but SurA is required for pilus biogenesis in Escherichia coli.周质肽基脯氨酰顺反异构酶对生存力并非必需,但SurA是大肠杆菌菌毛生物合成所必需的。
J Bacteriol. 2005 Nov;187(22):7680-6. doi: 10.1128/JB.187.22.7680-7686.2005.
2
Coordinate expression of fimbriae in uropathogenic Escherichia coli.尿路致病性大肠杆菌中菌毛的协同表达
Infect Immun. 2005 Nov;73(11):7588-96. doi: 10.1128/IAI.73.11.7588-7596.2005.
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Characterization of six lipoproteins in the sigmaE regulon.西格玛E调控子中六种脂蛋白的特性分析。
J Bacteriol. 2005 Jul;187(13):4552-61. doi: 10.1128/JB.187.13.4552-4561.2005.
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Identification of a multicomponent complex required for outer membrane biogenesis in Escherichia coli.鉴定大肠杆菌外膜生物合成所需的多组分复合物。
Cell. 2005 Apr 22;121(2):235-45. doi: 10.1016/j.cell.2005.02.015.
5
Effect of inactivation of the HtrA-like serine protease DegQ on the virulence of Salmonella enterica serovar Typhimurium in mice.类HtrA丝氨酸蛋白酶DegQ失活对鼠伤寒沙门氏菌在小鼠中致病性的影响。
Infect Immun. 2004 Dec;72(12):7357-9. doi: 10.1128/IAI.72.12.7357-7359.2004.
6
Transcriptome of uropathogenic Escherichia coli during urinary tract infection.泌尿道感染期间尿路致病性大肠杆菌的转录组
Infect Immun. 2004 Nov;72(11):6373-81. doi: 10.1128/IAI.72.11.6373-6381.2004.
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Role of HtrA in the virulence and competence of Streptococcus pneumoniae.HtrA在肺炎链球菌毒力和感受态中的作用
Infect Immun. 2004 Jun;72(6):3584-91. doi: 10.1128/IAI.72.6.3584-3591.2004.
8
New members of the Escherichia coli sigmaE regulon identified by a two-plasmid system.通过双质粒系统鉴定出的大肠杆菌σE调控子新成员。
FEMS Microbiol Lett. 2003 Aug 8;225(1):1-7. doi: 10.1016/S0378-1097(03)00480-4.
9
DegS is necessary for virulence and is among extraintestinal Escherichia coli genes induced in murine peritonitis.DegS对于毒力是必需的,并且属于在小鼠腹膜炎中诱导表达的肠外大肠杆菌基因。
Infect Immun. 2003 Jun;71(6):3088-96. doi: 10.1128/IAI.71.6.3088-3096.2003.
10
Extensive mosaic structure revealed by the complete genome sequence of uropathogenic Escherichia coli.尿路致病性大肠杆菌全基因组序列揭示的广泛镶嵌结构
Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):17020-4. doi: 10.1073/pnas.252529799. Epub 2002 Dec 5.

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.

DOI:10.1128/IAI.01984-05
PMID:16790776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1489677/
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。