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本文引用的文献

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Secrets of a secretin.缩胆囊素的秘密。
Structure. 2013 Dec 3;21(12):2098-9. doi: 10.1016/j.str.2013.11.002.
2
Structure of the dodecameric Yersinia enterocolitica secretin YscC and its trypsin-resistant core.十二聚体肠侵袭性大肠埃希氏菌分泌素 YscC 的结构及其胰蛋白酶抗性核心。
Structure. 2013 Dec 3;21(12):2152-61. doi: 10.1016/j.str.2013.09.012. Epub 2013 Oct 24.
3
The AlgZR two-component system recalibrates the RsmAYZ posttranscriptional regulatory system to inhibit expression of the Pseudomonas aeruginosa type III secretion system.AlgZR 双组分系统重新校准了 RsmAYZ 转录后调控系统,以抑制铜绿假单胞菌 III 型分泌系统的表达。
J Bacteriol. 2014 Jan;196(2):357-66. doi: 10.1128/JB.01199-13. Epub 2013 Nov 1.
4
Sequential inactivation of Rho GTPases and Lim kinase by Pseudomonas aeruginosa toxins ExoS and ExoT leads to endothelial monolayer breakdown.铜绿假单胞菌毒素 ExoS 和 ExoT 依次灭活 Rho GTPases 和 Lim 激酶导致内皮单层细胞破裂。
Cell Mol Life Sci. 2014 May;71(10):1927-41. doi: 10.1007/s00018-013-1451-9. Epub 2013 Aug 22.
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A refined model of the prototypical Salmonella SPI-1 T3SS basal body reveals the molecular basis for its assembly.一个精制的原型沙门氏菌 SPI-1 T3SS 基础体模型揭示了其组装的分子基础。
PLoS Pathog. 2013;9(4):e1003307. doi: 10.1371/journal.ppat.1003307. Epub 2013 Apr 25.
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Functional mapping of PilF and PilQ in the Pseudomonas aeruginosa type IV pilus system.在铜绿假单胞菌 IV 型菌毛系统中 PilF 和 PilQ 的功能映射。
Biochemistry. 2013 Apr 30;52(17):2914-23. doi: 10.1021/bi3015345. Epub 2013 Apr 18.
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Structure and biophysics of type III secretion in bacteria.细菌 III 型分泌系统的结构与生物物理学。
Biochemistry. 2013 Apr 16;52(15):2508-17. doi: 10.1021/bi400160a. Epub 2013 Apr 5.
8
Crystal structure of the pilotin from the enterohemorrhagic Escherichia coli type II secretion system.肠出血性大肠杆菌 II 型分泌系统 Pilotin 蛋白的晶体结构。
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9
Assembly of the type II secretion system such as found in Vibrio cholerae depends on the novel Pilotin AspS.装配 II 型分泌系统,如霍乱弧菌中的系统,依赖于新型的 Pilotin AspS。
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10
Deletion of invH gene in Salmonella enterica serovar Typhimurium limits the secretion of Sip effector proteins.肠沙门氏菌 Typhimurium 中 invH 基因的缺失限制了 Sip 效应蛋白的分泌。
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ExsB是铜绿假单胞菌III型分泌装置在细菌膜中正确组装以及在体内完全毒力所必需的。

ExsB is required for correct assembly of the Pseudomonas aeruginosa type III secretion apparatus in the bacterial membrane and full virulence in vivo.

作者信息

Perdu Caroline, Huber Philippe, Bouillot Stéphanie, Blocker Ariel, Elsen Sylvie, Attrée Ina, Faudry Eric

机构信息

Université Grenoble Alpes, Bacterial Pathogenesis and Cellular Responses Group, Grenoble, France CEA, iRTSV, Grenoble, France CNRS, ERL5261, Grenoble, France INSERM, U1036_S Biology of Cancer and Infection Laboratory, Grenoble, France.

Schools of Cellular & Molecular Medicine and Biochemistry, University of Bristol, Bristol, United Kingdom.

出版信息

Infect Immun. 2015 May;83(5):1789-98. doi: 10.1128/IAI.00048-15. Epub 2015 Feb 17.

DOI:10.1128/IAI.00048-15
PMID:25690097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4399059/
Abstract

Pseudomonas aeruginosa is responsible for high-morbidity infections of cystic fibrosis patients and is a major agent of nosocomial infections. One of its most potent virulence factors is a type III secretion system (T3SS) that injects toxins directly into the host cell cytoplasm. ExsB, a lipoprotein localized in the bacterial outer membrane, is one of the components of this machinery, of which the function remained elusive until now. The localization of the exsB gene within the exsCEBA regulatory gene operon suggested an implication in the T3SS regulation, while its similarity with yscW from Yersinia spp. argued in favor of a role in machinery assembly. The present work shows that ExsB is necessary for full in vivo virulence of P. aeruginosa. Furthermore, the requirement of ExsB for optimal T3SS assembly and activity is demonstrated using eukaryotic cell infection and in vitro assays. In particular, ExsB promotes the assembly of the T3SS secretin in the bacterial outer membrane, highlighting the molecular role of ExsB as a pilotin. This involvement in the regulation of the T3S apparatus assembly may explain the localization of the ExsB-encoding gene within the regulatory gene operon.

摘要

铜绿假单胞菌是导致囊性纤维化患者高发病率感染的病原体,也是医院感染的主要致病菌之一。其最有效的毒力因子之一是III型分泌系统(T3SS),该系统可将毒素直接注入宿主细胞质中。ExsB是一种位于细菌外膜的脂蛋白,是该系统的组成部分之一,其功能至今仍不清楚。exsB基因在exsCEBA调控基因操纵子中的定位表明它参与T3SS调控,而它与耶尔森氏菌属的yscW相似,这表明它在系统组装中发挥作用。目前的研究表明,ExsB对铜绿假单胞菌在体内的完全毒力是必需的。此外,利用真核细胞感染和体外试验证明了ExsB对T3SS最佳组装和活性的必要性。特别是,ExsB促进了细菌外膜中T3SS分泌素的组装,突出了ExsB作为引导素的分子作用。ExsB参与T3S装置组装的调控,这可能解释了编码ExsB的基因在调控基因操纵子中的定位。