• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

III型分泌系统:细菌与真核宿主细胞近距离作战的一种机制

Type III secretion: a bacterial device for close combat with cells of their eukaryotic host.

作者信息

Cornelis G R

机构信息

Microbial Pathogenesis Unit, Christian de Duve Institute of Cellular Pathology (ICP), Université Catholique de Louvain, Brussels, Belgium.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2000 May 29;355(1397):681-93. doi: 10.1098/rstb.2000.0608.

DOI:10.1098/rstb.2000.0608
PMID:10874740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1692769/
Abstract

Salmonella, Shigella, Yersinia, Pseudomonas aeruginosa, enteropathogenic Escherichia coli and several plant-pathogenic Gram-negative bacteria use a new type of systems called 'type III secretion' to attack their host. These systems are activated by contact with a eukaryotic cell membrane and they allow bacteria to inject bacterial proteins across the two bacterial membranes and the eukaryotic cell membrane to reach a given compartment and destroy or subvert the target cell. These systems consist of a secretion apparatus made up of about 25 individual proteins and a set of proteins released by this apparatus. Some of these released proteins are 'effectors' that are delivered by extracellular bacteria into the cytosol of the target cell while the others are 'translocators' that help the 'effectors' to cross the membrane of the eukaryotic cell. Most of the 'effectors' act on the cytoskeleton or on intracellular signalling cascades. One of the proteins injected by the enteropathogenic E. coli serves as a membrane receptor for the docking of the bacterium itself at the surface of the cell.

摘要

沙门氏菌、志贺氏菌、耶尔森氏菌、铜绿假单胞菌、肠道致病性大肠杆菌以及几种植物致病性革兰氏阴性菌利用一种名为“III型分泌系统”的新型系统来攻击它们的宿主。这些系统通过与真核细胞膜接触而被激活,它们使细菌能够将细菌蛋白穿过两层细菌膜和真核细胞膜,到达特定的区室,从而破坏或颠覆靶细胞。这些系统由一个由约25种不同蛋白质组成的分泌装置以及该装置释放的一组蛋白质构成。这些释放的蛋白质中,有些是“效应蛋白”,由胞外细菌递送至靶细胞的胞质溶胶中,而其他的则是“转运蛋白”,帮助“效应蛋白”穿过真核细胞的膜。大多数“效应蛋白”作用于细胞骨架或细胞内信号级联反应。肠道致病性大肠杆菌注入的一种蛋白质可作为细菌自身在细胞表面对接的膜受体。

相似文献

1
Type III secretion: a bacterial device for close combat with cells of their eukaryotic host.III型分泌系统:细菌与真核宿主细胞近距离作战的一种机制
Philos Trans R Soc Lond B Biol Sci. 2000 May 29;355(1397):681-93. doi: 10.1098/rstb.2000.0608.
2
Assembly and function of type III secretory systems.III型分泌系统的组装与功能。
Annu Rev Microbiol. 2000;54:735-74. doi: 10.1146/annurev.micro.54.1.735.
3
The bacterial injection kit: type III secretion systems.细菌注射试剂盒:III型分泌系统。
Ann Med. 2005;37(4):234-49. doi: 10.1080/07853890510037329.
4
Type III secretion: the bacteria-eukaryotic cell express.III型分泌:细菌与真核细胞的相互作用。 (原英文表述有误,推测正确表述可能是Type III secretion: the interaction between bacteria and eukaryotic cell,按照推测内容翻译的)
FEMS Microbiol Lett. 2005 Nov 1;252(1):1-10. doi: 10.1016/j.femsle.2005.08.036. Epub 2005 Sep 8.
5
The Yersinia Ysc-Yop 'type III' weaponry.耶尔森氏菌的Ysc-Yop“III型”武器装备。
Nat Rev Mol Cell Biol. 2002 Oct;3(10):742-52. doi: 10.1038/nrm932.
6
The Type III secretion system of Gram-negative bacteria: a potential therapeutic target?革兰氏阴性菌的III型分泌系统:一个潜在的治疗靶点?
Expert Opin Ther Targets. 2001 Jun;5(3):327-339. doi: 10.1517/14728222.5.3.327.
7
Protein secretion systems and adhesins: the molecular armory of Gram-negative pathogens.蛋白质分泌系统与黏附素:革兰氏阴性病原体的分子武器库。
Int J Med Microbiol. 2007 Oct;297(6):401-15. doi: 10.1016/j.ijmm.2007.03.017. Epub 2007 May 7.
8
The type III secretion system tip complex and translocon.III型分泌系统尖端复合体和转运孔蛋白
Mol Microbiol. 2008 Jun;68(5):1085-95. doi: 10.1111/j.1365-2958.2008.06237.x. Epub 2008 Apr 8.
9
Type III secretion systems: machines to deliver bacterial proteins into eukaryotic cells?III型分泌系统:将细菌蛋白输送到真核细胞中的机器?
Trends Microbiol. 1997 Apr;5(4):148-56. doi: 10.1016/S0966-842X(97)01029-9.
10
Insertion of the bacterial type III translocon: not your average needle stick.细菌III型分泌系统转运装置的插入:可不是一般的针刺。
Trends Microbiol. 2005 Mar;13(3):92-5. doi: 10.1016/j.tim.2005.01.008.

引用本文的文献

1
Some Examples of Bacterial Toxins as Tools.一些细菌毒素作为工具的例子。
Toxins (Basel). 2024 Apr 23;16(5):202. doi: 10.3390/toxins16050202.
2
Secretory System Components as Potential Prophylactic Targets for Bacterial Pathogens.分泌系统组件作为细菌病原体的潜在预防靶点。
Biomolecules. 2021 Jun 15;11(6):892. doi: 10.3390/biom11060892.
3
Immunoglobulin for Treating Bacterial Infections: One More Mechanism of Action.用于治疗细菌感染的免疫球蛋白:又一种作用机制。
Antibodies (Basel). 2019 Nov 3;8(4):52. doi: 10.3390/antib8040052.
4
Engineering toxin complex (PTC) into a recombinant injection nanomachine.将工程毒素复合物(PTC)构建到重组注射纳米机器中。
Life Sci Alliance. 2019 Sep 20;2(5). doi: 10.26508/lsa.201900485. Print 2019 Oct.
5
Blood feeding tsetse flies as hosts and vectors of mammals-pre-adapted African Trypanosoma: current and expected research directions.以哺乳动物为宿主和媒介的吸血采采蝇——适应非洲锥虫的前适应者:当前和预期的研究方向。
BMC Microbiol. 2018 Nov 23;18(Suppl 1):162. doi: 10.1186/s12866-018-1281-x.
6
Pseudomonas toxin pyocyanin triggers autophagy: Implications for pathoadaptive mutations.铜绿假单胞菌毒素绿脓菌素引发自噬:对致病适应性突变的影响。
Autophagy. 2016 Jun 2;12(6):1015-28. doi: 10.1080/15548627.2016.1170256. Epub 2016 May 9.
7
Transcriptomic dissection of the rice-Burkholderia glumae interaction.水稻与谷壳伯克霍尔德氏菌相互作用的转录组学剖析
BMC Genomics. 2014 Sep 3;15(1):755. doi: 10.1186/1471-2164-15-755.
8
Analysis of the prevalence, secretion and function of a cell cycle-inhibiting factor in the melioidosis pathogen Burkholderia pseudomallei.类鼻疽病原体伯克霍尔德菌中细胞周期抑制因子的患病率、分泌及功能分析
PLoS One. 2014 May 8;9(5):e96298. doi: 10.1371/journal.pone.0096298. eCollection 2014.
9
Mutations in hemG mediate resistance to salicylidene acylhydrazides, demonstrating a novel link between protoporphyrinogen oxidase (HemG) and Chlamydia trachomatis infectivity.突变体 hemG 介导对水杨酰腙的抗性,表明原卟啉原氧化酶(HemG)与沙眼衣原体感染之间存在新的联系。
J Bacteriol. 2013 Sep;195(18):4221-30. doi: 10.1128/JB.00506-13. Epub 2013 Jul 12.
10
IgG keeps virulent Salmonella from evading dendritic cell uptake.IgG 可阻止毒性沙门氏菌逃避树突状细胞摄取。
Immunology. 2012 Jul;136(3):291-305. doi: 10.1111/j.1365-2567.2012.03578.x.

本文引用的文献

1
Studies on the nutrition and physiology of Pasteurella pestis. VI. A differential plating medium for the estimation of the mutation rate to avirulence.鼠疫耶尔森氏菌的营养与生理学研究。VI. 一种用于评估无毒力突变率的鉴别平板培养基。
J Bacteriol. 1961 Apr;81(4):605-8. doi: 10.1128/jb.81.4.605-608.1961.
2
The effects of loss of different virulence determinants on the virulence and immunogenicity of strains of Pasteurella pestis.不同毒力决定因素缺失对鼠疫耶尔森氏菌菌株毒力和免疫原性的影响。
Br J Exp Pathol. 1958 Jun;39(3):278-91.
3
The Salmonella YopJ-homologue AvrA does not possess YopJ-like activity.鼠伤寒沙门氏菌YopJ同源物AvrA不具备类似YopJ的活性。
Microb Pathog. 2000 Feb;28(2):59-70. doi: 10.1006/mpat.1999.0324.
4
The Bpel locus encodes type III secretion machinery in Bordetella pertussis.Bpel基因座在百日咳博德特氏菌中编码III型分泌机制。
Microb Pathog. 1999 Dec;27(6):349-67. doi: 10.1006/mpat.1999.0307.
5
Yersinia enterocolitica type III secretion-translocation system: channel formation by secreted Yops.小肠结肠炎耶尔森菌III型分泌转运系统:分泌的耶尔森菌外膜蛋白形成通道
EMBO J. 1999 Dec 1;18(23):6793-9. doi: 10.1093/emboj/18.23.6793.
6
The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranes.福氏志贺菌的三方III型分泌系统将IpaB和IpaC插入宿主细胞膜。
J Cell Biol. 1999 Nov 1;147(3):683-93. doi: 10.1083/jcb.147.3.683.
7
Identification of CesT, a chaperone for the type III secretion of Tir in enteropathogenic Escherichia coli.鉴定CesT,一种肠道致病性大肠杆菌中TirⅢ型分泌的伴侣蛋白。
Mol Microbiol. 1999 Sep;33(6):1176-89. doi: 10.1046/j.1365-2958.1999.01559.x.
8
Enteropathogenic Escherichia coli translocated intimin receptor, Tir, requires a specific chaperone for stable secretion.肠道致病性大肠杆菌转位紧密素受体(Tir)需要一种特定的伴侣蛋白来实现稳定分泌。
Mol Microbiol. 1999 Sep;33(6):1162-75. doi: 10.1046/j.1365-2958.1999.01558.x.
9
Direct nucleation and bundling of actin by the SipC protein of invasive Salmonella.侵袭性沙门氏菌的SipC蛋白对肌动蛋白的直接成核与成束作用。
EMBO J. 1999 Sep 15;18(18):4926-34. doi: 10.1093/emboj/18.18.4926.
10
Insertion of a Yop translocation pore into the macrophage plasma membrane by Yersinia enterocolitica: requirement for translocators YopB and YopD, but not LcrG.小肠结肠炎耶尔森菌将Yop易位孔插入巨噬细胞质膜:需要易位蛋白YopB和YopD,但不需要LcrG。
Mol Microbiol. 1999 Sep;33(5):971-81. doi: 10.1046/j.1365-2958.1999.01537.x.