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本文引用的文献

1
Cytotoxicity and enterotoxicity of the thermostable direct hemolysin-deletion mutants of Vibrio parahaemolyticus.副溶血性弧菌耐热直接溶血素缺失突变体的细胞毒性和肠毒性
Microbiol Immunol. 2004;48(4):313-8. doi: 10.1111/j.1348-0421.2004.tb03512.x.
2
Genome sequence of Vibrio parahaemolyticus: a pathogenic mechanism distinct from that of V cholerae.副溶血性弧菌的基因组序列:一种与霍乱弧菌不同的致病机制。
Lancet. 2003 Mar 1;361(9359):743-9. doi: 10.1016/S0140-6736(03)12659-1.
3
An Inv/Mxi-Spa-like type III protein secretion system in Burkholderia pseudomallei modulates intracellular behaviour of the pathogen.类鼻疽伯克霍尔德菌中一种类似Inv/Mxi-Spa的III型蛋白分泌系统调节该病原体的细胞内行为。
Mol Microbiol. 2002 Nov;46(3):649-59. doi: 10.1046/j.1365-2958.2002.03190.x.
4
Characterization of the ysa pathogenicity locus in the chromosome of Yersinia enterocolitica and phylogeny analysis of type III secretion systems.小肠结肠炎耶尔森菌染色体上ysa致病位点的特征分析及Ⅲ型分泌系统的系统发育分析
J Mol Evol. 2002 Jul;55(1):37-51. doi: 10.1007/s00239-001-0089-7.
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Distribution of type III secretion gene clusters in Burkholderia pseudomallei, B. thailandensis and B. mallei.III型分泌基因簇在类鼻疽伯克霍尔德菌、泰国伯克霍尔德菌和鼻疽伯克霍尔德菌中的分布。
J Med Microbiol. 2002 May;51(5):374-384. doi: 10.1099/0022-1317-51-5-374.
6
The EspB protein of enterohaemorrhagic Escherichia coli interacts directly with alpha-catenin.肠出血性大肠杆菌的EspB蛋白直接与α-连环蛋白相互作用。
Cell Microbiol. 2002 Apr;4(4):213-22. doi: 10.1046/j.1462-5822.2002.00176.x.
7
Cortactin is necessary for F-actin accumulation in pedestal structures induced by enteropathogenic Escherichia coli infection.皮层肌动蛋白对于肠致病性大肠杆菌感染诱导的基座结构中F-肌动蛋白的积累是必需的。
Infect Immun. 2002 Apr;70(4):2206-9. doi: 10.1128/IAI.70.4.2206-2209.2002.
8
How and when are substrates selected for type III secretion?III型分泌的底物是如何以及何时被选择的?
Trends Microbiol. 2001 May;9(5):209-14. doi: 10.1016/s0966-842x(01)02014-5.
9
Complete genome sequence of enterohemorrhagic Escherichia coli O157:H7 and genomic comparison with a laboratory strain K-12.肠出血性大肠杆菌O157:H7全基因组序列及与实验室菌株K-12的基因组比较
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10
Type III secretion systems and pathogenicity islands.III型分泌系统与致病岛
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副溶血性弧菌两种III型分泌系统的功能特性

Functional characterization of two type III secretion systems of Vibrio parahaemolyticus.

作者信息

Park Kwon-Sam, Ono Takahiro, Rokuda Mitsuhiro, Jang Myoung-Ho, Okada Kazuhisa, Iida Tetsuya, Honda Takeshi

机构信息

Department of Bacterial Infections, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, 565-0871, Japan.

出版信息

Infect Immun. 2004 Nov;72(11):6659-65. doi: 10.1128/IAI.72.11.6659-6665.2004.

DOI:10.1128/IAI.72.11.6659-6665.2004
PMID:15501799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC523034/
Abstract

Vibrio parahaemolyticus, a gram-negative marine bacterium, is a worldwide cause of food-borne gastroenteritis. Recent genome sequencing of the clinical V. parahaemolyticus strain RIMD2210633 identified two sets of genes for the type III secretion system (TTSS), TTSS1 and TTSS2. Here, we constructed a series of mutant strains from RIMD2210633 to determine whether the two putative TTSS apparatus are functional. The cytotoxic activity of mutant strains having a deletion in one of the TTSS1 genes was significantly decreased compared with that of the parent and TTSS2-related mutant strains. In an enterotoxicity assay with the rabbit ileal loop test, intestinal fluid accumulation was diminished by deletion of the TTSS2-related genes while TTSS1-related mutants caused a level of fluid accumulation similar to that of the parent. VopD, a protein encoded in the proximity of the TTSS1 region and a homologue of the Yersinia YopD, was secreted in a TTSS1-dependent manner. In contrast, VopP, which is encoded by a pathogenicity island on chromosome 2 and is homologous to the Yersinia YopP, was secreted via the TTSS2 pathway. These results provide evidence that V. parahaemolyticus TTSSs function as secretion systems and may have a role in the pathogenicity of the organism. This is the first report of functional TTSSs in Vibrio species. The presence of TTSS apparatus gene homologues was demonstrated in other vibrios, such as Vibrio alginolyticus, Vibrio harveyi, and Vibrio tubiashii, suggesting that some other vibrios also contain TTSS and that the TTSS has a role in protein secretion in those organisms during interaction with eukaryotic cells.

摘要

副溶血性弧菌是一种革兰氏阴性海洋细菌,是全球食源性肠胃炎的致病原因。近期对临床副溶血性弧菌菌株RIMD2210633进行的基因组测序确定了Ⅲ型分泌系统(TTSS)的两组基因,即TTSS1和TTSS2。在此,我们从RIMD2210633构建了一系列突变菌株,以确定这两个假定的TTSS装置是否具有功能。与亲本和TTSS2相关突变菌株相比,在TTSS1基因之一中存在缺失的突变菌株的细胞毒性活性显著降低。在兔回肠袢试验的肠毒性测定中,缺失TTSS2相关基因会减少肠液积聚,而TTSS1相关突变体导致的液体积聚水平与亲本相似。VopD是一种在TTSS1区域附近编码的蛋白质,是耶尔森氏菌YopD的同源物,以TTSS1依赖的方式分泌。相比之下,VopP由2号染色体上的一个致病岛编码,与耶尔森氏菌YopP同源,通过TTSS2途径分泌。这些结果证明副溶血性弧菌的TTSS作为分泌系统发挥作用,并且可能在该生物体的致病性中起作用。这是关于弧菌属中功能性TTSS的首次报道。在其他弧菌如溶藻弧菌、哈维氏弧菌和塔氏弧菌中也证实了TTSS装置基因同源物的存在,这表明其他一些弧菌也含有TTSS,并且TTSS在这些生物体与真核细胞相互作用期间的蛋白质分泌中起作用。