Function and distribution of EspG2, a type III secretion system effector of enteropathogenic Escherichia coli

被引:16
作者
Smollett, Katherine
Shaw, Robert K.
Garmendia, Junkal
Knutton, Stuart
Franke, Gad
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Cell & Mol Biol, London SWZ 2AZ, England
[2] Univ Birmingham, Inst Child Hlth, Birmingham B4 6NH, W Midlands, England
基金
英国惠康基金;
关键词
EspG; EspG2; type III secretion system; micrombule network; infection; ENTEROCYTE EFFACEMENT; PROTEIN TRANSLOCATION; PATHOGENICITY ISLAND; GENES; TIR; IDENTIFICATION; VIRULENCE; PLASMID; BOVINE; LOCUS;
D O I
10.1016/j.micinf.2006.04.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The enteropathogenic Escherichia coli (EPEC) effector protein EspG, like the Shigella effector VirA, functions through disruption of the host cell microtubule network. Reports have differed as to whether the EspG homologue, EspG2, is also responsible for microtubule disruption. In this study we show that following translocation, EspG2 and VirA are localised under adherent bacteria and able to restore the microtubule disruption phenotype to an espG/espG2 double EPEC mutant. The espG/espG2 double mutant produced A/E lesions similar to wild-type EPEC on human intestinal in vitro organ cultures. Determining the distribution of espG and espG2 among clinical EPEC isolates revealed two different types of espG (espG alpha and espG beta) and espG2 (intact and pseudo genes), which were associated with specific EPEC serotypes and closely followed the EPEC lineage. This investigation has established a role for EspG2 in the disruption of the microtubule network and associated different espG and espG2 types with different groups of EPEC. (c) 2006 Elsevier SAS. All rights reserved.
引用
收藏
页码:2220 / 2227
页数:8
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