Modulation of chemokine gene expression by Shiga-toxin producing Escherichia coli belonging to various origins and serotypes

被引:13
作者
Gobert, Alain P. [1 ]
Coste, Alix [1 ]
Guzman, Carlos A. [2 ]
Vareille, Marjolaine [1 ]
Hindre, Thomas [1 ]
de Sablet, Thibaut [1 ]
Girardeau, Jean-Pierre [1 ]
Martin, Christine [1 ]
机构
[1] INRA, UR454, Microbiol Unit, Ctr Theix, F-63122 St Genes Champanelle, France
[2] Helmholtz Ctr Infect Res, Dept Vaccinol, D-38124 Braunschweig, Germany
关键词
epithelial cells; Shiga-toxin producing Escherichia coli; chemokine; locus of enterocyte effacement; flagellin;
D O I
10.1016/j.micinf.2007.10.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Infection with Shiga-toxin producing Escherichia coli (STEC) may result in the development of the haemolytic-uremic syndrome (HUS), the main cause of acute renal failure in children. While O157:H7 STEC are associated with large outbreaks of HUS, it is difficult to predict whether a non-O157:H7 isolate can be pathogenic for humans. The mucosal innate immune response plays a central role in the pathogenesis of HUS; therefore, we compared the induction of IL-8 and CCL20 in human colon epithelial cells infected with strains belonging to different serotypes, isolated from cattle or from HUS patients. No correlation was observed between strain virulence and chemokine gene expression. Rather, the genetic background of the strains seems to determine the chemokine gene expression profile. Investigating the contribution of different bacterial factors in this process, we show that the type III secretion system of O157:H7 bacteria, but not the intimate adhesion, is required to stimulate the cells. In addition, H7, H10, and H21 flagellins are potent inducers of chemokine gene expression when synthesized in large amount. (C) 2007 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:159 / 165
页数:7
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