Salmonella Typhimurium Type III Secretion Effectors Stimulate Innate Immune Responses in Cultured Epithelial Cells

被引:163
作者
Bruno, Vincent M. [1 ]
Hannemann, Sebastian [1 ]
Lara-Tejero, Maria [1 ]
Flavell, Richard A. [2 ]
Kleinstein, Steven H. [3 ,4 ]
Galan, Jorge E. [1 ]
机构
[1] Yale Univ, Sch Med, Sect Microbial Pathogenesis, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Howard Hughes Med Inst, Dept Immunobiol, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Interdept Program Computat Biol & Bioinformat, New Haven, CT USA
关键词
TOLL-LIKE RECEPTOR; HOST-CELL; SEROVAR TYPHIMURIUM; NUCLEAR RESPONSES; YERSINIA-ENTEROCOLITICA; NEGATIVE REGULATION; GENE-EXPRESSION; NEEDLE COMPLEX; PROTEINS SIPA; RHO GTPASES;
D O I
10.1371/journal.ppat.1000538
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Recognition of conserved bacterial products by innate immune receptors leads to inflammatory responses that control pathogen spread but that can also result in pathology. Intestinal epithelial cells are exposed to bacterial products and therefore must prevent signaling through innate immune receptors to avoid pathology. However, enteric pathogens are able to stimulate intestinal inflammation. We show here that the enteric pathogen Salmonella Typhimurium can stimulate innate immune responses in cultured epithelial cells by mechanisms that do not involve receptors of the innate immune system. Instead, S. Typhimurium stimulates these responses by delivering through its type III secretion system the bacterial effector proteins SopE, SopE2, and SopB, which in a redundant fashion stimulate Rho-family GTPases leading to the activation of mitogen-activated protein (MAP) kinase and NF-kappa B signaling. These observations have implications for the understanding of the mechanisms by which Salmonella Typhimurium induces intestinal inflammation as well as other intestinal inflammatory pathologies.
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页数:11
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