Salmonella AvrA effector inhibits the key proinflammatory, anti-apoptotic NF-κB pathway

被引:224
作者
Collier-Hyams, LS
Zeng, H
Sun, J
Tomlinson, AD
Bao, ZQ
Chen, H
Madara, JL
Orth, K
Neish, AS
机构
[1] Emory Univ, Sch Med, Dept Pathol & Lab Med, Epithelial Pathobiol Unit, Atlanta, GA 30322 USA
[2] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 41809 USA
[3] Univ Texas, SW Med Ctr, Dept Biol Mol, Dallas, TX 75390 USA
关键词
D O I
10.4049/jimmunol.169.6.2846
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Secreted prokaryotic effector proteins have evolved to modulate the cellular functions of specific eukaryotic hosts. Generally, these proteins are considered virulence factors that facilitate parasitism. However, in certain plant and insect eukaryotic/prokaryotic relationships, effector proteins are involved in the establishment of commensal or symbiotic interactions. In this study, we report that the AvrA protein from Salmonella typhimurium, a common enteropathogen of humans, is an effector molecule that inhibits activation of the key proinflammatory NF-kappaB transcription factor and augments apoptosis in human epithelial cells. This activity is similar but mechanistically distinct from that described for YopJ, an AvrA homolog expressed by the bacterial pathogen Yersinia. We suggest that AvrA may limit virulence in vertebrates in a manner analogous to avirulence factors in plants, and as such, is the first bacterial effector from a mammalian pathogen that has been ascribed such a function.
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页码:2846 / 2850
页数:5
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