The early transcriptional response of pig small intestinal mucosa to invasion by Salmonella enterica serovar typhimurium DT104

被引:37
作者
Niewold, Theo A.
Veldhuizen, Edwin J. A.
van der Meulen, Jan
Haagsman, Henk P.
de Wit, Agnes A. C.
Smits, Mari A.
Tersteeg, Monique H. G.
Hulst, Marcel M.
机构
[1] Univ Wageningen & Res Ctr, Anim Sci Grp, Lelystad, Netherlands
[2] Univ Utrecht, Fac Vet Med, Dept Infect Dis & Immunol, Utrecht, Netherlands
[3] Katholieke Univ Leuven, Nutr & Hlth Unit, Dept Biosyst, Fac Biosci Engn, B-3001 Heverlee, Belgium
关键词
Salmonella typhimurium; small intestine; intestinal immunity; microarray; transcriptomics;
D O I
10.1016/j.molimm.2006.05.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salmonella enterica serovar typhimurium (S. typhimurium) species are a leading cause of human invasive gastroenteritis. There is increasing in vitro evidence about Salmonella interaction with isolated cells or cell lines (macrophages, and enterocytes) on the molecular level, however, very little is known about in vivo interactions during actual invasion. We investigated the early interaction of S. typhimurium with intact small intestinal mucosa, in a pig model. Intestinal segments were infected with or without S. typhimurium DT104, and perfused. Whole mucosal gene expression was analyzed by cDNA array on 0, 2, 4, and 8 h post-infection. Invasion resulted in the upregulation of only eight transcripts in jejunal mucosa, among those the proinflammatory IL-8 (at 4 It only), and the anti inflammatory STAT3 (at 4 and 8 h). The limited number of differentially expressed genes found here in vivo compared to in vitro is most likely due to the presence of multiple, heterogenous cell interactions in intact mucosa. Furthermore, it is concluded that S. typhimurium evades strong host responses by downregulating the local inflammatory response. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1316 / 1322
页数:7
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