Quantitative analysis of the immune response upon Salmonella typhimurium infection along the porcine intestinal gut

被引:87
作者
Collado-Romero, Melania [1 ]
Arce, Cristina [1 ]
Ramirez-Boo, Maria [1 ]
Carvajal, Ana [2 ]
Garrido, Juan J. [1 ]
机构
[1] Univ Cordoba, Fac Vet, Dept Genet, Grp Genom & Mejora Anim, E-14071 Cordoba, Spain
[2] Univ Leon, Fac Vet, Dept Sanidad Anim, E-24071 Leon, Spain
关键词
Salmonella; pig; intestinal gut; immune response; real-time PCR; INNATE IMMUNITY; UP-REGULATION; CELLS; EXPRESSION; DEFENSINS; PIG; PATHOGENESIS; RECOGNITION; CASPASE-1; INVASION;
D O I
10.1051/vetres/2009072
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Salmonella enterica serovar Typhimurium causes enteric disease and compromises food safety. In pigs, the molecular response of the intestine to S. typhimurium has been traditionally characterized by in vitro models that do not reflect the actual immunological competence of the intestinal mucosa. In this work, we performed an oral S. typhimurium infection study to obtain insight into the in vitro response in three different sections (jejunum, ileum and colon) of the porcine intestine. For this, samples from one-month-old infected piglets were collected during a time course comprising 1, 2, and 6 days post inoculation to evaluate the intestinal response by quantifying the mRNA expression of gene coding for 28 innate immune system molecules using quantitative real-time PCR assays. In addition, samples from non-infected control animals were also employed to establish differences in the steady state gene expression between intestinal sections. The panel of quantified molecules included an assortment of cytokines, chemokines, pattern-recognition receptors, intracellular signaling molecules, transcription factors and antimicrobial molecules. Changes in gene expression occurred in the three different parts of the intestine and during the course of the S. typhimurium infection. Moreover, the high variation observed in expression patterns of genes coding for inflammatory mediators could indicate that each intestinal section responds differently to the infection. Thus, on the contrary to findings in the jejunum and colon, a down-regulation and lack of induction of some proinflammatory cytokine transcripts was observed in the ileum. Nevertheless, all chemoattractant cytokines assayed were up-regulated in the ileum and jejunum whereas only interleukin-8 and MIP-1 alpha mRNA were over expressed in the colon. In conclusion, our results reveal regional differences in gene expression profiles along the porcine intestinal gut as well as regional differences in the in. ammatory response to S. typhimurium infection. Taken together, these data should provide a basis for a complete understanding of the porcine intestinal response to bacterial infection.
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