Transcriptional analysis of porcine intestinal mucosa infected with Salmonella Typhimurium revealed a massive inflammatory response and disruption of bile acid absorption in ileum

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Author
Herrera Uribe, Juber
Collado-Romero, Melania
Zaldívar-López, Sara
Arce Jiménez, Cristina
Bautista, Rocío
Carvajal, Ana
Cirera, Susanna
Gonzalo Claros, M.
Garrido, Juan J.
Publisher
Biomed CentralDate
2016Subject
SalmonellosisInfected pork meat
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Infected pork meat is an important source of non-typhoidal human salmonellosis. Understanding of molecular
mechanisms involved in disease pathogenesis is important for the development of therapeutic and preventive strategies.
Thus, hereby we study the transcriptional profiles along the porcine intestine during infection with Salmonella
Typhimurium, as well as post-transcriptional gene modulation by microRNAs (miRNA). Sixteen piglets were orally challenged
with S. Typhimurium. Samples from jejunum, ileum and colon, collected 1, 2 and 6 days post infection (dpi)
were hybridized to mRNA and miRNA expression microarrays and analyzed. Jejunum showed a reduced transcriptional
response indicating mild inflammation only at 2 dpi. In ileum inflammatory genes were overexpressed (e.g.,
IL-1B, IL-6, IL-8, IL1RAP, TNFα), indicating a strong immune response at all times of infection. Infection also down-regulated
genes of the FXR pathway (e.g., NR1H4, FABP6, APOA1, SLC10A2), indicating disruption of the bile acid absorption
in ileum. This result was confirmed by decreased high-density lipoprotein cholesterol in serum of infected pigs. Ileal
inflammatory gene expression changes peaked at 2 dpi and tended to resolve at 6 dpi. Furthermore, miRNA analysis
of ileum at 2 dpi revealed 62 miRNAs potentially regulating target genes involved in this inflammatory process (e.g.,
miR-374 and miR-451). In colon, genes involved in epithelial adherence, proliferation and cellular reorganization were
down-regulated at 2 and 6 dpi. In summary, here we show the transcriptional changes occurring at the intestine
at different time points of the infection, which are mainly related to inflammation and disruption of the bile acid
metabolism.
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