Microbiota Composition and Immune Responses During Campylobacter Jejuni Infection in Conventionally Colonized IL-10 -/- Mice Lacking Nucleotide Oligomerization Domain 2.

Host immune responses are pivotal for combating enteropathogenic infections. We here assessed the impact of the innate receptor nucleotide oligomerization domain protein 2 (NOD2) in murine Campylobacter jejuni-infection. Conventionally colonized IL-10(-/-) mice lacking NOD2 and IL-10(-/-) controls were perorally challenged with C. jejuni strain 81-176 and displayed comparable pathogenic colonization of intestines until day 14 postinfection (p. i.). Whereas overall intestinal microbiota compositions were comparable in naive mice, NOD2(-/-)IL-10(-/-) mice exhibited less fecal bifidobacteria and lactobacilli than IL-10(-/-) counterparts after infection. Interestingly, NOD2(-/-)IL-10(-/-) mice were clinically more compromised during the early phase of infection, whereas, conversely, IL-10(-/-) animals exhibited more frequently bloody feces lateron. While colonic apoptotic cell and T lymphocyte numbers were comparable in either C. jejuni-infected mice, B lymphocytes were lower in the colon of infected NOD2(-/-)IL-10(-/-) mice versus controls. At day 14 p.i., colonic TNF and IL-23p19 mRNA levels were upregulated in NOD2(-/-)IL-10(-/-) mice only. Translocation rates of intestinal commensals to mesenteric lymphnodes and extra-intestinal compartments including liver and kidney were comparable, whereas viable bacteria were more frequently detected in spleens derived from IL-10(-/-) as compared to NOD2(-/-)IL-10(-/-) mice. In conclusion, NOD2 is involved during C. jejuni infection in conventionally colonized IL-10(-/-) mice in a time-dependent manner.