The Commensal Modulates Host Innate Immunity To Promote Oral Colonization.

, isolated from the oral cavity of wild-caught mice, does not colonize most inbred mouse strains. does weakly (50%) colonize C57BL/6J (B6) mice but readily colonizes CAST/EiJ (CAST) mice. In this study, we examined whether differences in the CAST and B6 host response could elucidate mechanisms governing colonization. In vivo stimulation of B6 or CAST splenocytes with wild type (WT) or LPS showed that CAST mice had a blunted inflammatory response, producing significantly lower levels of IL-6 than B6 mice. The use of specific genetic knockouts highlighted a need for an intact innate immune system to prevent colonization. B6-RAG-1 mice were colonized at a similar rate as WT B6 mice, whereas B6-MyD88 and TLR4 mice were readily colonized like CAST (100%) mice. Sequence analysis revealed a unique point mutation in TLR4 in CAST mice. However, crosses to TLR4 mice and analysis of recombinant inbred Collaborative Cross mice showed that TLR4 from CAST mice was not sufficient to allow colonization. In vitro stimulation of B6 bone marrow-derived macrophages or splenocytes with WT yielded low levels of IL-6 compared with LPS stimulation. Surprisingly, UV-inactivated induced high levels of IL-6, suggesting suppression of IL-6 production is an active bacterial process. Consistent with a critical role for IL-6 in preventing colonization, mice deficient for the IL-6 receptor were efficiently colonized, indicating host IL-6 production plays a critical role in determining host colonization susceptibility.