| Literature DB >> 31630178 |
Ichiro Takahashi1,2, Koji Hosomi2, Takahiro Nagatake2, Hirokazu Toubou1, Daiki Yamamoto1, Ikue Hayashi1, Yosuke Kurashima3, Shintaro Sato3, Naoko Shibata3, Yoshiyuki Goto3, Fumito Maruyama4, Ichiro Nakagawa4, Asaomi Kuwae5, Akio Abe5, Jun Kunisawa2,3,6,7, Hiroshi Kiyono3.
Abstract
Accumulating evidence has revealed that lymphoid tissue-resident commensal bacteria (e.g. Alcaligenes spp.) survive within dendritic cells. We extended our previous study by investigating microbes that persistently colonize colonic macrophages. 16S rRNA-based metagenome analysis using DNA purified from murine colonic macrophages revealed the presence of Stenotrophomonas maltophilia. The in situ intracellular colonization by S. maltophilia was recapitulated in vitro by using bone marrow-derived macrophages (BMDMs). Co-culture of BMDMs with clinically isolated S. maltophilia led to increased mitochondrial respiration and robust IL-10 production. We further identified a 25-kDa protein encoded by the gene assigned as smlt2713 (recently renamed as SMLT_RS12935) and secreted by S. maltophilia as the factor responsible for enhanced IL-10 production by BMDMs. IL-10 production is critical for maintenance of the symbiotic condition, because intracellular colonization by S. maltophilia was impaired in IL-10-deficient BMDMs, and smlt2713-deficient S. maltophilia failed to persistently colonize IL-10-competent BMDMs. These findings indicate a novel commensal network between colonic macrophages and S. maltophilia that is mediated by IL-10 and smlt2713.Entities:
Keywords: IL-10; colitis; gut-resident macrophage; intracellular commensal bacteria; symbiotic factor smlt2713
Year: 2020 PMID: 31630178 DOI: 10.1093/intimm/dxz071
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823