| Literature DB >> 27716507 |
Aleksey Chudnovskiy1, Arthur Mortha1, Veronika Kana1, Andrea Kennard2, Juan David Ramirez3, Adeeb Rahman4, Romain Remark1, Ilaria Mogno5, Ruby Ng6, Sasha Gnjatic7, El-Ad David Amir1, Alexander Solovyov8, Benjamin Greenbaum8, Jose Clemente4, Jeremiah Faith4, Yasmine Belkaid9, Michael E Grigg2, Miriam Merad10.
Abstract
While conventional pathogenic protists have been extensively studied, there is an underappreciated constitutive protist microbiota that is an integral part of the vertebrate microbiome. The impact of these species on the host and their potential contributions to mucosal immune homeostasis remain poorly studied. Here, we show that the protozoan Tritrichomonas musculis activates the host epithelial inflammasome to induce IL-18 release. Epithelial-derived IL-18 promotes dendritic cell-driven Th1 and Th17 immunity and confers dramatic protection from mucosal bacterial infections. Along with its role as a "protistic" antibiotic, colonization with T. musculis exacerbates the development of T-cell-driven colitis and sporadic colorectal tumors. Our findings demonstrate a novel mutualistic host-protozoan interaction that increases mucosal host defenses at the cost of an increased risk of inflammatory disease.Entities:
Keywords: IL-18; IL-1b; Tritrichomonas musculis; colon cancer; commensal protist; gut dendritic cells; gut macrophages; inflammasome; intestinal bacterial infection; microbiome
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Year: 2016 PMID: 27716507 PMCID: PMC5129837 DOI: 10.1016/j.cell.2016.08.076
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582