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Host-Protozoan Interactions Protect from Mucosal Infections through Activation of the Inflammasome
Author(s) -
Aleksey Chudnovskiy,
Arthur Mortha,
Veronika Kana,
Andrea Kennard,
Juan David Ramírez,
Adeeb Rahman,
Romain Remark,
Ilaria Mogno,
Ruby Ng,
Sacha Gnjatic,
El-ad David Amir,
Alexander Solovyov,
Benjamin Greenbaum,
José C. Clemente,
Jeremiah J. Faith,
Yasmine Belkaid,
Michael E. Grigg,
Miriam Mérad
Publication year - 2016
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2016.08.076
Subject(s) - biology , inflammasome , host (biology) , microbiology and biotechnology , commensalism , immunity , immunology , microbiome , protist , protozoan infection , immune system , colonisation resistance , inflammation , colonization , bacteria , gene , genetics
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.

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