IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
Author(s) -
Akira Nakajima,
Alexis Vogelzang,
Mikako Maruya,
Michio Miyajima,
Megumi Murata,
Aoi Son,
Tomomi Kuwahara,
Tatsuaki Tsuruyama,
Satoshi Yamada,
Minoru Matsuura,
Hiroshi Nakase,
Daniel A. Peterson,
Sidonia Fagarasan,
Keiichiro Suzuki
Publication year - 2018
Publication title -
the journal of experimental medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 8.483
H-Index - 448
eISSN - 1540-9538
pISSN - 0022-1007
DOI - 10.1084/jem.20180427
Subject(s) - mucus , bacteroidetes , bacteroides thetaiotaomicron , biology , firmicutes , gut flora , microbiology and biotechnology , bacteria , bacteroides , immunoglobulin a , microbiome , symbiosis , immunology , immune system , immunoglobulin g , genetics , 16s ribosomal rna , ecology
Immunoglobulin A (IgA) promotes health by regulating the composition and function of gut microbiota, but the molecular requirements for such homeostatic IgA function remain unknown. We found that a heavily glycosylated monoclonal IgA recognizing ovalbumin coats Bacteroides thetaiotaomicron ( B. theta ), a prominent gut symbiont of the phylum Bacteroidetes. In vivo, IgA alters the expression of polysaccharide utilization loci (PUL), including a functionally uncharacterized molecular family provisionally named Mucus-Associated Functional Factor (MAFF). In both mice and humans, MAFF is detected predominantly in mucus-resident bacteria, and its expression requires the presence of complex microbiota. Expression of the MAFF system facilitates symbiosis with other members of the phylum Firmicutes and promotes protection from a chemically induced model of colitis. Our data reveal a novel mechanism by which IgA promotes symbiosis and colonic homeostasis.
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