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IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria

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...

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Autores principales: Nakajima, Akira, Vogelzang, Alexis, Maruya, Mikako, Miyajima, Michio, Murata, Megumi, Son, Aoi, Kuwahara, Tomomi, Tsuruyama, Tatsuaki, Yamada, Satoshi, Matsuura, Minoru, Nakase, Hiroshi, Peterson, Daniel A., Fagarasan, Sidonia, Suzuki, Keiichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080902/
https://www.ncbi.nlm.nih.gov/pubmed/30042191
http://dx.doi.org/10.1084/jem.20180427
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author Nakajima, Akira
Vogelzang, Alexis
Maruya, Mikako
Miyajima, Michio
Murata, Megumi
Son, Aoi
Kuwahara, Tomomi
Tsuruyama, Tatsuaki
Yamada, Satoshi
Matsuura, Minoru
Nakase, Hiroshi
Peterson, Daniel A.
Fagarasan, Sidonia
Suzuki, Keiichiro
author_facet Nakajima, Akira
Vogelzang, Alexis
Maruya, Mikako
Miyajima, Michio
Murata, Megumi
Son, Aoi
Kuwahara, Tomomi
Tsuruyama, Tatsuaki
Yamada, Satoshi
Matsuura, Minoru
Nakase, Hiroshi
Peterson, Daniel A.
Fagarasan, Sidonia
Suzuki, Keiichiro
author_sort Nakajima, Akira
collection PubMed
description 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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spelling pubmed-60809022018-08-08 IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria Nakajima, Akira Vogelzang, Alexis Maruya, Mikako Miyajima, Michio Murata, Megumi Son, Aoi Kuwahara, Tomomi Tsuruyama, Tatsuaki Yamada, Satoshi Matsuura, Minoru Nakase, Hiroshi Peterson, Daniel A. Fagarasan, Sidonia Suzuki, Keiichiro J Exp Med Research Articles 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. Rockefeller University Press 2018-08-06 /pmc/articles/PMC6080902/ /pubmed/30042191 http://dx.doi.org/10.1084/jem.20180427 Text en © 2018 Nakajima et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Nakajima, Akira
Vogelzang, Alexis
Maruya, Mikako
Miyajima, Michio
Murata, Megumi
Son, Aoi
Kuwahara, Tomomi
Tsuruyama, Tatsuaki
Yamada, Satoshi
Matsuura, Minoru
Nakase, Hiroshi
Peterson, Daniel A.
Fagarasan, Sidonia
Suzuki, Keiichiro
IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
title IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
title_full IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
title_fullStr IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
title_full_unstemmed IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
title_short IgA regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
title_sort iga regulates the composition and metabolic function of gut microbiota by promoting symbiosis between bacteria
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080902/
https://www.ncbi.nlm.nih.gov/pubmed/30042191
http://dx.doi.org/10.1084/jem.20180427
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