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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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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. |
format | Online Article Text |
id | pubmed-6080902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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