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Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota
Mammalian gut microbiota are integral to host health. However, how this association began remains unclear. We show that in basal chordates the gut space is radially compartmentalized into a luminal part where food microbes pass and an almost axenic peripheral part, defined by membranous delamination...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109156/ https://www.ncbi.nlm.nih.gov/pubmed/30143642 http://dx.doi.org/10.1038/s41467-018-05884-0 |
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author | Nakashima, Keisuke Kimura, Satoshi Ogawa, Yu Watanabe, Soichi Soma, Satoshi Kaneko, Toyoji Yamada, Lixy Sawada, Hitoshi Tung, Che-Huang Lu, Tsai-Ming Yu, Jr-Kai Villar-Briones, Alejandro Kikuchi, Sakura Satoh, Noriyuki |
author_facet | Nakashima, Keisuke Kimura, Satoshi Ogawa, Yu Watanabe, Soichi Soma, Satoshi Kaneko, Toyoji Yamada, Lixy Sawada, Hitoshi Tung, Che-Huang Lu, Tsai-Ming Yu, Jr-Kai Villar-Briones, Alejandro Kikuchi, Sakura Satoh, Noriyuki |
author_sort | Nakashima, Keisuke |
collection | PubMed |
description | Mammalian gut microbiota are integral to host health. However, how this association began remains unclear. We show that in basal chordates the gut space is radially compartmentalized into a luminal part where food microbes pass and an almost axenic peripheral part, defined by membranous delamination of the gut epithelium. While this membrane, framed with chitin nanofibers, structurally resembles invertebrate peritrophic membranes, proteome supports its affinity to mammalian mucus layers, where gut microbiota colonize. In ray-finned fish, intestines harbor indigenous microbes, but chitinous membranes segregate these luminal microbes from the surrounding mucus layer. These data suggest that chitin-based barrier immunity is an ancient system, the loss of which, at least in mammals, provided mucus layers as a novel niche for microbial colonization. These findings provide a missing link for intestinal immune systems in animals, revealing disparate mucosal environment in model organisms and highlighting the loss of a proven system as innovation. |
format | Online Article Text |
id | pubmed-6109156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61091562018-08-27 Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota Nakashima, Keisuke Kimura, Satoshi Ogawa, Yu Watanabe, Soichi Soma, Satoshi Kaneko, Toyoji Yamada, Lixy Sawada, Hitoshi Tung, Che-Huang Lu, Tsai-Ming Yu, Jr-Kai Villar-Briones, Alejandro Kikuchi, Sakura Satoh, Noriyuki Nat Commun Article Mammalian gut microbiota are integral to host health. However, how this association began remains unclear. We show that in basal chordates the gut space is radially compartmentalized into a luminal part where food microbes pass and an almost axenic peripheral part, defined by membranous delamination of the gut epithelium. While this membrane, framed with chitin nanofibers, structurally resembles invertebrate peritrophic membranes, proteome supports its affinity to mammalian mucus layers, where gut microbiota colonize. In ray-finned fish, intestines harbor indigenous microbes, but chitinous membranes segregate these luminal microbes from the surrounding mucus layer. These data suggest that chitin-based barrier immunity is an ancient system, the loss of which, at least in mammals, provided mucus layers as a novel niche for microbial colonization. These findings provide a missing link for intestinal immune systems in animals, revealing disparate mucosal environment in model organisms and highlighting the loss of a proven system as innovation. Nature Publishing Group UK 2018-08-24 /pmc/articles/PMC6109156/ /pubmed/30143642 http://dx.doi.org/10.1038/s41467-018-05884-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nakashima, Keisuke Kimura, Satoshi Ogawa, Yu Watanabe, Soichi Soma, Satoshi Kaneko, Toyoji Yamada, Lixy Sawada, Hitoshi Tung, Che-Huang Lu, Tsai-Ming Yu, Jr-Kai Villar-Briones, Alejandro Kikuchi, Sakura Satoh, Noriyuki Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota |
title | Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota |
title_full | Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota |
title_fullStr | Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota |
title_full_unstemmed | Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota |
title_short | Chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota |
title_sort | chitin-based barrier immunity and its loss predated mucus-colonization by indigenous gut microbiota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109156/ https://www.ncbi.nlm.nih.gov/pubmed/30143642 http://dx.doi.org/10.1038/s41467-018-05884-0 |
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