Cargando…
Maternal diet and gut microbiome composition modulate early‐life immune development
In early life, the intestinal mucosa and immune system undergo a critical developmental process to contain the expanding gut microbiome while promoting tolerance toward commensals, yet the influence of maternal diet and microbial composition on offspring immune maturation remains poorly understood....
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405054/ https://www.ncbi.nlm.nih.gov/pubmed/37278126 http://dx.doi.org/10.15252/emmm.202217241 |
_version_ | 1785085438294228992 |
---|---|
author | Grant, Erica T Boudaud, Marie Muller, Arnaud Macpherson, Andrew J Desai, Mahesh S |
author_facet | Grant, Erica T Boudaud, Marie Muller, Arnaud Macpherson, Andrew J Desai, Mahesh S |
author_sort | Grant, Erica T |
collection | PubMed |
description | In early life, the intestinal mucosa and immune system undergo a critical developmental process to contain the expanding gut microbiome while promoting tolerance toward commensals, yet the influence of maternal diet and microbial composition on offspring immune maturation remains poorly understood. We colonized germ‐free mice with a consortium of 14 strains, fed them a standard fiber‐rich chow or a fiber‐free diet, and then longitudinally assessed offspring development during the weaning period. Unlike pups born to dams fed the fiber‐rich diet, pups of fiber‐deprived dams demonstrated delayed colonization with Akkermansia muciniphila, a mucin‐foraging bacterium that can also use milk oligosaccharides. The pups of fiber‐deprived dams exhibited an enrichment of colonic transcripts corresponding to defense response pathways and a peak in Il22 expression at weaning. Removal of A. muciniphila from the community, but maintenance on the fiber‐rich diet, was associated with reduced proportions of RORγt‐positive innate and adaptive immune cell subsets. Our results highlight the potent influence of maternal dietary fiber intake and discrete changes in microbial composition on the postnatal microbiome assemblage and early immune development. |
format | Online Article Text |
id | pubmed-10405054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104050542023-08-08 Maternal diet and gut microbiome composition modulate early‐life immune development Grant, Erica T Boudaud, Marie Muller, Arnaud Macpherson, Andrew J Desai, Mahesh S EMBO Mol Med Articles In early life, the intestinal mucosa and immune system undergo a critical developmental process to contain the expanding gut microbiome while promoting tolerance toward commensals, yet the influence of maternal diet and microbial composition on offspring immune maturation remains poorly understood. We colonized germ‐free mice with a consortium of 14 strains, fed them a standard fiber‐rich chow or a fiber‐free diet, and then longitudinally assessed offspring development during the weaning period. Unlike pups born to dams fed the fiber‐rich diet, pups of fiber‐deprived dams demonstrated delayed colonization with Akkermansia muciniphila, a mucin‐foraging bacterium that can also use milk oligosaccharides. The pups of fiber‐deprived dams exhibited an enrichment of colonic transcripts corresponding to defense response pathways and a peak in Il22 expression at weaning. Removal of A. muciniphila from the community, but maintenance on the fiber‐rich diet, was associated with reduced proportions of RORγt‐positive innate and adaptive immune cell subsets. Our results highlight the potent influence of maternal dietary fiber intake and discrete changes in microbial composition on the postnatal microbiome assemblage and early immune development. John Wiley and Sons Inc. 2023-06-06 /pmc/articles/PMC10405054/ /pubmed/37278126 http://dx.doi.org/10.15252/emmm.202217241 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Grant, Erica T Boudaud, Marie Muller, Arnaud Macpherson, Andrew J Desai, Mahesh S Maternal diet and gut microbiome composition modulate early‐life immune development |
title | Maternal diet and gut microbiome composition modulate early‐life immune development |
title_full | Maternal diet and gut microbiome composition modulate early‐life immune development |
title_fullStr | Maternal diet and gut microbiome composition modulate early‐life immune development |
title_full_unstemmed | Maternal diet and gut microbiome composition modulate early‐life immune development |
title_short | Maternal diet and gut microbiome composition modulate early‐life immune development |
title_sort | maternal diet and gut microbiome composition modulate early‐life immune development |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405054/ https://www.ncbi.nlm.nih.gov/pubmed/37278126 http://dx.doi.org/10.15252/emmm.202217241 |
work_keys_str_mv | AT grantericat maternaldietandgutmicrobiomecompositionmodulateearlylifeimmunedevelopment AT boudaudmarie maternaldietandgutmicrobiomecompositionmodulateearlylifeimmunedevelopment AT mullerarnaud maternaldietandgutmicrobiomecompositionmodulateearlylifeimmunedevelopment AT macphersonandrewj maternaldietandgutmicrobiomecompositionmodulateearlylifeimmunedevelopment AT desaimaheshs maternaldietandgutmicrobiomecompositionmodulateearlylifeimmunedevelopment |