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The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model

Newborns are colonized by maternal microbiota that is essential for offspring health and development. The composition of these pioneer communities exhibits individual differences, but the importance of this early-life heterogeneity to health outcomes is not understood. Here we validate a human micro...

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Autores principales: Jašarević, Eldin, Hill, Elizabeth M., Kane, Patrick J., Rutt, Lindsay, Gyles, Trevonn, Folts, Lillian, Rock, Kylie D., Howard, Christopher D., Morrison, Kathleen E., Ravel, Jacques, Bale, Tracy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560944/
https://www.ncbi.nlm.nih.gov/pubmed/34725359
http://dx.doi.org/10.1038/s41467-021-26634-9
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author Jašarević, Eldin
Hill, Elizabeth M.
Kane, Patrick J.
Rutt, Lindsay
Gyles, Trevonn
Folts, Lillian
Rock, Kylie D.
Howard, Christopher D.
Morrison, Kathleen E.
Ravel, Jacques
Bale, Tracy L.
author_facet Jašarević, Eldin
Hill, Elizabeth M.
Kane, Patrick J.
Rutt, Lindsay
Gyles, Trevonn
Folts, Lillian
Rock, Kylie D.
Howard, Christopher D.
Morrison, Kathleen E.
Ravel, Jacques
Bale, Tracy L.
author_sort Jašarević, Eldin
collection PubMed
description Newborns are colonized by maternal microbiota that is essential for offspring health and development. The composition of these pioneer communities exhibits individual differences, but the importance of this early-life heterogeneity to health outcomes is not understood. Here we validate a human microbiota-associated model in which fetal mice are cesarean delivered and gavaged with defined human vaginal microbial communities. This model replicates the inoculation that occurs during vaginal birth and reveals lasting effects on offspring metabolism, immunity, and the brain in a community-specific manner. This microbial effect is amplified by prior gestation in a maternal obesogenic or vaginal dysbiotic environment where placental and fetal ileum development are altered, and an augmented immune response increases rates of offspring mortality. Collectively, we describe a translationally relevant model to examine the defined role of specific human microbial communities on offspring health outcomes, and demonstrate that the prenatal environment dramatically shapes the postnatal response to inoculation.
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spelling pubmed-85609442021-11-15 The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model Jašarević, Eldin Hill, Elizabeth M. Kane, Patrick J. Rutt, Lindsay Gyles, Trevonn Folts, Lillian Rock, Kylie D. Howard, Christopher D. Morrison, Kathleen E. Ravel, Jacques Bale, Tracy L. Nat Commun Article Newborns are colonized by maternal microbiota that is essential for offspring health and development. The composition of these pioneer communities exhibits individual differences, but the importance of this early-life heterogeneity to health outcomes is not understood. Here we validate a human microbiota-associated model in which fetal mice are cesarean delivered and gavaged with defined human vaginal microbial communities. This model replicates the inoculation that occurs during vaginal birth and reveals lasting effects on offspring metabolism, immunity, and the brain in a community-specific manner. This microbial effect is amplified by prior gestation in a maternal obesogenic or vaginal dysbiotic environment where placental and fetal ileum development are altered, and an augmented immune response increases rates of offspring mortality. Collectively, we describe a translationally relevant model to examine the defined role of specific human microbial communities on offspring health outcomes, and demonstrate that the prenatal environment dramatically shapes the postnatal response to inoculation. Nature Publishing Group UK 2021-11-01 /pmc/articles/PMC8560944/ /pubmed/34725359 http://dx.doi.org/10.1038/s41467-021-26634-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jašarević, Eldin
Hill, Elizabeth M.
Kane, Patrick J.
Rutt, Lindsay
Gyles, Trevonn
Folts, Lillian
Rock, Kylie D.
Howard, Christopher D.
Morrison, Kathleen E.
Ravel, Jacques
Bale, Tracy L.
The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model
title The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model
title_full The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model
title_fullStr The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model
title_full_unstemmed The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model
title_short The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model
title_sort composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560944/
https://www.ncbi.nlm.nih.gov/pubmed/34725359
http://dx.doi.org/10.1038/s41467-021-26634-9
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