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Maternal gut microbiome regulates immunity to RSV infection in offspring
Development of the immune system can be influenced by diverse extrinsic and intrinsic factors that influence the risk of disease. Severe early life respiratory syncytial virus (RSV) infection is associated with persistent immune alterations. Previously, our group had shown that adult mice orally sup...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500238/ https://www.ncbi.nlm.nih.gov/pubmed/34613328 http://dx.doi.org/10.1084/jem.20210235 |
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author | Fonseca, Wendy Malinczak, Carrie-Anne Fujimura, Kei Li, Danny McCauley, Kathryn Li, Jia Best, Shannon K.K. Zhu, Diana Rasky, Andrew J. Johnson, Christine C. Bermick, Jennifer Zoratti, Edward M. Ownby, Dennis Lynch, Susan V. Lukacs, Nicholas W. Ptaschinski, Catherine |
author_facet | Fonseca, Wendy Malinczak, Carrie-Anne Fujimura, Kei Li, Danny McCauley, Kathryn Li, Jia Best, Shannon K.K. Zhu, Diana Rasky, Andrew J. Johnson, Christine C. Bermick, Jennifer Zoratti, Edward M. Ownby, Dennis Lynch, Susan V. Lukacs, Nicholas W. Ptaschinski, Catherine |
author_sort | Fonseca, Wendy |
collection | PubMed |
description | Development of the immune system can be influenced by diverse extrinsic and intrinsic factors that influence the risk of disease. Severe early life respiratory syncytial virus (RSV) infection is associated with persistent immune alterations. Previously, our group had shown that adult mice orally supplemented with Lactobacillus johnsonii exhibited decreased airway immunopathology following RSV infection. Here, we demonstrate that offspring of mice supplemented with L. johnsonii exhibit reduced airway mucus and Th2 cell–mediated response to RSV infection. Maternal supplementation resulted in a consistent gut microbiome in mothers and their offspring. Importantly, supplemented maternal plasma and breastmilk, and offspring plasma, exhibited decreased inflammatory metabolites. Cross-fostering studies showed that prenatal Lactobacillus exposure led to decreased Th2 cytokines and lung inflammation following RSV infection, while postnatal Lactobacillus exposure diminished goblet cell hypertrophy and mucus production in the lung in response to airway infection. These studies demonstrate that Lactobacillus modulation of the maternal microbiome and associated metabolic reprogramming enhance airway protection against RSV in neonates. |
format | Online Article Text |
id | pubmed-8500238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85002382022-05-01 Maternal gut microbiome regulates immunity to RSV infection in offspring Fonseca, Wendy Malinczak, Carrie-Anne Fujimura, Kei Li, Danny McCauley, Kathryn Li, Jia Best, Shannon K.K. Zhu, Diana Rasky, Andrew J. Johnson, Christine C. Bermick, Jennifer Zoratti, Edward M. Ownby, Dennis Lynch, Susan V. Lukacs, Nicholas W. Ptaschinski, Catherine J Exp Med Brief Definitive Report Development of the immune system can be influenced by diverse extrinsic and intrinsic factors that influence the risk of disease. Severe early life respiratory syncytial virus (RSV) infection is associated with persistent immune alterations. Previously, our group had shown that adult mice orally supplemented with Lactobacillus johnsonii exhibited decreased airway immunopathology following RSV infection. Here, we demonstrate that offspring of mice supplemented with L. johnsonii exhibit reduced airway mucus and Th2 cell–mediated response to RSV infection. Maternal supplementation resulted in a consistent gut microbiome in mothers and their offspring. Importantly, supplemented maternal plasma and breastmilk, and offspring plasma, exhibited decreased inflammatory metabolites. Cross-fostering studies showed that prenatal Lactobacillus exposure led to decreased Th2 cytokines and lung inflammation following RSV infection, while postnatal Lactobacillus exposure diminished goblet cell hypertrophy and mucus production in the lung in response to airway infection. These studies demonstrate that Lactobacillus modulation of the maternal microbiome and associated metabolic reprogramming enhance airway protection against RSV in neonates. Rockefeller University Press 2021-10-06 /pmc/articles/PMC8500238/ /pubmed/34613328 http://dx.doi.org/10.1084/jem.20210235 Text en © 2021 Fonseca et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Brief Definitive Report Fonseca, Wendy Malinczak, Carrie-Anne Fujimura, Kei Li, Danny McCauley, Kathryn Li, Jia Best, Shannon K.K. Zhu, Diana Rasky, Andrew J. Johnson, Christine C. Bermick, Jennifer Zoratti, Edward M. Ownby, Dennis Lynch, Susan V. Lukacs, Nicholas W. Ptaschinski, Catherine Maternal gut microbiome regulates immunity to RSV infection in offspring |
title | Maternal gut microbiome regulates immunity to RSV infection in offspring |
title_full | Maternal gut microbiome regulates immunity to RSV infection in offspring |
title_fullStr | Maternal gut microbiome regulates immunity to RSV infection in offspring |
title_full_unstemmed | Maternal gut microbiome regulates immunity to RSV infection in offspring |
title_short | Maternal gut microbiome regulates immunity to RSV infection in offspring |
title_sort | maternal gut microbiome regulates immunity to rsv infection in offspring |
topic | Brief Definitive Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500238/ https://www.ncbi.nlm.nih.gov/pubmed/34613328 http://dx.doi.org/10.1084/jem.20210235 |
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