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Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner
The microbiome is a regulator of host immunity, metabolism, neurodevelopment, and behavior. During early life, bacterial communities within maternal gut and vaginal compartments can have an impact on directing these processes. Maternal stress experience during pregnancy may impact offspring developm...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339804/ https://www.ncbi.nlm.nih.gov/pubmed/28266645 http://dx.doi.org/10.1038/srep44182 |
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author | Jašarević, Eldin Howard, Christopher D. Misic, Ana M. Beiting, Daniel P. Bale, Tracy L. |
author_facet | Jašarević, Eldin Howard, Christopher D. Misic, Ana M. Beiting, Daniel P. Bale, Tracy L. |
author_sort | Jašarević, Eldin |
collection | PubMed |
description | The microbiome is a regulator of host immunity, metabolism, neurodevelopment, and behavior. During early life, bacterial communities within maternal gut and vaginal compartments can have an impact on directing these processes. Maternal stress experience during pregnancy may impact offspring development by altering the temporal and spatial dynamics of the maternal microbiome during pregnancy. To examine the hypothesis that maternal stress disrupts gut and vaginal microbial dynamics during critical prenatal and postnatal windows, we used high-resolution 16S rRNA marker gene sequencing to examine outcomes in our mouse model of early prenatal stress. Consistent with predictions, maternal fecal communities shift across pregnancy, a process that is disrupted by stress. Vaginal bacterial community structure and composition exhibit lasting disruption following stress exposure. Comparison of maternal and offspring microbiota revealed that similarities in bacterial community composition was predicted by a complex interaction between maternal body niche and offspring age and sex. Importantly, early prenatal stress influenced offspring bacterial community assembly in a temporal and sex-specific manner. Taken together, our results demonstrate that early prenatal stress may influence offspring development through converging modifications to gut microbial composition during pregnancy and transmission of dysbiotic vaginal microbiome at birth. |
format | Online Article Text |
id | pubmed-5339804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53398042017-03-10 Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner Jašarević, Eldin Howard, Christopher D. Misic, Ana M. Beiting, Daniel P. Bale, Tracy L. Sci Rep Article The microbiome is a regulator of host immunity, metabolism, neurodevelopment, and behavior. During early life, bacterial communities within maternal gut and vaginal compartments can have an impact on directing these processes. Maternal stress experience during pregnancy may impact offspring development by altering the temporal and spatial dynamics of the maternal microbiome during pregnancy. To examine the hypothesis that maternal stress disrupts gut and vaginal microbial dynamics during critical prenatal and postnatal windows, we used high-resolution 16S rRNA marker gene sequencing to examine outcomes in our mouse model of early prenatal stress. Consistent with predictions, maternal fecal communities shift across pregnancy, a process that is disrupted by stress. Vaginal bacterial community structure and composition exhibit lasting disruption following stress exposure. Comparison of maternal and offspring microbiota revealed that similarities in bacterial community composition was predicted by a complex interaction between maternal body niche and offspring age and sex. Importantly, early prenatal stress influenced offspring bacterial community assembly in a temporal and sex-specific manner. Taken together, our results demonstrate that early prenatal stress may influence offspring development through converging modifications to gut microbial composition during pregnancy and transmission of dysbiotic vaginal microbiome at birth. Nature Publishing Group 2017-03-07 /pmc/articles/PMC5339804/ /pubmed/28266645 http://dx.doi.org/10.1038/srep44182 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jašarević, Eldin Howard, Christopher D. Misic, Ana M. Beiting, Daniel P. Bale, Tracy L. Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner |
title | Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner |
title_full | Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner |
title_fullStr | Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner |
title_full_unstemmed | Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner |
title_short | Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner |
title_sort | stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339804/ https://www.ncbi.nlm.nih.gov/pubmed/28266645 http://dx.doi.org/10.1038/srep44182 |
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