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The murine female intestinal microbiota does not shift throughout the estrous cycle
Pregnancy is accompanied by maternal physiological adaptations including metabolic, endocrine, immune, cardiovascular, skeletomuscular and neurological modifications that facilitate fetal and placental growth and development. Emerging evidence suggests that the maternal intestinal microbiota is modi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047814/ https://www.ncbi.nlm.nih.gov/pubmed/30011327 http://dx.doi.org/10.1371/journal.pone.0200729 |
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author | Wallace, Jessica G. Potts, Ryan H. Szamosi, Jake C. Surette, Michael G. Sloboda, Deborah M. |
author_facet | Wallace, Jessica G. Potts, Ryan H. Szamosi, Jake C. Surette, Michael G. Sloboda, Deborah M. |
author_sort | Wallace, Jessica G. |
collection | PubMed |
description | Pregnancy is accompanied by maternal physiological adaptations including metabolic, endocrine, immune, cardiovascular, skeletomuscular and neurological modifications that facilitate fetal and placental growth and development. Emerging evidence suggests that the maternal intestinal microbiota is modified over the course of healthy pregnancy. We have recently identified a maternal intestinal microbial shift within hours of conception; a shift that continued with advancing gestation. It is possible that maternal gut bacterial profiles might be associated with the known endocrine changes that accompany the female reproductive (estrous) cycle. Methods: To determine whether the estrous cycle influenced the shifts in the maternal intestinal microbiota, time-matched fecal pellets were collected daily for 3 consecutive estrous cycles from individually housed, non-pregnant female C57BL/6J mice (n = 10) fed a control diet. Estrous stage was identified by cell type predominance in vaginal cytological samples. The corresponding fecal pellets for each estrous stage were processed for bacterial 16S rRNA sequencing of the variable 3 (V3) region. Results: Estrous cycle stage accounted for a very small and not statistically significant proportion of the variation in the fecal microbiota according to PERMANOVA testing performed on Bray-Curtis dissimilarity scores. These values displayed no significant clustering of fecal microbial communities by estrous stage. Conclusion: The estrous cycle does not result in any significant shift in the intestinal microbial community in the reproductively mature, regularly cycling female mouse. |
format | Online Article Text |
id | pubmed-6047814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60478142018-07-26 The murine female intestinal microbiota does not shift throughout the estrous cycle Wallace, Jessica G. Potts, Ryan H. Szamosi, Jake C. Surette, Michael G. Sloboda, Deborah M. PLoS One Research Article Pregnancy is accompanied by maternal physiological adaptations including metabolic, endocrine, immune, cardiovascular, skeletomuscular and neurological modifications that facilitate fetal and placental growth and development. Emerging evidence suggests that the maternal intestinal microbiota is modified over the course of healthy pregnancy. We have recently identified a maternal intestinal microbial shift within hours of conception; a shift that continued with advancing gestation. It is possible that maternal gut bacterial profiles might be associated with the known endocrine changes that accompany the female reproductive (estrous) cycle. Methods: To determine whether the estrous cycle influenced the shifts in the maternal intestinal microbiota, time-matched fecal pellets were collected daily for 3 consecutive estrous cycles from individually housed, non-pregnant female C57BL/6J mice (n = 10) fed a control diet. Estrous stage was identified by cell type predominance in vaginal cytological samples. The corresponding fecal pellets for each estrous stage were processed for bacterial 16S rRNA sequencing of the variable 3 (V3) region. Results: Estrous cycle stage accounted for a very small and not statistically significant proportion of the variation in the fecal microbiota according to PERMANOVA testing performed on Bray-Curtis dissimilarity scores. These values displayed no significant clustering of fecal microbial communities by estrous stage. Conclusion: The estrous cycle does not result in any significant shift in the intestinal microbial community in the reproductively mature, regularly cycling female mouse. Public Library of Science 2018-07-16 /pmc/articles/PMC6047814/ /pubmed/30011327 http://dx.doi.org/10.1371/journal.pone.0200729 Text en © 2018 Wallace et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wallace, Jessica G. Potts, Ryan H. Szamosi, Jake C. Surette, Michael G. Sloboda, Deborah M. The murine female intestinal microbiota does not shift throughout the estrous cycle |
title | The murine female intestinal microbiota does not shift throughout the estrous cycle |
title_full | The murine female intestinal microbiota does not shift throughout the estrous cycle |
title_fullStr | The murine female intestinal microbiota does not shift throughout the estrous cycle |
title_full_unstemmed | The murine female intestinal microbiota does not shift throughout the estrous cycle |
title_short | The murine female intestinal microbiota does not shift throughout the estrous cycle |
title_sort | murine female intestinal microbiota does not shift throughout the estrous cycle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047814/ https://www.ncbi.nlm.nih.gov/pubmed/30011327 http://dx.doi.org/10.1371/journal.pone.0200729 |
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