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Transfer of oral bacteria to the fetus during late gestation
The fetus develops in a privileged environment, as the placenta serves as both a gateway for nutrients and a barrier for pathogen transfer to the fetus. Regardless, recent evidence suggests the presence of bacterial DNA in both placenta and fetus, and we have reported that DNA and protein from small...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804304/ https://www.ncbi.nlm.nih.gov/pubmed/33436911 http://dx.doi.org/10.1038/s41598-020-80653-y |
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author | Yu, Kevin Rodriguez, Michelle Paul, Zubin Gordon, Elizabeth Gu, Tongjun Rice, Kelly Triplett, Eric W. Keller-Wood, Maureen Wood, Charles E. |
author_facet | Yu, Kevin Rodriguez, Michelle Paul, Zubin Gordon, Elizabeth Gu, Tongjun Rice, Kelly Triplett, Eric W. Keller-Wood, Maureen Wood, Charles E. |
author_sort | Yu, Kevin |
collection | PubMed |
description | The fetus develops in a privileged environment, as the placenta serves as both a gateway for nutrients and a barrier for pathogen transfer to the fetus. Regardless, recent evidence suggests the presence of bacterial DNA in both placenta and fetus, and we have reported that DNA and protein from small numbers of bacteria gain access to the fetus from the maternal bloodstream. Other routes of environmental bacterial transfer from the mother to fetus remain unknown, as well as the physiological relevance of their presence. In these experiments, we examine multiple routes by which bacterial cellular components can enter the fetus and the fetal response to influx of bacterial DNA and protein. We inoculated maternal sheep with genetically-labeled S. aureus (Staphylococcus aureus) using three routes: intravenously, orally, and intra-vaginally. The inoculum did not produce sepsis or fever in the ewes, therefore mimicking incidental exposure to bacteria during pregnancy. 3–5 days post inoculation, we assessed the presence of bacterial components in the fetal tissues and analyzed fetal brain tissue to identify any alterations in gene expression. Our results demonstrate that components of bacteria that were introduced into the maternal mouth were detected in the fetal brain and that they stimulated changes in gene expression. We conclude that an oral route of transmission is relevant for transfer of bacterial cellular components to the fetus. |
format | Online Article Text |
id | pubmed-7804304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78043042021-01-13 Transfer of oral bacteria to the fetus during late gestation Yu, Kevin Rodriguez, Michelle Paul, Zubin Gordon, Elizabeth Gu, Tongjun Rice, Kelly Triplett, Eric W. Keller-Wood, Maureen Wood, Charles E. Sci Rep Article The fetus develops in a privileged environment, as the placenta serves as both a gateway for nutrients and a barrier for pathogen transfer to the fetus. Regardless, recent evidence suggests the presence of bacterial DNA in both placenta and fetus, and we have reported that DNA and protein from small numbers of bacteria gain access to the fetus from the maternal bloodstream. Other routes of environmental bacterial transfer from the mother to fetus remain unknown, as well as the physiological relevance of their presence. In these experiments, we examine multiple routes by which bacterial cellular components can enter the fetus and the fetal response to influx of bacterial DNA and protein. We inoculated maternal sheep with genetically-labeled S. aureus (Staphylococcus aureus) using three routes: intravenously, orally, and intra-vaginally. The inoculum did not produce sepsis or fever in the ewes, therefore mimicking incidental exposure to bacteria during pregnancy. 3–5 days post inoculation, we assessed the presence of bacterial components in the fetal tissues and analyzed fetal brain tissue to identify any alterations in gene expression. Our results demonstrate that components of bacteria that were introduced into the maternal mouth were detected in the fetal brain and that they stimulated changes in gene expression. We conclude that an oral route of transmission is relevant for transfer of bacterial cellular components to the fetus. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804304/ /pubmed/33436911 http://dx.doi.org/10.1038/s41598-020-80653-y Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yu, Kevin Rodriguez, Michelle Paul, Zubin Gordon, Elizabeth Gu, Tongjun Rice, Kelly Triplett, Eric W. Keller-Wood, Maureen Wood, Charles E. Transfer of oral bacteria to the fetus during late gestation |
title | Transfer of oral bacteria to the fetus during late gestation |
title_full | Transfer of oral bacteria to the fetus during late gestation |
title_fullStr | Transfer of oral bacteria to the fetus during late gestation |
title_full_unstemmed | Transfer of oral bacteria to the fetus during late gestation |
title_short | Transfer of oral bacteria to the fetus during late gestation |
title_sort | transfer of oral bacteria to the fetus during late gestation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804304/ https://www.ncbi.nlm.nih.gov/pubmed/33436911 http://dx.doi.org/10.1038/s41598-020-80653-y |
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