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Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice
The gut microbiota plays a central role in regulating host metabolism. While substantial progress has been made in discerning how the microbiota influences host functions post birth and beyond, little is known about how key members of the maternal gut microbiota can influence feto-placental growth....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236968/ https://www.ncbi.nlm.nih.gov/pubmed/35760917 http://dx.doi.org/10.1007/s00018-022-04379-y |
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author | Lopez-Tello, Jorge Schofield, Zoe Kiu, Raymond Dalby, Matthew J. van Sinderen, Douwe Le Gall, Gwénaëlle Sferruzzi-Perri, Amanda N. Hall, Lindsay J. |
author_facet | Lopez-Tello, Jorge Schofield, Zoe Kiu, Raymond Dalby, Matthew J. van Sinderen, Douwe Le Gall, Gwénaëlle Sferruzzi-Perri, Amanda N. Hall, Lindsay J. |
author_sort | Lopez-Tello, Jorge |
collection | PubMed |
description | The gut microbiota plays a central role in regulating host metabolism. While substantial progress has been made in discerning how the microbiota influences host functions post birth and beyond, little is known about how key members of the maternal gut microbiota can influence feto-placental growth. Notably, in pregnant women, Bifidobacterium represents a key beneficial microbiota genus, with levels observed to increase across pregnancy. Here, using germ-free and specific-pathogen-free mice, we demonstrate that the bacterium Bifidobacterium breve UCC2003 modulates maternal body adaptations, placental structure and nutrient transporter capacity, with implications for fetal metabolism and growth. Maternal and placental metabolome were affected by maternal gut microbiota (i.e. acetate, formate and carnitine). Histological analysis of the placenta confirmed that Bifidobacterium modifies placental structure via changes in Igf2P0, Dlk1, Mapk1 and Mapk14 expression. Additionally, B. breve UCC2003, acting through Slc2a1 and Fatp1-4 transporters, was shown to restore fetal glycaemia and fetal growth in association with changes in the fetal hepatic transcriptome. Our work emphasizes the importance of the maternal gut microbiota on feto-placental development and sets a foundation for future research towards the use of probiotics during pregnancy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04379-y. |
format | Online Article Text |
id | pubmed-9236968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-92369682022-06-29 Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice Lopez-Tello, Jorge Schofield, Zoe Kiu, Raymond Dalby, Matthew J. van Sinderen, Douwe Le Gall, Gwénaëlle Sferruzzi-Perri, Amanda N. Hall, Lindsay J. Cell Mol Life Sci Original Article The gut microbiota plays a central role in regulating host metabolism. While substantial progress has been made in discerning how the microbiota influences host functions post birth and beyond, little is known about how key members of the maternal gut microbiota can influence feto-placental growth. Notably, in pregnant women, Bifidobacterium represents a key beneficial microbiota genus, with levels observed to increase across pregnancy. Here, using germ-free and specific-pathogen-free mice, we demonstrate that the bacterium Bifidobacterium breve UCC2003 modulates maternal body adaptations, placental structure and nutrient transporter capacity, with implications for fetal metabolism and growth. Maternal and placental metabolome were affected by maternal gut microbiota (i.e. acetate, formate and carnitine). Histological analysis of the placenta confirmed that Bifidobacterium modifies placental structure via changes in Igf2P0, Dlk1, Mapk1 and Mapk14 expression. Additionally, B. breve UCC2003, acting through Slc2a1 and Fatp1-4 transporters, was shown to restore fetal glycaemia and fetal growth in association with changes in the fetal hepatic transcriptome. Our work emphasizes the importance of the maternal gut microbiota on feto-placental development and sets a foundation for future research towards the use of probiotics during pregnancy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04379-y. Springer International Publishing 2022-06-28 2022 /pmc/articles/PMC9236968/ /pubmed/35760917 http://dx.doi.org/10.1007/s00018-022-04379-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Lopez-Tello, Jorge Schofield, Zoe Kiu, Raymond Dalby, Matthew J. van Sinderen, Douwe Le Gall, Gwénaëlle Sferruzzi-Perri, Amanda N. Hall, Lindsay J. Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice |
title | Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice |
title_full | Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice |
title_fullStr | Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice |
title_full_unstemmed | Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice |
title_short | Maternal gut microbiota Bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice |
title_sort | maternal gut microbiota bifidobacterium promotes placental morphogenesis, nutrient transport and fetal growth in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236968/ https://www.ncbi.nlm.nih.gov/pubmed/35760917 http://dx.doi.org/10.1007/s00018-022-04379-y |
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