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Microbial embryonal colonization during pipefish male pregnancy

While originally acquired from the environment, a fraction of the microbiota is transferred from parents to offspring. The immune system shapes the microbial colonization, while commensal microbes may boost host immune defences. Parental transfer of microbes in viviparous animals remains ambiguous,...

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Autores principales: Beemelmanns, Anne, Poirier, Maude, Bayer, Till, Kuenzel, Sven, Roth, Olivia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327025/
https://www.ncbi.nlm.nih.gov/pubmed/30626884
http://dx.doi.org/10.1038/s41598-018-37026-3
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author Beemelmanns, Anne
Poirier, Maude
Bayer, Till
Kuenzel, Sven
Roth, Olivia
author_facet Beemelmanns, Anne
Poirier, Maude
Bayer, Till
Kuenzel, Sven
Roth, Olivia
author_sort Beemelmanns, Anne
collection PubMed
description While originally acquired from the environment, a fraction of the microbiota is transferred from parents to offspring. The immune system shapes the microbial colonization, while commensal microbes may boost host immune defences. Parental transfer of microbes in viviparous animals remains ambiguous, as the two transfer routes (transovarial vs. pregnancy) are intermingled within the maternal body. Pipefishes and seahorses (syngnathids) are ideally suited to disentangle transovarial microbial transfer from a contribution during pregnancy due to their maternal egg production and their unique male pregnancy. We assessed the persistency and the changes in the microbial communities of the maternal and paternal reproductive tracts over proceeding male pregnancy by sequencing microbial 16S rRNA genes of swabs from maternal gonads and brood pouches of non-pregnant and pregnant fathers. Applying parental immunological activation with heat-killed bacteria, we evaluated the impact of parental immunological status on microbial development. Our data indicate that maternal gonads and paternal brood pouches harbor distinct microbial communities, which could affect embryonal development in a sex-specific manner. Upon activation of the immune system, a shift of the microbial community was observed. The activation of the immune system induced the expansion of microbiota richness during late pregnancy, which corresponds to the time point of larval mouth opening, when initial microbial colonization must take place.
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spelling pubmed-63270252019-01-11 Microbial embryonal colonization during pipefish male pregnancy Beemelmanns, Anne Poirier, Maude Bayer, Till Kuenzel, Sven Roth, Olivia Sci Rep Article While originally acquired from the environment, a fraction of the microbiota is transferred from parents to offspring. The immune system shapes the microbial colonization, while commensal microbes may boost host immune defences. Parental transfer of microbes in viviparous animals remains ambiguous, as the two transfer routes (transovarial vs. pregnancy) are intermingled within the maternal body. Pipefishes and seahorses (syngnathids) are ideally suited to disentangle transovarial microbial transfer from a contribution during pregnancy due to their maternal egg production and their unique male pregnancy. We assessed the persistency and the changes in the microbial communities of the maternal and paternal reproductive tracts over proceeding male pregnancy by sequencing microbial 16S rRNA genes of swabs from maternal gonads and brood pouches of non-pregnant and pregnant fathers. Applying parental immunological activation with heat-killed bacteria, we evaluated the impact of parental immunological status on microbial development. Our data indicate that maternal gonads and paternal brood pouches harbor distinct microbial communities, which could affect embryonal development in a sex-specific manner. Upon activation of the immune system, a shift of the microbial community was observed. The activation of the immune system induced the expansion of microbiota richness during late pregnancy, which corresponds to the time point of larval mouth opening, when initial microbial colonization must take place. Nature Publishing Group UK 2019-01-09 /pmc/articles/PMC6327025/ /pubmed/30626884 http://dx.doi.org/10.1038/s41598-018-37026-3 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Beemelmanns, Anne
Poirier, Maude
Bayer, Till
Kuenzel, Sven
Roth, Olivia
Microbial embryonal colonization during pipefish male pregnancy
title Microbial embryonal colonization during pipefish male pregnancy
title_full Microbial embryonal colonization during pipefish male pregnancy
title_fullStr Microbial embryonal colonization during pipefish male pregnancy
title_full_unstemmed Microbial embryonal colonization during pipefish male pregnancy
title_short Microbial embryonal colonization during pipefish male pregnancy
title_sort microbial embryonal colonization during pipefish male pregnancy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327025/
https://www.ncbi.nlm.nih.gov/pubmed/30626884
http://dx.doi.org/10.1038/s41598-018-37026-3
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