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Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis

As metagenomic approaches for detecting infectious agents have improved, each tissue that was once thought to be sterile has been found to harbor a variety of microorganisms. Controversy still exists over the status of amniotic fluid, which is part of an immunologically privileged zone that is requi...

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Autores principales: Wang, HanChen, Yang, Gui Xiang, Hu, Yuxiang, Lam, Patricia, Sangha, Karan, Siciliano, Dawn, Swenerton, Anne, Miller, Ruth, Tilley, Peter, Von Dadelszen, Peter, Kalyan, Shirin, Tang, Patrick, Patel, Millan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046152/
https://www.ncbi.nlm.nih.gov/pubmed/35477737
http://dx.doi.org/10.1038/s41598-022-10869-7
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author Wang, HanChen
Yang, Gui Xiang
Hu, Yuxiang
Lam, Patricia
Sangha, Karan
Siciliano, Dawn
Swenerton, Anne
Miller, Ruth
Tilley, Peter
Von Dadelszen, Peter
Kalyan, Shirin
Tang, Patrick
Patel, Millan S.
author_facet Wang, HanChen
Yang, Gui Xiang
Hu, Yuxiang
Lam, Patricia
Sangha, Karan
Siciliano, Dawn
Swenerton, Anne
Miller, Ruth
Tilley, Peter
Von Dadelszen, Peter
Kalyan, Shirin
Tang, Patrick
Patel, Millan S.
author_sort Wang, HanChen
collection PubMed
description As metagenomic approaches for detecting infectious agents have improved, each tissue that was once thought to be sterile has been found to harbor a variety of microorganisms. Controversy still exists over the status of amniotic fluid, which is part of an immunologically privileged zone that is required to prevent maternal immune system rejection of the fetus. Due to this privilege, the exclusion of microbes has been proposed to be mandatory, leading to the sterile womb hypothesis. Since nucleic acid yields from amniotic fluid are very low, contaminating nucleic acid found in water, reagents and the laboratory environment frequently confound attempts to address this hypothesis. Here we present metagenomic criteria for microorganism detection and a metagenomic method able to be performed with small volumes of starting material, while controlling for exogenous contamination, to circumvent these and other pitfalls. We use this method to show that human mid-gestational amniotic fluid has no detectable virome or microbiome, supporting the sterile womb hypothesis.
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spelling pubmed-90461522022-04-29 Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis Wang, HanChen Yang, Gui Xiang Hu, Yuxiang Lam, Patricia Sangha, Karan Siciliano, Dawn Swenerton, Anne Miller, Ruth Tilley, Peter Von Dadelszen, Peter Kalyan, Shirin Tang, Patrick Patel, Millan S. Sci Rep Article As metagenomic approaches for detecting infectious agents have improved, each tissue that was once thought to be sterile has been found to harbor a variety of microorganisms. Controversy still exists over the status of amniotic fluid, which is part of an immunologically privileged zone that is required to prevent maternal immune system rejection of the fetus. Due to this privilege, the exclusion of microbes has been proposed to be mandatory, leading to the sterile womb hypothesis. Since nucleic acid yields from amniotic fluid are very low, contaminating nucleic acid found in water, reagents and the laboratory environment frequently confound attempts to address this hypothesis. Here we present metagenomic criteria for microorganism detection and a metagenomic method able to be performed with small volumes of starting material, while controlling for exogenous contamination, to circumvent these and other pitfalls. We use this method to show that human mid-gestational amniotic fluid has no detectable virome or microbiome, supporting the sterile womb hypothesis. Nature Publishing Group UK 2022-04-27 /pmc/articles/PMC9046152/ /pubmed/35477737 http://dx.doi.org/10.1038/s41598-022-10869-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, HanChen
Yang, Gui Xiang
Hu, Yuxiang
Lam, Patricia
Sangha, Karan
Siciliano, Dawn
Swenerton, Anne
Miller, Ruth
Tilley, Peter
Von Dadelszen, Peter
Kalyan, Shirin
Tang, Patrick
Patel, Millan S.
Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis
title Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis
title_full Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis
title_fullStr Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis
title_full_unstemmed Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis
title_short Comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis
title_sort comprehensive human amniotic fluid metagenomics supports the sterile womb hypothesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046152/
https://www.ncbi.nlm.nih.gov/pubmed/35477737
http://dx.doi.org/10.1038/s41598-022-10869-7
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