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Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation

Studies have shown that fetal immune cell activation may result from potential exposure to microbes, although the presence of microbes in fetus has been a controversial topic. Here, we combined metagenomic and virome techniques to investigate the presence of bacteria and viruses in fetal tissues (sm...

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Autores principales: Liu, Xu, He, Guolin, Lan, Yue, Guo, Weijie, Liu, Xuyuan, Li, Jing, Liu, Anqing, He, Miao, Liu, Xinhui, Fan, Zhenxin, Zhang, Yaoyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850102/
https://www.ncbi.nlm.nih.gov/pubmed/36685560
http://dx.doi.org/10.3389/fimmu.2022.1079294
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author Liu, Xu
He, Guolin
Lan, Yue
Guo, Weijie
Liu, Xuyuan
Li, Jing
Liu, Anqing
He, Miao
Liu, Xinhui
Fan, Zhenxin
Zhang, Yaoyao
author_facet Liu, Xu
He, Guolin
Lan, Yue
Guo, Weijie
Liu, Xuyuan
Li, Jing
Liu, Anqing
He, Miao
Liu, Xinhui
Fan, Zhenxin
Zhang, Yaoyao
author_sort Liu, Xu
collection PubMed
description Studies have shown that fetal immune cell activation may result from potential exposure to microbes, although the presence of microbes in fetus has been a controversial topic. Here, we combined metagenomic and virome techniques to investigate the presence of bacteria and viruses in fetal tissues (small intestine, cecum, and rectum). We found that the fetal gut is not a sterile environment and has a low abundance but metabolically rich microbiome. Specifically, Proteobacteria and Actinobacteria were the dominant bacteria phyla of fetal gut. In total, 700 species viruses were detected, and Human betaherpesvirus 5 was the most abundant eukaryotic viruses. Especially, we first identified Methanobrevibacter smithii in fetal gut. Through the comparison with adults’ gut microbiota we found that Firmicutes and Bacteroidetes gradually became the main force of gut microbiota during the process of growth and development. Interestingly, 6 antibiotic resistance genes were shared by the fetus and adults. Our results indicate the presence of microbes in the fetal gut and demonstrate the diversity of bacteria, archaea and viruses, which provide support for the studies related to early fetal immunity. This study further explores the specific composition of viruses in the fetal gut and the similarities between fetal and adults’ gut microbiota, which is valuable for understanding human fetal immunity development during gestation.
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spelling pubmed-98501022023-01-20 Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation Liu, Xu He, Guolin Lan, Yue Guo, Weijie Liu, Xuyuan Li, Jing Liu, Anqing He, Miao Liu, Xinhui Fan, Zhenxin Zhang, Yaoyao Front Immunol Immunology Studies have shown that fetal immune cell activation may result from potential exposure to microbes, although the presence of microbes in fetus has been a controversial topic. Here, we combined metagenomic and virome techniques to investigate the presence of bacteria and viruses in fetal tissues (small intestine, cecum, and rectum). We found that the fetal gut is not a sterile environment and has a low abundance but metabolically rich microbiome. Specifically, Proteobacteria and Actinobacteria were the dominant bacteria phyla of fetal gut. In total, 700 species viruses were detected, and Human betaherpesvirus 5 was the most abundant eukaryotic viruses. Especially, we first identified Methanobrevibacter smithii in fetal gut. Through the comparison with adults’ gut microbiota we found that Firmicutes and Bacteroidetes gradually became the main force of gut microbiota during the process of growth and development. Interestingly, 6 antibiotic resistance genes were shared by the fetus and adults. Our results indicate the presence of microbes in the fetal gut and demonstrate the diversity of bacteria, archaea and viruses, which provide support for the studies related to early fetal immunity. This study further explores the specific composition of viruses in the fetal gut and the similarities between fetal and adults’ gut microbiota, which is valuable for understanding human fetal immunity development during gestation. Frontiers Media S.A. 2023-01-05 /pmc/articles/PMC9850102/ /pubmed/36685560 http://dx.doi.org/10.3389/fimmu.2022.1079294 Text en Copyright © 2023 Liu, He, Lan, Guo, Liu, Li, Liu, He, Liu, Fan and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Liu, Xu
He, Guolin
Lan, Yue
Guo, Weijie
Liu, Xuyuan
Li, Jing
Liu, Anqing
He, Miao
Liu, Xinhui
Fan, Zhenxin
Zhang, Yaoyao
Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation
title Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation
title_full Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation
title_fullStr Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation
title_full_unstemmed Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation
title_short Virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation
title_sort virome and metagenomic analysis reveal the distinct distribution of microbiota in human fetal gut during gestation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850102/
https://www.ncbi.nlm.nih.gov/pubmed/36685560
http://dx.doi.org/10.3389/fimmu.2022.1079294
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