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Gut Microbiota Signatures in Gestational Anemia
Gestational diseases are associated with altered intestinal microbiota in pregnant women. Characterizing the gut microbiota of gestational anemia (GA) may describe a novel role of gut microbial abnormality in GA. In this study, we investigated differences in gut microbiota between GA patients and he...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947918/ https://www.ncbi.nlm.nih.gov/pubmed/33718259 http://dx.doi.org/10.3389/fcimb.2021.549678 |
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author | Long, Yan Liang, Fang Guo, Ruochun Zhu, Chunyan Zhao, Xueqin Wang, Xifan Liu, Fei Jiang, Min Liang, Qihua Zeng, Shanshui Han, Mengru Qin, Junjie Li, Shenghui Li, Shaochuan Yang, Hongling |
author_facet | Long, Yan Liang, Fang Guo, Ruochun Zhu, Chunyan Zhao, Xueqin Wang, Xifan Liu, Fei Jiang, Min Liang, Qihua Zeng, Shanshui Han, Mengru Qin, Junjie Li, Shenghui Li, Shaochuan Yang, Hongling |
author_sort | Long, Yan |
collection | PubMed |
description | Gestational diseases are associated with altered intestinal microbiota in pregnant women. Characterizing the gut microbiota of gestational anemia (GA) may describe a novel role of gut microbial abnormality in GA. In this study, we investigated differences in gut microbiota between GA patients and healthy pregnant women from the first trimester (n = 24 vs. 54) and the third trimester (n = 30 vs. 56) based on the 16S rRNA gene sequencing method. No statistically significant differences in α-diversity were identified between GA patients and controls in the first trimester of pregnancy, whereas the Shannon index and observed OTUs were significantly lower in GA patients than in healthy controls in the third trimester. Distance-based redundancy analysis revealed striking differences in microbial communities in the third trimester between GA patients and controls. Four genera were significantly different in relative abundance between GA patients and healthy controls, while 12 genera differentiated significantly between GA patients and healthy controls in the third trimester. At the operational taxonomic unit (OTU) level, 17 OTUs and 30 OTUs were identified to be different between GA patients and healthy controls in the first and third trimesters, respectively. Changes in gut microbial composition of GA patients suggest a potential relation with GA, and provide insights into the prediction and intervention of gestational anemia. |
format | Online Article Text |
id | pubmed-7947918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79479182021-03-12 Gut Microbiota Signatures in Gestational Anemia Long, Yan Liang, Fang Guo, Ruochun Zhu, Chunyan Zhao, Xueqin Wang, Xifan Liu, Fei Jiang, Min Liang, Qihua Zeng, Shanshui Han, Mengru Qin, Junjie Li, Shenghui Li, Shaochuan Yang, Hongling Front Cell Infect Microbiol Cellular and Infection Microbiology Gestational diseases are associated with altered intestinal microbiota in pregnant women. Characterizing the gut microbiota of gestational anemia (GA) may describe a novel role of gut microbial abnormality in GA. In this study, we investigated differences in gut microbiota between GA patients and healthy pregnant women from the first trimester (n = 24 vs. 54) and the third trimester (n = 30 vs. 56) based on the 16S rRNA gene sequencing method. No statistically significant differences in α-diversity were identified between GA patients and controls in the first trimester of pregnancy, whereas the Shannon index and observed OTUs were significantly lower in GA patients than in healthy controls in the third trimester. Distance-based redundancy analysis revealed striking differences in microbial communities in the third trimester between GA patients and controls. Four genera were significantly different in relative abundance between GA patients and healthy controls, while 12 genera differentiated significantly between GA patients and healthy controls in the third trimester. At the operational taxonomic unit (OTU) level, 17 OTUs and 30 OTUs were identified to be different between GA patients and healthy controls in the first and third trimesters, respectively. Changes in gut microbial composition of GA patients suggest a potential relation with GA, and provide insights into the prediction and intervention of gestational anemia. Frontiers Media S.A. 2021-02-25 /pmc/articles/PMC7947918/ /pubmed/33718259 http://dx.doi.org/10.3389/fcimb.2021.549678 Text en Copyright © 2021 Long, Liang, Guo, Zhu, Zhao, Wang, Liu, Jiang, Liang, Zeng, Han, Qin, Li, Li and Yang http://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 | Cellular and Infection Microbiology Long, Yan Liang, Fang Guo, Ruochun Zhu, Chunyan Zhao, Xueqin Wang, Xifan Liu, Fei Jiang, Min Liang, Qihua Zeng, Shanshui Han, Mengru Qin, Junjie Li, Shenghui Li, Shaochuan Yang, Hongling Gut Microbiota Signatures in Gestational Anemia |
title | Gut Microbiota Signatures in Gestational Anemia |
title_full | Gut Microbiota Signatures in Gestational Anemia |
title_fullStr | Gut Microbiota Signatures in Gestational Anemia |
title_full_unstemmed | Gut Microbiota Signatures in Gestational Anemia |
title_short | Gut Microbiota Signatures in Gestational Anemia |
title_sort | gut microbiota signatures in gestational anemia |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947918/ https://www.ncbi.nlm.nih.gov/pubmed/33718259 http://dx.doi.org/10.3389/fcimb.2021.549678 |
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