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Implication of the gut microbiome composition of type 2 diabetic patients from northern China
Emerging evidence has suggested the association of the gut microbiome with some human diseases, including type 2 diabetes (T2D). In this study, we analyzed the gut microbiota from a cohort of healthy and diabetic Chinese individuals from Northern China. Pyrosequencing of the V4V5 region of 16S rRNA...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096501/ https://www.ncbi.nlm.nih.gov/pubmed/32214153 http://dx.doi.org/10.1038/s41598-020-62224-3 |
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author | Li, Qian Chang, Yujun Zhang, Ke Chen, Hao Tao, Shiheng Zhang, Zhi |
author_facet | Li, Qian Chang, Yujun Zhang, Ke Chen, Hao Tao, Shiheng Zhang, Zhi |
author_sort | Li, Qian |
collection | PubMed |
description | Emerging evidence has suggested the association of the gut microbiome with some human diseases, including type 2 diabetes (T2D). In this study, we analyzed the gut microbiota from a cohort of healthy and diabetic Chinese individuals from Northern China. Pyrosequencing of the V4V5 region of 16S rRNA genes revealed a significant decrease in the gut microbiota diversity of diabetic patients as compared to healthy individuals. Butyrate-producing bacteria such as Bifidobacterium and Akkermansia were significantly decreased in diabetic patients. Furthermore, the abundance of Dorea was significantly increased in T2D individuals and negatively correlated with the abundance of butyrate-producing bacteria. The increase of Dorea could play a role in the development of T2D and has been previously overlooked. Importantly, functional analysis of the gut microbiome revealed for the first time that increased levels of butyrate production via transferases and the degradation of several amino acids due to gut microbial metabolism have strong correlations with T2D in Northern China. Moreover, the potential of gut microbiota-based classifiers to identify individuals with a high risk for T2D has been demonstrated in this study. Taken together, our findings have revealed a previously unappreciated association of the gut microbiome with T2D and have also suggested that changes in gut microbiota may be used to identify individuals at high risk for T2D. |
format | Online Article Text |
id | pubmed-7096501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70965012020-03-30 Implication of the gut microbiome composition of type 2 diabetic patients from northern China Li, Qian Chang, Yujun Zhang, Ke Chen, Hao Tao, Shiheng Zhang, Zhi Sci Rep Article Emerging evidence has suggested the association of the gut microbiome with some human diseases, including type 2 diabetes (T2D). In this study, we analyzed the gut microbiota from a cohort of healthy and diabetic Chinese individuals from Northern China. Pyrosequencing of the V4V5 region of 16S rRNA genes revealed a significant decrease in the gut microbiota diversity of diabetic patients as compared to healthy individuals. Butyrate-producing bacteria such as Bifidobacterium and Akkermansia were significantly decreased in diabetic patients. Furthermore, the abundance of Dorea was significantly increased in T2D individuals and negatively correlated with the abundance of butyrate-producing bacteria. The increase of Dorea could play a role in the development of T2D and has been previously overlooked. Importantly, functional analysis of the gut microbiome revealed for the first time that increased levels of butyrate production via transferases and the degradation of several amino acids due to gut microbial metabolism have strong correlations with T2D in Northern China. Moreover, the potential of gut microbiota-based classifiers to identify individuals with a high risk for T2D has been demonstrated in this study. Taken together, our findings have revealed a previously unappreciated association of the gut microbiome with T2D and have also suggested that changes in gut microbiota may be used to identify individuals at high risk for T2D. Nature Publishing Group UK 2020-03-25 /pmc/articles/PMC7096501/ /pubmed/32214153 http://dx.doi.org/10.1038/s41598-020-62224-3 Text en © The Author(s) 2020 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 Li, Qian Chang, Yujun Zhang, Ke Chen, Hao Tao, Shiheng Zhang, Zhi Implication of the gut microbiome composition of type 2 diabetic patients from northern China |
title | Implication of the gut microbiome composition of type 2 diabetic patients from northern China |
title_full | Implication of the gut microbiome composition of type 2 diabetic patients from northern China |
title_fullStr | Implication of the gut microbiome composition of type 2 diabetic patients from northern China |
title_full_unstemmed | Implication of the gut microbiome composition of type 2 diabetic patients from northern China |
title_short | Implication of the gut microbiome composition of type 2 diabetic patients from northern China |
title_sort | implication of the gut microbiome composition of type 2 diabetic patients from northern china |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096501/ https://www.ncbi.nlm.nih.gov/pubmed/32214153 http://dx.doi.org/10.1038/s41598-020-62224-3 |
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