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Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis
The human gut microbiota varies considerably among world populations due to a variety of factors including genetic background, diet, cultural habits and socioeconomic status. Here we characterized 110 healthy Mongolian adults gut microbiota by shotgun metagenomic sequencing and compared the intestin...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052615/ https://www.ncbi.nlm.nih.gov/pubmed/27708392 http://dx.doi.org/10.1038/srep34826 |
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author | Liu, Wenjun Zhang, Jiachao Wu, Chunyan Cai, Shunfeng Huang, Weiqiang Chen, Jing XI, Xiaoxia Liang, Zebin Hou, Qiangchuan Zhou, Bing Qin, Nan Zhang, Heping |
author_facet | Liu, Wenjun Zhang, Jiachao Wu, Chunyan Cai, Shunfeng Huang, Weiqiang Chen, Jing XI, Xiaoxia Liang, Zebin Hou, Qiangchuan Zhou, Bing Qin, Nan Zhang, Heping |
author_sort | Liu, Wenjun |
collection | PubMed |
description | The human gut microbiota varies considerably among world populations due to a variety of factors including genetic background, diet, cultural habits and socioeconomic status. Here we characterized 110 healthy Mongolian adults gut microbiota by shotgun metagenomic sequencing and compared the intestinal microbiome among Mongolians, the Hans and European cohorts. The results showed that the taxonomic profile of intestinal microbiome among cohorts revealed the Actinobaceria and Bifidobacterium were the key microbes contributing to the differences among Mongolians, the Hans and Europeans at the phylum level and genus level, respectively. Metagenomic species analysis indicated that Faecalibacterium prausnitzii and Coprococcus comeswere enrich in Mongolian people which might contribute to gut health through anti-inflammatory properties and butyrate production, respectively. On the other hand, the enriched genus Collinsella, biomarker in symptomatic atherosclerosis patients, might be associated with the high morbidity of cardiovascular and cerebrovascular diseases in Mongolian adults. At the functional level, a unique microbial metabolic pathway profile was present in Mongolian’s gut which mainly distributed in amino acid metabolism, carbohydrate metabolism, energy metabolism, lipid metabolism, glycan biosynthesis and metabolism. We can attribute the specific signatures of Mongolian gut microbiome to their unique genotype, dietary habits and living environment. |
format | Online Article Text |
id | pubmed-5052615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50526152016-10-19 Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis Liu, Wenjun Zhang, Jiachao Wu, Chunyan Cai, Shunfeng Huang, Weiqiang Chen, Jing XI, Xiaoxia Liang, Zebin Hou, Qiangchuan Zhou, Bing Qin, Nan Zhang, Heping Sci Rep Article The human gut microbiota varies considerably among world populations due to a variety of factors including genetic background, diet, cultural habits and socioeconomic status. Here we characterized 110 healthy Mongolian adults gut microbiota by shotgun metagenomic sequencing and compared the intestinal microbiome among Mongolians, the Hans and European cohorts. The results showed that the taxonomic profile of intestinal microbiome among cohorts revealed the Actinobaceria and Bifidobacterium were the key microbes contributing to the differences among Mongolians, the Hans and Europeans at the phylum level and genus level, respectively. Metagenomic species analysis indicated that Faecalibacterium prausnitzii and Coprococcus comeswere enrich in Mongolian people which might contribute to gut health through anti-inflammatory properties and butyrate production, respectively. On the other hand, the enriched genus Collinsella, biomarker in symptomatic atherosclerosis patients, might be associated with the high morbidity of cardiovascular and cerebrovascular diseases in Mongolian adults. At the functional level, a unique microbial metabolic pathway profile was present in Mongolian’s gut which mainly distributed in amino acid metabolism, carbohydrate metabolism, energy metabolism, lipid metabolism, glycan biosynthesis and metabolism. We can attribute the specific signatures of Mongolian gut microbiome to their unique genotype, dietary habits and living environment. Nature Publishing Group 2016-10-06 /pmc/articles/PMC5052615/ /pubmed/27708392 http://dx.doi.org/10.1038/srep34826 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Liu, Wenjun Zhang, Jiachao Wu, Chunyan Cai, Shunfeng Huang, Weiqiang Chen, Jing XI, Xiaoxia Liang, Zebin Hou, Qiangchuan Zhou, Bing Qin, Nan Zhang, Heping Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis |
title | Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis |
title_full | Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis |
title_fullStr | Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis |
title_full_unstemmed | Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis |
title_short | Unique Features of Ethnic Mongolian Gut Microbiome revealed by metagenomic analysis |
title_sort | unique features of ethnic mongolian gut microbiome revealed by metagenomic analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052615/ https://www.ncbi.nlm.nih.gov/pubmed/27708392 http://dx.doi.org/10.1038/srep34826 |
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