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Genomic variation landscape of the human gut microbiome
While large-scale efforts have rapidly advanced the understanding and practical impact of human genomic variation, the latter is largely unexplored in the human microbiome. We therefore developed a framework for metagenomic variation analysis and applied it to 252 fecal metagenomes of 207 individual...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3536929/ https://www.ncbi.nlm.nih.gov/pubmed/23222524 http://dx.doi.org/10.1038/nature11711 |
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author | Schloissnig, Siegfried Arumugam, Manimozhiyan Sunagawa, Shinichi Mitreva, Makedonka Tap, Julien Zhu, Ana Waller, Alison Mende, Daniel R. Kultima, Jens Roat Martin, John Kota, Karthik Sunyaev, Shamil R. Weinstock, George M. Bork, Peer |
author_facet | Schloissnig, Siegfried Arumugam, Manimozhiyan Sunagawa, Shinichi Mitreva, Makedonka Tap, Julien Zhu, Ana Waller, Alison Mende, Daniel R. Kultima, Jens Roat Martin, John Kota, Karthik Sunyaev, Shamil R. Weinstock, George M. Bork, Peer |
author_sort | Schloissnig, Siegfried |
collection | PubMed |
description | While large-scale efforts have rapidly advanced the understanding and practical impact of human genomic variation, the latter is largely unexplored in the human microbiome. We therefore developed a framework for metagenomic variation analysis and applied it to 252 fecal metagenomes of 207 individuals from Europe and North America. Using 7.4 billion reads aligned to 101 reference species, we detected 10.3 million single nucleotide polymorphisms (SNPs), 107,991 short indels, and 1,051 structural variants. The average ratio of non-synonymous to synonymous polymorphism rates of 0.11 was more variable between gut microbial species than across human hosts. Subjects sampled at varying time intervals exhibited individuality and temporal stability of SNP variation patterns, despite considerable composition changes of their gut microbiota. This implies that individual-specific strains are not easily replaced and that an individual might have a unique metagenomic genotype, which may be exploitable for personalized diet or drug intake. |
format | Online Article Text |
id | pubmed-3536929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-35369292013-07-03 Genomic variation landscape of the human gut microbiome Schloissnig, Siegfried Arumugam, Manimozhiyan Sunagawa, Shinichi Mitreva, Makedonka Tap, Julien Zhu, Ana Waller, Alison Mende, Daniel R. Kultima, Jens Roat Martin, John Kota, Karthik Sunyaev, Shamil R. Weinstock, George M. Bork, Peer Nature Article While large-scale efforts have rapidly advanced the understanding and practical impact of human genomic variation, the latter is largely unexplored in the human microbiome. We therefore developed a framework for metagenomic variation analysis and applied it to 252 fecal metagenomes of 207 individuals from Europe and North America. Using 7.4 billion reads aligned to 101 reference species, we detected 10.3 million single nucleotide polymorphisms (SNPs), 107,991 short indels, and 1,051 structural variants. The average ratio of non-synonymous to synonymous polymorphism rates of 0.11 was more variable between gut microbial species than across human hosts. Subjects sampled at varying time intervals exhibited individuality and temporal stability of SNP variation patterns, despite considerable composition changes of their gut microbiota. This implies that individual-specific strains are not easily replaced and that an individual might have a unique metagenomic genotype, which may be exploitable for personalized diet or drug intake. 2012-12-05 2013-01-03 /pmc/articles/PMC3536929/ /pubmed/23222524 http://dx.doi.org/10.1038/nature11711 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Schloissnig, Siegfried Arumugam, Manimozhiyan Sunagawa, Shinichi Mitreva, Makedonka Tap, Julien Zhu, Ana Waller, Alison Mende, Daniel R. Kultima, Jens Roat Martin, John Kota, Karthik Sunyaev, Shamil R. Weinstock, George M. Bork, Peer Genomic variation landscape of the human gut microbiome |
title | Genomic variation landscape of the human gut microbiome |
title_full | Genomic variation landscape of the human gut microbiome |
title_fullStr | Genomic variation landscape of the human gut microbiome |
title_full_unstemmed | Genomic variation landscape of the human gut microbiome |
title_short | Genomic variation landscape of the human gut microbiome |
title_sort | genomic variation landscape of the human gut microbiome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3536929/ https://www.ncbi.nlm.nih.gov/pubmed/23222524 http://dx.doi.org/10.1038/nature11711 |
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