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Individuality and temporal stability of the human gut microbiome

INTRODUCTION: The breakthrough of next generation sequencing-technologies has enabled large-scale studies of natural microbial communities and the 16S rRNA genes have been widely used as a phylogenetic marker to study community structure. However, major limitations of this approach are that neither...

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Autores principales: Sunagawa, Shinichi, Schloissnig, Siegfried, Arumugam, Manimozhiyan, Forslund, Kristoffer, Mitreva, Makedonka, Tap, Julien, Zhu, Ana, Waller, Alison, Mende, Daniel R., Kultima, Jens Roat, Martin, John, Kota, Karthik, Sunyaev, Shamil R., Typas, Athanasios, Weinstock, George M., Bork, Peer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: University Library System, University of Pittsburgh 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960903/
https://www.ncbi.nlm.nih.gov/pubmed/29805877
http://dx.doi.org/10.5195/cajgh.2013.120
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author Sunagawa, Shinichi
Schloissnig, Siegfried
Arumugam, Manimozhiyan
Forslund, Kristoffer
Mitreva, Makedonka
Tap, Julien
Zhu, Ana
Waller, Alison
Mende, Daniel R.
Kultima, Jens Roat
Martin, John
Kota, Karthik
Sunyaev, Shamil R.
Typas, Athanasios
Weinstock, George M.
Bork, Peer
author_facet Sunagawa, Shinichi
Schloissnig, Siegfried
Arumugam, Manimozhiyan
Forslund, Kristoffer
Mitreva, Makedonka
Tap, Julien
Zhu, Ana
Waller, Alison
Mende, Daniel R.
Kultima, Jens Roat
Martin, John
Kota, Karthik
Sunyaev, Shamil R.
Typas, Athanasios
Weinstock, George M.
Bork, Peer
author_sort Sunagawa, Shinichi
collection PubMed
description INTRODUCTION: The breakthrough of next generation sequencing-technologies has enabled large-scale studies of natural microbial communities and the 16S rRNA genes have been widely used as a phylogenetic marker to study community structure. However, major limitations of this approach are that neither strain-level resolution nor genomic context of microorganisms can be provided. This information, however, is crucial to answer fundamental questions about the temporal stability and distinctiveness of natural microbial communities. MATERIAL AND METHODS: We developed a methodological framework for metagenomic single nucleotide polymorphism (SNP) variation analysis and applied it to publicly available data from 252 human fecal samples from 207 European and North American individuals. We further analyzed samples from 43 healthy subjects that were sampled at least twice over time intervals of up to one year and measured population similarities of dominant gut species. RESULTS: We detected 10.3 million SNPs in 101 species, which nearly amounts to the number identified in more than 1,000 humans. CONCLUSION: The most striking result was that host-specific strains appear to be retained over long time periods. This indicates that individual-specific strains are not easily exchanged with the environment and furthermore, that an individuals appear to have a unique metagenomic genotype. This, in turn, is linked to implications for human gut physiology, such as the stability of antibiotic resistance potential.
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spelling pubmed-59609032018-05-25 Individuality and temporal stability of the human gut microbiome Sunagawa, Shinichi Schloissnig, Siegfried Arumugam, Manimozhiyan Forslund, Kristoffer Mitreva, Makedonka Tap, Julien Zhu, Ana Waller, Alison Mende, Daniel R. Kultima, Jens Roat Martin, John Kota, Karthik Sunyaev, Shamil R. Typas, Athanasios Weinstock, George M. Bork, Peer Cent Asian J Glob Health Articles INTRODUCTION: The breakthrough of next generation sequencing-technologies has enabled large-scale studies of natural microbial communities and the 16S rRNA genes have been widely used as a phylogenetic marker to study community structure. However, major limitations of this approach are that neither strain-level resolution nor genomic context of microorganisms can be provided. This information, however, is crucial to answer fundamental questions about the temporal stability and distinctiveness of natural microbial communities. MATERIAL AND METHODS: We developed a methodological framework for metagenomic single nucleotide polymorphism (SNP) variation analysis and applied it to publicly available data from 252 human fecal samples from 207 European and North American individuals. We further analyzed samples from 43 healthy subjects that were sampled at least twice over time intervals of up to one year and measured population similarities of dominant gut species. RESULTS: We detected 10.3 million SNPs in 101 species, which nearly amounts to the number identified in more than 1,000 humans. CONCLUSION: The most striking result was that host-specific strains appear to be retained over long time periods. This indicates that individual-specific strains are not easily exchanged with the environment and furthermore, that an individuals appear to have a unique metagenomic genotype. This, in turn, is linked to implications for human gut physiology, such as the stability of antibiotic resistance potential. University Library System, University of Pittsburgh 2014-03-27 /pmc/articles/PMC5960903/ /pubmed/29805877 http://dx.doi.org/10.5195/cajgh.2013.120 Text en New articles in this journal are licensed under a Creative Commons Attribution 3.0 License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Articles
Sunagawa, Shinichi
Schloissnig, Siegfried
Arumugam, Manimozhiyan
Forslund, Kristoffer
Mitreva, Makedonka
Tap, Julien
Zhu, Ana
Waller, Alison
Mende, Daniel R.
Kultima, Jens Roat
Martin, John
Kota, Karthik
Sunyaev, Shamil R.
Typas, Athanasios
Weinstock, George M.
Bork, Peer
Individuality and temporal stability of the human gut microbiome
title Individuality and temporal stability of the human gut microbiome
title_full Individuality and temporal stability of the human gut microbiome
title_fullStr Individuality and temporal stability of the human gut microbiome
title_full_unstemmed Individuality and temporal stability of the human gut microbiome
title_short Individuality and temporal stability of the human gut microbiome
title_sort individuality and temporal stability of the human gut microbiome
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960903/
https://www.ncbi.nlm.nih.gov/pubmed/29805877
http://dx.doi.org/10.5195/cajgh.2013.120
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