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Enterotypes of the human gut microbiome.


ABSTRACT: Our knowledge of species and functional composition of the human gut microbiome is rapidly increasing, but it is still based on very few cohorts and little is known about variation across the world. By combining 22 newly sequenced faecal metagenomes of individuals from four countries with previously published data sets, here we identify three robust clusters (referred to as enterotypes hereafter) that are not nation or continent specific. We also confirmed the enterotypes in two published, larger cohorts, indicating that intestinal microbiota variation is generally stratified, not continuous. This indicates further the existence of a limited number of well-balanced host-microbial symbiotic states that might respond differently to diet and drug intake. The enterotypes are mostly driven by species composition, but abundant molecular functions are not necessarily provided by abundant species, highlighting the importance of a functional analysis to understand microbial communities. Although individual host properties such as body mass index, age, or gender cannot explain the observed enterotypes, data-driven marker genes or functional modules can be identified for each of these host properties. For example, twelve genes significantly correlate with age and three functional modules with the body mass index, hinting at a diagnostic potential of microbial markers.

SUBMITTER: Arumugam M 

PROVIDER: S-EPMC3728647 | biostudies-literature | 2011 May

REPOSITORIES: biostudies-literature

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Enterotypes of the human gut microbiome.

Arumugam Manimozhiyan M   Raes Jeroen J   Pelletier Eric E   Le Paslier Denis D   Yamada Takuji T   Mende Daniel R DR   Fernandes Gabriel R GR   Tap Julien J   Bruls Thomas T   Batto Jean-Michel JM   Bertalan Marcelo M   Borruel Natalia N   Casellas Francesc F   Fernandez Leyden L   Gautier Laurent L   Hansen Torben T   Hattori Masahira M   Hayashi Tetsuya T   Kleerebezem Michiel M   Kurokawa Ken K   Leclerc Marion M   Levenez Florence F   Manichanh Chaysavanh C   Nielsen H Bjørn HB   Nielsen Trine T   Pons Nicolas N   Poulain Julie J   Qin Junjie J   Sicheritz-Ponten Thomas T   Tims Sebastian S   Torrents David D   Ugarte Edgardo E   Zoetendal Erwin G EG   Wang Jun J   Wang Jun J   Guarner Francisco F   Pedersen Oluf O   de Vos Willem M WM   Brunak Søren S   Doré Joel J   Antolín María M   Artiguenave François F   Blottiere Hervé M HM   Almeida Mathieu M   Brechot Christian C   Cara Carlos C   Chervaux Christian C   Cultrone Antonella A   Delorme Christine C   Denariaz Gérard G   Dervyn Rozenn R   Foerstner Konrad U KU   Friss Carsten C   van de Guchte Maarten M   Guedon Eric E   Haimet Florence F   Huber Wolfgang W   van Hylckama-Vlieg Johan J   Jamet Alexandre A   Juste Catherine C   Kaci Ghalia G   Knol Jan J   Lakhdari Omar O   Layec Severine S   Le Roux Karine K   Maguin Emmanuelle E   Mérieux Alexandre A   Melo Minardi Raquel R   M'rini Christine C   Muller Jean J   Oozeer Raish R   Parkhill Julian J   Renault Pierre P   Rescigno Maria M   Sanchez Nicolas N   Sunagawa Shinichi S   Torrejon Antonio A   Turner Keith K   Vandemeulebrouck Gaetana G   Varela Encarna E   Winogradsky Yohanan Y   Zeller Georg G   Weissenbach Jean J   Ehrlich S Dusko SD   Bork Peer P  

Nature 20110420 7346


Our knowledge of species and functional composition of the human gut microbiome is rapidly increasing, but it is still based on very few cohorts and little is known about variation across the world. By combining 22 newly sequenced faecal metagenomes of individuals from four countries with previously published data sets, here we identify three robust clusters (referred to as enterotypes hereafter) that are not nation or continent specific. We also confirmed the enterotypes in two published, large  ...[more]

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