Enterotypes of the human gut microbiome

被引:0
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作者
Manimozhiyan Arumugam
Jeroen Raes
Eric Pelletier
Denis Le Paslier
Takuji Yamada
Daniel R. Mende
Gabriel R. Fernandes
Julien Tap
Thomas Bruls
Jean-Michel Batto
Marcelo Bertalan
Natalia Borruel
Francesc Casellas
Leyden Fernandez
Laurent Gautier
Torben Hansen
Masahira Hattori
Tetsuya Hayashi
Michiel Kleerebezem
Ken Kurokawa
Marion Leclerc
Florence Levenez
Chaysavanh Manichanh
H. Bjørn Nielsen
Trine Nielsen
Nicolas Pons
Julie Poulain
Junjie Qin
Thomas Sicheritz-Ponten
Sebastian Tims
David Torrents
Edgardo Ugarte
Erwin G. Zoetendal
Jun Wang
Francisco Guarner
Oluf Pedersen
Willem M. de Vos
Søren Brunak
Joel Doré
Jean Weissenbach
S. Dusko Ehrlich
Peer Bork
机构
[1] European Molecular Biology Laboratory,Department of Biochemistry and Immunology
[2] Meyerhofstrasse 1,Division of Bioenvironmental Science
[3] VIB—Vrije Universiteit Brussel,Department of Biological Information
[4] Commissariat à l’Energie Atomique,Department of Biology
[5] Genoscope,Department of Biology
[6] Centre National de la Recherche Scientifique,undefined
[7] UMR8030,undefined
[8] Université d'Evry Val d'Essone 91000 Evry,undefined
[9] Universidade Federal de Minas Gerais,undefined
[10] Av. Antônio Carlos 6627,undefined
[11] 31270-901 Belo Horizonte,undefined
[12] Institut National de la Recherche Agronomique,undefined
[13] Center for Biological Sequence Analysis,undefined
[14] Technical University of Denmark,undefined
[15] Digestive System Research Unit,undefined
[16] University Hospital Vall d’Hebron,undefined
[17] Ciberehd,undefined
[18] Barcelona Supercomputing Center,undefined
[19] Jordi Girona 31,undefined
[20] Marie Krogh Center for Metabolic Research,undefined
[21] Section of Metabolic Genetics,undefined
[22] Faculty of Health Sciences,undefined
[23] University of Copenhagen,undefined
[24] Faculty of Health Sciences,undefined
[25] University of Southern Denmark,undefined
[26] Computational Biology Laboratory Bld,undefined
[27] The University of Tokyo Kashiwa Campus,undefined
[28] Kashiwa-no-ha 5-1-5,undefined
[29] Kashiwa,undefined
[30] Frontier Science Research Center,undefined
[31] University of Miyazaki,undefined
[32] 5200 Kiyotake,undefined
[33] Laboratory of Microbiology,undefined
[34] Wageningen University,undefined
[35] Tokyo Institute of Technology,undefined
[36] Graduate School of Bioscience and Biotechnology,undefined
[37] 4259 Nagatsuta-cho,undefined
[38] Midori-ku,undefined
[39] Yokohama-shi,undefined
[40] BGI-Shenzhen,undefined
[41] Novo Nordisk Foundation Center for Biosustainability,undefined
[42] Technical University of Denmark,undefined
[43] Institució Catalana de Recerca i Estudis Avançats (ICREA),undefined
[44] Pg. Lluís Companys 23,undefined
[45] University of Copenhagen,undefined
[46] Institute of Biomedical Science,undefined
[47] Faculty of Health Sciences,undefined
[48] University of Copenhagen,undefined
[49] Hagedorn Research Institute,undefined
[50] Faculty of Health Sciences,undefined
来源
Nature | 2011年 / 473卷
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摘要
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.
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页码:174 / 180
页数:6
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