A human gut microbial gene catalogue established by metagenomic sequencing

Junjie Qin(BGI Group (China)), Ruiqiang Li(BGI Group (China)), Jeroen Raes(Vrije Universiteit Brussel), Manimozhiyan Arumugam(European Molecular Biology Laboratory), Kristoffer Sølvsten Burgdorf, Chaysavanh Manichanh(Vall d'Hebron Hospital Universitari), Trine Nielsen, Nicolas Pons(Département Génétique Animale), Florence Levenez(Département Génétique Animale), Takuji Yamada(European Molecular Biology Laboratory), Daniel R. Mende(European Molecular Biology Laboratory), Junhua Li(BGI Group (China)), Junming Xu(BGI Group (China)), Shaochuan Li(BGI Group (China)), Dongfang Li(BGI Group (China)), Jianjun Cao(BGI Group (China)), Bo Wang(BGI Group (China)), Huiqing Liang(BGI Group (China)), Huisong Zheng(BGI Group (China)), Yinlong Xie(BGI Group (China)), Julien Tap(Département Génétique Animale), Patricia Lepage(Département Génétique Animale), Marcelo Bertalan(Technical University of Denmark), Jean-Michel Batto(Département Génétique Animale), Torben Hansen, Denis Le Paslier(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Allan Linneberg(Center for Clinical Research and Prevention), H. Bjørn Nielsen(Technical University of Denmark), Éric Pelletier(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Pierre Renault(Département Génétique Animale), Thomas Sicheritz‐Pontén(Technical University of Denmark), A. Keith Turner(Wellcome Sanger Institute), Hongmei Zhu(BGI Group (China)), Chang Yu(BGI Group (China)), Shengting Li(BGI Group (China)), Min Jian(BGI Group (China)), Yan Zhou(BGI Group (China)), Rui Li(BGI Group (China)), Xiuqing Zhang(BGI Group (China)), Songgang Li(BGI Group (China)), Nan Qin(BGI Group (China)), Huanming Yang(BGI Group (China)), Jian Wang(BGI Group (China)), Søren Brunak(Technical University of Denmark), Joël Doré(Département Génétique Animale), Francisco Guarner(Vall d'Hebron Hospital Universitari), Karsten Kristiansen(University of Copenhagen), Oluf Pedersen(University of Copenhagen), Julian Parkhill(Wellcome Sanger Institute), Jean Weissenbach(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Peer Bork(European Molecular Biology Laboratory), S. Dusko Ehrlich(Département Génétique Animale), Jun Wang(BGI Group (China))
Nature
March 1, 2010
Cited by 11,601Open Access
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Abstract

To understand the impact of gut microbes on human health and well-being it is crucial to assess their genetic potential. Here we describe the Illumina-based metagenomic sequencing, assembly and characterization of 3.3 million non-redundant microbial genes, derived from 576.7 gigabases of sequence, from faecal samples of 124 European individuals. The gene set, ∼150 times larger than the human gene complement, contains an overwhelming majority of the prevalent (more frequent) microbial genes of the cohort and probably includes a large proportion of the prevalent human intestinal microbial genes. The genes are largely shared among individuals of the cohort. Over 99% of the genes are bacterial, indicating that the entire cohort harbours between 1,000 and 1,150 prevalent bacterial species and each individual at least 160 such species, which are also largely shared. We define and describe the minimal gut metagenome and the minimal gut bacterial genome in terms of functions present in all individuals and most bacteria, respectively. The human body plays host to an estimated 100 trillion microbial cells, most of them in the gut where they have a profound influence on human physiology and nutrition — and are now regarded as crucial for human life. Gut microbes contribute to the energy harvest from food, and changes of gut microbiome may be associated with bowel diseases or obesity. Now the international MetaHIT (Metagenomics of the Human Intestinal Tract) project has published a gene catalogue of the human gut microbiome derived from 124 healthy, overweight and obese human adults, as well as inflammatory disease patients, from Denmark and Spain. The resulting data provide the first insights into this gene set — which is over 150 times larger than the human gene complement — and show that the genes are largely shared among individuals. Based on the variety of functions encoded by the gene set, it is possible to define both a minimal gut metagenome and a minimal gut bacterial genome. Deep metagenomic sequencing and characterization of the human gut microbiome from healthy and obese individuals, as well as those suffering from inflammatory bowel disease, provide the first insights into this gene set and how much of it is shared among individuals. The minimal gut metagenome as well as the minimal gut bacterial genome is also described.


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