Article open access publication

1,520 reference genomes from cultivated human gut bacteria enable functional microbiome analyses

Nature Biotechnology, Springer Nature, ISSN 1087-0156

Volume 37, 2, 2019

DOI:10.1038/s41587-018-0008-8, Dimensions: pub.1111907227, PMC: PMC6784896, PMID: 30718868,

Authors

Zou, Yuanqiang (1) (2)
Luo, Guangwen (2) (3)
Qin, Panpan (2) (4)
Xia, Yan (2) (4)
Liang, Suisha (2) (5)
Dai, Ying (2)
Su, Lili (2)
Liu, Chuan (2) (5)
Xu, Xun (2)
Hou, Yong (2)
Liu, Xin (2) (6)
Wang, Jian (2) (7)
Yang, Huanming (2) (7)
Kristiansen, Karsten (1) (2) (8)
Li, Junhua * (2) (9)
Jia, Huijue * (2) (10)
Xiao, Liang * (2) (5) (8) (11)

* Corresponding author

Affiliations

Organisations

  1. (1) University of Copenhagen, grid.5254.6, KU
  2. (2) Beijing Genomics Institute, grid.21155.32
  3. (3) Northeast Agricultural University, grid.412243.2
  4. (4) BGI Education Center, University of Chinese Academy of Sciences, Shenzhen, China
  5. (5) Shenzhen Engineering Laboratory of Detection and Intervention of Human Intestinal Microbiome, Shenzhen, China
  6. (6) BGI-Qingdao, BGI-Shenzhen, Qingdao, China
  7. (7) James D. Watson Institute of Genome Sciences, Hangzhou, China
  8. (8) Qingdao-Europe Advanced Institute for Life Sciences, Qingdao, China
  9. (9) South China University of Technology, grid.79703.3a
  10. (10) Macau University of Science and Technology, grid.259384.1
  11. (11) Huashan Hospital, grid.411405.5

Countries

Denmark

China

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Europe

Asia

Description

Reference genomes are essential for metagenomic analyses and functional characterization of the human gut microbiota. We present the Culturable Genome Reference (CGR), a collection of 1,520 nonredundant, high-quality draft genomes generated from >6,000 bacteria cultivated from fecal samples of healthy humans. Of the 1,520 genomes, which were chosen to cover all major bacterial phyla and genera in the human gut, 264 are not represented in existing reference genome catalogs. We show that this increase in the number of reference bacterial genomes improves the rate of mapping metagenomic sequencing reads from 50% to >70%, enabling higher-resolution descriptions of the human gut microbiome. We use the CGR genomes to annotate functions of 338 bacterial species, showing the utility of this resource for functional studies. We also carry out a pan-genome analysis of 38 important human gut species, which reveals the diversity and specificity of functional enrichment between their core and dispensable genomes.

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