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Human reference gut microbiome comprising 5,414 prokaryotic species, including newly assembled genomes from under-represented Asian metagenomes

Chan Yeong Kim, Muyoung Lee, Sunmo Yang, Kyungnam Kim, Dongeun Yong, Hye Ryun Kim, Insuk Lee
doi: https://doi.org/10.1101/2020.11.09.375873
Chan Yeong Kim
1Department of Biotechnology, College of Life Science & Biotechnology, Yonsei University, Seoul 03722, Korea
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Muyoung Lee
1Department of Biotechnology, College of Life Science & Biotechnology, Yonsei University, Seoul 03722, Korea
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Sunmo Yang
1Department of Biotechnology, College of Life Science & Biotechnology, Yonsei University, Seoul 03722, Korea
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Kyungnam Kim
2Department of Laboratory Medicine, Research Institute of Bacterial Resistance, College of Medicine, Yonsei University, Seoul 03722, Korea
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Dongeun Yong
2Department of Laboratory Medicine, Research Institute of Bacterial Resistance, College of Medicine, Yonsei University, Seoul 03722, Korea
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Hye Ryun Kim
3Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, College of Medicine, Yonsei University, Seoul 03722, Korea
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Insuk Lee
1Department of Biotechnology, College of Life Science & Biotechnology, Yonsei University, Seoul 03722, Korea
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  • For correspondence: insuklee@yonsei.ac.kr
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Abstract

Metagenome sampling bias for geographical location and lifestyle is partially responsible for the incomplete catalog of reference genomes of gut microbial species. Here, we present a substantially expanded microbiome catalog, the Human Reference Gut Microbiome (HRGM). Incorporating newly assembled 29,082 genomes from 845 fecal samples collected from three under-represented Asian countries—Korea, India, and Japan—the HRGM contains 232,098 non-redundant genomes of 5,414 representative prokaryotic species, >103 million unique proteins, and >274 million single-nucleotide variants. This is an over 10% increase from the largest reference database. The newly assembled genomes were enriched for members of the Bacteroidaceae family, including species associated with high-fiber and seaweed-rich diet. Single-nucleotide variant density was positively associated with the speciation rate of gut commensals. Ultra-deep sequencing facilitated the assembly of genomes of low-abundance taxa, and deep sequencing (>20 million read pairs) was needed for the profiling of low-abundance taxa. Importantly, the HRGM greatly improved the taxonomic and functional classification of sequencing reads from fecal samples. Finally, mapping homologous sequences for human auto-antigens onto the HRGM genomes revealed the association of commensal bacteria with high cross-reactivity potential with autoimmunity. The HRGM (www.mbiomenet.org/HRGM/) will facilitate the identification and functional analysis of disease-associated gut microbiota.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://www.mbiomenet.org/HRGM/

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted November 10, 2020.
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Human reference gut microbiome comprising 5,414 prokaryotic species, including newly assembled genomes from under-represented Asian metagenomes
Chan Yeong Kim, Muyoung Lee, Sunmo Yang, Kyungnam Kim, Dongeun Yong, Hye Ryun Kim, Insuk Lee
bioRxiv 2020.11.09.375873; doi: https://doi.org/10.1101/2020.11.09.375873
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Human reference gut microbiome comprising 5,414 prokaryotic species, including newly assembled genomes from under-represented Asian metagenomes
Chan Yeong Kim, Muyoung Lee, Sunmo Yang, Kyungnam Kim, Dongeun Yong, Hye Ryun Kim, Insuk Lee
bioRxiv 2020.11.09.375873; doi: https://doi.org/10.1101/2020.11.09.375873

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