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Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle
The body-wide human microbiome plays a role in health, but its full diversity remains uncharacterized, particularly outside of the gut and in international populations. We leveraged 9,428 metagenomes to reconstruct 154,723 microbial genomes (45% of high quality) spanning body sites, ages, countries,...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349461/ https://www.ncbi.nlm.nih.gov/pubmed/30661755 http://dx.doi.org/10.1016/j.cell.2019.01.001 |
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author | Pasolli, Edoardo Asnicar, Francesco Manara, Serena Zolfo, Moreno Karcher, Nicolai Armanini, Federica Beghini, Francesco Manghi, Paolo Tett, Adrian Ghensi, Paolo Collado, Maria Carmen Rice, Benjamin L. DuLong, Casey Morgan, Xochitl C. Golden, Christopher D. Quince, Christopher Huttenhower, Curtis Segata, Nicola |
author_facet | Pasolli, Edoardo Asnicar, Francesco Manara, Serena Zolfo, Moreno Karcher, Nicolai Armanini, Federica Beghini, Francesco Manghi, Paolo Tett, Adrian Ghensi, Paolo Collado, Maria Carmen Rice, Benjamin L. DuLong, Casey Morgan, Xochitl C. Golden, Christopher D. Quince, Christopher Huttenhower, Curtis Segata, Nicola |
author_sort | Pasolli, Edoardo |
collection | PubMed |
description | The body-wide human microbiome plays a role in health, but its full diversity remains uncharacterized, particularly outside of the gut and in international populations. We leveraged 9,428 metagenomes to reconstruct 154,723 microbial genomes (45% of high quality) spanning body sites, ages, countries, and lifestyles. We recapitulated 4,930 species-level genome bins (SGBs), 77% without genomes in public repositories (unknown SGBs [uSGBs]). uSGBs are prevalent (in 93% of well-assembled samples), expand underrepresented phyla, and are enriched in non-Westernized populations (40% of the total SGBs). We annotated 2.85 M genes in SGBs, many associated with conditions including infant development (94,000) or Westernization (106,000). SGBs and uSGBs permit deeper microbiome analyses and increase the average mappability of metagenomic reads from 67.76% to 87.51% in the gut (median 94.26%) and 65.14% to 82.34% in the mouth. We thus identify thousands of microbial genomes from yet-to-be-named species, expand the pangenomes of human-associated microbes, and allow better exploitation of metagenomic technologies. |
format | Online Article Text |
id | pubmed-6349461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63494612019-01-31 Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle Pasolli, Edoardo Asnicar, Francesco Manara, Serena Zolfo, Moreno Karcher, Nicolai Armanini, Federica Beghini, Francesco Manghi, Paolo Tett, Adrian Ghensi, Paolo Collado, Maria Carmen Rice, Benjamin L. DuLong, Casey Morgan, Xochitl C. Golden, Christopher D. Quince, Christopher Huttenhower, Curtis Segata, Nicola Cell Article The body-wide human microbiome plays a role in health, but its full diversity remains uncharacterized, particularly outside of the gut and in international populations. We leveraged 9,428 metagenomes to reconstruct 154,723 microbial genomes (45% of high quality) spanning body sites, ages, countries, and lifestyles. We recapitulated 4,930 species-level genome bins (SGBs), 77% without genomes in public repositories (unknown SGBs [uSGBs]). uSGBs are prevalent (in 93% of well-assembled samples), expand underrepresented phyla, and are enriched in non-Westernized populations (40% of the total SGBs). We annotated 2.85 M genes in SGBs, many associated with conditions including infant development (94,000) or Westernization (106,000). SGBs and uSGBs permit deeper microbiome analyses and increase the average mappability of metagenomic reads from 67.76% to 87.51% in the gut (median 94.26%) and 65.14% to 82.34% in the mouth. We thus identify thousands of microbial genomes from yet-to-be-named species, expand the pangenomes of human-associated microbes, and allow better exploitation of metagenomic technologies. Cell Press 2019-01-24 /pmc/articles/PMC6349461/ /pubmed/30661755 http://dx.doi.org/10.1016/j.cell.2019.01.001 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pasolli, Edoardo Asnicar, Francesco Manara, Serena Zolfo, Moreno Karcher, Nicolai Armanini, Federica Beghini, Francesco Manghi, Paolo Tett, Adrian Ghensi, Paolo Collado, Maria Carmen Rice, Benjamin L. DuLong, Casey Morgan, Xochitl C. Golden, Christopher D. Quince, Christopher Huttenhower, Curtis Segata, Nicola Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle |
title | Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle |
title_full | Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle |
title_fullStr | Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle |
title_full_unstemmed | Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle |
title_short | Extensive Unexplored Human Microbiome Diversity Revealed by Over 150,000 Genomes from Metagenomes Spanning Age, Geography, and Lifestyle |
title_sort | extensive unexplored human microbiome diversity revealed by over 150,000 genomes from metagenomes spanning age, geography, and lifestyle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349461/ https://www.ncbi.nlm.nih.gov/pubmed/30661755 http://dx.doi.org/10.1016/j.cell.2019.01.001 |
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