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The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing

The goal of the Human Microbiome Project (HMP) is to generate a comprehensive catalog of human-associated microorganisms including reference genomes representing the most common species. Toward this goal, the HMP has characterized the microbial communities at 18 body habitats in a cohort of over 200...

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Autores principales: Fodor, Anthony A., DeSantis, Todd Z., Wylie, Kristine M., Badger, Jonathan H., Ye, Yuzhen, Hepburn, Theresa, Hu, Ping, Sodergren, Erica, Liolios, Konstantinos, Huot-Creasy, Heather, Birren, Bruce W., Earl, Ashlee M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406062/
https://www.ncbi.nlm.nih.gov/pubmed/22848458
http://dx.doi.org/10.1371/journal.pone.0041294
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author Fodor, Anthony A.
DeSantis, Todd Z.
Wylie, Kristine M.
Badger, Jonathan H.
Ye, Yuzhen
Hepburn, Theresa
Hu, Ping
Sodergren, Erica
Liolios, Konstantinos
Huot-Creasy, Heather
Birren, Bruce W.
Earl, Ashlee M.
author_facet Fodor, Anthony A.
DeSantis, Todd Z.
Wylie, Kristine M.
Badger, Jonathan H.
Ye, Yuzhen
Hepburn, Theresa
Hu, Ping
Sodergren, Erica
Liolios, Konstantinos
Huot-Creasy, Heather
Birren, Bruce W.
Earl, Ashlee M.
author_sort Fodor, Anthony A.
collection PubMed
description The goal of the Human Microbiome Project (HMP) is to generate a comprehensive catalog of human-associated microorganisms including reference genomes representing the most common species. Toward this goal, the HMP has characterized the microbial communities at 18 body habitats in a cohort of over 200 healthy volunteers using 16S rRNA gene (16S) sequencing and has generated nearly 1,000 reference genomes from human-associated microorganisms. To determine how well current reference genome collections capture the diversity observed among the healthy microbiome and to guide isolation and future sequencing of microbiome members, we compared the HMP’s 16S data sets to several reference 16S collections to create a ‘most wanted’ list of taxa for sequencing. Our analysis revealed that the diversity of commonly occurring taxa within the HMP cohort microbiome is relatively modest, few novel taxa are represented by these OTUs and many common taxa among HMP volunteers recur across different populations of healthy humans. Taken together, these results suggest that it should be possible to perform whole-genome sequencing on a large fraction of the human microbiome, including the ‘most wanted’, and that these sequences should serve to support microbiome studies across multiple cohorts. Also, in stark contrast to other taxa, the ‘most wanted’ organisms are poorly represented among culture collections suggesting that novel culture- and single-cell-based methods will be required to isolate these organisms for sequencing.
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spelling pubmed-34060622012-07-30 The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing Fodor, Anthony A. DeSantis, Todd Z. Wylie, Kristine M. Badger, Jonathan H. Ye, Yuzhen Hepburn, Theresa Hu, Ping Sodergren, Erica Liolios, Konstantinos Huot-Creasy, Heather Birren, Bruce W. Earl, Ashlee M. PLoS One Research Article The goal of the Human Microbiome Project (HMP) is to generate a comprehensive catalog of human-associated microorganisms including reference genomes representing the most common species. Toward this goal, the HMP has characterized the microbial communities at 18 body habitats in a cohort of over 200 healthy volunteers using 16S rRNA gene (16S) sequencing and has generated nearly 1,000 reference genomes from human-associated microorganisms. To determine how well current reference genome collections capture the diversity observed among the healthy microbiome and to guide isolation and future sequencing of microbiome members, we compared the HMP’s 16S data sets to several reference 16S collections to create a ‘most wanted’ list of taxa for sequencing. Our analysis revealed that the diversity of commonly occurring taxa within the HMP cohort microbiome is relatively modest, few novel taxa are represented by these OTUs and many common taxa among HMP volunteers recur across different populations of healthy humans. Taken together, these results suggest that it should be possible to perform whole-genome sequencing on a large fraction of the human microbiome, including the ‘most wanted’, and that these sequences should serve to support microbiome studies across multiple cohorts. Also, in stark contrast to other taxa, the ‘most wanted’ organisms are poorly represented among culture collections suggesting that novel culture- and single-cell-based methods will be required to isolate these organisms for sequencing. Public Library of Science 2012-07-26 /pmc/articles/PMC3406062/ /pubmed/22848458 http://dx.doi.org/10.1371/journal.pone.0041294 Text en © 2012 Fodor et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fodor, Anthony A.
DeSantis, Todd Z.
Wylie, Kristine M.
Badger, Jonathan H.
Ye, Yuzhen
Hepburn, Theresa
Hu, Ping
Sodergren, Erica
Liolios, Konstantinos
Huot-Creasy, Heather
Birren, Bruce W.
Earl, Ashlee M.
The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing
title The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing
title_full The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing
title_fullStr The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing
title_full_unstemmed The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing
title_short The “Most Wanted” Taxa from the Human Microbiome for Whole Genome Sequencing
title_sort “most wanted” taxa from the human microbiome for whole genome sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406062/
https://www.ncbi.nlm.nih.gov/pubmed/22848458
http://dx.doi.org/10.1371/journal.pone.0041294
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