A core human microbiome as viewed through 16S rRNA sequence clusters.

We explore the microbiota of 18 body sites in over 200 individuals using sequences amplified V1-V3 and the V3-V5 small subunit ribosomal RNA (16S) hypervariable regions as part of the NIH Common Fund Human Microbiome Project. The body sites with the greatest number of core OTUs, defined as OTUs shar...

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Main Authors: Susan M Huse, Yuzhen Ye, Yanjiao Zhou, Anthony A Fodor
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3374614?pdf=render
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spelling doaj-d91659c549f3421f8ac2c983bb2ffaa02020-11-25T01:05:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0176e3424210.1371/journal.pone.0034242A core human microbiome as viewed through 16S rRNA sequence clusters.Susan M HuseYuzhen YeYanjiao ZhouAnthony A FodorWe explore the microbiota of 18 body sites in over 200 individuals using sequences amplified V1-V3 and the V3-V5 small subunit ribosomal RNA (16S) hypervariable regions as part of the NIH Common Fund Human Microbiome Project. The body sites with the greatest number of core OTUs, defined as OTUs shared amongst 95% or more of the individuals, were the oral sites (saliva, tongue, cheek, gums, and throat) followed by the nose, stool, and skin, while the vaginal sites had the fewest number of OTUs shared across subjects. We found that commonalities between samples based on taxonomy could sometimes belie variability at the sub-genus OTU level. This was particularly apparent in the mouth where a given genus can be present in many different oral sites, but the sub-genus OTUs show very distinct site selection, and in the vaginal sites, which are consistently dominated by the Lactobacillus genus but have distinctly different sub-genus V1-V3 OTU populations across subjects. Different body sites show approximately a ten-fold difference in estimated microbial richness, with stool samples having the highest estimated richness, followed by the mouth, throat and gums, then by the skin, nasal and vaginal sites. Richness as measured by the V1-V3 primers was consistently higher than richness measured by V3-V5. We also show that when such a large cohort is analyzed at the genus level, most subjects fit the stool "enterotype" profile, but other subjects are intermediate, blurring the distinction between the enterotypes. When analyzed at the finer-scale, OTU level, there was little or no segregation into stool enterotypes, but in the vagina distinct biotypes were apparent. Finally, we note that even OTUs present in nearly every subject, or that dominate in some samples, showed orders of magnitude variation in relative abundance emphasizing the highly variable nature across individuals.http://europepmc.org/articles/PMC3374614?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Susan M Huse
Yuzhen Ye
Yanjiao Zhou
Anthony A Fodor
spellingShingle Susan M Huse
Yuzhen Ye
Yanjiao Zhou
Anthony A Fodor
A core human microbiome as viewed through 16S rRNA sequence clusters.
PLoS ONE
author_facet Susan M Huse
Yuzhen Ye
Yanjiao Zhou
Anthony A Fodor
author_sort Susan M Huse
title A core human microbiome as viewed through 16S rRNA sequence clusters.
title_short A core human microbiome as viewed through 16S rRNA sequence clusters.
title_full A core human microbiome as viewed through 16S rRNA sequence clusters.
title_fullStr A core human microbiome as viewed through 16S rRNA sequence clusters.
title_full_unstemmed A core human microbiome as viewed through 16S rRNA sequence clusters.
title_sort core human microbiome as viewed through 16s rrna sequence clusters.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description We explore the microbiota of 18 body sites in over 200 individuals using sequences amplified V1-V3 and the V3-V5 small subunit ribosomal RNA (16S) hypervariable regions as part of the NIH Common Fund Human Microbiome Project. The body sites with the greatest number of core OTUs, defined as OTUs shared amongst 95% or more of the individuals, were the oral sites (saliva, tongue, cheek, gums, and throat) followed by the nose, stool, and skin, while the vaginal sites had the fewest number of OTUs shared across subjects. We found that commonalities between samples based on taxonomy could sometimes belie variability at the sub-genus OTU level. This was particularly apparent in the mouth where a given genus can be present in many different oral sites, but the sub-genus OTUs show very distinct site selection, and in the vaginal sites, which are consistently dominated by the Lactobacillus genus but have distinctly different sub-genus V1-V3 OTU populations across subjects. Different body sites show approximately a ten-fold difference in estimated microbial richness, with stool samples having the highest estimated richness, followed by the mouth, throat and gums, then by the skin, nasal and vaginal sites. Richness as measured by the V1-V3 primers was consistently higher than richness measured by V3-V5. We also show that when such a large cohort is analyzed at the genus level, most subjects fit the stool "enterotype" profile, but other subjects are intermediate, blurring the distinction between the enterotypes. When analyzed at the finer-scale, OTU level, there was little or no segregation into stool enterotypes, but in the vagina distinct biotypes were apparent. Finally, we note that even OTUs present in nearly every subject, or that dominate in some samples, showed orders of magnitude variation in relative abundance emphasizing the highly variable nature across individuals.
url http://europepmc.org/articles/PMC3374614?pdf=render
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