Abstract

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.

Highlights

  • While the microbiota that live on and in the human body have long been recognized as critical to understanding a variety of human diseases, we are only beginning to understand their critical role in maintaining human health

  • Study Set The Human Microbiome Project (HMP) 16S sequencing includes sequences amplified from the V3–V5 region, and in most cases amplified from the V1–V3 region as well

  • There were a total of,12 million V1–V3 and,15 million V3–V5 reads, and between 404 and 9,489 operational taxonomic units (OTUs) identified by body site, with an average sequencing depth of 5,709 tags (Table S1)

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Summary

Introduction

While the microbiota that live on and in the human body have long been recognized as critical to understanding a variety of human diseases, we are only beginning to understand their critical role in maintaining human health To facilitate this understanding, the National Institutes of Health launched the Human Microbiome Project (HMP) in 2008 [1] to sequence the microbiome of healthy human subjects The HMP is using both 16S rRNA tag sequencing to elucidate the types of microbes and their relative abundances and shotgun metagenomic sequencing to find out what functions these microbes may be performing These analyses, being published as an overview manuscript [3] and a series of companion papers, lay the groundwork for further research in the human microbiome: the similarities and differences between individuals and body sites, and through time the numbers and types of microbes and what role they play in human health

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