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Structure, function and diversity of the healthy human microbiome

J. Fah Sathirapongsasuti, Nicola Segata, Niall J. Lennon, Theresa A. Hepburn, Allison Griggs, Doyle V. Ward, Chandri Yandava, Dennis C. Friedrich, Sheila Fisher, Margaret Priest, Narmada Shenoy, Cristyn Kells, Diana Tabbaa, Curtis Huttenhower, Eric J. Alm

Nature · 2012 · ▲ 11,906 citations

Abstract

Studies of the human microbiome have revealed that even healthy individuals differ remarkably in the microbes that occupy habitats such as the gut, skin and vagina. Much of this diversity remains unexplained, although diet, environment, host genetics and early microbial exposure have all been implicated. Accordingly, to characterize the ecology of human-associated microbial communities, the Human Microbiome Project has analysed the largest cohort and set of distinct, clinically relevant body habitats so far. We found the diversity and abundance of each habitat’s signature microbes to vary widely even among healthy subjects, with strong niche specialization both within and among individuals. The project encountered an estimated 81–99% of the genera, enzyme families and community configurations occupied by the healthy Western microbiome. Metagenomic carriage of metabolic pathways was stable among individuals despite variation in community structure, and ethnic/racial background proved to be one of the strongest associations of both pathways and microbes with clinical metadata. These results thus delineate the range of structural and functional configurations normal in the microbial communities of a healthy population, enabling future characterization of the epidemiology, ecology and translational applications of the human microbiome. The Human Microbiome Project Consortium reports the first results of their analysis of microbial communities from distinct, clinically relevant body habitats in a human cohort; the insights into the microbial communities of a healthy population lay foundations for future exploration of the epidemiology, ecology and translational applications of the human microbiome. The Human Microbiome Project (HMP), supported by the National Institutes of Health Common Fund, has the goal of characterizing the microbial communities that inhabit and interact with the human body in sickness and in health. In two Articles in this issue of Nature, the HMP Consortium presents the first population-scale details of the organismal and functional composition of the microbiota across five areas of the body. An associated News & Views discusses the initial results — which, along with those of a series of co-publications, already constitute the most extensive catalogue of organisms and genes related to the human microbiome yet published — and highlights some of the major questions that the project will tackle in the next few years.

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Provenance

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OpenAlex
DOI
10.1038/nature11234
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2026-06-12 MST

Cite this

APA
Sathirapongsasuti, J.F., Segata, N., Lennon, N.J., Hepburn, T.A., Griggs, A., Ward, D.V., Yandava, C., Friedrich, D.C., Fisher, S., Priest, M., Shenoy, N., Kells, C., Tabbaa, D., Huttenhower, C., Alm, E.J., Gevers, D., Earl, A.M., Goldberg, J.M., Haas, B.J., &amp; Gujja, S. (2012). Structure, function and diversity of the healthy human microbiome. <em>Nature</em>. https://doi.org/10.1038/nature11234
Vancouver
Sathirapongsasuti JF, Segata N, Lennon NJ, Hepburn TA, Griggs A, Ward DV, et al. Structure, function and diversity of the healthy human microbiome. Nature. 2012. doi:10.1038/nature11234.
BibTeX
@article{j2012Struct, title = {Structure, function and diversity of the healthy human microbiome}, author = {J. Fah Sathirapongsasuti and Nicola Segata and Niall J. Lennon and Theresa A. Hepburn and Allison Griggs and Doyle V. Ward and Chandri Yandava and Dennis C. Friedrich and Sheila Fisher and Margaret Priest and Narmada Shenoy and Cristyn Kells and Diana Tabbaa and Curtis Huttenhower and Eric J. Alm and Dirk Gevers and Ashlee M. Earl and Jonathan M. Goldberg and Brian J. Haas and Sharvari Gujja and Susan J. Birren and Harindra Arachchi and M.A. Pearson}, journal = {Nature}, year = {2012}, doi = {10.1038/nature11234}, }

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