Mobile genes in the human microbiome are structured from global to individual scales
Authors
Ilana L. Brito, Massachusetts Institute of Technology
Suzan A. Yilmaz, Sandia National Laboratories
K. Huang, Broad Institute, Cambridge, United States
Liyi Xu, Broad Institute, Cambridge, United States
Stacy D. Jupiter, Wildlife Conservation Society, Suva, Fiji
Aaron P. Jenkins, Edith Cowan University
Waisea Naisilisili, Wildlife Conservation Society, Suva, Fiji
M. Tamminen, Eidgenossische Technische Hochschule Zurich
Chris S. Millie, Massachusetts Institute of Technology
Jennifer R. Wortman, Broad Institute, Cambridge, United States
Bruce W. Birren, Broad Institute, Cambridge, United States
Ramnik J. Xavier, Massachusetts General Hospital, Center for Computational and Integrative
Paul C. Blainey, Broad Institute, Cambridge, United States
A. K. Singh, Sandia National Laboratories, California
Dirk Gevers, Janssen Human Microbiome Institute, Cambridge, United States
Eric Alm, Massachusetts Institute of Technology
Document Type
Journal Article
Publication Title
Nature
Publisher
Nature
Place of Publication
United Kingdom
School
School of Medical and Health Sciences
RAS ID
24426
Abstract
Recent work has underscored the importance of the microbiome in human health, and has largely attributed differences in phenotype to differences in the species present among individuals. However, mobile genes can confer profoundly different phenotypes on different strains of the same species. Little is known about the function and distribution of mobile genes in the human microbiome, and in particular whether the gene pool is globally homogenous or constrained by human population structure. Here, we investigate this question by comparing the mobile genes found in the microbiomes of 81 metropolitan North Americans with those of 172 agrarian Fiji islanders using a combination of single-cell genomics and metagenomics. We find large differences in mobile gene content between the Fijian and North American microbiomes, with functional variation that mirrors known dietary differences such as the excess of plant-based starch degradation genes found in Fijian individuals. Notably, we also observed differences between the mobile gene pools of neighbouring Fijian villages, even though microbiome composition across villages is similar. Finally, we observe high rates of recombination leading to individual-specific mobile elements, suggesting that the abundance of some genes may reflect environmental selection rather than dispersal limitation. Together, these data support the hypothesis that human activities and behaviours provide selective pressures that shape mobile gene pools, and that acquisition of mobile genes is important for colonizing specific human populations.
DOI
10.1038/nature18927
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Comments
Brito, I. L., Yilmaz, S., Huang, K. Xu, L., Jupiter, S. D., Jenkins, A. P., . . . Alm E. J. (2016). Mobile genes in the human microbiome are structured from global to individual scales. Nature, 535, 435-439. Available here