Publication
Population-based metagenomics analysis reveals markers for gut microbiome composition and diversity
Zhernakova, A., Kurilshchikov, A., Bonder, M. J., Tigchelaar, E. F., Schirmer, M., Vatanen, T., Mujagic, Z., Vich Vila, A., Falony, G., Vieira-Silva, S., Wang, J., Imhann, F., Brandsma, E., Jankipersadsing, S. A., Joossens, M., Cenit, M. C., Deelen, P., Swertz, M. A., Weersma, R. K., Feskens, E. J. M., Netea, M. G., Gevers, D., Jonkers, D., Franke, L., Aulchenko, Y. S., Huttenhower, C., Raes, J., Hofker, M. H., Xavier, R. J., Wijmenga, C., Fu, J. & Lifelines Cohort Study, 29-Apr-2016, In : Science. 352, 6285, p. 565-569 5 p.Research output: Contribution to journal › Article › Academic › peer-review

Documents
- Population-based metagenomics analysis reveals markers for gut microbiome composition
Final publisher's version, 1.26 MB, PDF document
DOI
Deep sequencing of the gut microbiomes of 1135 participants from a Dutch population-based cohort shows relations between the microbiome and 126 exogenous and intrinsic host factors, including 31 intrinsic factors, 12 diseases, 19 drug groups, 4 smoking categories, and 60 dietary factors. These factors collectively explain 18.7% of the variation seen in the interindividual distance of microbial composition. We could associate 110 factors to 125 species and observed that fecal chromogranin A (CgA), a protein secreted by enteroendocrine cells, was exclusively associated with 61 microbial species whose abundance collectively accounted for 53% of microbial composition. Low CgA concentrations were seen in individuals with a more diverse microbiome. These results are an important step toward a better understanding of environment-diet-microbe-host interactions.
Original language | English |
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Pages (from-to) | 565-569 |
Number of pages | 5 |
Journal | Science |
Volume | 352 |
Issue number | 6285 |
Publication status | Published - 29-Apr-2016 |
- CHROMOGRANIN-A, ENTEROTYPES, POLYPHENOLS, METABOLISM, CHILDREN
Keywords
ID: 32087608