Host genetic variation impacts microbiome composition across human body sites

被引:501
作者
Blekhman, Ran [1 ,2 ]
Goodrich, Julia K. [3 ,4 ]
Huang, Katherine [5 ]
Sun, Qi [6 ]
Bukowski, Robert [6 ]
Bell, Jordana T. [7 ]
Spector, Timothy D. [7 ]
Keinan, Alon [8 ]
Ley, Ruth E. [3 ,4 ]
Gevers, Dirk [5 ]
Clark, Andrew G. [3 ]
机构
[1] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Ecol Evolut & Behav, St Paul, MN 55108 USA
[3] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
[4] Cornell Univ, Dept Microbiol, Ithaca, NY 14853 USA
[5] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[6] Cornell Univ, Inst Biotechnol, BRC Bioinformat Facil, Ithaca, NY 14853 USA
[7] Kings Coll London, Dept Twin Res & Genet Epidemiol, London, England
[8] Cornell Univ, Dept Biol Stat & Computat Biol, Ithaca, NY 14853 USA
来源
GENOME BIOLOGY | 2015年 / 16卷
基金
英国惠康基金;
关键词
GUT MICROBIOME; INTESTINAL MICROBIOTA; WIDE ASSOCIATION; LEPTIN RECEPTOR; INNATE IMMUNITY; EXPRESSION; POPULATION; SHAPE; DIET; DYSBIOSIS;
D O I
10.1186/s13059-015-0759-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The composition of bacteria in and on the human body varies widely across human individuals, and has been associated with multiple health conditions. While microbial communities are influenced by environmental factors, some degree of genetic influence of the host on the microbiome is also expected. This study is part of an expanding effort to comprehensively profile the interactions between human genetic variation and the composition of this microbial ecosystem on a genome- and microbiome-wide scale. Results: Here, we jointly analyze the composition of the human microbiome and host genetic variation. By mining the shotgun metagenomic data from the Human Microbiome Project for host DNA reads, we gathered information on host genetic variation for 93 individuals for whom bacterial abundance data are also available. Using this dataset, we identify significant associations between host genetic variation and microbiome composition in 10 of the 15 body sites tested. These associations are driven by host genetic variation in immunity-related pathways, and are especially enriched in host genes that have been previously associated with microbiome-related complex diseases, such as inflammatory bowel disease and obesity-related disorders. Lastly, we show that host genomic regions associated with the microbiome have high levels of genetic differentiation among human populations, possibly indicating host genomic adaptation to environment-specific microbiomes. Conclusions: Our results highlight the role of host genetic variation in shaping the composition of the human microbiome, and provide a starting point toward understanding the complex interaction between human genetics and the microbiome in the context of human evolution and disease.
引用
收藏
页数:12
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