Population Genetics in the Human Microbiome

被引:76
|
作者
Garud, Nandita R. [1 ]
Pollard, Katherine S. [2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90032 USA
[2] Gladstone Inst, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[4] Chan Zuckerberg Biohub, San Francisco, CA 94158 USA
基金
美国国家科学基金会;
关键词
GENOME-WIDE ASSOCIATION; COPY-NUMBER VARIATION; MOLECULAR EVOLUTION; ESCHERICHIA-COLI; GUT MICROBIOMES; MYCOBACTERIUM-TUBERCULOSIS; BACTERIAL TRANSMISSION; SPECIES DEFINITION; SELECTIVE SWEEPS; RAPID EVOLUTION;
D O I
10.1016/j.tig.2019.10.010
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
While the human microbiome's structure and function have been extensively studied, its within-species genetic diversity is less well understood. However, genetic mutations in the microbiome can confer biomedically relevant traits, such as the ability to extract nutrients from food, metabolize drugs, evade antibiotics, and communicate with the host immune system. The populatior genetic processes by which these traits evolve are complex, in part due to interacting ecological and evolutionary forces in the microbiome. Advances in metagenomic sequencing, coupled with bioinformatics tools and population genetic models, facilitate quantification of microbiome genetic variation and inferences about how this diversity arises, evolves, and correlates with trait of both n and hosts. In this review, we explore the population genetic forces (mutation , recombination, drift, and selection) that shape microbiome genetic diversity within and between hosts, as well as efforts towards predictive models that leverage microbiome genetics.
引用
收藏
页码:53 / 67
页数:15
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