From next-generation sequencing to systematic modeling of the gut microbiome

被引:69
|
作者
Ji, Boyang [1 ]
Nielsen, Jens [1 ]
机构
[1] Chalmers Univ Technol, Dept Biol & Biol Engn, Div Syst & Synthet Biol, SE-41296 Gothenburg, Sweden
关键词
FECAL MICROBIOTA; FAECALIBACTERIUM-PRAUSNITZII; INTESTINAL MICROBIOTA; PLASMODIUM-FALCIPARUM; DRUG TARGETS; HOST; BIOLOGY; DIET; DNA; INTEGRATION;
D O I
10.3389/fgene.2015.00219
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Changes in the human gut microbiome are associated with altered human metabolism and health, yet the mechanisms of interactions between microbial species and human metabolism have not been clearly elucidated. Next-generation sequencing has revolutionized the human gut microbiome research, but most current applications concentrate on studying the microbial diversity of communities and have at best provided associations between specific gut bacteria and human health. However, little is known about the inner metabolic mechanisms in the gut ecosystem. Here we review recent progress in modeling the metabolic interactions of gut microbiome, with special focus on the utilization of metabolic modeling to infer host microbe interactions and microbial species interactions. The systematic modeling of metabolic interactions could provide a predictive understanding of gut microbiome, and pave the way to synthetic microbiota design and personalized-microbiome medicine and healthcare. Finally, we discuss the integration of metabolic modeling and gut microbiome engineering, which offer a new way to explore metabolic interactions across members of the gut microbiota.
引用
收藏
页数:9
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