Diet, Genetics, and the Gut Microbiome Drive Dynamic Changes in Plasma Metabolites

被引:169
作者
Fujisaka, Shiho [1 ,2 ,3 ]
Avila-Pacheco, Julian [4 ]
Soto, Marion [1 ,2 ]
Kostic, Aleksandar [2 ,5 ]
Dreyfuss, Jonathan M. [2 ,6 ,7 ]
Pan, Hui [2 ,6 ,7 ]
Ussar, Siegfried [1 ,2 ,8 ]
Altindis, Emrah [1 ,2 ]
Li, Ning [9 ]
Bry, Lynn [9 ]
Clish, Clary B. [4 ]
Kahn, C. Ronald [1 ,2 ]
机构
[1] Joslin Diabet Ctr, Sect Integrat Physiol & Metab, Boston, MA 02215 USA
[2] Harvard Med Sch, Boston, MA 02215 USA
[3] Univ Toyama, Dept Internal Med 1, Toyama 9300194, Japan
[4] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[5] Joslin Diabet Ctr, Dept Microbiol & Immunobiol, Boston, MA 02215 USA
[6] Joslin Diabet Ctr, Bioinformat Core, Boston, MA 02215 USA
[7] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[8] Helmholtz Zentrum Munchen, Inst Diabet & Obes, D-85764 Neuherberg, Germany
[9] Brigham & Womens Hosp, Dept Pathol, Ctr Clin & Translat Metagen, 75 Francis St, Boston, MA 02115 USA
来源
CELL REPORTS | 2018年 / 22卷 / 11期
关键词
CHAIN FATTY-ACIDS; INSULIN-RESISTANCE; OBESE MICE; DISEASE; RISK; HEALTH; PHOSPHATIDYLCHOLINE; CONTRIBUTES; SENSITIVITY; PHYSIOLOGY;
D O I
10.1016/j.celrep.2018.02.060
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Diet, genetics, and the gut microbiome are determinants of metabolic status, in part through production of metabolites by the gut microbiota. To understand the mechanisms linking these factors, we performed LC-MS-based metabolomic analysis of cecal contents and plasma from C57BL/6J, 129S1/SvImJ, and 129S6/SvEvTac mice on chow or a high-fat diet (HFD) and HFD-treated with vancomycin or metronidazole. Prediction of the functional metagenome of gut bacteria by PICRUSt analysis of 16S sequences revealed dramatic differences in microbial metabolism. Cecal and plasma metabolites showed multifold differences reflecting the combined and integrated effects of diet, antibiotics, host background, and the gut microbiome. Eighteen plasma metabolites correlated positively or negatively with host insulin resistance across strains and diets. Over 1,000 still-unidentified metabolite peaks were also highly regulated by diet, antibiotics, and genetic background. Thus, diet, host genetics, and the gut microbiota interact to create distinct responses in plasma metabolites, which can contribute to regulation of metabolism and insulin resistance.
引用
收藏
页码:3072 / 3086
页数:15
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