An Integrated Multi‐Omics Analysis Defines Key Pathway Alterations in a Diet‐Induced Obesity Mouse Model

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  • Ulrik Kræmer Sundekilde
  • Christian Clement Yde, DuPont Nutrition Biosciences ApS, Brabrand
  • ,
  • Anders Hans Honoré, DuPont Nutrition Biosciences ApS, Brabrand
  • ,
  • Jessica M. Caverly Rae, E. I. duPont de Nemours and Company, Inc
  • ,
  • Frank R. Burns, E. I. duPont de Nemours and Company, Inc
  • ,
  • Pushkor Mukerji, E. I. duPont de Nemours and Company, Inc
  • ,
  • Michael P. Mawn, E. I. duPont de Nemours and Company, Inc
  • ,
  • Lotta Stenman, Dupont, Nutrition and Health, Kantvik, Finland
  • ,
  • Yvonne Dragan, E. I. duPont de Nemours and Company, Inc
  • ,
  • Kyle Glover, E. I. duPont de Nemours and Company, Inc
  • ,
  • Henrik Max Jensen, DuPont Nutrition Biosciences ApS, Brabrand, Danmark
Obesity is a multifactorial disease with many complications and related diseases and has become a global epidemic. To thoroughly understand the impact of obesity on whole organism homeostasis, it is helpful to utilize a systems biological approach combining gene expression and metabolomics across tissues and biofluids together with metagenomics of gut microbial diversity. Here, we present a multi-omics study on liver, muscle, adipose tissue, urine, plasma, and feces on mice fed a high-fat diet (HFD). Gene expression analyses showed alterations in genes related to lipid and energy metabolism and inflammation in liver and adipose tissue. The integration of metabolomics data across tissues and biofluids identified major differences in liver TCA cycle, where malate, succinate and oxaloacetate were found to be increased in HFD mice. This finding was supported by gene expression analysis of TCA-related enzymes in liver, where expression of malate dehydrogenase was found to be decreased. Investigations of the microbiome showed enrichment of Lachnospiraceae, Ruminococcaceae, Streptococcaceae and Lactobacillaceae in the HFD group. Our findings help elucidate how the whole organism metabolome and transcriptome are integrated and regulated during obesity.
OriginalsprogEngelsk
Artikelnummer80
TidsskriftMetabolites
Vol/bind10
Nummer3
Antal sider16
ISSN2218-1989
DOI
StatusUdgivet - feb. 2020

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