The gut microbiota modulates host amino acid and glutathione metabolism in mice

Autor: Cheng Cheng Zhang, Mattias Bergentall, Fredrik Bäckhed, Erik Larsson, Saeed Shoaie, Adil Mardinoglu, Jens Nielsen, Pouyan Ghaffari
Rok vydání: 2015
Předmět:
Male
genome-scale metabolic models
Adipose tissue
Ileum
White adipose tissue
Gut flora
digestive system
General Biochemistry
Genetics and Molecular Biology

Jejunum
Mice
transcriptomics
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
germ-free mice
Intestine
Small

Journal Article
medicine
Animals
Amino Acids
030304 developmental biology
0303 health sciences
General Immunology and Microbiology
biology
Microbiota
Research Support
Non-U.S. Gov't

Applied Mathematics
Biochemistry and Molecular Biology
Articles
glutathione metabolism
Glutathione
Metabolism
biology.organism_classification
metabolomics
Small intestine
Mice
Inbred C57BL

medicine.anatomical_structure
Computational Theory and Mathematics
chemistry
Biochemistry
General Agricultural and Biological Sciences
Cell and Molecular Biology
030217 neurology & neurosurgery
Information Systems
Zdroj: Molecular Systems Biology (1744-4292) vol.11(2015)
Mardinoglu, A, Bergentall, M, Ghaffari, P, Zhang, C, Larsson, E, Bäckhed, F, Nielsen, J & Shoaie, S 2015, ' The gut microbiota modulates host amino acid and glutathione metabolism in mice ', Molecular Systems Biology, vol. 11, no. 10, pp. 834 . https://doi.org/10.15252/msb.20156487
Molecular Systems Biology
ISSN: 1744-4292
DOI: 10.15252/msb.20156487
Popis: The gut microbiota has been proposed as an environmental factor that promotes the progression of metabolic diseases. Here, we investigated how the gut microbiota modulates the global metabolic differences in duodenum, jejunum, ileum, colon, liver, and two white adipose tissue depots obtained from conventionally raised (CONV-R) and germ-free (GF) mice using gene expression data and tissue-specific genome-scale metabolic models (GEMs). We created a generic mouse metabolic reaction (MMR) GEM, reconstructed 28 tissue-specific GEMs based on proteomics data, and manually curated GEMs for small intestine, colon, liver, and adipose tissues. We used these functional models to determine the global metabolic differences between CONV-R and GF mice. Based on gene expression data, we found that the gut microbiota affects the host amino acid (AA) metabolism, which leads to modifications in glutathione metabolism. To validate our predictions, we measured the level of AAs and N-acetylated AAs in the hepatic portal vein of CONV-R and GF mice. Finally, we simulated the metabolic differences between the small intestine of the CONV-R and GF mice accounting for the content of the diet and relative gene expression differences. Our analyses revealed that the gut microbiota influences host amino acid and glutathione metabolism in mice.
Databáze: OpenAIRE