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  • 标题:Murine Genetic Background Overcomes Gut Microbiota Changes to Explain Metabolic Response to High-Fat Diet
  • 本地全文:下载
  • 作者:Zahra Safari ; Aurélia Bruneau ; Magali Monnoye
  • 期刊名称:Nutrients
  • 电子版ISSN:2072-6643
  • 出版年度:2020
  • 卷号:12
  • 期号:2
  • 页码:287-304
  • DOI:10.3390/nu12020287
  • 出版社:MDPI Publishing
  • 摘要:Interactions of diet, gut microbiota, and host genetics play essential roles in the development of metabolic diseases. A/J and C57BL/6J (C57) are two mouse strains known to display different susceptibilities to metabolic disorders. In this context, we analyzed gut microbiota composition in A/J and C57 mice, and assessed its responses to high-fat diet (HFD) and antibiotic (AB) treatment. We also exchanged the gut microbiota between the two strains following AB treatment to evaluate its impact on the metabolism. We showed that A/J and C57 mice have different microbiome structure and composition at baseline. Moreover, A/J and C57 microbiomes responded differently to HFD and AB treatments. Exchange of the gut microbiota between the two strains was successful as recipients’ microbiota resembled donor-strain microbiota. Seven weeks after inoculation, the differences between recipients persisted and were still closer from the donor-strain microbiota. Despite effective microbiota transplants, the response to HFD was not markedly modified in C57 and A/J mice. Particularly, body weight gain and glucose intolerance in response to HFD remained different in the two mouse strains whatever the changes in microbiome composition. This indicated that genetic background has a much stronger impact on metabolic responses to HFD than gut microbiome composition.
  • 关键词:fecal microbiota transplantation (FMT); antibiotic treatment; high-fat diet (HFD); genetic background; metabolic disease; non-alcoholic fatty liver disease (NAFLD) fecal microbiota transplantation (FMT) ; antibiotic treatment ; high-fat diet (HFD) ; genetic background ; metabolic disease ; non-alcoholic fatty liver disease (NAFLD)
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