4.8 Article

Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice

期刊

CELL
卷 177, 期 6, 页码 1600-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2019.05.004

关键词

-

资金

  1. U.S. Department of Energy Office of Biological and Environmental Research
  2. DOE [DE-AC05-76RLO 1830]
  3. Autism Speaks Postdoctoral Fellowship in Translational Research [9718]
  4. Human Frontiers Science Program Long-Term Fellowship [2012/65]
  5. SFARI Bridge to Independence Award
  6. San Diego Diversity Fellowship
  7. National Biomedical Computation Resource
  8. NIH [GM124312-01, NS104925, HD055784, MH100027, MH100556]
  9. Autism Research Institute
  10. Emch Foundation
  11. Brenen Hornstein Autism Research AMP
  12. Education Foundation
  13. Simons Foundation
  14. Heritage Medical Research Institute

向作者/读者索取更多资源

Autism spectrum disorder (ASD) manifests as alterations in complex human behaviors including social communication and stereotypies. In addition to genetic risks, the gut microbiome differs between typically developing (TD) and ASD individuals, though it remains unclear whether the microbiome contributes to symptoms. We transplanted gut microbiota from human donors with ASD or TD controls into germfree mice and reveal that colonization with ASD microbiota is sufficient to induce hallmark autistic behaviors. The brains of mice colonized with ASD microbiota display alternative splicing of ASD-relevant genes. Microbiome and metabolome profiles of mice harboring human microbiota predict that specific bacterial taxa and their metabolites modulate ASD behaviors. Indeed, treatment of an ASD mouse model with candidate microbial metabolites improves behavioral abnormalities and modulates neuronal excitnhility in the brain. We propose that the gut microbiota regulates behaviors in mice via production of neuroactive metabolites, suggesting that gut-brain connections contribute to the pathophysiology of ASD.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据