自闭症谱系障碍
生物
微生物群
自闭症
代谢组
肠-脑轴
肠道菌群
人体微生物群
神经科学
遗传学
免疫学
生物信息学
代谢组学
心理学
发展心理学
作者
Gil Sharon,Nikki Jamie Cruz,Dae‐Wook Kang,Michael J. Gandal,Bo Wang,Young‐Mo Kim,Erika Zink,Cameron Casey,Bryn C. Taylor,Christianne J. Lane,Lisa Bramer,Nancy Isern,David Hoyt,Cecilia Noecker,Michael J. Sweredoski,Annie Moradian,Elhanan Borenstein,Janet Jansson,Rob Knight,Thomas Metz
出处
期刊:Cell
[Cell Press]
日期:2019-05-01
卷期号:177 (6): 1600-1618.e17
被引量:899
标识
DOI:10.1016/j.cell.2019.05.004
摘要
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 germ-free 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 excitability 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.
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