生物
肠道菌群
普雷沃菌属
自闭症谱系障碍
基因组
拟杆菌
自闭症
微生物群
神经发育障碍
粪便
蔷薇花
人口
遗传学
生物信息学
生理学
微生物学
免疫学
细菌
医学
精神科
基因
环境卫生
作者
Dan Zhou,Xuhua Mao,Qisha Liu,Mengchen Guo,Yaoyao Zhuang,Zhi Liu,Kun Chen,Junyu Chen,Rui Xu,Jun‐Ming Tang,Lianhong Qin,Bing Gu,Kangjian Liu,Chuan Su,Faming Zhang,Yankai Xia,Zhibin Hu,Xingyin Liu
出处
期刊:Gut microbes
[Informa]
日期:2020-04-21
卷期号:11 (5): 1246-1267
被引量:221
标识
DOI:10.1080/19490976.2020.1747329
摘要
Autism Spectrum Disorder (ASD) is a severe neurodevelopmental disorder. To enhance the understanding of the gut microbiota structure in ASD children at different ages as well as the relationship between gut microbiota and fecal metabolites, we first used the 16S rRNA sequencing to evaluate the gut microbial population in a cohort of 143 children aged 2–13 years old. We found that the α-diversity of ASD group showed no significant change with age, while the TD group showed increased α-diversity with age, which indicates that the compositional development of the gut microbiota in ASD varies at different ages in ways that are not consistent with TD group. Recent studies have shown that chronic constipation is one of the most commonly obvious gastrointestinal (GI) symptoms along with ASD core symptoms. To further investigate the potential interaction effects between ASD and GI symptoms, the 30 C-ASD and their aged-matched TD were picked out to perform metagenomics analysis. We observed that C-ASD group displayed decreased diversity, depletion of species of Sutterella, Prevotella, and Bacteroides as well as dysregulation of associated metabolism activities, which may involve in the pathogenesis of C-ASD. Consistent with metagenomic analysis, liquid chromatography-mass spectrometry (LC/MS) revealed some of the differential metabolites between C-ASD and TD group were involved in the metabolic network of neurotransmitters including serotonin, dopamine, histidine, and GABA. Furthermore, we found these differences in metabolites were associated with altered abundance of specific bacteria. The study suggested possible future modalities for ASD intervention through targeting the specific bacteria associated with neurotransmitter metabolism.
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