Wang Dilong, Jiang Youheng, Jiang Jian, Pan Yihang, Yang Yanming, Fang Xiaoyi, Liang Liyang, Li Hai, Dong Zepeng, Fan Shilu, Ma Daqing, Zhang Xue-Song, Li Huiliang, He Yulong, Li Ningning
Tomas Lindahl Nobel Laureate Laboratory, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong 518107, China; Department of Pediatrics, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510000, China.
Tomas Lindahl Nobel Laureate Laboratory, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong 518107, China; Center for Digestive Disease, Guangdong Provincial Key Laboratory of Digestive Cancer Research, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong 518107, China.
Cell Rep Med. 2025 Jan 21;6(1):101919. doi: 10.1016/j.xcrm.2024.101919. Epub 2025 Jan 13.
Gut microbiota (GM) alterations have been implicated in autism spectrum disorder (ASD), yet the specific functional architecture remains elusive. Here, employing multi-omics approaches, we investigate stool samples from two distinct cohorts comprising 203 children with mild ASD or typical development. In our screening cohort, regression-based analysis for metabolomic profiling identifies an elevated γ-aminobutyric acid (GABA) to glutamate (Glu) ratio as a metabolic signature of ASD, independent of age and gender. In the validating cohort, we affirm the GABA/Glu ratio as an ASD diagnostic indicator after adjusting for geography, age, gender, and specific food-consuming frequency. Integrated analysis of metabolomics, 16S rRNA sequencing, and metagenomics reveals a correlation between overrepresented Escherichia and disrupted GABA metabolism. Furthermore, we observe social behavioral impairments in weaning mice transplanted with E. coli, suggesting a potential link to ASD symptomatology. Collectively, these findings provide insights into potential diagnostic and therapeutic strategies aimed at evaluating and restoring gut microbial neurotransmitter homeostasis.
肠道微生物群(GM)的改变与自闭症谱系障碍(ASD)有关,但其具体的功能结构仍不清楚。在此,我们采用多组学方法,对来自两个不同队列的粪便样本进行了研究,这两个队列包括203名患有轻度ASD或发育正常的儿童。在我们的筛查队列中,基于回归的代谢组学分析确定,γ-氨基丁酸(GABA)与谷氨酸(Glu)的比值升高是ASD的一种代谢特征,与年龄和性别无关。在验证队列中,在调整了地理位置、年龄、性别和特定食物消费频率后,我们确认GABA/Glu比值可作为ASD的诊断指标。代谢组学、16S rRNA测序和宏基因组学的综合分析揭示了过量的大肠杆菌与GABA代谢紊乱之间的相关性。此外,我们观察到移植了大肠杆菌的断奶小鼠存在社会行为障碍,这表明其与ASD症状之间可能存在联系。总的来说,这些发现为旨在评估和恢复肠道微生物神经递质稳态的潜在诊断和治疗策略提供了见解。