A quasi-paired cohort strategy reveals the impaired detoxifying function of microbes in the gut of autistic children

Impairment in gut microbial detoxification is correlated with mitochondrial dysfunction and disease severity in autistic children. Growing evidence suggests that autism spectrum disorder (ASD) is strongly associated with dysbiosis in the gut microbiome, with the exact mechanisms still unclear. We ha...

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Published inScience advances Vol. 6; no. 43
Main Authors Zhang, Mengxiang, Chu, Yanan, Meng, Qingren, Ding, Rui, Shi, Xing, Wang, Zuqun, He, Yi, Zhang, Juan, Liu, Jing, Zhang, Jie, Yu, Jun, Kang, Yu, Wang, Juan
Format Journal Article
LanguageEnglish
Published United States American Association for the Advancement of Science 01.10.2020
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ISSN2375-2548
2375-2548
DOI10.1126/sciadv.aba3760

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Summary:Impairment in gut microbial detoxification is correlated with mitochondrial dysfunction and disease severity in autistic children. Growing evidence suggests that autism spectrum disorder (ASD) is strongly associated with dysbiosis in the gut microbiome, with the exact mechanisms still unclear. We have proposed a novel analytic strategy—quasi-paired cohort—and applied it to a metagenomic study of the ASD microbiome. By comparing paired samples of ASD and neurotypical subjects, we have identified significant deficiencies in ASD children in detoxifying enzymes and pathways, which show a strong correlation with biomarkers of mitochondrial dysfunction. Diagnostic models based on these detoxifying enzymes accurately distinguished ASD individuals from controls, and the dysfunction score inferred from the model increased with the clinical rating scores of ASD. In summary, our results suggest a previously undiscovered potential role of impaired intestinal microbial detoxification in toxin accumulation and mitochondrial dysfunction, a core component of ASD pathogenesis. These findings pave the way for designing future therapeutic strategies to restore microbial detoxification capabilities for patients with ASD.
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These authors contributed equally to this work.
ISSN:2375-2548
2375-2548
DOI:10.1126/sciadv.aba3760