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体外培养的人类肠道微生物菌群移植对改变肠道微生物菌群和改善自闭症谱系障碍相关症状的治疗效果。

Therapeutic Effects of the In Vitro Cultured Human Gut Microbiota as Transplants on Altering Gut Microbiota and Improving Symptoms Associated with Autism Spectrum Disorder.

机构信息

Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.

Zhongshan Hospital Department of Gastroenterology, Xiamen University, Xiamen, Fujian, China.

出版信息

Microb Ecol. 2020 Aug;80(2):475-486. doi: 10.1007/s00248-020-01494-w. Epub 2020 Feb 26.

DOI:10.1007/s00248-020-01494-w
PMID:32100127
Abstract

Autism spectrum disorder (ASD) is a brain-based neurodevelopmental disorder characterized by behavioral abnormalities. Accumulating studies show that the gut microbiota plays a vital role in the pathogenesis of ASD, and gut microbiota transplantation (GMT) is a promising technique for the treatment of ASD. In clinical applications of GMT, it is challenging to obtain effective transplants because of the high costs of donor selection and heterogeneity of donors' gut microbiota, which can cause different clinical responses. In vitro batch culture is a fast, easy-to-operate, and repeatable method to culture gut microbiota. Thus, the present study investigates the feasibility of treating ASD with in vitro cultured gut microbiota as transplants. We cultured gut microbiota via the in vitro batch culture method and performed GMT in the maternal immune activation (MIA)-induced ASD mouse model with original donor microbiota and in vitro cultured microbiota. Open field, three-chamber social, marble burying, and self-grooming tests were used for behavioral improvement assessment. Serum levels of chemokines were detected. Microbial total DNA was extracted from mouse fecal samples, and 16S rDNA was sequenced using Illumina. Our results showed that GMT treatment with original and cultured donor gut microbiota significantly ameliorated anxiety-like and repetitive behaviors and improved serum levels of chemokines including GRO-α (CXCL1), MIP-1α (CCL3), MCP-3 (CCL7), RANTES (CCL5), and Eotaxin (CCL11) in ASD mice. Meanwhile, the gut microbial communities of the two groups that received GMT treatment were changed compared with the ASD mice groups. In the group treated with in vitro cultured donor gut microbiota, there was a significant decrease in the relative abundance of key differential taxa, including S24-7, Clostridiaceae, Prevotella_other, and Candidatus Arthromitus. The relative abundance of these taxa reached close to the level of healthy mice. Prevotella_other also decreased in the group treated with original donor gut microbiota, with a significant increase in Ruminococcaceae and Oscillospira. The present study demonstrated that GMT with in vitro cultured microbiota also improved behavioral abnormalities and chemokine disorders in an ASD mouse model compared with GMT with original donor gut microbiota. In addition, it significantly modified several key differential taxa in gut microbial composition.

摘要

自闭症谱系障碍(ASD)是一种以行为异常为特征的基于大脑的神经发育障碍。越来越多的研究表明,肠道微生物群在 ASD 的发病机制中起着至关重要的作用,而肠道微生物群移植(GMT)是治疗 ASD 的一种有前途的技术。在 GMT 的临床应用中,由于供体选择成本高和供体肠道微生物群的异质性,获得有效的移植物具有挑战性,这可能导致不同的临床反应。体外批量培养是一种快速、易于操作且可重复的培养肠道微生物群的方法。因此,本研究探讨了使用体外培养的肠道微生物群作为移植物治疗 ASD 的可行性。我们通过体外批量培养法培养肠道微生物群,并在母体免疫激活(MIA)诱导的 ASD 小鼠模型中使用原始供体微生物群和体外培养的微生物群进行 GMT。通过旷场、三箱社交、埋珠和自我梳理试验评估行为改善情况。检测血清趋化因子水平。从小鼠粪便样本中提取微生物总 DNA,使用 Illumina 对 16S rDNA 进行测序。我们的结果表明,GMT 治疗用原始和培养的供体肠道微生物群显著改善 ASD 小鼠的焦虑样和重复行为,并改善趋化因子包括 GRO-α(CXCL1)、MIP-1α(CCL3)、MCP-3(CCL7)、RANTES(CCL5)和 Eotaxin(CCL11)的血清水平。同时,接受 GMT 治疗的两组小鼠的肠道微生物群落与 ASD 小鼠组相比发生了变化。在接受体外培养供体肠道微生物群治疗的组中,关键差异分类群的相对丰度显著降低,包括 S24-7、梭菌科、普雷沃氏菌属和 Arthromitus 属。这些分类群的相对丰度接近健康小鼠的水平。在接受原始供体肠道微生物群治疗的组中,Prevotella_other 的相对丰度也降低,而 Ruminococcaceae 和 Oscillospira 的相对丰度增加。本研究表明,与 GMT 治疗原始供体肠道微生物群相比,GMT 治疗体外培养的微生物群也改善了 ASD 小鼠模型的行为异常和趋化因子紊乱,并显著改变了肠道微生物组成的几个关键差异分类群。

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