Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Cell. 2013 Dec 19;155(7):1451-63. doi: 10.1016/j.cell.2013.11.024. Epub 2013 Dec 5.
Neurodevelopmental disorders, including autism spectrum disorder (ASD), are defined by core behavioral impairments; however, subsets of individuals display a spectrum of gastrointestinal (GI) abnormalities. We demonstrate GI barrier defects and microbiota alterations in the maternal immune activation (MIA) mouse model that is known to display features of ASD. Oral treatment of MIA offspring with the human commensal Bacteroides fragilis corrects gut permeability, alters microbial composition, and ameliorates defects in communicative, stereotypic, anxiety-like and sensorimotor behaviors. MIA offspring display an altered serum metabolomic profile, and B. fragilis modulates levels of several metabolites. Treating naive mice with a metabolite that is increased by MIA and restored by B. fragilis causes certain behavioral abnormalities, suggesting that gut bacterial effects on the host metabolome impact behavior. Taken together, these findings support a gut-microbiome-brain connection in a mouse model of ASD and identify a potential probiotic therapy for GI and particular behavioral symptoms in human neurodevelopmental disorders.
神经发育障碍,包括自闭症谱系障碍(ASD),以核心行为障碍为特征;然而,某些个体表现出一系列胃肠道(GI)异常。我们在已知具有 ASD 特征的母体免疫激活(MIA)小鼠模型中证明了 GI 屏障缺陷和微生物群改变。用人类共生拟杆菌对 MIA 后代进行口服治疗可纠正肠道通透性,改变微生物组成,并改善交流、刻板、焦虑样和感觉运动行为的缺陷。MIA 后代表现出改变的血清代谢组学特征,而 B. fragilis 调节几种代谢物的水平。用 MIA 增加和 B. fragilis 恢复的代谢物处理未处理的小鼠会引起某些行为异常,这表明肠道细菌对宿主代谢组的影响会影响行为。总之,这些发现支持 ASD 小鼠模型中的肠道-微生物组-大脑连接,并确定了一种用于人类神经发育障碍的 GI 和特定行为症状的潜在益生菌治疗方法。