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      Microbiota modulate behavioral and physiological abnormalities associated with neurodevelopmental disorders.

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          Abstract

          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.

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          Author and article information

          Journal
          Cell
          Cell
          Elsevier BV
          1097-4172
          0092-8674
          Dec 19 2013
          : 155
          : 7
          Affiliations
          [1 ] 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. Electronic address: ehsiao@caltech.edu.
          [2 ] Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
          [3 ] Alkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, Houston, TX 77030, USA.
          [4 ] Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
          [5 ] Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: php@caltech.edu.
          [6 ] Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: sarkis@caltech.edu.
          Article
          S0092-8674(13)01473-6 NIHMS543590
          10.1016/j.cell.2013.11.024
          3897394
          24315484
          55de5d85-04e5-4ea0-abc2-6eeade18cd12
          Copyright © 2013 Elsevier Inc. All rights reserved.
          History

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