Abstract

BackgroundGut microbiota has the capacity to impact the regular function of the brain, which can in turn affect the composition of microbiota. Autism spectrum disorder (ASD) patients suffer from gastrointestinal problems and experience changes in gut microbiota; however, it is not yet clear whether the change in the microbiota associated with ASD is a cause or a consequence of the disease.MethodsWe have investigated the species richness and microbial composition in a valproic acid (VPA)-induced rat model autism. Fecal samples from the rectum were collected at necropsy, microbial total DNA was extracted, 16 rRNA genes sequenced using Illumina, and the global microbial co-occurrence network was constructed using a random matrix theory-based pipeline. Collected rat microbiome data were compared to available data derived from cases of autism.ResultsWe found that VPA administration during pregnancy reduced fecal microbial richness, changed the gut microbial composition, and altered the metabolite potential of the fecal microbial community in a pattern similar to that seen in patients with ASD. However, the global network property and network composition as well as microbial co-occurrence patterns were largely preserved in the offspring of rats exposed to prenatal administration of VPA.ConclusionsOur data on the microbiota of the VPA rat model of autism indicate that this model, in addition to behaviorally and anatomically mimicking the autistic brain as previously shown, also mimics the microbiome features of autism, making it one of the best-suited rodent models for the study of autism and ASD.

Highlights

  • The gut and brain form the gut-brain axis through bidirectional nervous, endocrine, and immune communication

  • We demonstrated that when valproic acid (VPA) is administered via intraperitoneal injection to pregnant rats at a specific day of prenatal development with a specific dose (E 12.5, 400 mg/kg), the offspring of these rats (“400-E12 VPA rats”) experienced a decrease in the number of PV+ Ch and PV+ Baskets cells (Bsk) cells in their adult cerebral cortex similar to what we found in humans with autism

  • VPA reduces fecal microbial richness of the offspring A single IP injection of VPA during pregnancy in rats had a significant effect on fecal microbial richness in their offspring (P < 0.05, the Welch t test)

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Summary

Introduction

The gut and brain form the gut-brain axis through bidirectional nervous, endocrine, and immune communication. Rats exposed to VPA in utero present with an increased glutamatergic and a decreased GABAergic component in the cortex [9]. The VPA rat model of autism experiences behavioral, immune, and microbiota changes similar to those described in patients with autism. We demonstrated that when VPA is administered via intraperitoneal injection to pregnant rats at a specific day of prenatal development with a specific dose (E (embryonic day) 12.5, 400 mg/kg), the offspring of these rats (“400-E12 VPA rats”) experienced a decrease in the number of PV+ Ch and PV+ Bsk cells in their adult cerebral cortex similar to what we found in humans with autism (under revision). The 400-E12 VPA rats experienced behavioral changes similar to those exhibited by patients with autism (under revision). Gut microbiota has the capacity to impact the regular function of the brain, which can in turn affect the composition of microbiota. Autism spectrum disorder (ASD) patients suffer from gastrointestinal problems and experience changes in gut microbiota; it is not yet clear whether the change in the microbiota associated with ASD is a cause or a consequence of the disease

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