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A preliminary investigation on the relationship between gut microbiota and gene expressions in peripheral mononuclear cells of infants with autism spectrum disorders.
Inoue, Ryo; Sakaue, Yuko; Sawai, Chihiro; Sawai, Toshihiro; Ozeki, Motoyuki; Romero-Pérez, Gustavo A; Tsukahara, Takamitsu.
Affiliation
  • Inoue R; a Laboratory of Animal Science, Department of Agricultural and Life Sciences , Kyoto Prefectural University , Kyoto , Japan.
  • Sakaue Y; b Department of Pediatrics , Shiga University of Medical Science , Otsu , Japan.
  • Sawai C; b Department of Pediatrics , Shiga University of Medical Science , Otsu , Japan.
  • Sawai T; b Department of Pediatrics , Shiga University of Medical Science , Otsu , Japan.
  • Ozeki M; c Department of Informatics and Mediology , Mukogawa Women's University , Nishinomiya , Japan.
  • Romero-Pérez GA; d Kyoto Institute of Nutrition and Pathology , Kyoto , Japan.
  • Tsukahara T; a Laboratory of Animal Science, Department of Agricultural and Life Sciences , Kyoto Prefectural University , Kyoto , Japan.
Biosci Biotechnol Biochem ; 80(12): 2450-2458, 2016 Dec.
Article in En | MEDLINE | ID: mdl-27581276
Fecal and blood samples of infants with autism spectrum disorders (ASD) and healthy infants were analyzed to investigate the association of altered gut microbiota and ASD development. 16S rRNA gene-based sequencing found that, unlike those of healthy infants, feces of ASD infants had significantly higher and lower abundance of genera Faecalibacterium and Blautia, respectively. Moreover, DNA microarray analysis of peripheral blood mononuclear cells (PBMC) detected more highly than low expressed genes in ASD infants than in healthy infants. Gene Ontology analysis revealed that differentially expressed genes between ASD and healthy infants were involved in interferon (IFN)-γ and type-I IFN signaling pathways. Finally, strong positive correlations between expression of IFN signaling-associated genes in PBMC and fecal abundance of Faecalibacterium were found. Our results strongly suggested that altered gut microbiota in infants resulted from ASD development and was associated with systemic immunity dysregulation, especially chronic inflammation.
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Database: MEDLINE Main subject: Leukocytes, Mononuclear / Transcriptome / Autism Spectrum Disorder / Gastrointestinal Microbiome Type of study: Observational_studies / Risk_factors_studies Limits: Child, preschool / Humans / Infant Language: En Journal: Biosci Biotechnol Biochem Journal subject: BIOQUIMICA / BIOTECNOLOGIA Year: 2016 Type: Article Affiliation country: Japan
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Database: MEDLINE Main subject: Leukocytes, Mononuclear / Transcriptome / Autism Spectrum Disorder / Gastrointestinal Microbiome Type of study: Observational_studies / Risk_factors_studies Limits: Child, preschool / Humans / Infant Language: En Journal: Biosci Biotechnol Biochem Journal subject: BIOQUIMICA / BIOTECNOLOGIA Year: 2016 Type: Article Affiliation country: Japan