Imbalance of bacteriome profiles within the Finnish Diabetes Prediction and Prevention study: Parallel use of 16S profiling and virome sequencing in stool samples from children with islet autoimmunity and matched controls.

Background We set out to explore associations between the stool bacteriome profiles and early-onset islet autoimmunity, taking into account the interactions with the virus component of the microbiome. Methods Serial stool samples were longitudinally collected from 18 infants and toddlers with early-...

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Publicado en:Pediatric Diabetes Vol. 18; no. 7; pp. 588 - 599
Autores principales: Cinek, Ondrej, Kramna, Lenka, Lin, Jake, Oikarinen, Sami, Kolarova, Katerina, Ilonen, Jorma, Simell, Olli, Veijola, Riitta, Autio, Reija, Hyöty, Heikki
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Nov2017
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Nov2017
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1111/pedi.12468
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        atl: Imbalance of bacteriome profiles within the Finnish Diabetes Prediction and Prevention study: Parallel use of 16S profiling and virome sequencing in stool samples from children with islet autoimmunity and matched controls.
      aug:
        au:
          Cinek, Ondrej
          Kramna, Lenka
          Lin, Jake
          Oikarinen, Sami
          Kolarova, Katerina
          Ilonen, Jorma
          Simell, Olli
          Veijola, Riitta
          Autio, Reija
          Hyöty, Heikki
        affil: Department of Pediatrics, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague Czech Republic
      sug:
        subj:
          Gut Microbiota In Infancy and Childhood
          Feces Analysis
          Diabetes Mellitus, Type 1 Risk Factors
          Human
          Child
          DNA
          Correlation Coefficient
          RNA
          Child: 6-12 years
      ab: Background We set out to explore associations between the stool bacteriome profiles and early-onset islet autoimmunity, taking into account the interactions with the virus component of the microbiome. Methods Serial stool samples were longitudinally collected from 18 infants and toddlers with early-onset islet autoimmunity (median age 17.4 months) followed by type 1 diabetes, and 18 tightly matched controls from the Finnish Diabetes Prediction and Prevention ( DIPP) cohort. Three stool samples were analyzed, taken 3, 6, and 9 months before the first detection of serum autoantibodies in the case child. The risk of islet autoimmunity was evaluated in relation to the composition of the bacteriome 16S rDNA profiles assessed by mass sequencing, and to the composition of DNA and RNA viromes. Results Four operational taxonomic units were significantly less abundant in children who later on developed islet autoimmunity as compared to controls-most markedly the species of Bacteroides vulgatus and Bifidobacterium bifidum. The alpha or beta diversity, or the taxonomic levels of bacterial phyla, classes or genera, showed no differences between cases and controls. A correlation analysis suggested a possible relation between CrAssphage signals and quantities of Bacteroides dorei. No apparent associations were seen between development of islet autoimmunity and sequences of yet unknown origin. Conclusions The results confirm previous findings that an imbalance within the prevalent Bacteroides genus is associated with islet autoimmunity. The detected quantitative relation of the novel 'orphan' bacteriophage CrAssphage with a prevalent species of the Bacteroides genus may exemplify possible modifiers of the bacteriome.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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