Literature DB >> 28696303

Intestinal virome changes precede autoimmunity in type I diabetes-susceptible children.

Guoyan Zhao1, Tommi Vatanen2,3, Lindsay Droit4, Arnold Park4, Aleksandar D Kostic2, Tiffany W Poon2, Hera Vlamakis2, Heli Siljander5,6, Taina Härkönen5,6, Anu-Maaria Hämäläinen7, Aleksandr Peet8,9, Vallo Tillmann8,9, Jorma Ilonen10, David Wang4,11, Mikael Knip5,6,12,13, Ramnik J Xavier2,14, Herbert W Virgin1.   

Abstract

Viruses have long been considered potential triggers of autoimmune diseases. Here we defined the intestinal virome from birth to the development of autoimmunity in children at risk for type 1 diabetes (T1D). A total of 220 virus-enriched preparations from serially collected fecal samples from 11 children (cases) who developed serum autoantibodies associated with T1D (of whom five developed clinical T1D) were compared with samples from controls. Intestinal viromes of case subjects were less diverse than those of controls. Among eukaryotic viruses, we identified significant enrichment of Circoviridae-related sequences in samples from controls in comparison with cases. Enterovirus, kobuvirus, parechovirus, parvovirus, and rotavirus sequences were frequently detected but were not associated with autoimmunity. For bacteriophages, we found higher Shannon diversity and richness in controls compared with cases and observed that changes in the intestinal virome over time differed between cases and controls. Using Random Forests analysis, we identified disease-associated viral bacteriophage contigs after subtraction of age-associated contigs. These disease-associated contigs were statistically linked to specific components of the bacterial microbiome. Thus, changes in the intestinal virome preceded autoimmunity in this cohort. Specific components of the virome were both directly and inversely associated with the development of human autoimmune disease.

Entities:  

Keywords:  Circoviridae; bacteriophages; microbiome; type 1 diabetes; virome

Mesh:

Year:  2017        PMID: 28696303      PMCID: PMC5544325          DOI: 10.1073/pnas.1706359114

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  66 in total

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Authors:  P Kolehmainen; M Koskiniemi; S Oikarinen; R Veijola; O Simell; J Ilonen; M Knip; H Hyöty; S Tauriainen
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