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

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dc.contributor.author Zhao, Guoyan en
dc.contributor.author Vatanen, Tommi en
dc.contributor.author Droit, Lindsay en
dc.contributor.author Park, Arnold en
dc.contributor.author Kostic, Aleksandar D en
dc.contributor.author Poon, Tiffany W en
dc.contributor.author Vlamakis, Hera en
dc.contributor.author Siljander, Heli en
dc.contributor.author Härkönen, Taina en
dc.contributor.author Hämäläinen, Anu-Maaria en
dc.contributor.author Peet, Aleksandr en
dc.contributor.author Tillmann, Vallo en
dc.contributor.author Ilonen, Jorma en
dc.contributor.author Wang, David en
dc.contributor.author Knip, Mikael en
dc.contributor.author Xavier, Ramnik J en
dc.contributor.author Virgin, Herbert W en
dc.date.accessioned 2018-10-26T02:19:37Z en
dc.date.issued 2017-07-10 en
dc.identifier.citation Proceedings of the National Academy of Sciences of the United States of America 114(30):E6166-E6175 25 Jul 2017 en
dc.identifier.issn 0027-8424 en
dc.identifier.uri http://hdl.handle.net/2292/43513 en
dc.description.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. en
dc.format.medium Print-Electronic en
dc.language eng en
dc.relation.ispartofseries Proceedings of the National Academy of Sciences of the United States of America en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.rights.uri https://www.pnas.org/page/subscriptions/open-access en
dc.subject Intestines en
dc.subject Humans en
dc.subject Circoviridae en
dc.subject Diabetes Mellitus, Type 1 en
dc.subject Genetic Predisposition to Disease en
dc.subject Cohort Studies en
dc.subject Autoimmunity en
dc.subject Infant en
dc.subject Infant, Newborn en
dc.subject Gastrointestinal Microbiome en
dc.title Intestinal virome changes precede autoimmunity in type I diabetes-susceptible children. en
dc.type Journal Article en
dc.identifier.doi 10.1073/pnas.1706359114 en
pubs.issue 30 en
pubs.begin-page E6166 en
pubs.volume 114 en
dc.rights.holder Copyright: The authors en
dc.identifier.pmid 28696303 en
pubs.end-page E6175 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype Research Support, Non-U.S. Gov't en
pubs.subtype research-article en
pubs.subtype Journal Article en
pubs.subtype Research Support, N.I.H., Extramural en
pubs.elements-id 734567 en
pubs.org-id Liggins Institute en
dc.identifier.eissn 1091-6490 en
pubs.record-created-at-source-date 2017-07-12 en
pubs.dimensions-id 28696303 en


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