Gut Virome Sequencing in Children With Early Islet Autoimmunity

Author:

Kramná Lenka1,Kolářová Kateřina1,Oikarinen Sami2,Pursiheimo Juha-Pekka3,Ilonen Jorma4,Simell Olli5,Knip Mikael6789,Veijola Riitta10,Hyöty Heikki211,Cinek Ondrej1

Affiliation:

1. Department of Pediatrics, University Hospital Motol, and 2nd Faculty of Medicine, Charles University in Prague, Prague, Czech Republic

2. Department of Virology, School of Medicine, University of Tampere, Tampere, Finland

3. Department of Medical Biochemistry and Genetics, University of Turku, Turku, Finland

4. Department of Immunogenetics, University of Turku, Turku, Finland

5. Department of Pediatrics, Turku University Central Hospital, Turku, Finland

6. Children’s Hospital, University of Helsinki, and Helsinki University Central Hospital, Helsinki, Finland

7. Diabetes and Obesity Research Program, University of Helsinki, Helsinki, Finland

8. Department of Pediatrics, Tampere University Hospital, Tampere, Finland

9. Folklhälsan Research Center, Helsinki, Finland

10. Department of Pediatrics, Oulu University Hospital, and University of Oulu, Oulu, Finland

11. Fimlab Laboratories, Pirkanmaa Hospital District, Tampere, Finland

Abstract

OBJECTIVE This study used next-generation sequencing (NGS) technologies to characterize the gut virome at the onset of islet autoimmunity. RESEARCH DESIGN AND METHODS We conducted a case-control study nested within the Finnish Diabetes Prediction and Prevention (DIPP) cohort. The stool virome in 19 case children, who turned islet autoantibody positive before the age of 2 years and later developed clinical type 1 diabetes, and 19 tightly matched control subjects was analyzed using NGS performed from stool samples collected 3, 6, and 9 months before the onset of islet autoimmunity. Human virus findings were verified using real-time PCR. RESULTS One or more human viruses were present in 10.4% and bacteriophages were in 54% of the samples. The virome composition showed no association with islet autoimmunity. NGS was less sensitive and specific than real-time PCR. CONCLUSIONS The present data suggest no dramatic changes in the gut virome shortly before the emergence of islet autoimmunity and emphasize the need of verification of mass sequencing results when viral exposure is assessed in association studies.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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