Compromised Gut Microbiota Networks in Children With Anti-Islet Cell Autoimmunity

Author:

Endesfelder David12,zu Castell Wolfgang1,Ardissone Alexandria3,Davis-Richardson Austin G.3,Achenbach Peter2,Hagen Michael1,Pflueger Maren2,Gano Kelsey A.3,Fagen Jennie R.3,Drew Jennifer C.3,Brown Christopher T.3,Kolaczkowski Bryan3,Atkinson Mark4,Schatz Desmond4,Bonifacio Ezio56,Triplett Eric W.3,Ziegler Anette-G.2

Affiliation:

1. Scientific Computing Research Unit, Helmholtz Zentrum München, Germany

2. Institute of Diabetes Research, Helmholtz Zentrum München, and Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Germany

3. Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL

4. Department of Pediatrics, University of Florida, Gainesville, FL

5. Center for Regenerative Therapies, Dresden, and Paul Langerhans Institute Dresden, Technische Universität Dresden, Germany

6. Institute for Diabetes and Obesity, Helmholtz Zentrum München, Germany

Abstract

The gut microbiome is suggested to play a role in the pathogenesis of autoimmune disorders such as type 1 diabetes. Evidence of anti-islet cell autoimmunity in type 1 diabetes appears in the first years of life; however, little is known regarding the establishment of the gut microbiome in early infancy. Here, we sought to determine whether differences were present in early composition of the gut microbiome in children in whom anti-islet cell autoimmunity developed. We investigated the microbiome of 298 stool samples prospectively taken up to age 3 years from 22 case children in whom anti-islet cell autoantibodies developed, and 22 matched control children who remained islet cell autoantibody–negative in follow-up. The microbiome changed markedly during the first year of life, and was further affected by breast-feeding, food introduction, and birth delivery mode. No differences between anti-islet cell autoantibody–positive and –negative children were found in bacterial diversity, microbial composition, or single-genus abundances. However, substantial alterations in microbial interaction networks were observed at age 0.5 and 2 years in the children in whom anti-islet cell autoantibodies developed. The findings underscore a role of the microbiome in the pathogenesis of anti-islet cell autoimmunity and type 1 diabetes.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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