Early Childhood Gut Microbiomes Show Strong Geographic Differences Among Subjects at High Risk for Type 1 Diabetes

Gut microbiome dysbiosis is associated with numerous diseases, including type 1 diabetes. This pilot study determines how geographical location affects the microbiome of infants at high risk for type 1 diabetes in a population of homogenous HLA class II genotypes. High-throughput 16S rRNA sequencing...

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Published inDiabetes care Vol. 38; no. 2; pp. 329 - 332
Main Authors Kemppainen, Kaisa M., Ardissone, Alexandria N., Davis-Richardson, Austin G., Fagen, Jennie R., Gano, Kelsey A., León-Novelo, Luis G., Vehik, Kendra, Casella, George, Simell, Olli, Ziegler, Anette G., Rewers, Marian J., Lernmark, Åke, Hagopian, William, She, Jin-Xiong, Krischer, Jeffrey P., Akolkar, Beena, Schatz, Desmond A., Atkinson, Mark A., Triplett, Eric W.
Format Journal Article
LanguageEnglish
Published United States American Diabetes Association 01.02.2015
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Summary:Gut microbiome dysbiosis is associated with numerous diseases, including type 1 diabetes. This pilot study determines how geographical location affects the microbiome of infants at high risk for type 1 diabetes in a population of homogenous HLA class II genotypes. High-throughput 16S rRNA sequencing was performed on stool samples collected from 90 high-risk, nonautoimmune infants participating in The Environmental Determinants of Diabetes in the Young (TEDDY) study in the U.S., Germany, Sweden, and Finland. Study site-specific patterns of gut colonization share characteristics across continents. Finland and Colorado have a significantly lower bacterial diversity, while Sweden and Washington state are dominated by Bifidobacterium in early life. Bacterial community diversity over time is significantly different by geographical location. The microbiome of high-risk infants is associated with geographical location. Future studies aiming to identify the microbiome disease phenotype need to carefully consider the geographical origin of subjects.
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ISSN:0149-5992
1935-5548
1935-5548
DOI:10.2337/dc14-0850