The bacteriome at the onset of type 1 diabetes: A study from four geographically distant African and Asian countries
Language English Country Ireland Media print-electronic
Document type Journal Article
PubMed
30121305
DOI
10.1016/j.diabres.2018.08.010
PII: S0168-8227(18)30950-1
Knihovny.cz E-resources
- Keywords
- 16S rDNA sequencing, Africa, Asia, Bacteriome imbalance, Type 1 diabetes,
- MeSH
- Bacteria genetics MeSH
- RNA, Bacterial genetics MeSH
- Diabetes Mellitus, Type 1 epidemiology genetics microbiology MeSH
- Child MeSH
- Adult MeSH
- Feces microbiology MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Child, Preschool MeSH
- RNA, Ribosomal, 16S genetics MeSH
- Gastrointestinal Microbiome genetics MeSH
- High-Throughput Nucleotide Sequencing MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Africa epidemiology MeSH
- Asia epidemiology MeSH
- Names of Substances
- RNA, Bacterial MeSH
- RNA, Ribosomal, 16S MeSH
OBJECTIVES: Gut bacteriome profiling studies in type 1 diabetes (T1D) to date are mostly limited to populations of Europe, with two studies from China and one study each from Mexico and the USA. We therefore sought to characterize the stool bacteriome in children after onset of T1D along with age- and place-matched control subjects from four geographically distant African and Asian countries. METHODS: Samples were collected from 73 children and adolescents shortly after T1D onset (Azerbaijan 19, Jordan 20, Nigeria 14, Sudan 20) and 104 matched control subjects of similar age and locale. Genotyping of major T1D susceptibility genes was performed using saliva or blood samples. The bacteriome was profiled by next-generation sequencing of 16S rDNA. Negative binomial regression was used to model associations, with adjustment for the matched structure of the study. RESULTS: A significant positive association with T1D was noted for the genus Escherichia (class Gammaproteobacteria, phylum Proteobacteria), whereas Eubacterium and Roseburia, two genera of class Clostridia, phylum Firmicutes, were inversely associated with T1D. We also confirmed a previously observed inverse association with Clostridium clusters IV or XIVa. No associations were noted for richness, evenness, or enterotypes. CONCLUSIONS: Based on our results, some type of distortion of the gut bacteriome appears to be a global feature of T1D, and our findings for four distant populations add new candidates to the existing list of bacteria. It remains to be established whether the observed associations are markers or causative factors.
Department of Paediatrics and Child Health University of Khartoum Faculty of Medicine Khartoum Sudan
Department of Pediatrics School of Medicine University of Jordan Amman Jordan
Endocrine Centre Baku Str 1 Hashimov 4A AZ1114 Baku Azerbaijan
References provided by Crossref.org
Mutual Interactions of Silymarin and Colon Microbiota in Healthy Young and Healthy Elder Subjects