The bacteriome at the onset of type 1 diabetes: A study from four geographically distant African and Asian countries
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
30121305
DOI
10.1016/j.diabres.2018.08.010
PII: S0168-8227(18)30950-1
Knihovny.cz E-zdroje
- Klíčová slova
- 16S rDNA sequencing, Africa, Asia, Bacteriome imbalance, Type 1 diabetes,
- MeSH
- Bacteria genetika MeSH
- bakteriální RNA genetika MeSH
- diabetes mellitus 1. typu epidemiologie genetika mikrobiologie MeSH
- dítě MeSH
- dospělí MeSH
- feces mikrobiologie MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- předškolní dítě MeSH
- RNA ribozomální 16S genetika MeSH
- střevní mikroflóra genetika MeSH
- vysoce účinné nukleotidové sekvenování MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Afrika epidemiologie MeSH
- Asie epidemiologie MeSH
- Názvy látek
- bakteriální RNA MeSH
- RNA ribozomální 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
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