| Literature DB >> 25662751 |
Aleksandar D Kostic1, Dirk Gevers2, Heli Siljander3, Tommi Vatanen4, Tuulia Hyötyläinen5, Anu-Maaria Hämäläinen6, Aleksandr Peet7, Vallo Tillmann7, Päivi Pöhö8, Ismo Mattila5, Harri Lähdesmäki9, Eric A Franzosa10, Outi Vaarala11, Marcus de Goffau12, Hermie Harmsen12, Jorma Ilonen13, Suvi M Virtanen14, Clary B Clish2, Matej Orešič5, Curtis Huttenhower15, Mikael Knip16, Ramnik J Xavier17.
Abstract
Colonization of the fetal and infant gut microbiome results in dynamic changes in diversity, which can impact disease susceptibility. To examine the relationship between human gut microbiome dynamics throughout infancy and type 1 diabetes (T1D), we examined a cohort of 33 infants genetically predisposed to T1D. Modeling trajectories of microbial abundances through infancy revealed a subset of microbial relationships shared across most subjects. Although strain composition of a given species was highly variable between individuals, it was stable within individuals throughout infancy. Metabolic composition and metabolic pathway abundance remained constant across time. A marked drop in alpha-diversity was observed in T1D progressors in the time window between seroconversion and T1D diagnosis, accompanied by spikes in inflammation-favoring organisms, gene functions, and serum and stool metabolites. This work identifies trends in the development of the human infant gut microbiome along with specific alterations that precede T1D onset and distinguish T1D progressors from nonprogressors.Entities:
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Year: 2015 PMID: 25662751 PMCID: PMC4689191 DOI: 10.1016/j.chom.2015.01.001
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023