Strain-level translocation and enrichment mechanisms of oral bacteria in the lower gastrointestinal tract of stunted children
Simon YersiniD, Jean‐Chrysostome Gody, Florent MazeliD, Edgar Djimbele, Synthia Nazita Nigateloum, Bolmbaye Privat Gondje, Sonia Sandrine Vondo, Kaleb Jephté Estimé Kandou, Aline Raub, Youzheng TeoiD, Serge Ghislain DjorieiD, Nathalie KapeliD, Philippe Jean SansonettiiD, Pascale VonaeschiD, for the Afribiota Investigators, Jean-Marc Collard, Maria Doria, Darragh DuffyiD, Tamara Giles‐VernickiD, Jean-Chrysostome Gody, Milena HasaniD, Jean-Pierre Lombart, Synthia Nazita Nigatoloum, Laura Parfrey, Maheninasy RakotondrainipianaiD, , Ionela Gouandjika‐VasilacheiD
Abstract
Emerging evidence suggests that ectopic colonization of oral bacteria in the lower digestive tract may exacerbate gastrointestinal disorders. Nevertheless, it remains unclear whether bacteria of oral origin are continuously translocating from the oral cavity to the lower gastrointestinal tract or are locally adapted and persist in their respective niches. We investigated strain translocation dynamics in 44 healthy and stunted children from Bangui, Central African Republic. Using cross-sectional shotgun metagenomic sequencing of saliva, gastric, duodenal and fecal samples, and isolation and whole genome sequencing of 87 Streptococcus salivarius isolates, we showed translocation of members of the genera Streptococcus, Veillonella, Rothia and Haemophilus. Fecal isolates were more closely related to oral isolates from the same individuals than those from other individuals. Additionally, saliva showed higher S. salivarius nucleotide diversity compared to other compartments, suggesting a source-sink dynamic in which S. salivarius populations are continuously seeded from the oral cavity without durably establishing in the lower gastrointestinal tract. Last, we showed that overrepresentation of oral bacteria in the duodenum of stunted children is due to increased biomass, while in the colon it is linked to depletion of overall biomass, including in butyrate-producing strains. Our study quantifies mechanisms of oral-to-gut translocation and enrichment of oral taxa, providing key insights into microbiota disruption in stunted children.
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