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Natural Sciences›Biology›ecology

Resource landscape shapes the composition and stability of the human vaginal microbiota

Tsukushi KamiyaCentre National de la Recherche Scientifique

Mircea T. SofoneaInserm

Michael FranceUniversity of Maryland, Baltimore

Nicolas TessandierCentre National de la Recherche Scientifique

Ignacio G. BravoCentre National de la Recherche Scientifique

Carmen Lía MurallCentre National de la Recherche Scientifique

Jacques RavelUniversity of Maryland, Baltimore

Samuel AlizonCentre National de la Recherche Scientifique

PLoS Biology·February 3, 2026·1 citations

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Abstract

The vaginal microbiota is associated with the health of women and newborns alike. Despite its comparatively simple composition relative to other human microbiota systems, the mechanisms underpinning the dynamics and stability of vaginal microbial communities remain elusive. A crucial, yet so far underexplored, aspect of vaginal microbiota ecology is the role played by nutritional resources. Glycogen and its derivatives, produced by vaginal epithelia, are accessible to all bacterial constituents of the microbiota. Concurrently, free sialic acid and fucose offer supplementary nutritional resources to bacterial strains capable of cleaving them from glycans, which are structurally integral to mucus. Notably, bacteria adept at sialic acid exploitation are often correlated with adverse clinical outcomes and are frequently implicated in bacterial vaginosis (BV). In this study, we introduce a novel mathematical model tailored to human vaginal microbiota dynamics to explore the interactions between bacteria and their respective nutritional landscape. Our resource-based model examines the impact of the relative availability of glycogen derivatives (accessible to all bacterial species) and sialic acid (exclusive to some BV-associated bacteria) on the composition of the vaginal microbiota. Our findings elucidate that the success of BV-associated bacteria is intricately linked to their exclusive access to specific nutritional resources. This private access fortifies communities dominated by BV-associated bacteria, rendering them resilient to compositional transitions. We empirically corroborate our model prediction with longitudinal clinical data on microbiota composition and previously unpublished metabolomic profiles obtained from a North American cohort. The insights gleaned from this study shed light on potential pathways for BV prevention and treatment.

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