Competition against the intestinal microbiota selects for pathoadaptive traits in ESBL E. coli
Pramod Kumar JangiriD, Leonardo F. Lemos RochaiD, Marco MolariiD, Nicolas WenneriD, Cecilia FruetiD, Pablo ManfrediiD, Carlos FloresiD, Anna SintsovaiD, Roxanne Mouchet, Lisa Diner, Anouk BertolaiD, Svenja Förster, Elisa Lee, MiCayla Johnson, Malenka Kunz, Andrea RockeriD, Adrian EgliiD, Urs JenaliD, Christoph DehioiD, Anne‐Florence BitboliD, Médéric DiardiD
Abstract
The intestinal tract is a reservoir for Extended-Spectrum {beta}-Lactamase (ESBL)-producing Escherichia coli. Asymptomatic gut colonization by these pathobionts represents a major risk for extraintestinal infections. Despite clinical relevance, the genetic basis of gut colonization by ESBL E. coli remains poorly understood. Here, we determined how the microbiota shapes the fitness landscape of diverse ESBL E. coli strains, defining the functional requirements for intestinal colonization. In microbiota-depleted hosts, colonization relies mostly on metabolic functions. In contrast, in mice harbouring a microbiota, pathoadaptive functions associated with adhesion and biofilm formation are dominant determinants of E. coli fitness, together with accessory virulence functions. Consistent with these observations, experimental evolution in mice reveals convergent adaptation of ESBL E. coli to the presence of a complex microbiota through enhanced adhesion. These findings establish the microbiota as a major ecological driver of pathoadaptation in antibiotic-resistant pathobionts.
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