Ingestion of food- or waterborne antibiotic-resistant bacteria may lead to the dissemination of antibiotic-resistance genes in the gut microbiota and the development of antibiotic-resistant bacterial infection, a significant threat to animal and public health. Food or water may be contaminated with multiple resistant bacteria, but animal models on gene transfer were mainly based on single-strain infections. In this study, we investigated the mobility of β-lactam resistance following infection with single- versus multi-strain of resistant bacteria under ampicillin treatment. We characterized three bacterial strains isolated from food-animal production systems, O80:H26 and serovars Bredeney and Heidelberg. Each strain carries at least one conjugative plasmid that encodes a β-lactamase. We orally infected mice with each or all three bacterial strain(s) in the presence or absence of ampicillin treatment. We assessed plasmid transfer from the three donor bacteria to an introduced CV601gfp recipient in the mouse gut, and evaluated the impacts of the bacterial infection on gut microbiota and gut health. In the absence of ampicillin treatment, none of the donor or recipient bacteria established in the normal gut microbiota and plasmid transfer was not detected. In contrast, the ampicillin treatment disrupted the gut microbiota and enabled . Bredeney and Heidelberg to colonize and transfer their plasmids to the CV601gfp recipient. O80:H26 on its own failed to colonize the mouse gut. However, during co-infection with the two strains, O80:H26 colonized and transferred its plasmid to the CV601gfp recipient and a residential O2:H6 strain. The co-infection significantly increased plasmid transfer frequency, enhanced Proteobacteria expansion and resulted in inflammation in the mouse gut. Our findings suggest that single-strain infection models for evaluating gene transfer may underrepresent the consequences of multi-strain infections following the consumption of heavily contaminated food or water.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358583PMC
http://dx.doi.org/10.3389/fmicb.2020.01591DOI Listing

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