Bacteriocin production facilitates nosocomial emergence of vancomycin-resistant Enterococcus faecium
Mills, E. G.; Smith, A. B.; Griffith, M. P.; Hewlett, K.; Pless, L.; Sundermann, A. J.; Harrison, L. H.; Zackular, J. P.; Van Tyne, D.
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Vancomycin-resistant Enterococcus faecium (VREfm) is a prevalent healthcare-acquired pathogen. Gastrointestinal colonization can lead to difficult-to-treat bloodstream infections with high mortality rates. Prior studies have investigated VREfm population structure within healthcare centers. However, little is known about how and why hospital-adapted VREfm populations change over time. We sequenced 710 healthcare-associated VREfm clinical isolates from 2017-2022 from a large tertiary care center as part of the Enhanced Detection System for Healthcare-Associated Transmission (EDS-HAT) program. Although the VREfm population in our center was polyclonal, 46% of isolates formed genetically related clusters, suggesting a high transmission rate. We compared our collection to 15,631 publicly available VREfm genomes spanning 20 years. Our findings describe a drastic shift in lineage replacement within nosocomial VREfm populations at both the local and global level. Functional and genomic analysis revealed, antimicrobial peptide, bacteriocin T8 may be a driving feature of strain emergence and persistence in the hospital setting. SummaryThis study shows local and global lineage replacement of vancomycin-resistant Enterococcus faecium. Bacteriocin T8 is enriched in emergent lineages and provides a strong competitive advantage in vitro and in vivo.
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