Bacteriocin production facilitates nosocomial emergence of vancomycin-resistant Enterococcus faecium

Emma G Mills1, Alexander B Smith2, Marissa P Griffith1,3,4

  • 1Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Insights

Vancomycin-resistant Enterococcus faecium (VREfm) hospital strains show significant lineage shifts over time. Bacteriocin T8 may drive VREfm emergence and persistence in healthcare settings, impacting infection control strategies.

Area of Science:

  • Microbiology
  • Genomics
  • Epidemiology

Background:

  • Vancomycin-resistant Enterococcus faecium (VREfm) is a major healthcare-associated pathogen.
  • Gastrointestinal colonization by VREfm can lead to severe bloodstream infections with high mortality.
  • Understanding VREfm population dynamics in hospitals is crucial for infection control.

Purpose of the Study:

  • To investigate temporal changes in hospital-adapted VREfm populations.
  • To identify factors driving the emergence and persistence of VREfm strains in healthcare settings.
  • To compare local VREfm evolution with global trends.

Main Methods:

  • Whole-genome sequencing of 710 clinical VREfm isolates from 2017-2022.
  • Comparative genomic analysis with 15,631 publicly available VREfm genomes.
  • Functional analysis to identify strain-specific adaptive features.

Main Results:

  • The VREfm population was polyclonal, with 46% of isolates forming genetically related clusters, indicating high transmission.
  • A significant shift in VREfm lineage replacement was observed both locally and globally over a 20-year period.
  • Antimicrobial peptide bacteriocin T8 was identified as a potential driver for VREfm strain emergence and persistence.

Conclusions:

  • Hospital-adapted VREfm populations undergo substantial temporal shifts in lineage composition.
  • Bacteriocin T8 may play a critical role in the success of specific VREfm strains within the hospital environment.
  • These findings have implications for developing targeted interventions against VREfm transmission and infection.

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