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Published on: December 23, 2022
Comparative genomics and pangenomics of vancomycin-resistant and susceptible Enterococcus faecium from Irish
Robert J Leigh1, Chloe McKenna1, Robert McWade2
1Department of Biology, Maynooth University, Mariavilla, Maynooth, Co. Kildare, Ireland.
Abstract:
Introduction. Enterococcus faecium has emerged as an important nosocomial pathogen, which is increasingly difficult to treat due to the genetic acquisition of vancomycin resistance. Ireland has a recalcitrant vancomycin-resistant bloodstream infection rate compared to other developed countries.Hypothesis/Gap statement. Vancomycin resistance rates persist amongst E. faecium isolates from Irish hospitals. The evolutionary genomics governing these trends have not been fully elucidated.Methodology. A set of 28 vancomycin-resistant isolates was sequenced to construct a dataset alongside 61 other publicly available Irish genomes. This dataset was extensively analysed using in silico methodologies (comparative genomics, pangenomics, phylogenetics, genotypics and comparative functional analyses) to uncover distinct evolutionary, coevolutionary and clinically relevant population trends.Results. These results suggest that a stable (in terms of genome size, GC% and number of genes), yet genetically diverse population (in terms of gene content) of E. faecium persists in Ireland with acquired resistance arising via plasmid acquisition (vanA) or, to a lesser extent, chromosomal recombination (vanB). Population analysis revealed five clusters with one cluster partitioned into four clades which transcend isolation dates. Pangenomic and recombination analyses revealed an open (whole genome and chromosomal specific) pangenome illustrating a rampant evolutionary pattern. Comparative resistomics and virulomics uncovered distinct chromosomal and mobilomal propensity for multidrug resistance, widespread chromosomal point-mutation-mediated resistance and chromosomally harboured arsenals of virulence factors. Interestingly, a potential difference in biofilm formation strategies was highlighted by coevolutionary analysis, suggesting differential biofilm genotypes between vanA and vanB isolates.Conclusions. These results highlight the evolutionary history of Irish E. faecium isolates and may provide insight into underlying infection dynamics in a clinical setting. Due to the apparent ease of vancomycin resistance acquisition over time, susceptible E. faecium should be concurrently reduced in Irish hospitals to mitigate potential resistant infections.
Insights
Vancomycin-resistant Enterococcus faecium in Ireland shows genetic diversity and rapid evolution. Resistance is acquired via plasmids or chromosomal changes, highlighting the need to reduce susceptible strains to prevent infections.
Area of Science:
- * Medical Microbiology
- * Evolutionary Genomics
- * Infectious Diseases
Background:
- * Enterococcus faecium is a significant hospital-acquired pathogen.
- * Increasing vancomycin resistance in E. faecium poses treatment challenges.
- * Ireland exhibits high rates of vancomycin-resistant bloodstream infections.
Purpose of the Study:
- * Investigate the evolutionary genomics of vancomycin-resistant E. faecium in Ireland.
- * Elucidate population trends and resistance acquisition mechanisms.
- * Understand the genetic basis of virulence and resistance.
Main Methods:
- * Whole-genome sequencing of 28 vancomycin-resistant E. faecium isolates.
- * Comparative genomics, pangenomics, and phylogenetic analyses.
- * In silico analysis of resistance and virulence factors.
Main Results:
- * A genetically diverse yet stable E. faecium population exists in Ireland.
- * Vancomycin resistance (vanA, vanB) acquired via plasmids or chromosomal recombination.
- * Open pangenome indicates rampant evolution; distinct resistance and virulence profiles identified.
Conclusions:
- * Evolutionary history of Irish E. faecium isolates revealed.
- * Insights into clinical infection dynamics and resistance acquisition.
- * Reducing susceptible E. faecium is crucial to mitigate future resistant infections.
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