The global dissemination of hospital clones of Enterococcus faecium

Author:

van Hal Sebastiaan J.ORCID, ,Willems Rob J. L.,Gouliouris Theodore,Ballard Susan A.,Coque Teresa M.,Hammerum Anette M.,Hegstad Kristin,Westh Hendrik T.,Howden Benjamin P.,Malhotra-Kumar Surbhi,Werner Guido,Yanagihara Katsunori,Earl Ashlee M.,Raven Katherine E.,Corander Jukka,Bowden Rory

Abstract

AbstractBackgroundThe hospital-adapted A1 group ofEnterococcus faeciumremains an organism of significant concern in the context of drug-resistant hospital-associated infections. How this pathogen evolves and disseminates remains poorly understood.MethodsA large, globally representative collection of short-read genomic data from the hospital-associated A1 group ofEnterococcus faeciumwas assembled (n = 973). We analysed, using a novel analysis approach, global diversity in terms of both the dynamics of the accessory genome and homologous recombination among conserved genes.ResultsTwo main modes of genomic evolution continue to shapeE. faecium: the acquisition and loss of genes, including antimicrobial resistance genes, through mobile genetic elements including plasmids, and homologous recombination of the core genome. These events lead to new clones emerging at the local level, followed by the erosion of signals of clonality through recombination, and in some identifiable cases producing new clonal clusters. These patterns lead to new, emerging lineages which are able to spread globally over relatively short timeframes.ConclusionsThe ability of A1E. faeciumto continually present new combinations of genes for potential selection suggests that controlling this pathogen will remain challenging but establishing a framework for understanding genomic evolution is likely to aid in tracking the threats posed by newly emerging lineages.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine

Reference37 articles.

1. Weiner LM, Webb AK, Limbago B, Dudeck MA, Patel J, Kallen AJ, Edwards JR, Sievert DM. Antimicrobial-resistant pathogens associated with healthcare-associated infections: summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2011-2014. Infect Control Hosp Epidemiol. 2016;37(11):1288–301. https://doi.org/10.1017/ice.2016.174.

2. van Hal SJ, Ip CLC, Ansari MA, Wilson DJ, Espedido BA, Jensen SO, et al. Evolutionary dynamics of Enterococcus faecium reveals complex genomic relationships between isolates with independent emergence of vancomycin resistance. Microb Genom. 2016;2(1):e000048. https://doi.org/10.1099/mgen.0.000048.

3. van Hal SJ, Beukers AG, Timms VJ, Ellem JA, Taylor P, Maley MW, Newton PJ, Ferguson JK, Lee A, Chen SC, Sintchenko V. Relentless spread and adaptation of non-typeable vanA vancomycin-resistant Enterococcus faecium: a genome-wide investigation. J Antimicrob Chemother. 2018;73(6):1487–91. https://doi.org/10.1093/jac/dky074.

4. Bender JK, Kalmbach A, Fleige C, Klare I, Fuchs S, Werner G. Population structure and acquisition of the vanB resistance determinant in German clinical isolates of Enterococcus faecium ST192. Sci Rep. 2016;6(1):21847. https://doi.org/10.1038/srep21847.

5. Ayobami O, Willrich N, Reuss A, Eckmanns T, Markwart R. The ongoing challenge of vancomycin-resistant Enterococcus faecium and Enterococcus faecalis in Europe: an epidemiological analysis of bloodstream infections. Emerg Microbes Infect. 2020;9(1):1180–93. https://doi.org/10.1080/22221751.2020.1769500.

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