Emergence and spread of vancomycin resistance among enterococci in Europe

Author:

Werner G1,Coque T M2,Hammerum A M3,Hope R4,Hryniewicz W5,Johnson A4,Klare I1,Kristinsson K G6,Leclercq R7,Lester C H3,Lillie M4,Novais C89,Olsson-Liljequist B10,Peixe L V9,Sadowy E5,Simonsen G S11,Top J12,Vuopio-Varkila J13,Willems R J12,Witte W1,Woodford N4

Affiliation:

1. Robert Koch-Institute, Wernigerode Branch, Wernigerode, Germany

2. University Hospital Ramón y Cajal, Madrid, Spain

3. Statens Serum Institute, Copenhagen, Denmark

4. Health Protection Agency Centre for Infections, London, United Kingdom

5. National Medicines Institute, Warsaw, Poland

6. Department of Clinical Microbiology, Landspitali University Hospital, Reykjavik, Iceland

7. National Reference Centre for Antimicrobial Resistance, Laboratory for Enterococci, University Hospital, Caen, France

8. Faculty of Health Sciences, Fernando Pessoa University, Porto, Portugal

9. REQUIMTE, Faculty of Pharmacy, University of Porto, Portugal

10. Swedish Institute for Infectious Disease Control, Stockholm, Sweden

11. Norwegian Surveillance System for Antimicrobial Resistance, University Hospital of North Norway, Tromsø, Norway

12. University Medical Centre Utrecht, Utrecht, the Netherlands

13. National Public Health Institute (KTL), Helsinki, Finland

Abstract

Vancomycin-resistant enterococci (VRE) first appeared in the late 1980s in a few European countries. Nowadays, six types of acquired vancomycin resistance in enterococci are known; however, only VanA and to a lesser extent VanB are widely prevalent. Various genes encode acquired vancomycin resistance and these are typically associated with mobile genetic elements which allow resistance to spread clonally and laterally. The major reservoir of acquired vancomycin resistance is Enterococcus faecium; vancomycin-resistant Enterococcus faecalis are still rare. Population analysis of E. faecium has revealed a distinct subpopulation of hospital-acquired strain types, which can be differentiated by molecular typing methods (MLVA, MLST) from human commensal and animal strains. Hospital-acquired E. faecium have additional genomic content (accessory genome) including several factors known or supposed to be virulence-associated. Acquired ampicillin resistance is a major phenotypic marker of hospital-acquired E. faecium in Europe and experience has shown that it often precedes increasing rates of VRE with a delay of several years. Several factors are known to promote VRE colonisation and transmission; however, despite having populations with similar predispositions and preconditions, rates of VRE vary all over Europe.

Publisher

European Centre for Disease Control and Prevention (ECDC)

Subject

Virology,Public Health, Environmental and Occupational Health,Epidemiology

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