| Literature DB >> 30447411 |
Jennifer K Bender1, Vincent Cattoir2, Kristin Hegstad3, Ewa Sadowy4, Teresa M Coque5, Henrik Westh6, Anette M Hammerum7, Kirsten Schaffer8, Karen Burns9, Stephen Murchan10, Carla Novais11, Ana R Freitas11, Luísa Peixe11, Maria Del Grosso12, Annalisa Pantosti12, Guido Werner13.
Abstract
Vancomycin-resistant enterococci (VRE) are important nosocomial pathogens. Invasive VRE infections are difficult to treat since common therapeutic options including ampicillin and glycopeptides often fail. In vitro, most VRE remain susceptible to last-resort antibiotics such as linezolid, tigecycline and daptomycin. However, neither tigecycline nor linezolid act in a bactericidal manner, and daptomycin has proven activity only at high dosages licensed for treating enterococcal endocarditis. Despite these pharmacological and therapeutic limitations, reports on resistance to these last-resort drugs in VRE, and enterococci in general, have increased in recent years. In this review, we briefly recapitulate the current knowledge on the mode of action as well as the known and novel mechanisms of resistance and describe surveillance data on resistance to linezolid, tigecycline and daptomycin in enterococci. In addition, we also suggest a common nomenclature for designating enterococci and VRE with resistances to these important last-resort antibiotics.Entities:
Keywords: Daptomycin; Linezolid; Tigecycline; VRE; vanA; vanB
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Year: 2018 PMID: 30447411 DOI: 10.1016/j.drup.2018.10.002
Source DB: PubMed Journal: Drug Resist Updat ISSN: 1368-7646 Impact factor: 18.500