替加环素
达托霉素
利奈唑啉
医学
重症监护医学
抗生素
肠球菌
抗生素耐药性
万古霉素
微生物学
生物
金黄色葡萄球菌
细菌
遗传学
作者
Jennifer K. Bender,Vincent Cattoir,Kristin Hegstad,Ewa Sadowy,Teresa M. Coque,Henrik Westh,Anette M. Hammerum,Kirsten Schaffer,Karen Burns,S. Murchan,Carla Novais,Ana R. Freitas,Luı́sa Peixe,María Del Grosso,Annalisa Pantosti,Guido Werner
标识
DOI:10.1016/j.drup.2018.10.002
摘要
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.
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