首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Note: In Vitro Activities of Daptomycin Vancomycin Linezolid and Quinupristin-Dalfopristin against Staphylococci and Enterococci Including Vancomycin- Intermediate and -Resistant Strains
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Note: In Vitro Activities of Daptomycin Vancomycin Linezolid and Quinupristin-Dalfopristin against Staphylococci and Enterococci Including Vancomycin- Intermediate and -Resistant Strains

机译:注意:达托霉素万古霉素利奈唑胺和奎奴普丁-达福普汀对葡萄球菌和肠球菌的体外活性包括中度和耐万古霉素菌株

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摘要

The in vitro activity of daptomycin was compared with those of vancomycin, linezolid, and quinupristin-dalfopristin against a variety (n = 203) of gram-positive bacteria, including methicillin-resistant Staphylococcus aureus and S. epidermidis (MRSA and MRSE, respectively), vancomycin-resistant enterococci (VRE), and vancomycin-intermediate S. aureus (VISA). Overall, daptomycin was more active against all organisms tested, except Enterococcus faecium and VISA, against which its activity was similar to that of quinupristin-dalfopristin. In time-kill studies with MRSA, MRSE, VRE, and VISA, daptomycin demonstrated greater bactericidal activity than all other drugs tested, killing ≥3 log CFU/ml by 8 h. Daptomycin may be a potential alternative drug therapy for multidrug-resistant gram-positive organisms and warrants further investigation.
机译:比较了达托霉素与万古霉素,利奈唑胺和奎奴普丁-达福普汀对多种革兰氏阳性细菌(包括耐甲氧西林的金黄色葡萄球菌和表皮葡萄球菌(分别为MRSA和MRSE))的体外活性。 ,耐万古霉素的肠球菌(VRE)和耐万古霉素的金黄色葡萄球菌(VISA)。总体而言,达托霉素对所有测试的生物体都具有更高的活性,粪便肠球菌和VISA除外,后者的活性与奎奴普丁-达福普汀相似。在使用MRSA,MRSE,VRE和VISA进行的时间杀灭研究中,达托霉素的杀菌活性高于所有其他测试药物,在8小时内杀死≥3 log CFU / ml。达托霉素可能是耐多药革兰氏阳性生物的潜在替代药物疗法,值得进一步研究。

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