首页> 外文期刊>Antimicrobial agents and chemotherapy. >In vitro activities of daptomycin, vancomycin, linezolid, and quinupristin-dalfopristin against Staphylococci and Enterococci, including vancomycin- intermediate and -resistant strains.
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In vitro activities of daptomycin, vancomycin, linezolid, and quinupristin-dalfopristin against Staphylococci and Enterococci, including vancomycin- intermediate and -resistant strains.

机译: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,包括万古霉素中等和耐药菌株。

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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 > or =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 h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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