Lopez Sara, Hackbarth Corinne, Romanò Gabriella, Trias Joaquim, Jabes Daniela, Goldstein Beth P
Vicuron Pharmaceuticals, Fremont, CA, USA.
J Antimicrob Chemother. 2005 Mar;55 Suppl 2:ii21-4. doi: 10.1093/jac/dki007.
Dalbavancin is a novel, semi-synthetic glycopeptide antibiotic. The aim of this study was to further explore its activity against staphylococci.
The bactericidal activity of dalbavancin was studied using MBC and time-kill methods. The potential for resistance to dalbavancin was examined using single-step and serial-passage experiments.
Dalbavancin was bactericidal against methicillin-susceptible and -resistant Staphylococcus aureus, in both the presence and absence of human serum. No resistance was seen with any isolate tested. After serial passage, bacterial populations were more homogeneous in their susceptibility to dalbavancin than to vancomycin or teicoplanin.
Dalbavancin is bactericidal for staphylococci. Resistance to this semi-synthetic glycopeptide is not readily developed in vitro.
达巴万星是一种新型半合成糖肽类抗生素。本研究的目的是进一步探究其对葡萄球菌的活性。
采用最低杀菌浓度(MBC)和时间杀菌法研究达巴万星的杀菌活性。通过单步和连续传代实验检测对达巴万星产生耐药性的可能性。
无论有无人血清存在,达巴万星对甲氧西林敏感和耐药的金黄色葡萄球菌均具有杀菌作用。对所有测试菌株均未观察到耐药性。连续传代后,细菌群体对达巴万星的敏感性比万古霉素或替考拉宁更均匀。
达巴万星对葡萄球菌具有杀菌作用。在体外不易产生对这种半合成糖肽的耐药性。