Kaatz G W, Seo S M
Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan 48201.
Antimicrob Agents Chemother. 1990 Jul;34(7):1376-80. doi: 10.1128/AAC.34.7.1376.
WIN 57273 is a new fluoroquinolone with excellent in vitro activity versus gram-positive pathogens, including methicillin-susceptible and -resistant Staphylococcus aureus and Staphylococcus epidermidis and gentamicin-susceptible and -resistant Enterococcus faecalis. We compared the microdilution MICs and MBCs of this compound to those of other antimicrobial agents for more than 30 clinical isolates of each of these groups of organisms and found that with few exceptions, it was at least 10 times more active than all other drugs tested. Selection for resistance to ciprofloxacin (greater than or equal to 5 micrograms/ml) or WIN 57273 (greater than or equal to 0.16 microgram/ml) by the gradient plate method produced mutants with diminished susceptibility to the other fluoroquinolone; however, the MICs and MBCs of WIN 57273 for such strains were still quite low and remained below the preliminary susceptibility breakpoint (less than or equal to 2 micrograms/ml). Spontaneous mutations conferring resistance to two and five times the WIN 57273 MIC were detectable at low frequencies for S. aureus and S. epidermidis; such mutations were virtually undetectable for E. faecalis. Further testing is necessary to establish if the effectiveness of WIN 57273 is maintained in vivo, first in animals and then in humans with infections caused by methicillin-susceptible and -resistant strains of S. aureus and S. epidermidis or gentamicin-susceptible and -resistant strains of E. faecalis.
WIN 57273是一种新型氟喹诺酮类药物,对革兰氏阳性病原体具有优异的体外活性,包括对甲氧西林敏感和耐药的金黄色葡萄球菌、表皮葡萄球菌,以及对庆大霉素敏感和耐药的粪肠球菌。我们将该化合物与其他抗菌药物对这些菌群中30多种临床分离株的微量稀释法最低抑菌浓度(MIC)和最低杀菌浓度(MBC)进行了比较,发现除少数例外情况外,它的活性至少比所有其他受试药物高10倍。通过梯度平板法筛选对环丙沙星(大于或等于5微克/毫升)或WIN 57273(大于或等于0.16微克/毫升)耐药的菌株,产生了对另一种氟喹诺酮类药物敏感性降低的突变体;然而,WIN 57273对这类菌株的MIC和MBC仍然相当低,且仍低于初步敏感性断点(小于或等于2微克/毫升)。对于金黄色葡萄球菌和表皮葡萄球菌,能在低频下检测到对两倍和五倍WIN 57273 MIC产生耐药性的自发突变;而对于粪肠球菌,几乎检测不到此类突变。有必要进一步进行试验,以确定WIN 57273在体内是否仍保持有效性,首先在动物中进行,然后在感染了对甲氧西林敏感和耐药的金黄色葡萄球菌及表皮葡萄球菌菌株,或对庆大霉素敏感和耐药的粪肠球菌菌株的人类中进行。