首页> 外文期刊>International journal of antimicrobial agents >Comparison of minimal inhibitory and mutant prevention drug concentrations of 4 fluoroquinolones against clinical isolates of methicillin-susceptible and -resistant Staphylococcus aureus
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Comparison of minimal inhibitory and mutant prevention drug concentrations of 4 fluoroquinolones against clinical isolates of methicillin-susceptible and -resistant Staphylococcus aureus

机译:4种氟喹诺酮类药物对甲氧西林敏感和耐药金黄色葡萄球菌临床分离株的最低抑菌和预防突变药物浓度的比较

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Staphylococcus aureus remains an important human pathogen affecting both outpatients and those hospitalized. Increasing antimicrobial resistance is global but prevalence rates are variable for different geographical areas. Fluoroquinotones have been used to treat S. aureus infections and the newer quinolones have enhanced in vitro activity against this organism. The mutant prevention concentration (MPC) defines the antimicrobial drug concentration threshold that would require an organism to simultaneously possess two mutations for growth in the presence of the drug. We tested clinical isolates of methicillin-susceptible (MSSA) and methicillin-resistant (MRSA) S. aureus by minimum inhibitory concentration (MIC) and MPC against gatifloxacin, gemifloxacin, levofloxacin and moxifloxacin. For MSSA strains, the rank order of potency based on MIC90 values were gemifloxacin (0.063 mg/l) = moxifloxacin (0.063 mg/l) > gatifloxacin (0.05 mg/l) = levofloxacin (0.25 mg/l) and by MPC values moxifloxacin (0.25 mg/l) > gemifloxacin (0.5 mg/l) > gatifloxacin (1 mg/l) = levofloxacin (1 mg/l). For 87% of the isolates the MPC value was 0.5 mg/l for gatifloxacin. The rank order of potency based on the time the serum drug concentration exceeded the MPC90, was as follows: moxifloxacin (> 24 h) > levofloxacin (> 18 h) > gatifloxacin (12 h) > gemifloxacin (9 h). Serum drug concentration remained in excess of the MPC87 for 24 h for gatifloxacin. Both MIC90 and MPC90 values were higher against MRSA strains and the time above the MPC90 was significantly shorter for all agents. (C) 2004 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
机译:金黄色葡萄球菌仍然是影响门诊和住院患者的重要人类病原体。抗菌素耐药性的增加是全球性的,但不同地区的流行率是可变的。氟喹诺酮类药物已用于治疗金黄色葡萄球菌感染,新型喹诺酮类药物已增强了针对这种生物的体外活性。突变预防浓度(MPC)定义了抗菌药物浓度阈值,该阈值要求生物体在药物存在下同时具有两个突变才能生长。我们通过对加替沙星,吉非沙星,左氧氟沙星和莫西沙星的最小抑菌浓度(MIC)和MPC测试了耐甲氧西林(MSSA)和耐甲氧西林(MRSA)的金黄色葡萄球菌的临床分离株。对于MSSA菌株,基于MIC90值的效力排名为吉非沙星(0.063 mg / l)=莫西沙星(0.063 mg / l)>加替沙星(0.05 mg / l)=左氧氟沙星(0.25 mg / l),MPC值为莫西沙星(0.25 mg / l)>吉非沙星(0.5 mg / l)>加替沙星(1 mg / l)=左氧氟沙星(1 mg / l)。对于87%的分离物,加替沙星的MPC值为0.5 mg / l。基于血清药物浓度超过MPC90的时间,效力的等级顺序如下:莫西沙星(> 24小时)>左氧氟沙星(> 18小时)>加替沙星(12小时)>吉非沙星(9小时)。加替沙星的血清药物浓度在24小时内仍超过MPC87。相对于MRSA菌株,MIC90和MPC90值均较高,并且所有试剂均高于MPC90的时间明显更短。 (C)2004年Elsevier B.V.和国际化学疗法学会。版权所有。

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