Edelstein P H, Edelstein M A, Lehr K H, Ren J
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104-4283, USA.
J Antimicrob Chemother. 1996 Jan;37(1):117-26. doi: 10.1093/jac/37.1.117.
The activities of levofloxacin and ofloxacin against 22 clinical legionella isolates was determined by microbroth dilution susceptibility testing. Growth inhibition of two Legionella pneumophila strains grown in guinea pig alveolar macrophages by levofloxacin, ofloxacin, or erythromycin was also determined. The drug concentrations required to inhibit 90% of strains tested was 0.032 mg/L for levofloxacin or ofloxacin, and was 0.016 mg/L for ciprofloxacin. BYE alpha broth significantly inhibited the activities of all three drugs tested, as judged by the susceptibility of control Escherichia coli strains. Levofloxacin (0.25 mg/L) reduced bacterial counts of two L. pneumophila strains grown in guinea pig alveolar macrophages by 1 log10, but regrowth occurred over a 3 day period; levofloxacin (1 mg/L) reduced bacterial counts by 2-3 log10 cfu/mL. Levofloxacin was significantly more active than erythromycin, and as active as ofloxacin or ciprofloxacin in this assay. Pharmacokinetic and therapy studies of levofloxacin and ofloxacin were performed in guinea pigs with L. pneumophila pneumonia. For the pharmacokinetic study, levofloxacin was given (10 mg/kg) by the intraperitoneal route to infected guinea pigs; mean peak plasma and lung concentrations were 3.4 mg/L and 1.4 micrograms/g, respectively, at 0.5 h and 2.6 mg/L and 0.6 micrograms/g at 1 h. The terminal half-life phase of elimination from plasma and lung was c. 1 h. All 15 infected guinea pigs treated with levofloxacin (10 mg/kg/day given ip once daily) for 5 days survived for 9 days after antimicrobial therapy, as did all 14 guinea pigs treated with the same dose of ofloxacin. None of 13 animals treated with saline survived. Levofloxacin is effective against L. pneumophila in vitro and in a guinea pig model of legionnaire's disease. Levofloxacin should be evaluated as a treatment of human legionnaires' disease.
通过微量肉汤稀释药敏试验测定了左氧氟沙星和氧氟沙星对22株临床嗜肺军团菌分离株的活性。还测定了左氧氟沙星、氧氟沙星或红霉素对在豚鼠肺泡巨噬细胞中生长的两株嗜肺军团菌菌株的生长抑制作用。抑制90%受试菌株所需的药物浓度,左氧氟沙星或氧氟沙星为0.032mg/L,环丙沙星为0.016mg/L。根据对照大肠杆菌菌株的药敏情况判断,BYEα肉汤显著抑制了所测试的三种药物的活性。左氧氟沙星(0.25mg/L)使在豚鼠肺泡巨噬细胞中生长的两株嗜肺军团菌菌株的细菌计数降低了1个对数级,但在3天内出现了细菌再生长;左氧氟沙星(1mg/L)使细菌计数降低了2 - 3个对数级cfu/mL。在该试验中,左氧氟沙星的活性显著高于红霉素,与氧氟沙星或环丙沙星的活性相当。在患有嗜肺军团菌肺炎的豚鼠中进行了左氧氟沙星和氧氟沙星的药代动力学及治疗研究。对于药代动力学研究,给感染的豚鼠腹腔注射左氧氟沙星(10mg/kg);在0.5小时时,血浆和肺的平均峰值浓度分别为3.4mg/L和1.4μg/g,在1小时时分别为2.6mg/L和0.6μg/g。从血浆和肺中消除的终末半衰期约为1小时。所有15只接受左氧氟沙星(10mg/kg/天,腹腔注射,每日一次)治疗5天的感染豚鼠在抗菌治疗后存活了9天,接受相同剂量氧氟沙星治疗的所有14只豚鼠也是如此。13只用生理盐水治疗的动物均未存活。左氧氟沙星在体外和豚鼠军团病模型中对嗜肺军团菌有效。应评估左氧氟沙星作为人类军团病治疗药物的效果。