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通过最低抑菌浓度(MIC)和时间杀菌曲线研究20株对青霉素敏感及耐药的肺炎球菌对左氧氟沙星、环丙沙星、氧氟沙星、红霉素、阿奇霉素和克拉霉素的敏感性。

Susceptibility of twenty penicillin-susceptible and -resistant pneumococci to levofloxacin, ciprofloxacin, ofloxacin, erythromycin, azithromycin, and clarithromycin by MIC and time-kill.

作者信息

Visalli M A, Jacobs M R, Appelbaum P C

机构信息

Department of Pathology (Clinical Microbiology), Hershey Medical Center, Pennsylvania 17033, USA.

出版信息

Diagn Microbiol Infect Dis. 1997 Jul;28(3):131-7. doi: 10.1016/s0732-8893(97)00017-5.

DOI:10.1016/s0732-8893(97)00017-5
PMID:9294703
Abstract

This study uses MIC and time-kill methodology to examine the antipneumococcal activity of levofloxacin, ciprofloxacin, ofloxacin, erythromycin, azithromycin, and clarithromycin against 20 pneumococci. Ten strains had levofloxacin MICs of 1.0 microgram/ml, and ten levofloxacin MICs of 2.0 micrograms/ml. Five strains in each group were macrolide susceptible, and five were macrolide resistant. MICs for ciprofloxacin and ofloxacin ranged from 0.5 to 4.0 micrograms/ml and 1.0 to 8.0 micrograms/ml, respectively. MICs of erythromycin, azithromycin, and clarithromycin were similar for macrolide susceptible strains, ranging between 0.004 to 0.06 microgram/ml, and were > or = 128.0 micrograms/ml for macrolide resistant strains. The three quinolones were bactericidal (99.9% killing) for all macrolide-susceptible strains at 2 x MIC at 24 h. The three quinolones yielded 99% killing of all strains after 12 h at 2 x MIC, and 90% killing of all strains after 6 h at the MIC of levofloxacin and ciprofloxacin and 2 x MIC for ofloxacin. Levofloxacin yielded 90% killing of all strains after 4 h at 2 x MIC and ofloxacin at 4 x MIC. For macrolide-susceptible strains, erythromycin and clarithromycin were bactericidal for 9 of 10 strains after 24 h at 4 x and 2 x MIC, respectively, and azithromycin was bactericidal after 24 h at 2 x MIC for 8 of 10 strains. All three macrolides were bactericidal after 12 h only, while 90% killing occurred in 9 of 10 strains at 8 x MIC after 6 h. Quinolone kill kinetics were similar for the 10 macrolide-resistant strains. For macrolide-resistant strains, at 64 to 128.0 micrograms/ml, virtually no decrease in count was seen, with no bactericidal effect.

摘要

本研究采用最低抑菌浓度(MIC)和杀菌动力学方法,检测左氧氟沙星、环丙沙星、氧氟沙星、红霉素、阿奇霉素和克拉霉素对20株肺炎球菌的抗肺炎球菌活性。10株菌株的左氧氟沙星MIC为1.0微克/毫升,另外10株的左氧氟沙星MIC为2.0微克/毫升。每组中有5株对大环内酯类敏感,5株对大环内酯类耐药。环丙沙星和氧氟沙星的MIC分别为0.5至4.0微克/毫升和1.0至8.0微克/毫升。对大环内酯类敏感的菌株,红霉素、阿奇霉素和克拉霉素的MIC相似,范围在0.004至0.06微克/毫升之间,而对大环内酯类耐药的菌株,其MIC大于或等于128.0微克/毫升。三种喹诺酮类药物在24小时时对所有大环内酯类敏感菌株在2倍MIC浓度下均有杀菌作用(杀菌率达99.9%)。三种喹诺酮类药物在2倍MIC浓度下12小时后对所有菌株的杀菌率达99%,在左氧氟沙星和环丙沙星的MIC浓度以及氧氟沙星的2倍MIC浓度下6小时后对所有菌株的杀菌率达90%。左氧氟沙星在2倍MIC浓度下4小时后以及氧氟沙星在4倍MIC浓度下4小时后对所有菌株的杀菌率达90%。对于大环内酯类敏感菌株,红霉素和克拉霉素分别在4倍和2倍MIC浓度下24小时后对10株中的9株有杀菌作用,阿奇霉素在2倍MIC浓度下24小时后对10株中的8株有杀菌作用。所有三种大环内酯类药物仅在12小时后有杀菌作用,而在6小时后8倍MIC浓度下10株中有9株的杀菌率达90%。喹诺酮类药物对10株大环内酯类耐药菌株的杀菌动力学相似。对于大环内酯类耐药菌株,在64至128.0微克/毫升浓度下,菌数几乎没有减少,无杀菌作用。

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