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采用时间杀菌法对青霉素G、RP 59500、红霉素、司帕沙星、环丙沙星和万古霉素的抗肺炎球菌活性进行比较研究。

Study of comparative antipneumococcal activities of penicillin G, RP 59500, erythromycin, sparfloxacin, ciprofloxacin, and vancomycin by using time-kill methodology.

作者信息

Pankuch G A, Jacobs M R, Appelbaum P C

机构信息

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

出版信息

Antimicrob Agents Chemother. 1994 Sep;38(9):2065-72. doi: 10.1128/AAC.38.9.2065.

Abstract

Time-kill studies were used to examine the in vitro activities of penicillin G, RP 59500, erythromycin, ciprofloxacin, sparfloxacin, and vancomycin against 10 pneumococci expressing various degrees of susceptibility to penicillin and erythromycin. RP 59500 MICs for all strains were 0.5 to 2.0 micrograms/ml, while erythromycin MICs were 0.008 to 0.06 microgram/ml for erythromycin-susceptible strains and 32.0 to 64.0 micrograms/ml for erythromycin-resistant strains. Strains were more susceptible to sparfloxacin (0.125 to 0.5 microgram/ml) than to ciprofloxacin (0.5 to 4.0 micrograms/ml), and all were inhibited by vancomycin at MICs of 0.25 to 0.5 microgram/ml. Time-kill studies showed that antibiotic concentrations greater than the MIC were bactericidal for each strain, with the following exceptions. Erythromycin was bactericidal for one penicillin-resistant strain at 6 h, with regrowth after 12 and 24 h. Three penicillin-susceptible strains were bacteriostatically inhibited by erythromycin at concentrations greater than or equal to the MIC by 6 h. One penicillin-susceptible strain (penicillin MIC, 0.06 microgram/ml) was bacteriostatically inhibited by penicillin G at 24 h at the MIC or at one-half the MIC; a bactericidal effect was found only with penicillin G at concentrations of > or = 0.25 microgram/ml. At 10 min after inoculation a 1- to 3-log10-unit reduction (90 to 99.9%) in the original inoculum was seen for 6 of 10 strains with RP 59500 at concentrations greater than or equal to the MIC. This effect was not found with any of the other compounds tested. A bactericidal effect was found at > or = 6 h with RP 59500 at concentrations of one-half to one-quarter the MIC in 7 of 10 strains, and a bacteriostatic effect was found in 3 or 10 strains, with regrowth at 24 h. One penicillin-resistant strain was examined by the time-kill methodology at 0, 1, 2, and 3 h. RP 59500 at a concentration equal to the MIC was bactericidal within 1 h, and at a concentration of one-half the MIC it was bactericidal within 3 h. This phenomenon was not seen with the other antimicrobial agents tested. Regrowth of strains at ciprofloxacin concentrations equal to the MIC or at a one-half to one-quarter the MIC was found. For sparfloxacin, three of the four penicillin-susceptible strains and two of four penicillin-resistant strains were bacteriostatically inhibited by 6 h. Bactericidal effects were found at 6, 12, and 24 h with both intermediate-resistant, one penicillin-susceptible, and two penicillin-resistant strains. Complete killing was observed with vancomycin at concentrations greater than MIC. Of the new compounds tested, RP 59500 and sparfloxacin show promise for the treatment of infections caused by penicillin-susceptible and -resistant pneumococci. The clinical significance of rapid killing by RP 59500 remains to be determined.

摘要

采用时间-杀菌研究来检测青霉素G、RP 59500、红霉素、环丙沙星、司帕沙星和万古霉素对10株对青霉素和红霉素呈现不同程度敏感性的肺炎球菌的体外活性。所有菌株的RP 59500 MIC值为0.5至2.0微克/毫升,而红霉素敏感菌株的红霉素MIC值为0.008至0.06微克/毫升,红霉素耐药菌株的红霉素MIC值为32.0至64.0微克/毫升。菌株对司帕沙星(0.125至0.5微克/毫升)的敏感性高于环丙沙星(0.5至4.0微克/毫升),所有菌株均被万古霉素在0.25至0.5微克/毫升的MIC值下抑制。时间-杀菌研究表明,抗生素浓度高于MIC时对各菌株具有杀菌作用,但有以下例外情况。红霉素对1株青霉素耐药菌株在6小时时具有杀菌作用,但在12小时和24小时后出现再生长。3株青霉素敏感菌株在6小时时被红霉素在大于或等于MIC的浓度下抑菌。1株青霉素敏感菌株(青霉素MIC为0.06微克/毫升)在24小时时被青霉素G在MIC或MIC的一半浓度下抑菌;仅在青霉素G浓度大于或等于0.25微克/毫升时发现杀菌作用。接种后10分钟,10株菌株中有6株在RP 59500浓度大于或等于MIC时,原始接种菌量减少1至3个对数10单位(90%至99.9%)。在测试的其他化合物中未发现这种效果。10株菌株中有7株在RP 59500浓度为MIC的一半至四分之一时,在大于或等于6小时时发现杀菌作用,3株菌株发现抑菌作用,在24小时时出现再生长。对1株青霉素耐药菌株在0、1、2和3小时采用时间-杀菌方法进行检测。RP 59500在等于MIC的浓度下1小时内具有杀菌作用,在MIC的一半浓度下3小时内具有杀菌作用。在测试的其他抗菌药物中未观察到这种现象。发现菌株在环丙沙星浓度等于MIC或MIC的一半至四分之一时出现再生长。对于司帕沙星,4株青霉素敏感菌株中有3株和4株青霉素耐药菌株中有2株在6小时时被抑菌。对于中度耐药、1株青霉素敏感和2株青霉素耐药菌株,在6、12和24小时时发现杀菌作用。在浓度大于MIC时,万古霉素可实现完全杀灭。在所测试的新化合物中,RP 59500和司帕沙星在治疗由青霉素敏感和耐药肺炎球菌引起的感染方面显示出前景。RP快速杀菌的临床意义仍有待确定。

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