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半合成青霉素的活性及其与美西林对拟杆菌属细菌的协同作用。

Activity of semisynthetic penicillins and synergism with mecillinam against Bacteroides species.

作者信息

Trestman I, Kaye D, Levison M E

出版信息

Antimicrob Agents Chemother. 1979 Sep;16(3):283-6. doi: 10.1128/AAC.16.3.283.

Abstract

The minimal inhibitory concentrations (MIC) of six penicillins (ampicillin, carbenicillin, ticarcillin, piperacillin, mezlocillin, and Bay k 4999) against 29 clinical isolates of Bacteriodes spp. (including Bacteroides fragilis, Bacteroides thetaiotaomicron, and Bacteroides vulgatus) were determined by an agar dilution method. Bay k 4999 was most active, followed in descending order by ampicillin, piperacillin, mezlocillin, ticarcillin, and carbenicillin. Mecillinam, a 6 beta-amidino-penicillanic acid, inhibited no strains at 50 micrograms/ml, but when compared with ampicillin, a fourfold or greater increase in MIC for ampicillin (antagonism) was noted in 3 of 29 strains, with no effect on MIC for 26 strains, whereas when combined with carbenicillin, a fourfold or greater decrease in MIC for both antibiotics (synergism) was noted in 12 strains, 4 of which had an MIC of greater than or equal to 250 micrograms/ml for carbenicillin alone. These studies demonstrate the increased activity of some newer semisynthetic penicillins and the potential synergy obtained with mecillinam and carbenicillin against Bacteroides sp.

摘要

采用琼脂稀释法测定了六种青霉素(氨苄西林、羧苄西林、替卡西林、哌拉西林、美洛西林和Bay k 4999)对29株拟杆菌属临床分离株(包括脆弱拟杆菌、多形拟杆菌和普通拟杆菌)的最低抑菌浓度(MIC)。Bay k 4999活性最强,其次依次为氨苄西林、哌拉西林、美洛西林、替卡西林和羧苄西林。甲烯氨苄青霉素,一种6β-脒基青霉烷酸,在50微克/毫升时对所有菌株均无抑制作用,但是与氨苄西林相比,29株菌株中有3株氨苄西林的MIC增加了四倍或更多(拮抗作用),26株菌株的MIC没有变化,而与羧苄西林联合使用时,12株菌株中两种抗生素的MIC均降低了四倍或更多(协同作用),其中4株单独使用羧苄西林时MIC大于或等于250微克/毫升。这些研究表明一些新型半合成青霉素的活性增强,以及甲烯氨苄青霉素和羧苄西林对拟杆菌属的潜在协同作用。

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