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妥布霉素与哌拉西林联合使用对根除铜绿假单胞菌固着生物膜细胞的活性增强。

Enhanced activity of combination of tobramycin and piperacillin for eradication of sessile biofilm cells of Pseudomonas aeruginosa.

作者信息

Anwar H, Costerton J W

机构信息

Department of Microbiology, University of Alberta, Edmonton, Canada.

出版信息

Antimicrob Agents Chemother. 1990 Sep;34(9):1666-71. doi: 10.1128/AAC.34.9.1666.

Abstract

An in vitro chemostat system in which Pseudomonas aeruginosa can be cultivated at a slow growth rate and under iron limitation conditions was used to study the susceptibilities of sessile bacteria of mucoid and nonmucoid P. aeruginosa strains to tobramycin and piperacillin. Planktonic cells of both mucoid and nonmucoid P. aeruginosa strains were susceptible to tobramycin and piperacillin. None of the cells was found to be viable after 2 h of exposure to 200 micrograms of piperacillin plus 10 micrograms of tobramycin per ml. Young sessile bacteria were slightly more resistant to piperacillin or tobramycin than the planktonic cells were. However, eradication of young sessile bacteria could be achieved with a combination of piperacillin and tobramycin. None of these young biofilm bacteria were found to be viable after a 2-h exposure to 200 micrograms of piperacillin plus 10 micrograms of tobramycin per ml. Old sessile bacteria were very resistant to these antibiotics. Eradication of old sessile bacteria could not be achieved with either tobramycin (200 micrograms/ml) or piperacillin (200 micrograms/ml) alone. Combination of higher concentrations of tobramycin with piperacillin resulted in an enhancement of killing of the old sessile bacteria. Exposure of old sessile bacteria to 200 micrograms of piperacillin plus 100 micrograms of tobramycin per ml resulted in the reduction of the viable count to approximately 0.02%. The data suggest that the eradication of biofilm-associated infections is best carried out as early as possible. Enhanced activities against the sessile bacteria were achieved when higher concentrations of aminoglycosides were combined with beta-lactam antibiotics.

摘要

利用一种体外恒化器系统,在该系统中铜绿假单胞菌能够在缓慢生长速率和铁限制条件下进行培养,以研究黏液型和非黏液型铜绿假单胞菌菌株的固着细菌对妥布霉素和哌拉西林的敏感性。黏液型和非黏液型铜绿假单胞菌菌株的浮游细胞对妥布霉素和哌拉西林敏感。每毫升暴露于200微克哌拉西林加10微克妥布霉素2小时后,未发现有细胞存活。年轻的固着细菌对哌拉西林或妥布霉素的耐药性略高于浮游细胞。然而,哌拉西林和妥布霉素联合使用可根除年轻的固着细菌。每毫升暴露于200微克哌拉西林加10微克妥布霉素2小时后,未发现这些年轻的生物膜细菌有存活的。老龄固着细菌对这些抗生素具有很强的耐药性。单独使用妥布霉素(200微克/毫升)或哌拉西林(200微克/毫升)均无法根除老龄固着细菌。更高浓度的妥布霉素与哌拉西林联合使用可增强对老龄固着细菌的杀灭作用。老龄固着细菌每毫升暴露于200微克哌拉西林加100微克妥布霉素后,活菌数减少至约0.02%。数据表明,生物膜相关感染的根除最好尽早进行。当更高浓度的氨基糖苷类药物与β-内酰胺类抗生素联合使用时,对固着细菌的活性增强。

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