Soboh F, Khoury A E, Zamboni A C, Davidson D, Mittelman M W
Centre for Infection and Biomaterials Research, Toronto Hospital, Ontario, Canada.
Antimicrob Agents Chemother. 1995 Jun;39(6):1281-6. doi: 10.1128/AAC.39.6.1281.
Infection is a common complication associated with the use of transcutaneous and implanted medical devices. These infections are generally difficult to treat and frequently require removal of the biomaterial before the infection can be completely eradicated. The presence of a bacterial biofilm recalcitrant to treatment often mediates these infections. We studied the influence of a polycationic protein, protamine sulfate, on the efficacy of the fluoroquinolone ciprofloxacin against a clinical isolate of Pseudomonas aeruginosa. A P. aeruginosa biofilm was developed on 1-cm sections of red rubber catheter material and then treated with various combinations of protamine sulfate and ciprofloxacin. The present work demonstrated that ciprofloxacin in combination with protamine was more effective against biofilms than was ciprofloxacin alone. Protamine sulfate at 50 micrograms/ml combined with antibiotic at 0.5 microgram/ml reduced the number of viable cells by an average of 98.97%, while protamine sulfate at 50 micrograms/ml alone resulted in an average 107.8% increase and antibiotic alone resulted in an average 58.6% reduction after 24 h. Furthermore, protamine sulfate, in combination with ciprofloxacin, inhibited P. aeruginosa in a dose-dependent fashion. It was further observed that treatment with the combination of protamine sulfate and ciprofloxacin had a more drastic effect on planktonic organisms as compared with the P. aeruginosa biofilms; the MBC was reduced to < 0.05 microgram/ml in the presence of 25 micrograms of protamine sulfate per ml. These findings were substantiated by ultrastructure studies of treated cells using scanning and transmission electron microscopy. The synergism between ciprofloxacin and protamine sulfate significantly enhanced the efficacy of ciprofloxacin against planktonic and biofilm P. aeruginosa.
感染是经皮和植入式医疗设备使用过程中常见的并发症。这些感染通常难以治疗,并且在感染完全根除之前常常需要移除生物材料。对治疗具有抗性的细菌生物膜的存在常常介导这些感染。我们研究了聚阳离子蛋白硫酸鱼精蛋白对氟喹诺酮类药物环丙沙星抗铜绿假单胞菌临床分离株疗效的影响。在红色橡胶导管材料的1厘米切片上形成铜绿假单胞菌生物膜,然后用硫酸鱼精蛋白和环丙沙星的各种组合进行处理。目前的研究表明,环丙沙星与鱼精蛋白联合使用对生物膜的效果比单独使用环丙沙星更有效。50微克/毫升的硫酸鱼精蛋白与0.5微克/毫升的抗生素联合使用可使活细胞数量平均减少98.97%,而单独使用50微克/毫升的硫酸鱼精蛋白导致24小时后活细胞数量平均增加107.8%,单独使用抗生素则导致活细胞数量平均减少58.6%。此外,硫酸鱼精蛋白与环丙沙星联合使用以剂量依赖的方式抑制铜绿假单胞菌。进一步观察到,与铜绿假单胞菌生物膜相比,硫酸鱼精蛋白和环丙沙星联合处理对浮游生物的影响更大;在每毫升含有25微克硫酸鱼精蛋白的情况下,最低杀菌浓度降至< 0.05微克/毫升。使用扫描电子显微镜和透射电子显微镜对处理后的细胞进行超微结构研究证实了这些发现。环丙沙星和硫酸鱼精蛋白之间的协同作用显著增强了环丙沙星对浮游和生物膜形式的铜绿假单胞菌的疗效。