Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Mail stop C-16, 1600 Clifton Rd., Atlanta, GA 30333, USA.
Antimicrob Agents Chemother. 2010 Jan;54(1):397-404. doi: 10.1128/AAC.00669-09. Epub 2009 Oct 12.
Microorganisms develop biofilms on indwelling medical devices and are associated with device-related infections, resulting in substantial morbidity and mortality. This study investigated the effect of pretreating hydrogel-coated catheters with Pseudomonas aeruginosa bacteriophages on biofilm formation by P. aeruginosa in an in vitro model. Hydrogel-coated catheters were exposed to a 10 log(10) PFU ml(-1) lysate of P. aeruginosa phage M4 for 2 h at 37 degrees C prior to bacterial inoculation. The mean viable biofilm count on untreated catheters was 6.87 log(10) CFU cm(-2) after 24 h. The pretreatment of catheters with phage reduced this value to 4.03 log(10) CFU cm(-2) (P < 0.001). Phage treatment immediately following bacterial inoculation also reduced biofilm viable counts (4.37 log(10) CFU cm(-2) reduction; P < 0.001). The regrowth of biofilms on phage-treated catheters occurred between 24 and 48 h, but supplemental treatment with phage at 24 h significantly reduced biofilm regrowth (P < 0.001). Biofilm isolates resistant to phage M4 were recovered from catheters pretreated with phage. The phage susceptibility profiles of these isolates were used to guide the development of a five-phage cocktail from a larger library of P. aeruginosa phages. The pretreatment of catheters with this cocktail reduced the 48-h mean biofilm cell density by 99.9% (from 7.13 to 4.13 log(10) CFU cm(-2); P < 0.001), but fewer biofilm isolates were resistant to these phages. These results suggest the potential of applying phages, especially phage cocktails, to the surfaces of indwelling medical devices for mitigating biofilm formation by clinically relevant bacteria.
微生物在留置医疗器械上形成生物膜,并与器械相关感染有关,导致发病率和死亡率显著增加。本研究在体外模型中研究了用绿脓杆菌噬菌体预处理水凝胶涂层导管对绿脓杆菌生物膜形成的影响。水凝胶涂层导管在 37°C 下用 10 log(10) PFU ml(-1)的绿脓杆菌噬菌体 M4 裂解物孵育 2 小时,然后接种细菌。未经处理的导管在 24 小时后生物膜活菌计数的平均值为 6.87 log(10) CFU cm(-2)。用噬菌体预处理导管可将该值降低至 4.03 log(10) CFU cm(-2)(P < 0.001)。细菌接种后立即用噬菌体处理也减少了生物膜活菌计数(减少 4.37 log(10) CFU cm(-2);P < 0.001)。噬菌体处理的导管上生物膜的再生长发生在 24 至 48 小时之间,但在 24 小时时用噬菌体进行补充处理可显著减少生物膜的再生长(P < 0.001)。从用噬菌体预处理的导管中回收了对噬菌体 M4 具有抗性的生物膜分离物。这些分离物的噬菌体敏感性谱用于指导从更大的绿脓杆菌噬菌体文库中开发五噬菌体鸡尾酒。用该鸡尾酒预处理导管可将 48 小时平均生物膜细胞密度降低 99.9%(从 7.13 降至 4.13 log(10) CFU cm(-2);P < 0.001),但对这些噬菌体具有抗性的生物膜分离物较少。这些结果表明,应用噬菌体,特别是噬菌体鸡尾酒,对留置医疗器械表面进行处理以减少临床相关细菌形成生物膜的潜力。