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Bacteriophage Cocktail for the Prevention of Biofilm Formation by Pseudomonas aeruginosa on Catheters in an In Vitro Model System

生物膜 铜绿假单胞菌 微生物学 噬菌体 体外 噬菌体疗法 溶解 接种 细菌 生物 菌落形成单位 化学 分子生物学 大肠杆菌 免疫学 生物化学 遗传学 基因
作者
Weiling Fu,Terri S. Forster,Oren Mayer,John J. Curtin,Susan M. Lehman,Rodney M. Donlan
出处
期刊:Antimicrobial Agents and Chemotherapy [American Society for Microbiology]
卷期号:54 (1): 397-404 被引量:342
标识
DOI:10.1128/aac.00669-09
摘要

ABSTRACT 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°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.
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