Work

Impact of Pseudomonas aeruginosa biofilm exopolysaccharide composition on bacteriophage and bacteriophage-antibiotic combination activity

Year: 2025

Type: article

Abstract: ABSTRACT Multidrug-resistant Pseudomonas aeruginosa is a leading cause of hospital-acquired infections, including medical device infections, partially due to the organism’s ability to produce biofilm on prosthetic material. Increased antibiotic tolerance of bacteria within biofilm, along with the increasing prevalence of infections caused by multidrug-resistant P. aeruginosa , including extensively drug-resistant phenotypes, results in scenarios where conventional antibiotics may fail to effectively treat these infections. Bacteriophage (phage) therapy is a promising alternative to conventional antimicrobial therapy that can provide potent antibiofilm activity, particularly when combined with antibiotics. The impact of P. aeruginosa biofilm phenotype on the efficacy of phage-antibiotic combinations remains unclear. We characterized the biofilms of a panel of 10 clinical and two laboratory P. aeruginosa isolates by determining the minimum biofilm inhibitory concentrations, biofilm production capabilities, and phage activity. Furthermore, we quantified the exopolysaccharide content of P. aeruginosa strains PAO1 and PA14 and confirmed they produced Class II and Class I biofilm, respectively. We then selected a triple-phage cocktail with broad activity across all P. aeruginosa strains for evaluation of antibiofilm activity against PAO1 and PA14 in vitro . Through spectrophotometric growth suppression and time-kill analyses, we found the triple-phage cocktail + ciprofloxacin to be more efficacious in biofilm eradication than either modality alone. Phage 109 displayed potent antibiofilm activity against both strains irrespective of planktonic activity, whereas phages E2005-C and EM-T3762627-2_AH displayed distinct antibiofilm activity based on biofilm phenotype. These data warrant further investigation into the impact of P. aeruginosa biofilm phenotype on phage antibiofilm activity.

Source: Antimicrobial Agents and Chemotherapy

DOI: 10.1128/aac.00925-25