Synergistic Therapeutic Strategies for Pseudomonas aeruginosa
Cystic fibrosis (CF) is a genetic disorder characterized by defective chloride ion transport, leading to thickened mucus in the airways. This viscous environment predisposes patients to persistent respiratory infections, with Pseudomonas aeruginosa representing the most common and difficult-to-eradicate pathogen. Chronic colonization by P. aeruginosa significantly accelerates pulmonary decline, increases hospitalization frequency, and contributes to morbidity