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The factors that contribute to worse outcomes in individuals with cystic fibrosis (CF) with chronicPseudomonas aeruginosa infections are not well understood. Therefore, there is a need to understand environmental factors within the CF airway that contribute toP. aeruginosa colonization and infection.

Calprotectin-Mediated Zinc Chelation Inhibits Pseudomonas aeruginosa Protease Activity in Cystic Fibrosis Sputum