Cystic Fibrosis

Natural products shape microbial ecology and disease in the cystic fibrosis airway

Cystic fibrosis (CF) is a life-shortening autosomal recessive genetic disorder caused by mutation in the gene encoding the CF transmembrane conductance regulator (CFTR). Dysfunction in CFTR leads to the accumulation of thick and dehydrated mucus in …

Differential Metabolite Production Underlies Disruption of the Cystic Fibrosis Airway Microbiota by Pathogens

Cystic fibrosis (CF) is a multisystem disease characterized by the accumulation of mucus in the airways that promotes pathogen colonization, leading to respiratory exacerbations, lung failure, and death. Culture-independent approaches have revealed …

Achromobacter spp.: Emerging pathogens in the cystic fibrosis lung

What are Achromobacter spp. and how do they infect the lungs of people with cystic fibrosis?