Two recent studies have demonstrated the presence of biologically significant amounts of cyanide within the airways of cystic fibrosis (CF) patients infected with Pseudomonas aeruginosa. Whilst environmental strains of P. aeruginosa are known to synthesise cyanide, there has been a relative lack of investigation into bacterial cyanogenesis from a medical viewpoint, despite the role P. aeruginosa plays in many serious infection settings and especially in CF lung disease. This review discusses the implications of cyanogenesis in the CF airway in terms of bacterial ecology, host immune response, progression of lung disease and potential treatment options
Cystic fibrosis (CF) is a genetic disease that results in the accumulation of dense, dehydrated mucu...
Recent data indicate that cystic fibrosis (CF) airway mucus is anaerobic. This suggests that Pseudom...
The patients with Cystic Fibrosis (CF), an inherent genetic disorder, suffer from chronic bacterial ...
AbstractTwo recent studies have demonstrated the presence of biologically significant amounts of cya...
The cystic fibrosis (CF) lung environment is poorly defined, but data suggest that bacteria may enco...
Lung disease is the most lethal manifestation of Cystic Fibrosis (CF). The bacterium Pseudomonas aer...
Most cystic fibrosis (CF) sufferers will die before reaching their mid thirties as a result of life ...
BACKGROUND: Pseudomonas aeruginosa (PA) and Burkholderia cepacia complex (Bcc), commonly found in th...
Background: Pseudomonas aeruginosa (PA) and Burkholderia cepacia complex (Bcc), commonly found in th...
Anaerobic bacteria are not only normal commensals, but are also considered opportunistic pathogens a...
The airways of cystic fibrosis (CF) patients are chronically colonized by patient-specific polymicro...
The cystic fibrosis (CF) airway is characteristically colonized with a mucoid Pseudomonas aeruginosa...
© 2014, American Society for Microbiology. Cystic fibrosis (CF) patients have increased susceptibili...
complex (Bcc), commonly found in the lungs of cystic fibrosis (CF) patients, often produce cyanide ...
Recent evidence indicates that Pseudomonas aeruginosa residing as biofilms in airway mucus of cystic...
Cystic fibrosis (CF) is a genetic disease that results in the accumulation of dense, dehydrated mucu...
Recent data indicate that cystic fibrosis (CF) airway mucus is anaerobic. This suggests that Pseudom...
The patients with Cystic Fibrosis (CF), an inherent genetic disorder, suffer from chronic bacterial ...
AbstractTwo recent studies have demonstrated the presence of biologically significant amounts of cya...
The cystic fibrosis (CF) lung environment is poorly defined, but data suggest that bacteria may enco...
Lung disease is the most lethal manifestation of Cystic Fibrosis (CF). The bacterium Pseudomonas aer...
Most cystic fibrosis (CF) sufferers will die before reaching their mid thirties as a result of life ...
BACKGROUND: Pseudomonas aeruginosa (PA) and Burkholderia cepacia complex (Bcc), commonly found in th...
Background: Pseudomonas aeruginosa (PA) and Burkholderia cepacia complex (Bcc), commonly found in th...
Anaerobic bacteria are not only normal commensals, but are also considered opportunistic pathogens a...
The airways of cystic fibrosis (CF) patients are chronically colonized by patient-specific polymicro...
The cystic fibrosis (CF) airway is characteristically colonized with a mucoid Pseudomonas aeruginosa...
© 2014, American Society for Microbiology. Cystic fibrosis (CF) patients have increased susceptibili...
complex (Bcc), commonly found in the lungs of cystic fibrosis (CF) patients, often produce cyanide ...
Recent evidence indicates that Pseudomonas aeruginosa residing as biofilms in airway mucus of cystic...
Cystic fibrosis (CF) is a genetic disease that results in the accumulation of dense, dehydrated mucu...
Recent data indicate that cystic fibrosis (CF) airway mucus is anaerobic. This suggests that Pseudom...
The patients with Cystic Fibrosis (CF), an inherent genetic disorder, suffer from chronic bacterial ...