Background: Cystic fibrosis (CF) is associated with significant morbidity and early mortality due to recurrent acute and chronic lung infections. The chronic use of multiple antibiotics increases the possibility of multidrug resistance (MDR). Antibiotic susceptibility determined by culture-based techniques may not fully represent the resistance profile. The study objective was to detect additional antibiotic resistance using molecular methods and relate the presence of MDR to airway microbiome diversity and pulmonary function. Methods: Bacterial DNA was extracted from sputum samples and amplified for the V4 region of the 16S rRNA gene. An qPCR array was used to detect antibiotic resistance genes. Clinical culture results and pulmonary funct...
Background: Chronic infection and concomitant airway inflammation is the leading cause of morbidity ...
In persons with cystic fibrosis (CF), decreased airway microbial diversity is associated with lower ...
35 p.Despite significant advances in treatment strategies targeting the underlying defect in cystic ...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
<div><p>Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of t...
Repeated pulmonary exacerbation and progressive lung function decline characterize cystic fibrosis (...
Chronic airway colonisation by Pseudomonas aeruginosa, a hallmark of cystic fibrosis (CF) lung disea...
Cystic fibrosis (CF) is an autosomal recessive disease associated with recurrent lung infections tha...
The evolution of pulmonary disease in cystic fibrosis (CF) usually beginswhenbacteria get trapped in...
Recent reports document an increasing incidence of new Gram-negative pathogens such as Stenotrophomo...
Thesis (Ph.D.)--University of Washington, 2020Cystic fibrosis (CF) is a genetic disease resulting in...
Bacteria that infect the airways of persons with cystic fibrosis (CF) include a group of well-descri...
Cystic Fibrosis (CF) is an autosomal recessive disease caused by a mutated Cystic Fibrosis Transmemb...
<div><p>Bacteria that infect the airways of persons with cystic fibrosis (CF) include a group of wel...
Cystic fibrosis (CF) is a life-limiting hereditary disease characterised by recurrent polymicrobial ...
Background: Chronic infection and concomitant airway inflammation is the leading cause of morbidity ...
In persons with cystic fibrosis (CF), decreased airway microbial diversity is associated with lower ...
35 p.Despite significant advances in treatment strategies targeting the underlying defect in cystic ...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
<div><p>Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of t...
Repeated pulmonary exacerbation and progressive lung function decline characterize cystic fibrosis (...
Chronic airway colonisation by Pseudomonas aeruginosa, a hallmark of cystic fibrosis (CF) lung disea...
Cystic fibrosis (CF) is an autosomal recessive disease associated with recurrent lung infections tha...
The evolution of pulmonary disease in cystic fibrosis (CF) usually beginswhenbacteria get trapped in...
Recent reports document an increasing incidence of new Gram-negative pathogens such as Stenotrophomo...
Thesis (Ph.D.)--University of Washington, 2020Cystic fibrosis (CF) is a genetic disease resulting in...
Bacteria that infect the airways of persons with cystic fibrosis (CF) include a group of well-descri...
Cystic Fibrosis (CF) is an autosomal recessive disease caused by a mutated Cystic Fibrosis Transmemb...
<div><p>Bacteria that infect the airways of persons with cystic fibrosis (CF) include a group of wel...
Cystic fibrosis (CF) is a life-limiting hereditary disease characterised by recurrent polymicrobial ...
Background: Chronic infection and concomitant airway inflammation is the leading cause of morbidity ...
In persons with cystic fibrosis (CF), decreased airway microbial diversity is associated with lower ...
35 p.Despite significant advances in treatment strategies targeting the underlying defect in cystic ...