The airway fluids of cystic fibrosis (CF) patients contain local pH gradients and are more acidic than those of healthy individuals. pH is a critical factor that is often overlooked in studies seeking to recapitulate the infection microenvironment. We sought to determine the impact of pH on the physiology of a ubiqituous yet understudied microbe, Stenotrophomonas maltophilia Phylogenomics was first used to reconstruct evolutionary relationships between 74 strains of S. maltophilia (59 from CF patients). Neither the core genome (2,158 genes) nor the accessory genome (11,978 genes) distinguish the CF and non-CF isolates; however, strains from similar isolation sources grouped into the same subclades. We grew two human and six CF S. maltophili...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
<div><p>Introduction</p><p>Cystic fibrosis (CF) airways are colonized by a polymicrobial community o...
In patients afflicted with cystic fibrosis (CF), morbidity and mortality are primarily associated wi...
The airway fluids of cystic fibrosis (CF) patients contain local pH gradients and are more acidic th...
Cystic fibrosis (CF) is a genetic disease that results in the accumulation of dense, dehydrated mucu...
Pseudomonas aeruginosa (P. aeruginosa) can chronically colonize in immunocompromised hosts, especial...
The present study was carried out to understand the adaptive strategies developed by Stenotrophomona...
Due to the continuous exposure to a challenging environment and repeated antibiotic treatment course...
The cystic fibrosis (CF) lung contains thick mucus colonized by opportunistic pathogens which adapt ...
Stenotrophomonas maltophilia is an emerging nosocomial bacterial pathogen which is currently isolate...
Stenotrophomonas maltophilia is an emerging nosocomial bacterial pathogen which is currently isolate...
Cystic fibrosis (CF) is an autosomal recessive disease caused by CFTR mutations. It is characterized...
International audienceIn patients with cystic fibrosis (CF), the lung is a remarkable ecological nic...
Mutations in the human genome may result in altered phenotypes. The cystic fibrosis (CF) patient, fo...
Cystic fibrosis (CF) is a progressive, genetic disease characterized by mutations in the CF transmem...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
<div><p>Introduction</p><p>Cystic fibrosis (CF) airways are colonized by a polymicrobial community o...
In patients afflicted with cystic fibrosis (CF), morbidity and mortality are primarily associated wi...
The airway fluids of cystic fibrosis (CF) patients contain local pH gradients and are more acidic th...
Cystic fibrosis (CF) is a genetic disease that results in the accumulation of dense, dehydrated mucu...
Pseudomonas aeruginosa (P. aeruginosa) can chronically colonize in immunocompromised hosts, especial...
The present study was carried out to understand the adaptive strategies developed by Stenotrophomona...
Due to the continuous exposure to a challenging environment and repeated antibiotic treatment course...
The cystic fibrosis (CF) lung contains thick mucus colonized by opportunistic pathogens which adapt ...
Stenotrophomonas maltophilia is an emerging nosocomial bacterial pathogen which is currently isolate...
Stenotrophomonas maltophilia is an emerging nosocomial bacterial pathogen which is currently isolate...
Cystic fibrosis (CF) is an autosomal recessive disease caused by CFTR mutations. It is characterized...
International audienceIn patients with cystic fibrosis (CF), the lung is a remarkable ecological nic...
Mutations in the human genome may result in altered phenotypes. The cystic fibrosis (CF) patient, fo...
Cystic fibrosis (CF) is a progressive, genetic disease characterized by mutations in the CF transmem...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
<div><p>Introduction</p><p>Cystic fibrosis (CF) airways are colonized by a polymicrobial community o...
In patients afflicted with cystic fibrosis (CF), morbidity and mortality are primarily associated wi...