LasR variant cystic fibrosis isolates reveal an adaptable quorum-sensing hierarchy in Pseudomonas aeruginosa

JB Feltner, DJ Wolter, CE Pope, MC Groleau… - MBio, 2016 - Am Soc Microbiol
Chronic Pseudomonas aeruginosa infections cause significant morbidity in patients with
cystic fibrosis (CF). Over years to decades, P. aeruginosa adapts genetically as it establishes …

Staphylococcus aureus Small-Colony Variants Are Independently Associated With Worse Lung Disease in Children With Cystic Fibrosis

…, CE Pope, M Blackledge, E Déziel… - Clinical Infectious …, 2013 - academic.oup.com
Background. Cystic fibrosis (CF) lung disease is associated with diverse bacteria chronically
infecting the airways. Slow-growing, antibiotic-resistant mutants of Staphylococcus aureus …

[PDF][PDF] Human and extracellular DNA depletion for metagenomic analysis of complex clinical infection samples yields optimized viable microbiome profiles

MT Nelson, CE Pope, RL Marsh, DJ Wolter, EJ Weiss… - Cell reports, 2019 - cell.com
Metagenomic sequencing is a promising approach for identifying and characterizing organisms
and their functional characteristics in complex, polymicrobial infections, such as airway …

Pseudomonas aeruginosa In Vitro Phenotypes Distinguish Cystic Fibrosis Infection Stages and Outcomes

…, W Morgan, DJ Wolter, CE Pope… - American journal of …, 2014 - atsjournals.org
Rationale: Pseudomonas aeruginosa undergoes phenotypic changes during cystic fibrosis (CF)
lung infection. Although mucoidy is traditionally associated with transition to chronic …

Human gut bacteria contain acquired interbacterial defence systems

…, AJ Verster, MC Radey, DT Schmidtke, CE Pope… - Nature, 2019 - nature.com
The human gastrointestinal tract consists of a dense and diverse microbial community, the
composition of which is intimately linked to health. Extrinsic factors such as diet and host …

[HTML][HTML] Metagenomic evidence for taxonomic dysbiosis and functional imbalance in the gastrointestinal tracts of children with cystic fibrosis

O Manor, R Levy, CE Pope, HS Hayden… - Scientific reports, 2016 - nature.com
Cystic fibrosis (CF) results in inflammation, malabsorption of fats and other nutrients, and
obstruction in the gastrointestinal (GI) tract, yet the mechanisms linking these disease …

Escherichia coli Dysbiosis Correlates With Gastrointestinal Dysfunction in Children With Cystic Fibrosis

LR Hoffman, CE Pope, HS Hayden… - Clinical infectious …, 2014 - academic.oup.com
Cystic fibrosis gastrointestinal disease includes nutrient malabsorption and intestinal
inflammation. We show that the abundances of Escherichia coli in fecal microbiota were …

Fecal dysbiosis in infants with cystic fibrosis is associated with early linear growth failure

HS Hayden, A Eng, CE Pope, MJ Brittnacher, AT Vo… - Nature medicine, 2020 - nature.com
Most infants with cystic fibrosis (CF) have pancreatic exocrine insufficiency that results in
nutrient malabsorption and requires oral pancreatic enzyme replacement. Newborn screening …

[HTML][HTML] CFTR dysregulation drives active selection of the gut microbiome

…, EJ Weiss, PM Treuting, N Tolley, CE Pope… - PLoS …, 2020 - journals.plos.org
Patients with cystic fibrosis (CF) have altered fecal microbiomes compared to those of healthy
controls. The magnitude of this dysbiosis correlates with measures of CF gastrointestinal (…

Pseudomonas aeruginosa Phenotypes Associated With Eradication Failure in Children With Cystic Fibrosis

…, DJ Wolter, LS Houston, CE Pope… - Clinical infectious …, 2014 - academic.oup.com
We measured in vitro phenotypes of early Pseudomonas aeruginosa isolates from children
with cystic fibrosis in an antibiotic eradication therapy trial. Isolates frequently exhibited …