Cargando…

Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth

People with cystic fibrosis (CF) who develop related diabetes (CFRD) have accelerated pulmonary decline, increased infection with antibiotic-resistant Pseudomonas aeruginosa and increased pulmonary exacerbations. We have previously shown that glucose concentrations are elevated in airway surface liq...

Descripción completa

Detalles Bibliográficos
Autores principales: Garnett, James P., Gray, Michael A., Tarran, Robert, Brodlie, Malcolm, Ward, Christopher, Baker, Emma H., Baines, Deborah L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790714/
https://www.ncbi.nlm.nih.gov/pubmed/24124542
http://dx.doi.org/10.1371/journal.pone.0076283
_version_ 1782286631691091968
author Garnett, James P.
Gray, Michael A.
Tarran, Robert
Brodlie, Malcolm
Ward, Christopher
Baker, Emma H.
Baines, Deborah L.
author_facet Garnett, James P.
Gray, Michael A.
Tarran, Robert
Brodlie, Malcolm
Ward, Christopher
Baker, Emma H.
Baines, Deborah L.
author_sort Garnett, James P.
collection PubMed
description People with cystic fibrosis (CF) who develop related diabetes (CFRD) have accelerated pulmonary decline, increased infection with antibiotic-resistant Pseudomonas aeruginosa and increased pulmonary exacerbations. We have previously shown that glucose concentrations are elevated in airway surface liquid (ASL) of people with CF, particularly in those with CFRD. We therefore explored the hypotheses that glucose homeostasis is altered in CF airway epithelia and that elevation of glucose flux into ASL drives increased bacterial growth, with an effect over and above other cystic fibrosis transmembrane conductance regulator (CFTR)-related ASL abnormalities. The aim of this study was to compare the mechanisms governing airway glucose homeostasis in CF and non-CF primary human bronchial epithelial (HBE) monolayers, under normal conditions and in the presence of Ps. aeruginosa filtrate. HBE-bacterial co-cultures were performed in the presence of 5 mM or 15 mM basolateral glucose to investigate how changes in blood glucose, such as those seen in CFRD, affects luminal Ps. aeruginosa growth. Calu-3 cell monolayers were used to evaluate the potential importance of glucose on Ps. aeruginosa growth, in comparison to other hallmarks of the CF ASL, namely mucus hyperviscosity and impaired CFTR-dependent fluid secretions. We show that elevation of basolateral glucose promotes the apical growth of Ps. aeruginosa on CF airway epithelial monolayers more than non-CF monolayers. Ps. aeruginosa secretions elicited more glucose flux across CF airway epithelial monolayers compared to non-CF monolayers which we propose increases glucose availability in ASL for bacterial growth. In addition, elevating basolateral glucose increased Ps. aeruginosa growth over and above any CFTR-dependent effects and the presence or absence of mucus in Calu-3 airway epithelia-bacteria co-cultures. Together these studies highlight the importance of glucose as an additional factor in promoting Ps. aeruginosa growth and respiratory infection in CF disease.
format Online
Article
Text
id pubmed-3790714
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37907142013-10-11 Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth Garnett, James P. Gray, Michael A. Tarran, Robert Brodlie, Malcolm Ward, Christopher Baker, Emma H. Baines, Deborah L. PLoS One Research Article People with cystic fibrosis (CF) who develop related diabetes (CFRD) have accelerated pulmonary decline, increased infection with antibiotic-resistant Pseudomonas aeruginosa and increased pulmonary exacerbations. We have previously shown that glucose concentrations are elevated in airway surface liquid (ASL) of people with CF, particularly in those with CFRD. We therefore explored the hypotheses that glucose homeostasis is altered in CF airway epithelia and that elevation of glucose flux into ASL drives increased bacterial growth, with an effect over and above other cystic fibrosis transmembrane conductance regulator (CFTR)-related ASL abnormalities. The aim of this study was to compare the mechanisms governing airway glucose homeostasis in CF and non-CF primary human bronchial epithelial (HBE) monolayers, under normal conditions and in the presence of Ps. aeruginosa filtrate. HBE-bacterial co-cultures were performed in the presence of 5 mM or 15 mM basolateral glucose to investigate how changes in blood glucose, such as those seen in CFRD, affects luminal Ps. aeruginosa growth. Calu-3 cell monolayers were used to evaluate the potential importance of glucose on Ps. aeruginosa growth, in comparison to other hallmarks of the CF ASL, namely mucus hyperviscosity and impaired CFTR-dependent fluid secretions. We show that elevation of basolateral glucose promotes the apical growth of Ps. aeruginosa on CF airway epithelial monolayers more than non-CF monolayers. Ps. aeruginosa secretions elicited more glucose flux across CF airway epithelial monolayers compared to non-CF monolayers which we propose increases glucose availability in ASL for bacterial growth. In addition, elevating basolateral glucose increased Ps. aeruginosa growth over and above any CFTR-dependent effects and the presence or absence of mucus in Calu-3 airway epithelia-bacteria co-cultures. Together these studies highlight the importance of glucose as an additional factor in promoting Ps. aeruginosa growth and respiratory infection in CF disease. Public Library of Science 2013-10-04 /pmc/articles/PMC3790714/ /pubmed/24124542 http://dx.doi.org/10.1371/journal.pone.0076283 Text en © 2013 Garnett et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Garnett, James P.
Gray, Michael A.
Tarran, Robert
Brodlie, Malcolm
Ward, Christopher
Baker, Emma H.
Baines, Deborah L.
Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth
title Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth
title_full Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth
title_fullStr Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth
title_full_unstemmed Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth
title_short Elevated Paracellular Glucose Flux across Cystic Fibrosis Airway Epithelial Monolayers Is an Important Factor for Pseudomonas aeruginosa Growth
title_sort elevated paracellular glucose flux across cystic fibrosis airway epithelial monolayers is an important factor for pseudomonas aeruginosa growth
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790714/
https://www.ncbi.nlm.nih.gov/pubmed/24124542
http://dx.doi.org/10.1371/journal.pone.0076283
work_keys_str_mv AT garnettjamesp elevatedparacellularglucosefluxacrosscysticfibrosisairwayepithelialmonolayersisanimportantfactorforpseudomonasaeruginosagrowth
AT graymichaela elevatedparacellularglucosefluxacrosscysticfibrosisairwayepithelialmonolayersisanimportantfactorforpseudomonasaeruginosagrowth
AT tarranrobert elevatedparacellularglucosefluxacrosscysticfibrosisairwayepithelialmonolayersisanimportantfactorforpseudomonasaeruginosagrowth
AT brodliemalcolm elevatedparacellularglucosefluxacrosscysticfibrosisairwayepithelialmonolayersisanimportantfactorforpseudomonasaeruginosagrowth
AT wardchristopher elevatedparacellularglucosefluxacrosscysticfibrosisairwayepithelialmonolayersisanimportantfactorforpseudomonasaeruginosagrowth
AT bakeremmah elevatedparacellularglucosefluxacrosscysticfibrosisairwayepithelialmonolayersisanimportantfactorforpseudomonasaeruginosagrowth
AT bainesdeborahl elevatedparacellularglucosefluxacrosscysticfibrosisairwayepithelialmonolayersisanimportantfactorforpseudomonasaeruginosagrowth