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Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung

Chronic colonization of the lungs by Pseudomonas aeruginosa is one of the major causes of morbidity and mortality in cystic fibrosis (CF) patients. To gain insights into the characteristic biofilm phenotype of P. aeruginosa in the CF lungs, mimicking the CF lung environment is critical. We previousl...

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Autores principales: Dingemans, Jozef, Monsieurs, Pieter, Yu, Sung-Huan, Crabbé, Aurélie, Förstner, Konrad U., Malfroot, Anne, Cornelis, Pierre, Van Houdt, Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981712/
https://www.ncbi.nlm.nih.gov/pubmed/27486191
http://dx.doi.org/10.1128/mBio.00813-16
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author Dingemans, Jozef
Monsieurs, Pieter
Yu, Sung-Huan
Crabbé, Aurélie
Förstner, Konrad U.
Malfroot, Anne
Cornelis, Pierre
Van Houdt, Rob
author_facet Dingemans, Jozef
Monsieurs, Pieter
Yu, Sung-Huan
Crabbé, Aurélie
Förstner, Konrad U.
Malfroot, Anne
Cornelis, Pierre
Van Houdt, Rob
author_sort Dingemans, Jozef
collection PubMed
description Chronic colonization of the lungs by Pseudomonas aeruginosa is one of the major causes of morbidity and mortality in cystic fibrosis (CF) patients. To gain insights into the characteristic biofilm phenotype of P. aeruginosa in the CF lungs, mimicking the CF lung environment is critical. We previously showed that growth of the non-CF-adapted P. aeruginosa PAO1 strain in a rotating wall vessel, a device that simulates the low fluid shear (LS) conditions present in the CF lung, leads to the formation of in-suspension, self-aggregating biofilms. In the present study, we determined the phenotypic and transcriptomic changes associated with the growth of a highly adapted, transmissible P. aeruginosa CF strain in artificial sputum medium under LS conditions. Robust self-aggregating biofilms were observed only under LS conditions. Growth under LS conditions resulted in the upregulation of genes involved in stress response, alginate biosynthesis, denitrification, glycine betaine biosynthesis, glycerol metabolism, and cell shape maintenance, while genes involved in phenazine biosynthesis, type VI secretion, and multidrug efflux were downregulated. In addition, a number of small RNAs appeared to be involved in the response to shear stress. Finally, quorum sensing was found to be slightly but significantly affected by shear stress, resulting in higher production of autoinducer molecules during growth under high fluid shear (HS) conditions. In summary, our study revealed a way to modulate the behavior of a highly adapted P. aeruginosa CF strain by means of introducing shear stress, driving it from a biofilm lifestyle to a more planktonic lifestyle.
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spelling pubmed-49817122016-08-17 Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung Dingemans, Jozef Monsieurs, Pieter Yu, Sung-Huan Crabbé, Aurélie Förstner, Konrad U. Malfroot, Anne Cornelis, Pierre Van Houdt, Rob mBio Research Article Chronic colonization of the lungs by Pseudomonas aeruginosa is one of the major causes of morbidity and mortality in cystic fibrosis (CF) patients. To gain insights into the characteristic biofilm phenotype of P. aeruginosa in the CF lungs, mimicking the CF lung environment is critical. We previously showed that growth of the non-CF-adapted P. aeruginosa PAO1 strain in a rotating wall vessel, a device that simulates the low fluid shear (LS) conditions present in the CF lung, leads to the formation of in-suspension, self-aggregating biofilms. In the present study, we determined the phenotypic and transcriptomic changes associated with the growth of a highly adapted, transmissible P. aeruginosa CF strain in artificial sputum medium under LS conditions. Robust self-aggregating biofilms were observed only under LS conditions. Growth under LS conditions resulted in the upregulation of genes involved in stress response, alginate biosynthesis, denitrification, glycine betaine biosynthesis, glycerol metabolism, and cell shape maintenance, while genes involved in phenazine biosynthesis, type VI secretion, and multidrug efflux were downregulated. In addition, a number of small RNAs appeared to be involved in the response to shear stress. Finally, quorum sensing was found to be slightly but significantly affected by shear stress, resulting in higher production of autoinducer molecules during growth under high fluid shear (HS) conditions. In summary, our study revealed a way to modulate the behavior of a highly adapted P. aeruginosa CF strain by means of introducing shear stress, driving it from a biofilm lifestyle to a more planktonic lifestyle. American Society for Microbiology 2016-08-02 /pmc/articles/PMC4981712/ /pubmed/27486191 http://dx.doi.org/10.1128/mBio.00813-16 Text en Copyright © 2016 Dingemans et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Dingemans, Jozef
Monsieurs, Pieter
Yu, Sung-Huan
Crabbé, Aurélie
Förstner, Konrad U.
Malfroot, Anne
Cornelis, Pierre
Van Houdt, Rob
Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung
title Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung
title_full Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung
title_fullStr Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung
title_full_unstemmed Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung
title_short Effect of Shear Stress on Pseudomonas aeruginosa Isolated from the Cystic Fibrosis Lung
title_sort effect of shear stress on pseudomonas aeruginosa isolated from the cystic fibrosis lung
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981712/
https://www.ncbi.nlm.nih.gov/pubmed/27486191
http://dx.doi.org/10.1128/mBio.00813-16
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