The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis

Abstract The exopolysaccharide Psl contributes to biofilm structure and antibiotic tolerance and may play a role in the failure to eradicate Pseudomonas aeruginosa from cystic fibrosis (CF) airways. The study objective was to determine whether there were any differences in Psl in P. aeruginosa isola...

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Autores principales: Amanda J. Morris, Lindsay Jackson, Yvonne CW Yau, Courtney Reichhardt, Trevor Beaudoin, Stephanie Uwumarenogie, Kevin M. Guttman, P. Lynne Howell, Matthew R. Parsek, Lucas R. Hoffman, Dao Nguyen, Antonio DiGiandomenico, David S. Guttman, Daniel J. Wozniak, Valerie J. Waters
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:e854128294d24e40bec501038888f54b2021-12-02T16:34:05ZThe role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis10.1038/s41522-021-00234-32055-5008https://doaj.org/article/e854128294d24e40bec501038888f54b2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41522-021-00234-3https://doaj.org/toc/2055-5008Abstract The exopolysaccharide Psl contributes to biofilm structure and antibiotic tolerance and may play a role in the failure to eradicate Pseudomonas aeruginosa from cystic fibrosis (CF) airways. The study objective was to determine whether there were any differences in Psl in P. aeruginosa isolates that were successfully eradicated compared to those that persisted, despite inhaled tobramycin treatment, in children with CF. Initial P. aeruginosa isolates were collected from children with CF undergoing eradication treatment, grown as biofilms and labeled with 3 anti-Psl monoclonal antibodies (Cam003/Psl0096, WapR001, WapR016) before confocal microscopy visualization. When grown as biofilms, P. aeruginosa isolates from children who failed antibiotic eradication therapy, had significantly increased Psl0096 binding compared to isolates from those who cleared P. aeruginosa. This was confirmed in P. aeruginosa isolates from the SickKids Eradication Cohort as well as the Early Pseudomonas Infection Control (EPIC) trial. Increased anti-Psl antibody binding was associated with bacterial aggregation and tobramycin tolerance. The biofilm matrix represents a potential therapeutic target to improve P. aeruginosa eradication treatment.Amanda J. MorrisLindsay JacksonYvonne CW YauCourtney ReichhardtTrevor BeaudoinStephanie UwumarenogieKevin M. GuttmanP. Lynne HowellMatthew R. ParsekLucas R. HoffmanDao NguyenAntonio DiGiandomenicoDavid S. GuttmanDaniel J. WozniakValerie J. WatersNature PortfolioarticleMicrobial ecologyQR100-130ENnpj Biofilms and Microbiomes, Vol 7, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Microbial ecology
QR100-130
spellingShingle Microbial ecology
QR100-130
Amanda J. Morris
Lindsay Jackson
Yvonne CW Yau
Courtney Reichhardt
Trevor Beaudoin
Stephanie Uwumarenogie
Kevin M. Guttman
P. Lynne Howell
Matthew R. Parsek
Lucas R. Hoffman
Dao Nguyen
Antonio DiGiandomenico
David S. Guttman
Daniel J. Wozniak
Valerie J. Waters
The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis
description Abstract The exopolysaccharide Psl contributes to biofilm structure and antibiotic tolerance and may play a role in the failure to eradicate Pseudomonas aeruginosa from cystic fibrosis (CF) airways. The study objective was to determine whether there were any differences in Psl in P. aeruginosa isolates that were successfully eradicated compared to those that persisted, despite inhaled tobramycin treatment, in children with CF. Initial P. aeruginosa isolates were collected from children with CF undergoing eradication treatment, grown as biofilms and labeled with 3 anti-Psl monoclonal antibodies (Cam003/Psl0096, WapR001, WapR016) before confocal microscopy visualization. When grown as biofilms, P. aeruginosa isolates from children who failed antibiotic eradication therapy, had significantly increased Psl0096 binding compared to isolates from those who cleared P. aeruginosa. This was confirmed in P. aeruginosa isolates from the SickKids Eradication Cohort as well as the Early Pseudomonas Infection Control (EPIC) trial. Increased anti-Psl antibody binding was associated with bacterial aggregation and tobramycin tolerance. The biofilm matrix represents a potential therapeutic target to improve P. aeruginosa eradication treatment.
format article
author Amanda J. Morris
Lindsay Jackson
Yvonne CW Yau
Courtney Reichhardt
Trevor Beaudoin
Stephanie Uwumarenogie
Kevin M. Guttman
P. Lynne Howell
Matthew R. Parsek
Lucas R. Hoffman
Dao Nguyen
Antonio DiGiandomenico
David S. Guttman
Daniel J. Wozniak
Valerie J. Waters
author_facet Amanda J. Morris
Lindsay Jackson
Yvonne CW Yau
Courtney Reichhardt
Trevor Beaudoin
Stephanie Uwumarenogie
Kevin M. Guttman
P. Lynne Howell
Matthew R. Parsek
Lucas R. Hoffman
Dao Nguyen
Antonio DiGiandomenico
David S. Guttman
Daniel J. Wozniak
Valerie J. Waters
author_sort Amanda J. Morris
title The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis
title_short The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis
title_full The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis
title_fullStr The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis
title_full_unstemmed The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis
title_sort role of psl in the failure to eradicate pseudomonas aeruginosa biofilms in children with cystic fibrosis
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/e854128294d24e40bec501038888f54b
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