Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis Patients

Cystic fibrosis (CF) patients often acquire chronic respiratory tract infections due to Pseudomonas aeruginosa and Burkholderia cepacia complex (Bcc) species. In the CF lung, these bacteria grow as multicellular aggregates termed biofilms. Biofilms demonstrate increased (adaptive) resistance to conv...

Full description

Bibliographic Details
Main Authors: César de la Fuente-Núñez, Sarah C. Mansour, Zhejun Wang, Lucy Jiang, Elena B.M. Breidenstein, Melissa Elliott, Fany Reffuveille, David P. Speert, Shauna L. Reckseidler-Zenteno, Ya Shen, Markus Haapasalo, Robert E.W. Hancock
Format: Article
Language:English
Published: MDPI AG 2014-10-01
Series:Antibiotics
Subjects:
Online Access:http://www.mdpi.com/2079-6382/3/4/509
id doaj-1120db610f2e4160b89de1b518988b83
record_format Article
spelling doaj-1120db610f2e4160b89de1b518988b832020-11-24T22:43:32ZengMDPI AGAntibiotics2079-63822014-10-013450952610.3390/antibiotics3040509antibiotics3040509Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis PatientsCésar de la Fuente-Núñez0Sarah C. Mansour1Zhejun Wang2Lucy Jiang3Elena B.M. Breidenstein4Melissa Elliott5Fany Reffuveille6David P. Speert7Shauna L. Reckseidler-Zenteno8Ya Shen9Markus Haapasalo10Robert E.W. Hancock11Centre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaCentre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaDivision of Endodontics, Department of Oral Biological and Medical Sciences, Faculty of Dentistry, University of British Columbia, Vancouver, BC, V6T 1Z3, CanadaCentre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaCentre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaCentre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaCentre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaDepartment of Pediatrics, University of British Columbia, Vancouver, BC, V6H 3V4, CanadaAthabasca University, Athabasca, AB, T9S 3A3, CanadaDivision of Endodontics, Department of Oral Biological and Medical Sciences, Faculty of Dentistry, University of British Columbia, Vancouver, BC, V6T 1Z3, CanadaDivision of Endodontics, Department of Oral Biological and Medical Sciences, Faculty of Dentistry, University of British Columbia, Vancouver, BC, V6T 1Z3, CanadaCentre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaCystic fibrosis (CF) patients often acquire chronic respiratory tract infections due to Pseudomonas aeruginosa and Burkholderia cepacia complex (Bcc) species. In the CF lung, these bacteria grow as multicellular aggregates termed biofilms. Biofilms demonstrate increased (adaptive) resistance to conventional antibiotics, and there are currently no available biofilm-specific therapies. Using plastic adherent, hydroxyapatite and flow cell biofilm models coupled with confocal and scanning electron microscopy, it was demonstrated that an anti-biofilm peptide 1018 prevented biofilm formation, eradicated mature biofilms and killed biofilms formed by a wide range of P. aeruginosa and B. cenocepacia clinical isolates. New peptide derivatives were designed that, compared to their parent peptide 1018, showed similar or decreased anti-biofilm activity against P. aeruginosa biofilms, but increased activity against biofilms formed by the Gram-positive bacterium methicillin resistant Staphylococcus aureus. In addition, some of these new peptide derivatives retained the immunomodulatory activity of 1018 since they induced the production of the chemokine monocyte chemotactic protein-1 (MCP-1) and suppressed lipopolysaccharide-mediated tumor necrosis factor-α (TNF-α) production by human peripheral blood mononuclear cells (PBMC) and were non-toxic towards these cells. Peptide 1018 and its derivatives provide promising leads for the treatment of chronic biofilm infections and hyperinflammatory lung disease in CF patients.http://www.mdpi.com/2079-6382/3/4/509anti-biofilmimmunomodulationpeptidesantibiotic-resistancecystic fibrosis
collection DOAJ
language English
format Article
sources DOAJ
author César de la Fuente-Núñez
Sarah C. Mansour
Zhejun Wang
Lucy Jiang
Elena B.M. Breidenstein
Melissa Elliott
Fany Reffuveille
David P. Speert
Shauna L. Reckseidler-Zenteno
Ya Shen
Markus Haapasalo
Robert E.W. Hancock
spellingShingle César de la Fuente-Núñez
Sarah C. Mansour
Zhejun Wang
Lucy Jiang
Elena B.M. Breidenstein
Melissa Elliott
Fany Reffuveille
David P. Speert
Shauna L. Reckseidler-Zenteno
Ya Shen
Markus Haapasalo
Robert E.W. Hancock
Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis Patients
Antibiotics
anti-biofilm
immunomodulation
peptides
antibiotic-resistance
cystic fibrosis
author_facet César de la Fuente-Núñez
Sarah C. Mansour
Zhejun Wang
Lucy Jiang
Elena B.M. Breidenstein
Melissa Elliott
Fany Reffuveille
David P. Speert
Shauna L. Reckseidler-Zenteno
Ya Shen
Markus Haapasalo
Robert E.W. Hancock
author_sort César de la Fuente-Núñez
title Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis Patients
title_short Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis Patients
title_full Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis Patients
title_fullStr Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis Patients
title_full_unstemmed Anti-Biofilm and Immunomodulatory Activities of Peptides That Inhibit Biofilms Formed by Pathogens Isolated from Cystic Fibrosis Patients
title_sort anti-biofilm and immunomodulatory activities of peptides that inhibit biofilms formed by pathogens isolated from cystic fibrosis patients
publisher MDPI AG
series Antibiotics
issn 2079-6382
publishDate 2014-10-01
description Cystic fibrosis (CF) patients often acquire chronic respiratory tract infections due to Pseudomonas aeruginosa and Burkholderia cepacia complex (Bcc) species. In the CF lung, these bacteria grow as multicellular aggregates termed biofilms. Biofilms demonstrate increased (adaptive) resistance to conventional antibiotics, and there are currently no available biofilm-specific therapies. Using plastic adherent, hydroxyapatite and flow cell biofilm models coupled with confocal and scanning electron microscopy, it was demonstrated that an anti-biofilm peptide 1018 prevented biofilm formation, eradicated mature biofilms and killed biofilms formed by a wide range of P. aeruginosa and B. cenocepacia clinical isolates. New peptide derivatives were designed that, compared to their parent peptide 1018, showed similar or decreased anti-biofilm activity against P. aeruginosa biofilms, but increased activity against biofilms formed by the Gram-positive bacterium methicillin resistant Staphylococcus aureus. In addition, some of these new peptide derivatives retained the immunomodulatory activity of 1018 since they induced the production of the chemokine monocyte chemotactic protein-1 (MCP-1) and suppressed lipopolysaccharide-mediated tumor necrosis factor-α (TNF-α) production by human peripheral blood mononuclear cells (PBMC) and were non-toxic towards these cells. Peptide 1018 and its derivatives provide promising leads for the treatment of chronic biofilm infections and hyperinflammatory lung disease in CF patients.
topic anti-biofilm
immunomodulation
peptides
antibiotic-resistance
cystic fibrosis
url http://www.mdpi.com/2079-6382/3/4/509
work_keys_str_mv AT cesardelafuentenunez antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT sarahcmansour antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT zhejunwang antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT lucyjiang antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT elenabmbreidenstein antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT melissaelliott antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT fanyreffuveille antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT davidpspeert antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT shaunalreckseidlerzenteno antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT yashen antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT markushaapasalo antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
AT robertewhancock antibiofilmandimmunomodulatoryactivitiesofpeptidesthatinhibitbiofilmsformedbypathogensisolatedfromcysticfibrosispatients
_version_ 1725695255019257856