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Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients

[Image: see text] Lung infection is the leading cause of morbidity and mortality in cystic fibrosis (CF) patients and is mainly dominated by Pseudomonas aeruginosa. Treatment of CF-associated lung infections is problematic because the drugs are vulnerable to multidrug-resistant pathogens, many of wh...

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Autores principales: Ben Hur, Daniel, Kapach, Gal, Wani, Naiem Ahmad, Kiper, Edo, Ashkenazi, Moshe, Smollan, Gill, Keller, Natan, Efrati, Ori, Shai, Yechiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289885/
https://www.ncbi.nlm.nih.gov/pubmed/35759644
http://dx.doi.org/10.1021/acs.jmedchem.2c00270
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author Ben Hur, Daniel
Kapach, Gal
Wani, Naiem Ahmad
Kiper, Edo
Ashkenazi, Moshe
Smollan, Gill
Keller, Natan
Efrati, Ori
Shai, Yechiel
author_facet Ben Hur, Daniel
Kapach, Gal
Wani, Naiem Ahmad
Kiper, Edo
Ashkenazi, Moshe
Smollan, Gill
Keller, Natan
Efrati, Ori
Shai, Yechiel
author_sort Ben Hur, Daniel
collection PubMed
description [Image: see text] Lung infection is the leading cause of morbidity and mortality in cystic fibrosis (CF) patients and is mainly dominated by Pseudomonas aeruginosa. Treatment of CF-associated lung infections is problematic because the drugs are vulnerable to multidrug-resistant pathogens, many of which are major biofilm producers like P. aeruginosa. Antimicrobial peptides (AMPs) are essential components in all life forms and exhibit antimicrobial activity. Here we investigated a series of AMPs (d,l-K(6)L(9)), each composed of six lysines and nine leucines but differing in their sequence composed of l- and d-amino acids. The d,l-K(6)L(9) peptides showed antimicrobial and antibiofilm activities against P. aeruginosa from CF patients. Furthermore, the data revealed that the d,l-K(6)L(9) peptides are stable and resistant to degradation by CF sputum proteases and maintain their activity in a CF sputum environment. Additionally, the d,l-K(6)L(9) peptides do not induce bacterial resistance. Overall, these findings should assist in the future development of alternative treatments against resistant bacterial biofilms.
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spelling pubmed-92898852022-07-19 Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients Ben Hur, Daniel Kapach, Gal Wani, Naiem Ahmad Kiper, Edo Ashkenazi, Moshe Smollan, Gill Keller, Natan Efrati, Ori Shai, Yechiel J Med Chem [Image: see text] Lung infection is the leading cause of morbidity and mortality in cystic fibrosis (CF) patients and is mainly dominated by Pseudomonas aeruginosa. Treatment of CF-associated lung infections is problematic because the drugs are vulnerable to multidrug-resistant pathogens, many of which are major biofilm producers like P. aeruginosa. Antimicrobial peptides (AMPs) are essential components in all life forms and exhibit antimicrobial activity. Here we investigated a series of AMPs (d,l-K(6)L(9)), each composed of six lysines and nine leucines but differing in their sequence composed of l- and d-amino acids. The d,l-K(6)L(9) peptides showed antimicrobial and antibiofilm activities against P. aeruginosa from CF patients. Furthermore, the data revealed that the d,l-K(6)L(9) peptides are stable and resistant to degradation by CF sputum proteases and maintain their activity in a CF sputum environment. Additionally, the d,l-K(6)L(9) peptides do not induce bacterial resistance. Overall, these findings should assist in the future development of alternative treatments against resistant bacterial biofilms. American Chemical Society 2022-06-27 2022-07-14 /pmc/articles/PMC9289885/ /pubmed/35759644 http://dx.doi.org/10.1021/acs.jmedchem.2c00270 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Ben Hur, Daniel
Kapach, Gal
Wani, Naiem Ahmad
Kiper, Edo
Ashkenazi, Moshe
Smollan, Gill
Keller, Natan
Efrati, Ori
Shai, Yechiel
Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients
title Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients
title_full Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients
title_fullStr Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients
title_full_unstemmed Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients
title_short Antimicrobial Peptides against Multidrug-Resistant Pseudomonas aeruginosa Biofilm from Cystic Fibrosis Patients
title_sort antimicrobial peptides against multidrug-resistant pseudomonas aeruginosa biofilm from cystic fibrosis patients
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289885/
https://www.ncbi.nlm.nih.gov/pubmed/35759644
http://dx.doi.org/10.1021/acs.jmedchem.2c00270
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