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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-9289885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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