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Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus
Staphylococcus aureus is one of the most common pathogens associated with infection in wounds. The current standard of care uses a combination of disinfection and drainage followed by conventional antibiotics such as methicillin. Methicillin and vancomycin resistance has rendered these treatments in...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241801/ https://www.ncbi.nlm.nih.gov/pubmed/35467395 http://dx.doi.org/10.1128/spectrum.00534-22 |
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author | Benjamin, Aaron B. Moule, Madeleine G. Didwania, Maruti K. Hardy, Jonathan Saenkham-Huntsinger, Panatda Sule, Preeti Nielsen, Josefine Eilsø Lin, Jennifer S. Contag, Christopher H. Barron, Annelise E. Cirillo, Jeffrey D. |
author_facet | Benjamin, Aaron B. Moule, Madeleine G. Didwania, Maruti K. Hardy, Jonathan Saenkham-Huntsinger, Panatda Sule, Preeti Nielsen, Josefine Eilsø Lin, Jennifer S. Contag, Christopher H. Barron, Annelise E. Cirillo, Jeffrey D. |
author_sort | Benjamin, Aaron B. |
collection | PubMed |
description | Staphylococcus aureus is one of the most common pathogens associated with infection in wounds. The current standard of care uses a combination of disinfection and drainage followed by conventional antibiotics such as methicillin. Methicillin and vancomycin resistance has rendered these treatments ineffective, often causing the reemergence of infection. This study examines the use of antimicrobial peptoids (sequence-specific poly-N-substituted glycines) designed to mimic naturally occurring cationic, amphipathic host defense peptides, as an alternative to conventional antibiotics. These peptoids also show efficient and fast (<30 min) killing of methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA) at low micromolar concentrations without having apparent cytotoxic side effects in vivo. Additionally, these novel peptoids show excellent efficacy against biofilm formation and detachment for both MSSA and MRSA. In comparison, conventional antibiotics were unable to detach or prevent formation of biofilms. One cationic 12mer, Peptoid 1, shows great promise, as it could prevent formation of and detach biofilms at concentrations as low as 1.6 μM. The use of a bioluminescent S. aureus murine incision wound model demonstrated clearance of infection in peptoid-treated mice within 8 days, conveying another advantage these peptoids have over conventional antibiotics. These results provide clear evidence of the potential for antimicrobial peptoids for the treatment of S. aureus wound infections. IMPORTANCE Staphylococcus aureus resistance is a consistent problem with a large impact on the health care system. Infections with resistant S. aureus can cause serious adverse effects and can result in death. These antimicrobial peptoids show efficient killing of bacteria both as a biofilm and as free bacteria, often doing so in less than 30 min. As such, these antimicrobials have the potential to alleviate the burden that Staphylococcus infections have on the health care system and cause better outcomes for infected patients. |
format | Online Article Text |
id | pubmed-9241801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92418012022-06-30 Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus Benjamin, Aaron B. Moule, Madeleine G. Didwania, Maruti K. Hardy, Jonathan Saenkham-Huntsinger, Panatda Sule, Preeti Nielsen, Josefine Eilsø Lin, Jennifer S. Contag, Christopher H. Barron, Annelise E. Cirillo, Jeffrey D. Microbiol Spectr Research Article Staphylococcus aureus is one of the most common pathogens associated with infection in wounds. The current standard of care uses a combination of disinfection and drainage followed by conventional antibiotics such as methicillin. Methicillin and vancomycin resistance has rendered these treatments ineffective, often causing the reemergence of infection. This study examines the use of antimicrobial peptoids (sequence-specific poly-N-substituted glycines) designed to mimic naturally occurring cationic, amphipathic host defense peptides, as an alternative to conventional antibiotics. These peptoids also show efficient and fast (<30 min) killing of methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA) at low micromolar concentrations without having apparent cytotoxic side effects in vivo. Additionally, these novel peptoids show excellent efficacy against biofilm formation and detachment for both MSSA and MRSA. In comparison, conventional antibiotics were unable to detach or prevent formation of biofilms. One cationic 12mer, Peptoid 1, shows great promise, as it could prevent formation of and detach biofilms at concentrations as low as 1.6 μM. The use of a bioluminescent S. aureus murine incision wound model demonstrated clearance of infection in peptoid-treated mice within 8 days, conveying another advantage these peptoids have over conventional antibiotics. These results provide clear evidence of the potential for antimicrobial peptoids for the treatment of S. aureus wound infections. IMPORTANCE Staphylococcus aureus resistance is a consistent problem with a large impact on the health care system. Infections with resistant S. aureus can cause serious adverse effects and can result in death. These antimicrobial peptoids show efficient killing of bacteria both as a biofilm and as free bacteria, often doing so in less than 30 min. As such, these antimicrobials have the potential to alleviate the burden that Staphylococcus infections have on the health care system and cause better outcomes for infected patients. American Society for Microbiology 2022-04-25 /pmc/articles/PMC9241801/ /pubmed/35467395 http://dx.doi.org/10.1128/spectrum.00534-22 Text en Copyright © 2022 Benjamin et al. https://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 (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Benjamin, Aaron B. Moule, Madeleine G. Didwania, Maruti K. Hardy, Jonathan Saenkham-Huntsinger, Panatda Sule, Preeti Nielsen, Josefine Eilsø Lin, Jennifer S. Contag, Christopher H. Barron, Annelise E. Cirillo, Jeffrey D. Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus |
title | Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus |
title_full | Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus |
title_fullStr | Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus |
title_full_unstemmed | Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus |
title_short | Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus |
title_sort | efficacy of cathelicidin-mimetic antimicrobial peptoids against staphylococcus aureus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241801/ https://www.ncbi.nlm.nih.gov/pubmed/35467395 http://dx.doi.org/10.1128/spectrum.00534-22 |
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