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The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections

Dramatic increase in bacterial resistance towards conventional antibiotics emphasises the importance to identify novel, more potent antimicrobial therapies. Antimicrobial peptides (AMPs) have emerged as a promising new group to be evaluated in therapeutic intervention of infectious diseases. Here we...

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Autores principales: Myhrman, Emma, Håkansson, Joakim, Lindgren, Kerstin, Björn, Camilla, Sjöstrand, Veronika, Mahlapuu, Margit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602619/
https://www.ncbi.nlm.nih.gov/pubmed/23053090
http://dx.doi.org/10.1007/s00253-012-4439-8
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author Myhrman, Emma
Håkansson, Joakim
Lindgren, Kerstin
Björn, Camilla
Sjöstrand, Veronika
Mahlapuu, Margit
author_facet Myhrman, Emma
Håkansson, Joakim
Lindgren, Kerstin
Björn, Camilla
Sjöstrand, Veronika
Mahlapuu, Margit
author_sort Myhrman, Emma
collection PubMed
description Dramatic increase in bacterial resistance towards conventional antibiotics emphasises the importance to identify novel, more potent antimicrobial therapies. Antimicrobial peptides (AMPs) have emerged as a promising new group to be evaluated in therapeutic intervention of infectious diseases. Here we describe a novel AMP, PXL150, which demonstrates in vitro a broad spectrum microbicidal action against both Gram-positive and Gram-negative bacteria, including resistant strains. The potent microbicidal activity and broad antibacterial spectrum of PXL150 were not associated with any hemolytic activity. Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) failed to develop resistance towards PXL150 during continued selection pressure. PXL150 caused a rapid depolarisation of cytoplasmic membrane of S. aureus, and dissipating membrane potential is likely one mechanism for PXL150 to kill its target bacteria. Studies in human cell lines indicated that PXL150 has anti-inflammatory properties, which might be of additional benefit. PXL150 demonstrated pronounced anti-infectious effect in an in vivo model of full thickness wounds infected with MRSA in rats and in an ex vivo model of pig skin infected with S. aureus. Subcutaneous or topical application of the peptide in rats did not lead to any adverse reactions. In conclusion, PXL150 may constitute a new therapeutic alternative for local treatment of infections, and further studies are warranted to evaluate the applicability of this AMP in clinical settings. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-012-4439-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-36026192013-03-20 The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections Myhrman, Emma Håkansson, Joakim Lindgren, Kerstin Björn, Camilla Sjöstrand, Veronika Mahlapuu, Margit Appl Microbiol Biotechnol Applied Microbial and Cell Physiology Dramatic increase in bacterial resistance towards conventional antibiotics emphasises the importance to identify novel, more potent antimicrobial therapies. Antimicrobial peptides (AMPs) have emerged as a promising new group to be evaluated in therapeutic intervention of infectious diseases. Here we describe a novel AMP, PXL150, which demonstrates in vitro a broad spectrum microbicidal action against both Gram-positive and Gram-negative bacteria, including resistant strains. The potent microbicidal activity and broad antibacterial spectrum of PXL150 were not associated with any hemolytic activity. Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) failed to develop resistance towards PXL150 during continued selection pressure. PXL150 caused a rapid depolarisation of cytoplasmic membrane of S. aureus, and dissipating membrane potential is likely one mechanism for PXL150 to kill its target bacteria. Studies in human cell lines indicated that PXL150 has anti-inflammatory properties, which might be of additional benefit. PXL150 demonstrated pronounced anti-infectious effect in an in vivo model of full thickness wounds infected with MRSA in rats and in an ex vivo model of pig skin infected with S. aureus. Subcutaneous or topical application of the peptide in rats did not lead to any adverse reactions. In conclusion, PXL150 may constitute a new therapeutic alternative for local treatment of infections, and further studies are warranted to evaluate the applicability of this AMP in clinical settings. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-012-4439-8) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-10-04 2013 /pmc/articles/PMC3602619/ /pubmed/23053090 http://dx.doi.org/10.1007/s00253-012-4439-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Applied Microbial and Cell Physiology
Myhrman, Emma
Håkansson, Joakim
Lindgren, Kerstin
Björn, Camilla
Sjöstrand, Veronika
Mahlapuu, Margit
The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections
title The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections
title_full The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections
title_fullStr The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections
title_full_unstemmed The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections
title_short The novel antimicrobial peptide PXL150 in the local treatment of skin and soft tissue infections
title_sort novel antimicrobial peptide pxl150 in the local treatment of skin and soft tissue infections
topic Applied Microbial and Cell Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602619/
https://www.ncbi.nlm.nih.gov/pubmed/23053090
http://dx.doi.org/10.1007/s00253-012-4439-8
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