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Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides
Modern medicine is challenged continuously by the increasing prevalence of antibiotic resistant bacteria. Cationic antimicrobial peptides and their derivatives are interesting potential alternatives to antibiotics due to their rapid action, broad-spectrum of antimicrobial activity and limited emerge...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799255/ https://www.ncbi.nlm.nih.gov/pubmed/29402952 http://dx.doi.org/10.1038/s41598-018-20912-1 |
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author | Jodoin, Joelle Hincke, Maxwell T. |
author_facet | Jodoin, Joelle Hincke, Maxwell T. |
author_sort | Jodoin, Joelle |
collection | PubMed |
description | Modern medicine is challenged continuously by the increasing prevalence of antibiotic resistant bacteria. Cationic antimicrobial peptides and their derivatives are interesting potential alternatives to antibiotics due to their rapid action, broad-spectrum of antimicrobial activity and limited emergence of bacterial resistance. This study reports the novel antimicrobial properties of histone H5, purified from chicken erythrocytes, and histone H5-derived synthetic peptides. Broth microdilution assays revealed that histone H5 has potent broad-spectrum antimicrobial activity against Gram-positive and Gram-negative planktonic bacteria (MIC range: 1.9 ± 1.8 to 4.9 ± 1.5 µg/mL), including vancomycin-resistant Enterococcus (VRE) and methicillin-resistant Staphylococcus aureus (MRSA). Moreover, histone H5 displayed anti-biofilm activity against established Listeria monocytogenes and Pseudomonas aeruginosa biofilms. Scanning electron microscopy demonstrated bacterial membrane damage after histone H5 treatment, while a hemolytic assay revealed that histone H5 is non-toxic towards mammalian erythrocytes, even at a concentration of 1 mg/mL. Although the predicted H5-derived antimicrobial peptides tested in this study were located within the antimicrobial domain of histone H5, their synthetic versions did not possess more potent antimicrobial activity than the full length protein. Overall, this study demonstrates that histone H5 is a potent antimicrobial and therefore a promising template for the development of novel histone H5-derived antimicrobial peptides. |
format | Online Article Text |
id | pubmed-5799255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57992552018-02-14 Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides Jodoin, Joelle Hincke, Maxwell T. Sci Rep Article Modern medicine is challenged continuously by the increasing prevalence of antibiotic resistant bacteria. Cationic antimicrobial peptides and their derivatives are interesting potential alternatives to antibiotics due to their rapid action, broad-spectrum of antimicrobial activity and limited emergence of bacterial resistance. This study reports the novel antimicrobial properties of histone H5, purified from chicken erythrocytes, and histone H5-derived synthetic peptides. Broth microdilution assays revealed that histone H5 has potent broad-spectrum antimicrobial activity against Gram-positive and Gram-negative planktonic bacteria (MIC range: 1.9 ± 1.8 to 4.9 ± 1.5 µg/mL), including vancomycin-resistant Enterococcus (VRE) and methicillin-resistant Staphylococcus aureus (MRSA). Moreover, histone H5 displayed anti-biofilm activity against established Listeria monocytogenes and Pseudomonas aeruginosa biofilms. Scanning electron microscopy demonstrated bacterial membrane damage after histone H5 treatment, while a hemolytic assay revealed that histone H5 is non-toxic towards mammalian erythrocytes, even at a concentration of 1 mg/mL. Although the predicted H5-derived antimicrobial peptides tested in this study were located within the antimicrobial domain of histone H5, their synthetic versions did not possess more potent antimicrobial activity than the full length protein. Overall, this study demonstrates that histone H5 is a potent antimicrobial and therefore a promising template for the development of novel histone H5-derived antimicrobial peptides. Nature Publishing Group UK 2018-02-05 /pmc/articles/PMC5799255/ /pubmed/29402952 http://dx.doi.org/10.1038/s41598-018-20912-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jodoin, Joelle Hincke, Maxwell T. Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides |
title | Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides |
title_full | Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides |
title_fullStr | Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides |
title_full_unstemmed | Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides |
title_short | Histone H5 is a potent Antimicrobial Agent and a template for novel Antimicrobial Peptides |
title_sort | histone h5 is a potent antimicrobial agent and a template for novel antimicrobial peptides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799255/ https://www.ncbi.nlm.nih.gov/pubmed/29402952 http://dx.doi.org/10.1038/s41598-018-20912-1 |
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