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Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin
Of the thousands of natural product antibiotics discovered to date, only a handful have been developed for the treatment of bacterial infection. The clinically unexploited majority likely include compounds with untapped potential as antibacterial drugs, and in view of the ever-growing unmet medical...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727142/ https://www.ncbi.nlm.nih.gov/pubmed/29234001 http://dx.doi.org/10.1038/s41598-017-17232-1 |
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author | Nass, Nada M. Farooque, Sannia Hind, Charlotte Wand, Matthew E. Randall, Christopher P. Sutton, J. Mark Seipke, Ryan F. Rayner, Christopher M. O’Neill, Alex J. |
author_facet | Nass, Nada M. Farooque, Sannia Hind, Charlotte Wand, Matthew E. Randall, Christopher P. Sutton, J. Mark Seipke, Ryan F. Rayner, Christopher M. O’Neill, Alex J. |
author_sort | Nass, Nada M. |
collection | PubMed |
description | Of the thousands of natural product antibiotics discovered to date, only a handful have been developed for the treatment of bacterial infection. The clinically unexploited majority likely include compounds with untapped potential as antibacterial drugs, and in view of the ever-growing unmet medical need for such agents, warrant systematic re-evaluation. Here we revisit the actinorhodins, a class that was first reported 70 years ago, but which remains poorly characterized. We show that γ-actinorhodin possesses many of the requisite properties of an antibacterial drug, displaying potent and selective bactericidal activity against key Gram-positive pathogens (including Staphylococcus aureus and enterococci), a mode of action distinct from that of other agents in clinical use, an extremely low potential for the development of resistance, and a degree of in vivo efficacy in an invertebrate model of infection. Our findings underscore the utility of revisiting unexploited antibiotics as a source of novel antibacterial drug candidates. |
format | Online Article Text |
id | pubmed-5727142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57271422017-12-13 Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin Nass, Nada M. Farooque, Sannia Hind, Charlotte Wand, Matthew E. Randall, Christopher P. Sutton, J. Mark Seipke, Ryan F. Rayner, Christopher M. O’Neill, Alex J. Sci Rep Article Of the thousands of natural product antibiotics discovered to date, only a handful have been developed for the treatment of bacterial infection. The clinically unexploited majority likely include compounds with untapped potential as antibacterial drugs, and in view of the ever-growing unmet medical need for such agents, warrant systematic re-evaluation. Here we revisit the actinorhodins, a class that was first reported 70 years ago, but which remains poorly characterized. We show that γ-actinorhodin possesses many of the requisite properties of an antibacterial drug, displaying potent and selective bactericidal activity against key Gram-positive pathogens (including Staphylococcus aureus and enterococci), a mode of action distinct from that of other agents in clinical use, an extremely low potential for the development of resistance, and a degree of in vivo efficacy in an invertebrate model of infection. Our findings underscore the utility of revisiting unexploited antibiotics as a source of novel antibacterial drug candidates. Nature Publishing Group UK 2017-12-12 /pmc/articles/PMC5727142/ /pubmed/29234001 http://dx.doi.org/10.1038/s41598-017-17232-1 Text en © The Author(s) 2017 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 Nass, Nada M. Farooque, Sannia Hind, Charlotte Wand, Matthew E. Randall, Christopher P. Sutton, J. Mark Seipke, Ryan F. Rayner, Christopher M. O’Neill, Alex J. Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin |
title | Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin |
title_full | Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin |
title_fullStr | Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin |
title_full_unstemmed | Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin |
title_short | Revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin |
title_sort | revisiting unexploited antibiotics in search of new antibacterial drug candidates: the case of γ-actinorhodin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727142/ https://www.ncbi.nlm.nih.gov/pubmed/29234001 http://dx.doi.org/10.1038/s41598-017-17232-1 |
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