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The use of resazurin as a novel antimicrobial agent against Francisella tularensis
The highly infectious and deadly pathogen, Francisella tularensis, is classified by the CDC as a Category A bioterrorism agent. Inhalation of a single bacterium results in an acute pneumonia with a 30–60% mortality rate without treatment. Due to the prevalence of antibiotic resistance, there is a st...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853850/ https://www.ncbi.nlm.nih.gov/pubmed/24367766 http://dx.doi.org/10.3389/fcimb.2013.00093 |
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author | Schmitt, Deanna M. O'Dee, Dawn M. Cowan, Brianna N. Birch, James W.-M. Mazzella, Leanne K. Nau, Gerard J. Horzempa, Joseph |
author_facet | Schmitt, Deanna M. O'Dee, Dawn M. Cowan, Brianna N. Birch, James W.-M. Mazzella, Leanne K. Nau, Gerard J. Horzempa, Joseph |
author_sort | Schmitt, Deanna M. |
collection | PubMed |
description | The highly infectious and deadly pathogen, Francisella tularensis, is classified by the CDC as a Category A bioterrorism agent. Inhalation of a single bacterium results in an acute pneumonia with a 30–60% mortality rate without treatment. Due to the prevalence of antibiotic resistance, there is a strong need for new types of antibacterial drugs. Resazurin is commonly used to measure bacterial and eukaryotic cell viability through its reduction to the fluorescent product resorufin. When tested on various bacterial taxa at the recommended concentration of 44 μM, a potent bactericidal effect was observed against various Francisella and Neisseria species, including the human pathogens type A F. tularensis (Schu S4) and N. gonorrhoeae. As low as 4.4 μM resazurin was sufficient for a 10-fold reduction in F. tularensis growth. In broth culture, resazurin was reduced to resorufin by F. tularensis. Resorufin also suppressed the growth of F. tularensis suggesting that this compound is the biologically active form responsible for decreasing the viability of F. tularensis LVS bacteria. Replication of F. tularensis in primary human macrophages and non-phagocytic cells was abolished following treatment with 44 μM resazurin indicating this compound could be an effective therapy for tularemia in vivo. |
format | Online Article Text |
id | pubmed-3853850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38538502013-12-23 The use of resazurin as a novel antimicrobial agent against Francisella tularensis Schmitt, Deanna M. O'Dee, Dawn M. Cowan, Brianna N. Birch, James W.-M. Mazzella, Leanne K. Nau, Gerard J. Horzempa, Joseph Front Cell Infect Microbiol Microbiology The highly infectious and deadly pathogen, Francisella tularensis, is classified by the CDC as a Category A bioterrorism agent. Inhalation of a single bacterium results in an acute pneumonia with a 30–60% mortality rate without treatment. Due to the prevalence of antibiotic resistance, there is a strong need for new types of antibacterial drugs. Resazurin is commonly used to measure bacterial and eukaryotic cell viability through its reduction to the fluorescent product resorufin. When tested on various bacterial taxa at the recommended concentration of 44 μM, a potent bactericidal effect was observed against various Francisella and Neisseria species, including the human pathogens type A F. tularensis (Schu S4) and N. gonorrhoeae. As low as 4.4 μM resazurin was sufficient for a 10-fold reduction in F. tularensis growth. In broth culture, resazurin was reduced to resorufin by F. tularensis. Resorufin also suppressed the growth of F. tularensis suggesting that this compound is the biologically active form responsible for decreasing the viability of F. tularensis LVS bacteria. Replication of F. tularensis in primary human macrophages and non-phagocytic cells was abolished following treatment with 44 μM resazurin indicating this compound could be an effective therapy for tularemia in vivo. Frontiers Media S.A. 2013-12-06 /pmc/articles/PMC3853850/ /pubmed/24367766 http://dx.doi.org/10.3389/fcimb.2013.00093 Text en Copyright © 2013 Schmitt, O'Dee, Cowan, Birch, Mazzella, Nau and Horzempa. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Schmitt, Deanna M. O'Dee, Dawn M. Cowan, Brianna N. Birch, James W.-M. Mazzella, Leanne K. Nau, Gerard J. Horzempa, Joseph The use of resazurin as a novel antimicrobial agent against Francisella tularensis |
title | The use of resazurin as a novel antimicrobial agent against Francisella tularensis |
title_full | The use of resazurin as a novel antimicrobial agent against Francisella tularensis |
title_fullStr | The use of resazurin as a novel antimicrobial agent against Francisella tularensis |
title_full_unstemmed | The use of resazurin as a novel antimicrobial agent against Francisella tularensis |
title_short | The use of resazurin as a novel antimicrobial agent against Francisella tularensis |
title_sort | use of resazurin as a novel antimicrobial agent against francisella tularensis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853850/ https://www.ncbi.nlm.nih.gov/pubmed/24367766 http://dx.doi.org/10.3389/fcimb.2013.00093 |
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