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Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection
Infection with aerosolized Francisella tularensis or Yersinia pestis can lead to lethal disease in humans if treatment is not initiated promptly. Finafloxacin is a novel fluoroquinolone which has demonstrated broad-spectrum activity against a range of bacterial species in vitro, in vivo, and in huma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315961/ https://www.ncbi.nlm.nih.gov/pubmed/33753342 http://dx.doi.org/10.1128/AAC.02294-20 |
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author | Barnes, Kay B. Richards, Mark I. Laws, Thomas R. Núñez, Alejandro Thwaite, Joanne E. Bentley, Christine Harding, Sarah V. |
author_facet | Barnes, Kay B. Richards, Mark I. Laws, Thomas R. Núñez, Alejandro Thwaite, Joanne E. Bentley, Christine Harding, Sarah V. |
author_sort | Barnes, Kay B. |
collection | PubMed |
description | Infection with aerosolized Francisella tularensis or Yersinia pestis can lead to lethal disease in humans if treatment is not initiated promptly. Finafloxacin is a novel fluoroquinolone which has demonstrated broad-spectrum activity against a range of bacterial species in vitro, in vivo, and in humans, activity which is superior in acidic, infection-relevant conditions. Human-equivalent doses of finafloxacin or ciprofloxacin were delivered at 24 h (representing prophylaxis) or at 72 or 38 h (representing treatment) postchallenge with F. tularensis or Y. pestis, respectively, in BALB/c mouse models. In addition, a short course of therapy (3 days) was compared to a longer course (7 days). Both therapies provided a high level of protection against both infections when administered at 24 h postchallenge, irrespective of the length of the dosing regimen; however, differences were observed when therapy was delayed. A benefit was demonstrated with finafloxacin compared to ciprofloxacin in both models when therapy was delivered later in the infection. These studies suggest that finafloxacin is an effective alternative therapeutic for the prophylaxis and treatment of inhalational infections with F. tularensis or Y. pestis. |
format | Online Article Text |
id | pubmed-8315961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-83159612021-11-18 Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection Barnes, Kay B. Richards, Mark I. Laws, Thomas R. Núñez, Alejandro Thwaite, Joanne E. Bentley, Christine Harding, Sarah V. Antimicrob Agents Chemother Experimental Therapeutics Infection with aerosolized Francisella tularensis or Yersinia pestis can lead to lethal disease in humans if treatment is not initiated promptly. Finafloxacin is a novel fluoroquinolone which has demonstrated broad-spectrum activity against a range of bacterial species in vitro, in vivo, and in humans, activity which is superior in acidic, infection-relevant conditions. Human-equivalent doses of finafloxacin or ciprofloxacin were delivered at 24 h (representing prophylaxis) or at 72 or 38 h (representing treatment) postchallenge with F. tularensis or Y. pestis, respectively, in BALB/c mouse models. In addition, a short course of therapy (3 days) was compared to a longer course (7 days). Both therapies provided a high level of protection against both infections when administered at 24 h postchallenge, irrespective of the length of the dosing regimen; however, differences were observed when therapy was delayed. A benefit was demonstrated with finafloxacin compared to ciprofloxacin in both models when therapy was delivered later in the infection. These studies suggest that finafloxacin is an effective alternative therapeutic for the prophylaxis and treatment of inhalational infections with F. tularensis or Y. pestis. American Society for Microbiology 2021-05-18 /pmc/articles/PMC8315961/ /pubmed/33753342 http://dx.doi.org/10.1128/AAC.02294-20 Text en © Crown copyright 2021. 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 | Experimental Therapeutics Barnes, Kay B. Richards, Mark I. Laws, Thomas R. Núñez, Alejandro Thwaite, Joanne E. Bentley, Christine Harding, Sarah V. Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection |
title | Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection |
title_full | Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection |
title_fullStr | Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection |
title_full_unstemmed | Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection |
title_short | Finafloxacin Is an Effective Treatment for Inhalational Tularemia and Plague in Mouse Models of Infection |
title_sort | finafloxacin is an effective treatment for inhalational tularemia and plague in mouse models of infection |
topic | Experimental Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315961/ https://www.ncbi.nlm.nih.gov/pubmed/33753342 http://dx.doi.org/10.1128/AAC.02294-20 |
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