Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Barnes, Kay B., Richards, Mark I., Laws, Thomas R., Núñez, Alejandro, Thwaite, Joanne E., Bentley, Christine, Harding, Sarah V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
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
_version_ 1783729800015249408
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
work_keys_str_mv AT barneskayb finafloxacinisaneffectivetreatmentforinhalationaltularemiaandplagueinmousemodelsofinfection
AT richardsmarki finafloxacinisaneffectivetreatmentforinhalationaltularemiaandplagueinmousemodelsofinfection
AT lawsthomasr finafloxacinisaneffectivetreatmentforinhalationaltularemiaandplagueinmousemodelsofinfection
AT nunezalejandro finafloxacinisaneffectivetreatmentforinhalationaltularemiaandplagueinmousemodelsofinfection
AT thwaitejoannee finafloxacinisaneffectivetreatmentforinhalationaltularemiaandplagueinmousemodelsofinfection
AT bentleychristine finafloxacinisaneffectivetreatmentforinhalationaltularemiaandplagueinmousemodelsofinfection
AT hardingsarahv finafloxacinisaneffectivetreatmentforinhalationaltularemiaandplagueinmousemodelsofinfection