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Mucosal Challenge Ferret Models of Ebola Virus Disease

Recent studies have shown the domestic ferret (Mustela putorius furo) to be a promising small animal model for the study of Ebola virus (EBOV) disease and medical countermeasure evaluation. To date, most studies have focused on traditional challenge routes, predominantly intramuscular and intranasal...

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Autores principales: Brasel, Trevor, Comer, Jason E., Massey, Shane, Smith, Jeanon, Smith, Jennifer, Hyde, Matthew, Kocsis, Andrew, Gainey, Melicia, Niemuth, Nancy, Triplett, Cheryl, Rudge, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001755/
https://www.ncbi.nlm.nih.gov/pubmed/33806375
http://dx.doi.org/10.3390/pathogens10030292
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author Brasel, Trevor
Comer, Jason E.
Massey, Shane
Smith, Jeanon
Smith, Jennifer
Hyde, Matthew
Kocsis, Andrew
Gainey, Melicia
Niemuth, Nancy
Triplett, Cheryl
Rudge, Thomas
author_facet Brasel, Trevor
Comer, Jason E.
Massey, Shane
Smith, Jeanon
Smith, Jennifer
Hyde, Matthew
Kocsis, Andrew
Gainey, Melicia
Niemuth, Nancy
Triplett, Cheryl
Rudge, Thomas
author_sort Brasel, Trevor
collection PubMed
description Recent studies have shown the domestic ferret (Mustela putorius furo) to be a promising small animal model for the study of Ebola virus (EBOV) disease and medical countermeasure evaluation. To date, most studies have focused on traditional challenge routes, predominantly intramuscular and intranasal administration. Here, we present results from a non-clinical pathogenicity study examining oronasal, oral, and ocular mucosal challenge routes in ferrets. Animals were challenged with 1, 10, or 100 plaque forming units EBOV followed by monitoring of disease progression and biosampling. Ferrets administered virus via oronasal and oral routes met euthanasia criteria due to advanced disease 5–10 days post-challenge. Conversely, all ferrets dosed via the ocular route survived until the scheduled study termination 28-day post-challenge. In animals that succumbed to disease, a dose/route response was not observed; increases in disease severity, febrile responses, serum and tissue viral load, alterations in clinical pathology, and gross/histopathology findings were similar between subjects. Disease progression in ferrets challenged via ocular administration was unremarkable throughout the study period. Results from this study further support the ferret as a model for EBOV disease following oral and nasal mucosa exposure.
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spelling pubmed-80017552021-03-28 Mucosal Challenge Ferret Models of Ebola Virus Disease Brasel, Trevor Comer, Jason E. Massey, Shane Smith, Jeanon Smith, Jennifer Hyde, Matthew Kocsis, Andrew Gainey, Melicia Niemuth, Nancy Triplett, Cheryl Rudge, Thomas Pathogens Article Recent studies have shown the domestic ferret (Mustela putorius furo) to be a promising small animal model for the study of Ebola virus (EBOV) disease and medical countermeasure evaluation. To date, most studies have focused on traditional challenge routes, predominantly intramuscular and intranasal administration. Here, we present results from a non-clinical pathogenicity study examining oronasal, oral, and ocular mucosal challenge routes in ferrets. Animals were challenged with 1, 10, or 100 plaque forming units EBOV followed by monitoring of disease progression and biosampling. Ferrets administered virus via oronasal and oral routes met euthanasia criteria due to advanced disease 5–10 days post-challenge. Conversely, all ferrets dosed via the ocular route survived until the scheduled study termination 28-day post-challenge. In animals that succumbed to disease, a dose/route response was not observed; increases in disease severity, febrile responses, serum and tissue viral load, alterations in clinical pathology, and gross/histopathology findings were similar between subjects. Disease progression in ferrets challenged via ocular administration was unremarkable throughout the study period. Results from this study further support the ferret as a model for EBOV disease following oral and nasal mucosa exposure. MDPI 2021-03-04 /pmc/articles/PMC8001755/ /pubmed/33806375 http://dx.doi.org/10.3390/pathogens10030292 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Brasel, Trevor
Comer, Jason E.
Massey, Shane
Smith, Jeanon
Smith, Jennifer
Hyde, Matthew
Kocsis, Andrew
Gainey, Melicia
Niemuth, Nancy
Triplett, Cheryl
Rudge, Thomas
Mucosal Challenge Ferret Models of Ebola Virus Disease
title Mucosal Challenge Ferret Models of Ebola Virus Disease
title_full Mucosal Challenge Ferret Models of Ebola Virus Disease
title_fullStr Mucosal Challenge Ferret Models of Ebola Virus Disease
title_full_unstemmed Mucosal Challenge Ferret Models of Ebola Virus Disease
title_short Mucosal Challenge Ferret Models of Ebola Virus Disease
title_sort mucosal challenge ferret models of ebola virus disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001755/
https://www.ncbi.nlm.nih.gov/pubmed/33806375
http://dx.doi.org/10.3390/pathogens10030292
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