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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Published in | Pathogens (Basel) Vol. 10; no. 3; p. 292 |
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Main Authors | , , , , , , , , , , |
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04.03.2021
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Abstract | 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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AbstractList | 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. 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.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. Recent studies have shown the domestic ferret ( ) 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. 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. |
Author | Smith, Jeanon Gainey, Melicia Kocsis, Andrew Massey, Shane Hyde, Matthew Smith, Jennifer Comer, Jason E. Brasel, Trevor Triplett, Cheryl Niemuth, Nancy Rudge, Thomas |
AuthorAffiliation | 3 Animal Resources Center, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77573, USA; mahyde@utmb.edu (M.H.); agkocsis@utmb.edu (A.K.) 1 Department of Microbiology and Immunology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77573, USA; jscomer@utmb.edu (J.E.C.); chmassey@utmb.edu (S.M.); jensmit1@utmb.edu (J.S.) 4 Battelle, 1425 Plain City-Georgesville Road, NE, West Jefferson, OH 43162, USA; GaineyM@battelle.org (M.G.); niemuth@battelle.org (N.N.); triplettc@battelle.org (C.T.); rudget@battelle.org (T.R.J.) 2 Department of Pathology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77573, USA; jeksmith@utmb.edu |
AuthorAffiliation_xml | – name: 4 Battelle, 1425 Plain City-Georgesville Road, NE, West Jefferson, OH 43162, USA; GaineyM@battelle.org (M.G.); niemuth@battelle.org (N.N.); triplettc@battelle.org (C.T.); rudget@battelle.org (T.R.J.) – name: 2 Department of Pathology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77573, USA; jeksmith@utmb.edu – name: 1 Department of Microbiology and Immunology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77573, USA; jscomer@utmb.edu (J.E.C.); chmassey@utmb.edu (S.M.); jensmit1@utmb.edu (J.S.) – name: 3 Animal Resources Center, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77573, USA; mahyde@utmb.edu (M.H.); agkocsis@utmb.edu (A.K.) |
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Cites_doi | 10.1093/infdis/jiy141 10.1136/bmj.g7348 10.1007/s00134-014-3515-1 10.24272/j.issn.2095-8137.2017.053 10.1016/j.chom.2018.12.005 10.1080/17460441.2018.1527827 10.1371/journal.ppat.1002569 10.1128/JVI.01067-14 10.1242/dmm.000471 10.1128/mSphere.00309-18 10.1093/infdis/jiw209 10.1128/JVI.01033-16 10.3390/v4123511 10.18632/oncotarget.17694 10.3390/v11020137 10.3201/eid0805.010284 10.1016/j.antiviral.2019.03.001 |
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References | Jaax (ref_3) 1996; 120 Beeching (ref_17) 2014; 349 Cross (ref_7) 2018; 13 Belser (ref_21) 2014; 88 Bente (ref_5) 2009; 2 Yan (ref_19) 2019; 165 ref_13 ref_23 Cross (ref_9) 2016; 214 ref_11 Fletcher (ref_18) 2014; 40 ref_20 Shurtleff (ref_22) 2012; 4 Geisbert (ref_2) 2002; 8 Ragland (ref_4) 2017; 67 Siragam (ref_8) 2018; 39 Kroeker (ref_15) 2017; 8 ref_16 Cross (ref_10) 2018; 218 Kozak (ref_12) 2016; 90 Bennett (ref_1) 2017; 411 ref_6 Bornholdt (ref_14) 2019; 25 |
References_xml | – ident: ref_13 doi: 10.1093/infdis/jiy141 – ident: ref_6 – volume: 349 start-page: g7348 year: 2014 ident: ref_17 article-title: Ebola virus disease publication-title: BMJ doi: 10.1136/bmj.g7348 – volume: 40 start-page: 1936 year: 2014 ident: ref_18 article-title: Understanding organ dysfunction in Ebola virus disease publication-title: Intensiv. Care Med. doi: 10.1007/s00134-014-3515-1 – volume: 39 start-page: 15 year: 2018 ident: ref_8 article-title: Animal models for filovirus infections publication-title: Zool Res. doi: 10.24272/j.issn.2095-8137.2017.053 – volume: 25 start-page: 49 year: 2019 ident: ref_14 article-title: A Two-Antibody Pan-Ebolavirus Cocktail Confers Broad Therapeutic Protection in Ferrets and Nonhuman Primates publication-title: Cell Host Microbe doi: 10.1016/j.chom.2018.12.005 – volume: 13 start-page: 1027 year: 2018 ident: ref_7 article-title: Small animal models of filovirus disease: Recent advances and future directions publication-title: Expert Opin. Drug Discov. doi: 10.1080/17460441.2018.1527827 – volume: 67 start-page: 253 year: 2017 ident: ref_4 article-title: Animal Models of Ebolavirus Infection publication-title: Comp. Med. – ident: ref_20 doi: 10.1371/journal.ppat.1002569 – ident: ref_16 – volume: 88 start-page: 9647 year: 2014 ident: ref_21 article-title: Influenza Virus Infectivity and Virulence following Ocular-Only Aerosol Inoculation of Ferrets publication-title: J. Virol. doi: 10.1128/JVI.01067-14 – volume: 120 start-page: 140 year: 1996 ident: ref_3 article-title: Lethal experimental infection of rhesus monkeys with Ebola-Zaire (Mayinga) virus by the oral and conjunctival route of exposure publication-title: Arch. Pathol. Lab. Med. – volume: 2 start-page: 12 year: 2009 ident: ref_5 article-title: Disease modeling for Ebola and Marburg viruses publication-title: Dis. Model. Mech. doi: 10.1242/dmm.000471 – ident: ref_11 doi: 10.1128/mSphere.00309-18 – volume: 218 start-page: S486 year: 2018 ident: ref_10 article-title: Comparative Transcriptomics in Ebola Makona-Infected Ferrets, Nonhuman Primates, and Humans publication-title: J. Infect. Dis. – volume: 214 start-page: 565 year: 2016 ident: ref_9 article-title: The Domestic Ferret (Mustela putorius furo) as a Lethal Infection Model for 3 Species of Ebola virus publication-title: J. Infect. Dis. doi: 10.1093/infdis/jiw209 – volume: 90 start-page: 9209 year: 2016 ident: ref_12 article-title: Ferrets Infected with Bundibugyo Virus or Ebola Virus Recapitulate Important Aspects of Human Filovirus Disease publication-title: J. Virol. doi: 10.1128/JVI.01033-16 – volume: 4 start-page: 3511 year: 2012 ident: ref_22 article-title: Standardization of the Filovirus Plaque Assay for Use in Preclinical Studies publication-title: Viruses doi: 10.3390/v4123511 – volume: 8 start-page: 46262 year: 2017 ident: ref_15 article-title: Characterization of Sudan Ebolavirus infection in ferrets publication-title: Oncotarget doi: 10.18632/oncotarget.17694 – ident: ref_23 doi: 10.3390/v11020137 – volume: 8 start-page: 503 year: 2002 ident: ref_2 article-title: Evaluation in Nonhuman Primates of Vaccines against Ebola Virus publication-title: Emerg. Infect. Dis. doi: 10.3201/eid0805.010284 – volume: 165 start-page: 1 year: 2019 ident: ref_19 article-title: Characterization of Reston virus infection in ferrets publication-title: Antivir. Res. doi: 10.1016/j.antiviral.2019.03.001 – volume: 411 start-page: 171 year: 2017 ident: ref_1 article-title: Nonhuman Primate Models of Ebola Virus Disease publication-title: Curr. Top. Microbiol. Immunol. |
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Snippet | 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... Recent studies have shown the domestic ferret ( ) to be a promising small animal model for the study of Ebola virus (EBOV) disease and medical countermeasure... 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... |
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SubjectTerms | animal models blood serum disease progression Ebola virus Ebolavirus euthanasia ferret ferrets histopathology intranasal administration mucosal challenge nasal mucosa pathogenicity viral load viruses |
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Title | Mucosal Challenge Ferret Models of Ebola Virus Disease |
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