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...

Full description

Saved in:
Bibliographic Details
Published inPathogens (Basel) Vol. 10; no. 3; p. 292
Main Authors Brasel, Trevor, Comer, Jason E., Massey, Shane, Smith, Jeanon, Smith, Jennifer, Hyde, Matthew, Kocsis, Andrew, Gainey, Melicia, Niemuth, Nancy, Triplett, Cheryl, Rudge, Thomas
Format Journal Article
LanguageEnglish
Published Switzerland MDPI 04.03.2021
MDPI AG
Subjects
Online AccessGet full text

Cover

Loading…
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.
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.)
Author_xml – sequence: 1
  givenname: Trevor
  surname: Brasel
  fullname: Brasel, Trevor
– sequence: 2
  givenname: Jason E.
  surname: Comer
  fullname: Comer, Jason E.
– sequence: 3
  givenname: Shane
  surname: Massey
  fullname: Massey, Shane
– sequence: 4
  givenname: Jeanon
  surname: Smith
  fullname: Smith, Jeanon
– sequence: 5
  givenname: Jennifer
  surname: Smith
  fullname: Smith, Jennifer
– sequence: 6
  givenname: Matthew
  surname: Hyde
  fullname: Hyde, Matthew
– sequence: 7
  givenname: Andrew
  surname: Kocsis
  fullname: Kocsis, Andrew
– sequence: 8
  givenname: Melicia
  orcidid: 0000-0003-0993-8284
  surname: Gainey
  fullname: Gainey, Melicia
– sequence: 9
  givenname: Nancy
  surname: Niemuth
  fullname: Niemuth, Nancy
– sequence: 10
  givenname: Cheryl
  surname: Triplett
  fullname: Triplett, Cheryl
– sequence: 11
  givenname: Thomas
  surname: Rudge
  fullname: Rudge, Thomas
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33806375$$D View this record in MEDLINE/PubMed
BookMark eNqNks1u1DAUhS3UipbSB2CDsmQzcB07trNBQkMLlVqxAbbWjX0z48oTD3ZSibcnw7RVS6UKb_x3zudj-75iB0MaiLE3HN4L0cKHLY7rtKKhcAABdVu_YMc1aLUAw_XBg_EROy3lGuZmYDd_yY6EMKCEbo6ZuppcKhir5RpjpGFF1TnlTGN1lTzFUqW-OutSxOpnyFOpPodCWOg1O-wxFjq97U_Yj_Oz78uvi8tvXy6Wny4XTrZmXHjuiAxqUlzUrTSCZO-5lxwIvNHUa4UNce20A9UCaM-FcbLjva-dakCcsIs91ye8ttscNph_24TB_l1IeWUxj8FFsmp3lDRSd7yTrpOola-RK6nmFFrjzPq4Z22nbkPe0TBmjI-gj3eGsLardGPnZ-O6aWbAu1tATr8mKqPdhOIoRhwoTcXWjQSplWnq_5CCaZRsWz1L3z6MdZ_n7o9mAd8LXE6lZOrvJRzsrhTsk1KYPfofjwsjjiHtbhbiM84_99K6AA
CitedBy_id crossref_primary_10_1038_s41598_023_31027_7
crossref_primary_10_1038_s41598_022_11851_z
crossref_primary_10_1128_JVI_00833_21
crossref_primary_10_1128_jvi_01888_22
crossref_primary_10_3390_v16121806
crossref_primary_10_1038_s41392_024_01917_x
crossref_primary_10_1016_j_virs_2024_03_010
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
ContentType Journal Article
Copyright 2021 by the authors. 2021
Copyright_xml – notice: 2021 by the authors. 2021
DBID AAYXX
CITATION
NPM
7X8
7S9
L.6
5PM
DOA
DOI 10.3390/pathogens10030292
DatabaseName CrossRef
PubMed
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals (Freely Accessible)
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
DatabaseTitleList AGRICOLA
CrossRef

MEDLINE - Academic
PubMed

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 2076-0817
ExternalDocumentID oai_doaj_org_article_6cee84847b1b4cb4a76d2a1646d1c77a
PMC8001755
33806375
10_3390_pathogens10030292
Genre Journal Article
GrantInformation_xml – fundername: Department of Health and Human Services, National institute of Allergy and Infectious Disease
  grantid: HHSN272201200003I/HHSN27200015
– fundername: NIH HHS
  grantid: HHSN272201200003I/HHSN27200015
GroupedDBID 53G
5VS
8FE
8FH
AADQD
AAHBH
AAYXX
ADBBV
AFKRA
AFZYC
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BBNVY
BCNDV
BENPR
BHPHI
CCPQU
CITATION
DIK
GROUPED_DOAJ
HCIFZ
HYE
IAO
IHR
ITC
KQ8
LK8
M48
M7P
MODMG
M~E
OK1
PGMZT
PHGZM
PHGZT
PIMPY
PROAC
RPM
NPM
7X8
PQGLB
7S9
L.6
5PM
PUEGO
ID FETCH-LOGICAL-c498t-d1cee8a7e61329483e4fd1d410e0d87ef76a5e17c7c069007d138c4b1fd2c6503
IEDL.DBID M48
ISSN 2076-0817
IngestDate Wed Aug 27 01:29:11 EDT 2025
Thu Aug 21 17:59:38 EDT 2025
Fri Jul 11 13:26:40 EDT 2025
Thu Jul 10 18:15:30 EDT 2025
Thu Jan 02 22:57:07 EST 2025
Tue Jul 01 04:15:39 EDT 2025
Thu Apr 24 23:13:04 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords Ebola virus
ferret
mucosal challenge
Language English
License 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/).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c498t-d1cee8a7e61329483e4fd1d410e0d87ef76a5e17c7c069007d138c4b1fd2c6503
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0003-0993-8284
OpenAccessLink https://doaj.org/article/6cee84847b1b4cb4a76d2a1646d1c77a
PMID 33806375
PQID 2508564997
PQPubID 23479
ParticipantIDs doaj_primary_oai_doaj_org_article_6cee84847b1b4cb4a76d2a1646d1c77a
pubmedcentral_primary_oai_pubmedcentral_nih_gov_8001755
proquest_miscellaneous_2540476852
proquest_miscellaneous_2508564997
pubmed_primary_33806375
crossref_primary_10_3390_pathogens10030292
crossref_citationtrail_10_3390_pathogens10030292
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20210304
PublicationDateYYYYMMDD 2021-03-04
PublicationDate_xml – month: 3
  year: 2021
  text: 20210304
  day: 4
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
PublicationTitle Pathogens (Basel)
PublicationTitleAlternate Pathogens
PublicationYear 2021
Publisher MDPI
MDPI AG
Publisher_xml – name: MDPI
– name: MDPI AG
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.
SSID ssj0000800817
Score 2.1870644
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...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 292
SubjectTerms animal models
blood serum
disease progression
Ebola virus
Ebolavirus
euthanasia
ferret
ferrets
histopathology
intranasal administration
mucosal challenge
nasal mucosa
pathogenicity
viral load
viruses
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals (Freely Accessible)
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1LS8NAEF6kIHgR38YXK3gSgtlkXz1qbSmCnqz0FpLdDa2UVJr24L93JklLo1Iv3kIyCbMzu5mZ7JdvCLkxZcVlMt-6AD_dWO4nJsKf3YWxcJQlrkT5vsj-gD8NxXCt1Rdiwip64MpwdxLe4prDOzRlKTcpT5S0YYKsWJYZpcrUCGLeWjH1XudBmqlqGzOCuh7x1aMp-KRgOK_DdtgIRCVf_29J5nes5Frw6e2R3TprpPeVtvtky-UHZLvqI_l5SOQz4s5BoLNsjUJ7DiG4FFudTQo6zWg3hSKWvo1ni4I-VrsyR2TQ6752-n7dEME3vK3nPowYjJEoJ7E9PNeR45lllrPABVYrlymZCMeUUQYJiANlWaQNT1lmQwOpWHRMWvk0d6eEZk7DapYBPFBxWLipi7iWxnIeOm2iwCPB0jqxqdnCsWnFJIaqAQ0a_zCoR25Xt3xUVBmbhB_Q5CtBZLkuT4Dv49r38V--98j10mExrArc6khyN10UMSR2Wkio5tQmGRg4VFsClDmpnLxSBwp3yN2U8IhquL-hb_NKPh6V7NwaA78QZ_8xwHOyEyKGBjFv_IK05rOFu4QkaJ5elfP9C5pjBts
  priority: 102
  providerName: Directory of Open Access Journals
Title Mucosal Challenge Ferret Models of Ebola Virus Disease
URI https://www.ncbi.nlm.nih.gov/pubmed/33806375
https://www.proquest.com/docview/2508564997
https://www.proquest.com/docview/2540476852
https://pubmed.ncbi.nlm.nih.gov/PMC8001755
https://doaj.org/article/6cee84847b1b4cb4a76d2a1646d1c77a
Volume 10
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1LS8NAEB5Ki-BFfFsfJYInIZLHZnc9iFhtKUJFxIq3kOxufFASbVrQf-9MkharRfAWkk3YfLuT-b7dyQzAkSoUl0psbRxautHMjpRPP7sHSuNREpkiyveG9wbs-jF4rMG0vFUFYL5Q2lE9qcFoePLx_nmOBn9GihMlO4VOP2cId-7SlPVO8YvcQMckyE77Fdt_rciRLGrweqjebTou9zkXP2XOUxUJ_Rex0J_BlN-8U3cVVipaaV2U82ANaiZdh6Wy0OTnBvA-BaZjg8tp7RSrayhG16JaaMPcyhKrEyMU1sPLaJJbV-W2zSYMup37y55dVUywFTuVY1u76PNkJAyn-vFM-oYl2tXMdYyjpTCJ4FFgXKGEogzFjtCuLxWL3UR7CrmavwX1NEvNDliJkWju3MEHCoaWHRufSa40Y56Rynea4EzRCVWVTpyqWgxDlBUEaPgL0CYcz255K3Np_NW4TZDPGlIa7OJENnoKK6sKOb0uQwcbuzFTMYsE115EKdMQCSGiJhxOByxEs6G9kCg12SQPkfnJgKPcE3-1wRdHORZgZ7bLQZ51B5U9kjsRNEHMDf9cf-evpC_PRfpuScwgCHb_g8YeLHsUTEPBb2wf6uPRxBwgGxrHLWi0Oze3d61iNaFVzPgvaMoL0A
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Mucosal+Challenge+Ferret+Models+of+Ebola+Virus+Disease&rft.jtitle=Pathogens+%28Basel%29&rft.au=Brasel%2C+Trevor&rft.au=Comer%2C+Jason+E.&rft.au=Massey%2C+Shane&rft.au=Smith%2C+Jeanon&rft.date=2021-03-04&rft.issn=2076-0817&rft.eissn=2076-0817&rft.volume=10&rft.issue=3&rft.spage=292&rft_id=info:doi/10.3390%2Fpathogens10030292&rft.externalDBID=n%2Fa&rft.externalDocID=10_3390_pathogens10030292
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2076-0817&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2076-0817&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2076-0817&client=summon