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dc.contributor.authorRosenke, K
dc.contributor.authorMeade-White, K
dc.contributor.authorLetko, M
dc.contributor.authorClancy, C
dc.contributor.authorHansen, F
dc.contributor.authorLiu, Y
dc.contributor.authorOkumura, A
dc.contributor.authorTang-Huau, T-L
dc.contributor.authorLi, R
dc.contributor.authorSaturday, G
dc.contributor.authorFeldmann, F
dc.contributor.authorScott, D
dc.contributor.authorWang, Z
dc.contributor.authorMunster, V
dc.contributor.authorJarvis, MA
dc.contributor.authorFeldmann, H
dc.date.accessioned2021-08-09T12:44:05Z
dc.date.available2021-08-09T12:44:05Z
dc.date.issued2020-12-25
dc.identifier.issn2222-1751
dc.identifier.issn2222-1751
dc.identifier.urihttp://hdl.handle.net/10026.1/17499
dc.description.abstract

Following emergence in late 2019, SARS-CoV-2 rapidly became pandemic and is presently responsible for millions of infections and hundreds of thousands of deaths worldwide. There is currently no approved vaccine to halt the spread of SARS-CoV-2 and only very few treatment options are available to manage COVID-19 patients. For development of preclinical countermeasures, reliable and well-characterized small animal disease models will be of paramount importance. Here we show that intranasal inoculation of SARS-CoV-2 into Syrian hamsters consistently caused moderate broncho-interstitial pneumonia, with high viral lung loads and extensive virus shedding, but animals only displayed transient mild disease. We determined the infectious dose 50 to be only five infectious particles, making the Syrian hamster a highly susceptible model for SARS-CoV-2 infection. Neither hamster age nor sex had any impact on the severity of disease or course of infection. Finally, prolonged viral persistence in interleukin 2 receptor gamma chain knockout hamsters revealed susceptibility of SARS-CoV-2 to adaptive immune control. In conclusion, the Syrian hamster is highly susceptible to SARS-CoV-2 making it a very suitable infection model for COVID-19 countermeasure development.

dc.format.extent2673-2684
dc.format.mediumPrint
dc.languageen
dc.language.isoen
dc.publisherInforma UK Limited
dc.subjectSARS-CoV-2
dc.subjecthamster
dc.subjectinfection model
dc.subjectsusceptible
dc.subjectpneumonia
dc.titleDefining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33251966
plymouth.issue1
plymouth.volume9
plymouth.publication-statusPublished
plymouth.journalEmerging Microbes & Infections
dc.identifier.doi10.1080/22221751.2020.1858177
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Biomedical Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeUnited States
dcterms.dateAccepted2020-11-26
dc.rights.embargodate2021-8-11
dc.identifier.eissn2222-1751
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1080/22221751.2020.1858177
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2020-12-25
rioxxterms.typeJournal Article/Review


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