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Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection

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 man...

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Autores principales: Rosenke, Kyle, Meade-White, Kimberly, Letko, Michael, Clancy, Chad, Hansen, Frederick, Liu, Yanan, Okumura, Atsushi, Tang-Huau, Tsing-Lee, Li, Rong, Saturday, Greg, Feldmann, Friederike, Scott, Dana, Wang, Zhongde, Munster, Vincent, Jarvis, Michael A., Feldmann, Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523093/
https://www.ncbi.nlm.nih.gov/pubmed/32995767
http://dx.doi.org/10.1101/2020.09.25.314070
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author Rosenke, Kyle
Meade-White, Kimberly
Letko, Michael
Clancy, Chad
Hansen, Frederick
Liu, Yanan
Okumura, Atsushi
Tang-Huau, Tsing-Lee
Li, Rong
Saturday, Greg
Feldmann, Friederike
Scott, Dana
Wang, Zhongde
Munster, Vincent
Jarvis, Michael A.
Feldmann, Heinz
author_facet Rosenke, Kyle
Meade-White, Kimberly
Letko, Michael
Clancy, Chad
Hansen, Frederick
Liu, Yanan
Okumura, Atsushi
Tang-Huau, Tsing-Lee
Li, Rong
Saturday, Greg
Feldmann, Friederike
Scott, Dana
Wang, Zhongde
Munster, Vincent
Jarvis, Michael A.
Feldmann, Heinz
author_sort Rosenke, Kyle
collection PubMed
description 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.
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spelling pubmed-75230932020-09-30 Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection Rosenke, Kyle Meade-White, Kimberly Letko, Michael Clancy, Chad Hansen, Frederick Liu, Yanan Okumura, Atsushi Tang-Huau, Tsing-Lee Li, Rong Saturday, Greg Feldmann, Friederike Scott, Dana Wang, Zhongde Munster, Vincent Jarvis, Michael A. Feldmann, Heinz bioRxiv Article 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. Cold Spring Harbor Laboratory 2020-09-27 /pmc/articles/PMC7523093/ /pubmed/32995767 http://dx.doi.org/10.1101/2020.09.25.314070 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY-NC-ND 4.0 International license (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Article
Rosenke, Kyle
Meade-White, Kimberly
Letko, Michael
Clancy, Chad
Hansen, Frederick
Liu, Yanan
Okumura, Atsushi
Tang-Huau, Tsing-Lee
Li, Rong
Saturday, Greg
Feldmann, Friederike
Scott, Dana
Wang, Zhongde
Munster, Vincent
Jarvis, Michael A.
Feldmann, Heinz
Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection
title Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection
title_full Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection
title_fullStr Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection
title_full_unstemmed Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection
title_short Defining the Syrian hamster as a highly susceptible preclinical model for SARS-CoV-2 infection
title_sort defining the syrian hamster as a highly susceptible preclinical model for sars-cov-2 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523093/
https://www.ncbi.nlm.nih.gov/pubmed/32995767
http://dx.doi.org/10.1101/2020.09.25.314070
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