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The SARS-CoV ferret model in an infection–challenge study
Phase I human clinical studies involving therapeutics for emerging and biodefense pathogens with low incidence, such as the severe acute respiratory syndrome coronavirus (SARS-CoV), requires at a minimum preclinical evaluation of efficacy in two well-characterized and robust animal models. Thus, a f...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2831213/ https://www.ncbi.nlm.nih.gov/pubmed/18234270 http://dx.doi.org/10.1016/j.virol.2007.12.032 |
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author | Chu, Yong-Kyu Ali, Georgia D. Jia, Fuli Li, Qianjun Kelvin, David Couch, Ronald C. Harrod, Kevin S. Hutt, Julie A. Cameron, Cheryl Weiss, Susan R. Jonsson, Colleen B. |
author_facet | Chu, Yong-Kyu Ali, Georgia D. Jia, Fuli Li, Qianjun Kelvin, David Couch, Ronald C. Harrod, Kevin S. Hutt, Julie A. Cameron, Cheryl Weiss, Susan R. Jonsson, Colleen B. |
author_sort | Chu, Yong-Kyu |
collection | PubMed |
description | Phase I human clinical studies involving therapeutics for emerging and biodefense pathogens with low incidence, such as the severe acute respiratory syndrome coronavirus (SARS-CoV), requires at a minimum preclinical evaluation of efficacy in two well-characterized and robust animal models. Thus, a ferret SARS-CoV model was evaluated over a period of 58 days following extensive optimization and characterization of the model in order to validate clinical, histopathological, virological and immunological endpoints. Ferrets that were infected intranasally with 10(3) TCID(50) SARS-CoV showed higher body temperature (2–6 d.p.i.), sneezing (5–10 d.p.i.), lesions (5–7 d.p.i.) and decreased WBC/lymphocytes (2–5 d.p.i.). SARS-CoV was detected up to 7 d.p.i. in various tissues and excreta, while neutralizing antibody titers rose at 7 d.p.i. and peaked at 14 d.p.i. At 29 d.p.i., one group was challenged with 10(3) TCID(50) SARS-CoV, and an anamnestic response in neutralizing antibodies was evident with no detectable virus. This study supports the validity of the ferret model for use in evaluating efficacy of potential therapeutics to treat SARS. |
format | Text |
id | pubmed-2831213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-28312132010-03-03 The SARS-CoV ferret model in an infection–challenge study Chu, Yong-Kyu Ali, Georgia D. Jia, Fuli Li, Qianjun Kelvin, David Couch, Ronald C. Harrod, Kevin S. Hutt, Julie A. Cameron, Cheryl Weiss, Susan R. Jonsson, Colleen B. Virology Article Phase I human clinical studies involving therapeutics for emerging and biodefense pathogens with low incidence, such as the severe acute respiratory syndrome coronavirus (SARS-CoV), requires at a minimum preclinical evaluation of efficacy in two well-characterized and robust animal models. Thus, a ferret SARS-CoV model was evaluated over a period of 58 days following extensive optimization and characterization of the model in order to validate clinical, histopathological, virological and immunological endpoints. Ferrets that were infected intranasally with 10(3) TCID(50) SARS-CoV showed higher body temperature (2–6 d.p.i.), sneezing (5–10 d.p.i.), lesions (5–7 d.p.i.) and decreased WBC/lymphocytes (2–5 d.p.i.). SARS-CoV was detected up to 7 d.p.i. in various tissues and excreta, while neutralizing antibody titers rose at 7 d.p.i. and peaked at 14 d.p.i. At 29 d.p.i., one group was challenged with 10(3) TCID(50) SARS-CoV, and an anamnestic response in neutralizing antibodies was evident with no detectable virus. This study supports the validity of the ferret model for use in evaluating efficacy of potential therapeutics to treat SARS. Elsevier Inc. 2008-04-25 2008-01-29 /pmc/articles/PMC2831213/ /pubmed/18234270 http://dx.doi.org/10.1016/j.virol.2007.12.032 Text en Copyright © 2008 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Chu, Yong-Kyu Ali, Georgia D. Jia, Fuli Li, Qianjun Kelvin, David Couch, Ronald C. Harrod, Kevin S. Hutt, Julie A. Cameron, Cheryl Weiss, Susan R. Jonsson, Colleen B. The SARS-CoV ferret model in an infection–challenge study |
title | The SARS-CoV ferret model in an infection–challenge study |
title_full | The SARS-CoV ferret model in an infection–challenge study |
title_fullStr | The SARS-CoV ferret model in an infection–challenge study |
title_full_unstemmed | The SARS-CoV ferret model in an infection–challenge study |
title_short | The SARS-CoV ferret model in an infection–challenge study |
title_sort | sars-cov ferret model in an infection–challenge study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2831213/ https://www.ncbi.nlm.nih.gov/pubmed/18234270 http://dx.doi.org/10.1016/j.virol.2007.12.032 |
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