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Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection
Ferrets were experimentally inoculated with SARS-CoV-2 (severe acute respiratory syndrome (SARS)-related coronavirus 2) to assess infection dynamics and host response. During the resulting subclinical infection, viral RNA was monitored between 2 and 21 days post-inoculation (dpi), and reached a peak...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830262/ https://www.ncbi.nlm.nih.gov/pubmed/33467732 http://dx.doi.org/10.3390/v13010113 |
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author | Everett, Helen E. Lean, Fabian Z. X. Byrne, Alexander M. P. van Diemen, Pauline M. Rhodes, Shelley James, Joe Mollett, Benjamin Coward, Vivien J. Skinner, Paul Warren, Caroline J. Bewley, Kevin R. Watson, Samantha Hurley, Shellene Ryan, Kathryn A. Hall, Yper Simmons, Hugh Núñez, Alejandro Carroll, Miles W. Brown, Ian H. Brookes, Sharon M. |
author_facet | Everett, Helen E. Lean, Fabian Z. X. Byrne, Alexander M. P. van Diemen, Pauline M. Rhodes, Shelley James, Joe Mollett, Benjamin Coward, Vivien J. Skinner, Paul Warren, Caroline J. Bewley, Kevin R. Watson, Samantha Hurley, Shellene Ryan, Kathryn A. Hall, Yper Simmons, Hugh Núñez, Alejandro Carroll, Miles W. Brown, Ian H. Brookes, Sharon M. |
author_sort | Everett, Helen E. |
collection | PubMed |
description | Ferrets were experimentally inoculated with SARS-CoV-2 (severe acute respiratory syndrome (SARS)-related coronavirus 2) to assess infection dynamics and host response. During the resulting subclinical infection, viral RNA was monitored between 2 and 21 days post-inoculation (dpi), and reached a peak in the upper respiratory cavity between 4 and 6 dpi. Viral genomic sequence analysis in samples from three animals identified the Y453F nucleotide substitution relative to the inoculum. Viral RNA was also detected in environmental samples, specifically in swabs of ferret fur. Microscopy analysis revealed viral protein and RNA in upper respiratory tract tissues, notably in cells of the respiratory and olfactory mucosae of the nasal turbinates, including olfactory neuronal cells. Antibody responses to the spike and nucleoprotein were detected from 21 dpi, but virus-neutralizing activity was low. A second intranasal inoculation (re-exposure) of two ferrets after a 17-day interval did not produce re-initiation of viral RNA shedding, but did amplify the humoral response in one animal. Therefore, ferrets can be experimentally infected with SARS-CoV-2 to model human asymptomatic infection. |
format | Online Article Text |
id | pubmed-7830262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78302622021-01-26 Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection Everett, Helen E. Lean, Fabian Z. X. Byrne, Alexander M. P. van Diemen, Pauline M. Rhodes, Shelley James, Joe Mollett, Benjamin Coward, Vivien J. Skinner, Paul Warren, Caroline J. Bewley, Kevin R. Watson, Samantha Hurley, Shellene Ryan, Kathryn A. Hall, Yper Simmons, Hugh Núñez, Alejandro Carroll, Miles W. Brown, Ian H. Brookes, Sharon M. Viruses Article Ferrets were experimentally inoculated with SARS-CoV-2 (severe acute respiratory syndrome (SARS)-related coronavirus 2) to assess infection dynamics and host response. During the resulting subclinical infection, viral RNA was monitored between 2 and 21 days post-inoculation (dpi), and reached a peak in the upper respiratory cavity between 4 and 6 dpi. Viral genomic sequence analysis in samples from three animals identified the Y453F nucleotide substitution relative to the inoculum. Viral RNA was also detected in environmental samples, specifically in swabs of ferret fur. Microscopy analysis revealed viral protein and RNA in upper respiratory tract tissues, notably in cells of the respiratory and olfactory mucosae of the nasal turbinates, including olfactory neuronal cells. Antibody responses to the spike and nucleoprotein were detected from 21 dpi, but virus-neutralizing activity was low. A second intranasal inoculation (re-exposure) of two ferrets after a 17-day interval did not produce re-initiation of viral RNA shedding, but did amplify the humoral response in one animal. Therefore, ferrets can be experimentally infected with SARS-CoV-2 to model human asymptomatic infection. MDPI 2021-01-15 /pmc/articles/PMC7830262/ /pubmed/33467732 http://dx.doi.org/10.3390/v13010113 Text en © 2021 by the authors. 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/). |
spellingShingle | Article Everett, Helen E. Lean, Fabian Z. X. Byrne, Alexander M. P. van Diemen, Pauline M. Rhodes, Shelley James, Joe Mollett, Benjamin Coward, Vivien J. Skinner, Paul Warren, Caroline J. Bewley, Kevin R. Watson, Samantha Hurley, Shellene Ryan, Kathryn A. Hall, Yper Simmons, Hugh Núñez, Alejandro Carroll, Miles W. Brown, Ian H. Brookes, Sharon M. Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection |
title | Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection |
title_full | Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection |
title_fullStr | Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection |
title_full_unstemmed | Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection |
title_short | Intranasal Infection of Ferrets with SARS-CoV-2 as a Model for Asymptomatic Human Infection |
title_sort | intranasal infection of ferrets with sars-cov-2 as a model for asymptomatic human infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830262/ https://www.ncbi.nlm.nih.gov/pubmed/33467732 http://dx.doi.org/10.3390/v13010113 |
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