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Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats
Several reports demonstrated the susceptibility of domestic cats to SARS-CoV-2 infection. Here, we describe a thorough investigation of the immune responses in cats after experimental SARS-CoV-2 inoculation, along with the characterization of infection kinetics and pathological lesions. Specific pat...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222871/ https://www.ncbi.nlm.nih.gov/pubmed/37243138 http://dx.doi.org/10.3390/v15051052 |
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author | Vreman, Sandra van der Heijden, Elisabeth M. D. L. Ravesloot, Lars Ludwig, Irene S. van den Brand, Judith M. A. Harders, Frank Kampfraath, Andries A. Egberink, Herman F. Gonzales, Jose L. Oreshkova, Nadia Broere, Femke van der Poel, Wim H. M. Gerhards, Nora M. |
author_facet | Vreman, Sandra van der Heijden, Elisabeth M. D. L. Ravesloot, Lars Ludwig, Irene S. van den Brand, Judith M. A. Harders, Frank Kampfraath, Andries A. Egberink, Herman F. Gonzales, Jose L. Oreshkova, Nadia Broere, Femke van der Poel, Wim H. M. Gerhards, Nora M. |
author_sort | Vreman, Sandra |
collection | PubMed |
description | Several reports demonstrated the susceptibility of domestic cats to SARS-CoV-2 infection. Here, we describe a thorough investigation of the immune responses in cats after experimental SARS-CoV-2 inoculation, along with the characterization of infection kinetics and pathological lesions. Specific pathogen-free domestic cats (n = 12) were intranasally inoculated with SARS-CoV-2 and subsequently sacrificed on DPI (days post-inoculation) 2, 4, 7 and 14. None of the infected cats developed clinical signs. Only mild histopathologic lung changes associated with virus antigen expression were observed mainly on DPI 4 and 7. Viral RNA was present until DPI 7, predominantly in nasal and throat swabs. The infectious virus could be isolated from the nose, trachea and lungs until DPI 7. In the swab samples, no biologically relevant SARS-CoV-2 mutations were observed over time. From DPI 7 onwards, all cats developed a humoral immune response. The cellular immune responses were limited to DPI 7. Cats showed an increase in CD8+ cells, and the subsequent RNA sequence analysis of CD4+ and CD8+ subsets revealed a prominent upregulation of antiviral and inflammatory genes on DPI 2. In conclusion, infected domestic cats developed a strong antiviral response and cleared the virus within the first week after infection without overt clinical signs and relevant virus mutations. |
format | Online Article Text |
id | pubmed-10222871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102228712023-05-28 Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats Vreman, Sandra van der Heijden, Elisabeth M. D. L. Ravesloot, Lars Ludwig, Irene S. van den Brand, Judith M. A. Harders, Frank Kampfraath, Andries A. Egberink, Herman F. Gonzales, Jose L. Oreshkova, Nadia Broere, Femke van der Poel, Wim H. M. Gerhards, Nora M. Viruses Article Several reports demonstrated the susceptibility of domestic cats to SARS-CoV-2 infection. Here, we describe a thorough investigation of the immune responses in cats after experimental SARS-CoV-2 inoculation, along with the characterization of infection kinetics and pathological lesions. Specific pathogen-free domestic cats (n = 12) were intranasally inoculated with SARS-CoV-2 and subsequently sacrificed on DPI (days post-inoculation) 2, 4, 7 and 14. None of the infected cats developed clinical signs. Only mild histopathologic lung changes associated with virus antigen expression were observed mainly on DPI 4 and 7. Viral RNA was present until DPI 7, predominantly in nasal and throat swabs. The infectious virus could be isolated from the nose, trachea and lungs until DPI 7. In the swab samples, no biologically relevant SARS-CoV-2 mutations were observed over time. From DPI 7 onwards, all cats developed a humoral immune response. The cellular immune responses were limited to DPI 7. Cats showed an increase in CD8+ cells, and the subsequent RNA sequence analysis of CD4+ and CD8+ subsets revealed a prominent upregulation of antiviral and inflammatory genes on DPI 2. In conclusion, infected domestic cats developed a strong antiviral response and cleared the virus within the first week after infection without overt clinical signs and relevant virus mutations. MDPI 2023-04-25 /pmc/articles/PMC10222871/ /pubmed/37243138 http://dx.doi.org/10.3390/v15051052 Text en © 2023 by the authors. 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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vreman, Sandra van der Heijden, Elisabeth M. D. L. Ravesloot, Lars Ludwig, Irene S. van den Brand, Judith M. A. Harders, Frank Kampfraath, Andries A. Egberink, Herman F. Gonzales, Jose L. Oreshkova, Nadia Broere, Femke van der Poel, Wim H. M. Gerhards, Nora M. Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats |
title | Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats |
title_full | Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats |
title_fullStr | Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats |
title_full_unstemmed | Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats |
title_short | Immune Responses and Pathogenesis following Experimental SARS-CoV-2 Infection in Domestic Cats |
title_sort | immune responses and pathogenesis following experimental sars-cov-2 infection in domestic cats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222871/ https://www.ncbi.nlm.nih.gov/pubmed/37243138 http://dx.doi.org/10.3390/v15051052 |
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