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SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity
Epidemiological studies have revealed the emergence of multiple SARS-CoV-2 variants of concern (VOC), including the lineage B.1.1.7 that is rapidly replacing old variants. The B.1.1.7 variant has been linked to increased morbidity rates, transmissibility, and potentially mortality (1). To assess vir...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020966/ https://www.ncbi.nlm.nih.gov/pubmed/33821266 http://dx.doi.org/10.1101/2021.04.02.438186 |
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author | Nuñez, Ivette A. Lien, Christopher Z. Selvaraj, Prabhuanand Stauft, Charles B. Liu, Shufeng Starost, Matthew F. Wang, Tony T. |
author_facet | Nuñez, Ivette A. Lien, Christopher Z. Selvaraj, Prabhuanand Stauft, Charles B. Liu, Shufeng Starost, Matthew F. Wang, Tony T. |
author_sort | Nuñez, Ivette A. |
collection | PubMed |
description | Epidemiological studies have revealed the emergence of multiple SARS-CoV-2 variants of concern (VOC), including the lineage B.1.1.7 that is rapidly replacing old variants. The B.1.1.7 variant has been linked to increased morbidity rates, transmissibility, and potentially mortality (1). To assess viral fitness in vivo and to address whether the B.1.1.7 variant is capable of immune escape, we conducted infection and re-infection studies in naïve and convalescent Syrian hamsters (>10 months old). Hamsters infected by either a B.1.1.7 variant or a B.1 (G614) variant exhibited comparable viral loads and pathology. Convalescent hamsters that were previously infected by the original D614 variant were protected from disease following B.1.1.7 challenge with no observable clinical signs or lung pathology. Altogether, our study did not find that the B.1.1.7 variant significantly differs from the B.1 variant in pathogenicity in hamsters and that natural infection-induced immunity confers protection against a secondary challenge by the B1.1.7 variant. |
format | Online Article Text |
id | pubmed-8020966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-80209662021-04-06 SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity Nuñez, Ivette A. Lien, Christopher Z. Selvaraj, Prabhuanand Stauft, Charles B. Liu, Shufeng Starost, Matthew F. Wang, Tony T. bioRxiv Article Epidemiological studies have revealed the emergence of multiple SARS-CoV-2 variants of concern (VOC), including the lineage B.1.1.7 that is rapidly replacing old variants. The B.1.1.7 variant has been linked to increased morbidity rates, transmissibility, and potentially mortality (1). To assess viral fitness in vivo and to address whether the B.1.1.7 variant is capable of immune escape, we conducted infection and re-infection studies in naïve and convalescent Syrian hamsters (>10 months old). Hamsters infected by either a B.1.1.7 variant or a B.1 (G614) variant exhibited comparable viral loads and pathology. Convalescent hamsters that were previously infected by the original D614 variant were protected from disease following B.1.1.7 challenge with no observable clinical signs or lung pathology. Altogether, our study did not find that the B.1.1.7 variant significantly differs from the B.1 variant in pathogenicity in hamsters and that natural infection-induced immunity confers protection against a secondary challenge by the B1.1.7 variant. Cold Spring Harbor Laboratory 2021-04-02 /pmc/articles/PMC8020966/ /pubmed/33821266 http://dx.doi.org/10.1101/2021.04.02.438186 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Article Nuñez, Ivette A. Lien, Christopher Z. Selvaraj, Prabhuanand Stauft, Charles B. Liu, Shufeng Starost, Matthew F. Wang, Tony T. SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity |
title | SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity |
title_full | SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity |
title_fullStr | SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity |
title_full_unstemmed | SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity |
title_short | SARS-CoV-2 B.1.1.7 infection of Syrian hamster does not cause more severe disease and is protected by naturally acquired immunity |
title_sort | sars-cov-2 b.1.1.7 infection of syrian hamster does not cause more severe disease and is protected by naturally acquired immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020966/ https://www.ncbi.nlm.nih.gov/pubmed/33821266 http://dx.doi.org/10.1101/2021.04.02.438186 |
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