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The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection

The ongoing emergence of SARS-CoV-2 virus variants remains a source of concern because it is accompanied by the potential for increased virulence as well as evasion of immunity. Here we show that, although having an almost identical spike gene sequence as another Omicron variant (BA.5.2.1), a BA.4 i...

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Autores principales: Davies, Elizabeth R., Ryan, Kathryn A., Bewley, Kevin R., Coombes, Naomi S., Salguero, Francisco J., Carnell, Oliver T., Biddlecombe, Sarah, Charlton, Michael, Challis, Amy, Cross, Eleanor S., Handley, Alastair, Ngabo, Didier, Weldon, Thomas M., Hall, Yper, Funnell, Simon G. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10224153/
https://www.ncbi.nlm.nih.gov/pubmed/37243219
http://dx.doi.org/10.3390/v15051133
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author Davies, Elizabeth R.
Ryan, Kathryn A.
Bewley, Kevin R.
Coombes, Naomi S.
Salguero, Francisco J.
Carnell, Oliver T.
Biddlecombe, Sarah
Charlton, Michael
Challis, Amy
Cross, Eleanor S.
Handley, Alastair
Ngabo, Didier
Weldon, Thomas M.
Hall, Yper
Funnell, Simon G. P.
author_facet Davies, Elizabeth R.
Ryan, Kathryn A.
Bewley, Kevin R.
Coombes, Naomi S.
Salguero, Francisco J.
Carnell, Oliver T.
Biddlecombe, Sarah
Charlton, Michael
Challis, Amy
Cross, Eleanor S.
Handley, Alastair
Ngabo, Didier
Weldon, Thomas M.
Hall, Yper
Funnell, Simon G. P.
author_sort Davies, Elizabeth R.
collection PubMed
description The ongoing emergence of SARS-CoV-2 virus variants remains a source of concern because it is accompanied by the potential for increased virulence as well as evasion of immunity. Here we show that, although having an almost identical spike gene sequence as another Omicron variant (BA.5.2.1), a BA.4 isolate lacked all the typical disease characteristics of other isolates seen in the Golden Syrian hamster model despite replicating almost as effectively. Animals infected with BA.4 had similar viral shedding profiles to those seen with BA.5.2.1 (up to day 6 post-infection), but they all failed to lose weight or present with any other significant clinical signs. We hypothesize that this lack of detectable signs of disease during infection with BA.4 was due to a small (nine nucleotide) deletion (∆686–694) in the viral genome (ORF1ab) responsible for the production of non-structural protein 1, which resulted in the loss of three amino acids (aa 141–143).
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spelling pubmed-102241532023-05-28 The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection Davies, Elizabeth R. Ryan, Kathryn A. Bewley, Kevin R. Coombes, Naomi S. Salguero, Francisco J. Carnell, Oliver T. Biddlecombe, Sarah Charlton, Michael Challis, Amy Cross, Eleanor S. Handley, Alastair Ngabo, Didier Weldon, Thomas M. Hall, Yper Funnell, Simon G. P. Viruses Article The ongoing emergence of SARS-CoV-2 virus variants remains a source of concern because it is accompanied by the potential for increased virulence as well as evasion of immunity. Here we show that, although having an almost identical spike gene sequence as another Omicron variant (BA.5.2.1), a BA.4 isolate lacked all the typical disease characteristics of other isolates seen in the Golden Syrian hamster model despite replicating almost as effectively. Animals infected with BA.4 had similar viral shedding profiles to those seen with BA.5.2.1 (up to day 6 post-infection), but they all failed to lose weight or present with any other significant clinical signs. We hypothesize that this lack of detectable signs of disease during infection with BA.4 was due to a small (nine nucleotide) deletion (∆686–694) in the viral genome (ORF1ab) responsible for the production of non-structural protein 1, which resulted in the loss of three amino acids (aa 141–143). MDPI 2023-05-10 /pmc/articles/PMC10224153/ /pubmed/37243219 http://dx.doi.org/10.3390/v15051133 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
Davies, Elizabeth R.
Ryan, Kathryn A.
Bewley, Kevin R.
Coombes, Naomi S.
Salguero, Francisco J.
Carnell, Oliver T.
Biddlecombe, Sarah
Charlton, Michael
Challis, Amy
Cross, Eleanor S.
Handley, Alastair
Ngabo, Didier
Weldon, Thomas M.
Hall, Yper
Funnell, Simon G. P.
The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection
title The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection
title_full The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection
title_fullStr The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection
title_full_unstemmed The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection
title_short The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection
title_sort omicron sub-variant ba.4 displays a remarkable lack of clinical signs in a golden syrian hamster model of sars-cov-2 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10224153/
https://www.ncbi.nlm.nih.gov/pubmed/37243219
http://dx.doi.org/10.3390/v15051133
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