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Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant

The mutation profile of the SARS-CoV-2 Omicron (lineage BA.1) variant posed a concern for naturally acquired and vaccine-induced immunity. We investigated the ability of prior infection with an early SARS-CoV-2 ancestral isolate (Australia/VIC01/2020, VIC01) to protect against disease caused by BA.1...

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Autores principales: Ryan, Kathryn A., Bewley, Kevin R., Watson, Robert J., Burton, Christopher, Carnell, Oliver, Cavell, Breeze E., Challis, Amy, Coombes, Naomi S., Davies, Elizabeth R., Edun-Huges, Jack, Emery, Kirsty, Fell, Rachel, Fotheringham, Susan A., Gooch, Karen E., Gowan, Kathryn, Handley, Alastair, Harris, Debbie J., Hesp, Richard, Hunter, Laura, Humphreys, Richard, Johnson, Rachel, Kennard, Chelsea, Knott, Daniel, Lister, Sian, Morley, Daniel, Ngabo, Didier, Osman, Karen L., Paterson, Jemma, Penn, Elizabeth J., Pullan, Steven T., Richards, Kevin S., Summers, Sian, Thomas, Stephen R., Weldon, Thomas, Wiblin, Nathan R., Rayner, Emma L., Vipond, Richard T., Hallis, Bassam, Salguero, Francisco J., Funnell, Simon G. P., Hall, Yper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104347/
https://www.ncbi.nlm.nih.gov/pubmed/37014911
http://dx.doi.org/10.1371/journal.ppat.1011293
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author Ryan, Kathryn A.
Bewley, Kevin R.
Watson, Robert J.
Burton, Christopher
Carnell, Oliver
Cavell, Breeze E.
Challis, Amy
Coombes, Naomi S.
Davies, Elizabeth R.
Edun-Huges, Jack
Emery, Kirsty
Fell, Rachel
Fotheringham, Susan A.
Gooch, Karen E.
Gowan, Kathryn
Handley, Alastair
Harris, Debbie J.
Hesp, Richard
Hunter, Laura
Humphreys, Richard
Johnson, Rachel
Kennard, Chelsea
Knott, Daniel
Lister, Sian
Morley, Daniel
Ngabo, Didier
Osman, Karen L.
Paterson, Jemma
Penn, Elizabeth J.
Pullan, Steven T.
Richards, Kevin S.
Summers, Sian
Thomas, Stephen R.
Weldon, Thomas
Wiblin, Nathan R.
Rayner, Emma L.
Vipond, Richard T.
Hallis, Bassam
Salguero, Francisco J.
Funnell, Simon G. P.
Hall, Yper
author_facet Ryan, Kathryn A.
Bewley, Kevin R.
Watson, Robert J.
Burton, Christopher
Carnell, Oliver
Cavell, Breeze E.
Challis, Amy
Coombes, Naomi S.
Davies, Elizabeth R.
Edun-Huges, Jack
Emery, Kirsty
Fell, Rachel
Fotheringham, Susan A.
Gooch, Karen E.
Gowan, Kathryn
Handley, Alastair
Harris, Debbie J.
Hesp, Richard
Hunter, Laura
Humphreys, Richard
Johnson, Rachel
Kennard, Chelsea
Knott, Daniel
Lister, Sian
Morley, Daniel
Ngabo, Didier
Osman, Karen L.
Paterson, Jemma
Penn, Elizabeth J.
Pullan, Steven T.
Richards, Kevin S.
Summers, Sian
Thomas, Stephen R.
Weldon, Thomas
Wiblin, Nathan R.
Rayner, Emma L.
Vipond, Richard T.
Hallis, Bassam
Salguero, Francisco J.
Funnell, Simon G. P.
Hall, Yper
author_sort Ryan, Kathryn A.
collection PubMed
description The mutation profile of the SARS-CoV-2 Omicron (lineage BA.1) variant posed a concern for naturally acquired and vaccine-induced immunity. We investigated the ability of prior infection with an early SARS-CoV-2 ancestral isolate (Australia/VIC01/2020, VIC01) to protect against disease caused by BA.1. We established that BA.1 infection in naïve Syrian hamsters resulted in a less severe disease than a comparable dose of the ancestral virus, with fewer clinical signs including less weight loss. We present data to show that these clinical observations were almost absent in convalescent hamsters challenged with the same dose of BA.1 50 days after an initial infection with ancestral virus. These data provide evidence that convalescent immunity against ancestral SARS-CoV-2 is protective against BA.1 in the Syrian hamster model of infection. Comparison with published pre-clinical and clinical data supports consistency of the model and its predictive value for the outcome in humans. Further, the ability to detect protection against the less severe disease caused by BA.1 demonstrates continued value of the Syrian hamster model for evaluation of BA.1-specific countermeasures.
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spelling pubmed-101043472023-04-15 Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant Ryan, Kathryn A. Bewley, Kevin R. Watson, Robert J. Burton, Christopher Carnell, Oliver Cavell, Breeze E. Challis, Amy Coombes, Naomi S. Davies, Elizabeth R. Edun-Huges, Jack Emery, Kirsty Fell, Rachel Fotheringham, Susan A. Gooch, Karen E. Gowan, Kathryn Handley, Alastair Harris, Debbie J. Hesp, Richard Hunter, Laura Humphreys, Richard Johnson, Rachel Kennard, Chelsea Knott, Daniel Lister, Sian Morley, Daniel Ngabo, Didier Osman, Karen L. Paterson, Jemma Penn, Elizabeth J. Pullan, Steven T. Richards, Kevin S. Summers, Sian Thomas, Stephen R. Weldon, Thomas Wiblin, Nathan R. Rayner, Emma L. Vipond, Richard T. Hallis, Bassam Salguero, Francisco J. Funnell, Simon G. P. Hall, Yper PLoS Pathog Research Article The mutation profile of the SARS-CoV-2 Omicron (lineage BA.1) variant posed a concern for naturally acquired and vaccine-induced immunity. We investigated the ability of prior infection with an early SARS-CoV-2 ancestral isolate (Australia/VIC01/2020, VIC01) to protect against disease caused by BA.1. We established that BA.1 infection in naïve Syrian hamsters resulted in a less severe disease than a comparable dose of the ancestral virus, with fewer clinical signs including less weight loss. We present data to show that these clinical observations were almost absent in convalescent hamsters challenged with the same dose of BA.1 50 days after an initial infection with ancestral virus. These data provide evidence that convalescent immunity against ancestral SARS-CoV-2 is protective against BA.1 in the Syrian hamster model of infection. Comparison with published pre-clinical and clinical data supports consistency of the model and its predictive value for the outcome in humans. Further, the ability to detect protection against the less severe disease caused by BA.1 demonstrates continued value of the Syrian hamster model for evaluation of BA.1-specific countermeasures. Public Library of Science 2023-04-04 /pmc/articles/PMC10104347/ /pubmed/37014911 http://dx.doi.org/10.1371/journal.ppat.1011293 Text en © 2023 Ryan et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ryan, Kathryn A.
Bewley, Kevin R.
Watson, Robert J.
Burton, Christopher
Carnell, Oliver
Cavell, Breeze E.
Challis, Amy
Coombes, Naomi S.
Davies, Elizabeth R.
Edun-Huges, Jack
Emery, Kirsty
Fell, Rachel
Fotheringham, Susan A.
Gooch, Karen E.
Gowan, Kathryn
Handley, Alastair
Harris, Debbie J.
Hesp, Richard
Hunter, Laura
Humphreys, Richard
Johnson, Rachel
Kennard, Chelsea
Knott, Daniel
Lister, Sian
Morley, Daniel
Ngabo, Didier
Osman, Karen L.
Paterson, Jemma
Penn, Elizabeth J.
Pullan, Steven T.
Richards, Kevin S.
Summers, Sian
Thomas, Stephen R.
Weldon, Thomas
Wiblin, Nathan R.
Rayner, Emma L.
Vipond, Richard T.
Hallis, Bassam
Salguero, Francisco J.
Funnell, Simon G. P.
Hall, Yper
Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant
title Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant
title_full Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant
title_fullStr Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant
title_full_unstemmed Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant
title_short Syrian hamster convalescence from prototype SARS-CoV-2 confers measurable protection against the attenuated disease caused by the Omicron variant
title_sort syrian hamster convalescence from prototype sars-cov-2 confers measurable protection against the attenuated disease caused by the omicron variant
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104347/
https://www.ncbi.nlm.nih.gov/pubmed/37014911
http://dx.doi.org/10.1371/journal.ppat.1011293
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