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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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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. |
format | Online Article Text |
id | pubmed-10104347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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