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Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters
The emergence of the SARS-CoV-2 Omicron (B.1.1.529) variant with a surprising number of spike mutations raises concerns about reduced sensitivity of this virus to antibody neutralization and subsequent vaccine breakthrough infections. Here, we infect Moderna mRNA-vaccinated or previously infected ha...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s).
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958134/ https://www.ncbi.nlm.nih.gov/pubmed/35421378 http://dx.doi.org/10.1016/j.celrep.2022.110688 |
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author | Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Chiba, Shiho Armbrust, Tammy Wright, Ryan Balaram, Ariane Florek, Kelsey R. Bateman, Allen C. Kawaoka, Yoshihiro |
author_facet | Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Chiba, Shiho Armbrust, Tammy Wright, Ryan Balaram, Ariane Florek, Kelsey R. Bateman, Allen C. Kawaoka, Yoshihiro |
author_sort | Halfmann, Peter J. |
collection | PubMed |
description | The emergence of the SARS-CoV-2 Omicron (B.1.1.529) variant with a surprising number of spike mutations raises concerns about reduced sensitivity of this virus to antibody neutralization and subsequent vaccine breakthrough infections. Here, we infect Moderna mRNA-vaccinated or previously infected hamsters with the Omicron BA.1 variant. While the Moderna mRNA vaccine reduces viral loads in the respiratory tissues upon challenge with an early S-614G isolate, the vaccine efficacy is not as pronounced after infection with the Omicron variant. Previous infection with the early SARS-CoV-2 isolate prevents replication after rechallenge with either virus in the lungs of previously infected hamsters, but the Omicron variant replicates efficiently in nasal turbinate tissue. These results experimentally demonstrate in an animal model that the antigenic changes in the Omicron variant are responsible for vaccine breakthrough and re-infection. |
format | Online Article Text |
id | pubmed-8958134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Author(s). |
record_format | MEDLINE/PubMed |
spelling | pubmed-89581342022-03-28 Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Chiba, Shiho Armbrust, Tammy Wright, Ryan Balaram, Ariane Florek, Kelsey R. Bateman, Allen C. Kawaoka, Yoshihiro Cell Rep Report The emergence of the SARS-CoV-2 Omicron (B.1.1.529) variant with a surprising number of spike mutations raises concerns about reduced sensitivity of this virus to antibody neutralization and subsequent vaccine breakthrough infections. Here, we infect Moderna mRNA-vaccinated or previously infected hamsters with the Omicron BA.1 variant. While the Moderna mRNA vaccine reduces viral loads in the respiratory tissues upon challenge with an early S-614G isolate, the vaccine efficacy is not as pronounced after infection with the Omicron variant. Previous infection with the early SARS-CoV-2 isolate prevents replication after rechallenge with either virus in the lungs of previously infected hamsters, but the Omicron variant replicates efficiently in nasal turbinate tissue. These results experimentally demonstrate in an animal model that the antigenic changes in the Omicron variant are responsible for vaccine breakthrough and re-infection. The Author(s). 2022-04-19 2022-03-28 /pmc/articles/PMC8958134/ /pubmed/35421378 http://dx.doi.org/10.1016/j.celrep.2022.110688 Text en © 2022 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Report Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Chiba, Shiho Armbrust, Tammy Wright, Ryan Balaram, Ariane Florek, Kelsey R. Bateman, Allen C. Kawaoka, Yoshihiro Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters |
title | Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters |
title_full | Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters |
title_fullStr | Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters |
title_full_unstemmed | Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters |
title_short | Efficacy of vaccination and previous infection against the Omicron BA.1 variant in Syrian hamsters |
title_sort | efficacy of vaccination and previous infection against the omicron ba.1 variant in syrian hamsters |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958134/ https://www.ncbi.nlm.nih.gov/pubmed/35421378 http://dx.doi.org/10.1016/j.celrep.2022.110688 |
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