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SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain
The emergence and rapid spread of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (BA.1.1) has attracted global attention. The numerous mutations in the spike protein suggest that it may have altered susceptibility to immune protection elicited by the existing corona...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200063/ https://www.ncbi.nlm.nih.gov/pubmed/37178794 http://dx.doi.org/10.1016/j.virusres.2023.199131 |
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author | Li, Jianhua Li, Xiaoyan Mao, Haiyan Huang, Chen Sun, Yi Miao, Liangbin Li, Jiaxuan Song, Wanchen Zhang, Yanjun Huang, Jinsong Chen, Keda |
author_facet | Li, Jianhua Li, Xiaoyan Mao, Haiyan Huang, Chen Sun, Yi Miao, Liangbin Li, Jiaxuan Song, Wanchen Zhang, Yanjun Huang, Jinsong Chen, Keda |
author_sort | Li, Jianhua |
collection | PubMed |
description | The emergence and rapid spread of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (BA.1.1) has attracted global attention. The numerous mutations in the spike protein suggest that it may have altered susceptibility to immune protection elicited by the existing coronavirus disease 2019 (COVID-19) infection. We used a live virus neutralization test and SARS-CoV-2 pseudotype vesicular stomatitis virus vector-based neutralization assay to assess the degree of immune escape efficiency of the original, Delta (B1.617.2), and Omicron strains against the serum antibodies from 64 unvaccinated patients who had recovered from COVID-19 and the results were strongly correlated. The convalescent serum neutralization was more markedly reduced against the Omicron variant (9.4–57.9-fold) than the Delta variant (2.0–4.5-fold) as compared with the original strain. Our results demonstrate the reduced fusion and notable immune evasion capabilities of the Omicron variants, highlighting the importance of accelerating the development of vaccines targeting them. |
format | Online Article Text |
id | pubmed-10200063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102000632023-05-22 SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain Li, Jianhua Li, Xiaoyan Mao, Haiyan Huang, Chen Sun, Yi Miao, Liangbin Li, Jiaxuan Song, Wanchen Zhang, Yanjun Huang, Jinsong Chen, Keda Virus Res Short Communication The emergence and rapid spread of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (BA.1.1) has attracted global attention. The numerous mutations in the spike protein suggest that it may have altered susceptibility to immune protection elicited by the existing coronavirus disease 2019 (COVID-19) infection. We used a live virus neutralization test and SARS-CoV-2 pseudotype vesicular stomatitis virus vector-based neutralization assay to assess the degree of immune escape efficiency of the original, Delta (B1.617.2), and Omicron strains against the serum antibodies from 64 unvaccinated patients who had recovered from COVID-19 and the results were strongly correlated. The convalescent serum neutralization was more markedly reduced against the Omicron variant (9.4–57.9-fold) than the Delta variant (2.0–4.5-fold) as compared with the original strain. Our results demonstrate the reduced fusion and notable immune evasion capabilities of the Omicron variants, highlighting the importance of accelerating the development of vaccines targeting them. Elsevier 2023-05-21 /pmc/articles/PMC10200063/ /pubmed/37178794 http://dx.doi.org/10.1016/j.virusres.2023.199131 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Short Communication Li, Jianhua Li, Xiaoyan Mao, Haiyan Huang, Chen Sun, Yi Miao, Liangbin Li, Jiaxuan Song, Wanchen Zhang, Yanjun Huang, Jinsong Chen, Keda SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain |
title | SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain |
title_full | SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain |
title_fullStr | SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain |
title_full_unstemmed | SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain |
title_short | SARS-CoV-2 omicron BA.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain |
title_sort | sars-cov-2 omicron ba.1.1 is highly resistant to antibody neutralization of convalescent serum from the origin strain |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200063/ https://www.ncbi.nlm.nih.gov/pubmed/37178794 http://dx.doi.org/10.1016/j.virusres.2023.199131 |
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