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Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2
There is currently a lack of biological tools to study the replication cycle and pathogenesis of SARS-CoV-2, the etiological agent of COVID-19. Repurposing the existing tools, including antibodies of SARS-CoV, is an effective way to accelerate the development of therapeutics for COVID-19. Here, we e...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402058/ https://www.ncbi.nlm.nih.gov/pubmed/32766589 http://dx.doi.org/10.1101/2020.07.30.229377 |
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author | Bates, Timothy A. Weinstein, Jules B. Farley, Scotland E. Leier, Hans C. Messer, William B. Tafesse, Fikadu G. |
author_facet | Bates, Timothy A. Weinstein, Jules B. Farley, Scotland E. Leier, Hans C. Messer, William B. Tafesse, Fikadu G. |
author_sort | Bates, Timothy A. |
collection | PubMed |
description | There is currently a lack of biological tools to study the replication cycle and pathogenesis of SARS-CoV-2, the etiological agent of COVID-19. Repurposing the existing tools, including antibodies of SARS-CoV, is an effective way to accelerate the development of therapeutics for COVID-19. Here, we extensively characterized antibodies of the SARS-CoV structural proteins for their cross-reactivity, experimental utility, and neutralization of SARS-CoV-2. We assessed a total of 10 antibodies (six for Spike, two for Membrane, and one for Nucleocapsid and Envelope viral protein). We evaluated the utility of these antibodies against SARS-CoV-2 in a variety of assays, including immunofluorescence, ELISA, biolayer interferometry, western blots, and micro-neutralization. Remarkably, a high proportion of the antibodies we tested showed cross-reactivity, indicating a potentially generalizable theme of cross-reactivity between SARS-CoV and SARS-CoV-2 antibodies. These antibodies should help facilitate further research into SARS-CoV-2 basic biology. Moreover, our study provides critical information about the propensity of SARS-CoV antibodies to cross-react with SARS-CoV-2 and highlights its relevance in defining the clinical significance of such antibodies to improve testing and guide the development of novel vaccines and therapeutics. |
format | Online Article Text |
id | pubmed-7402058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-74020582020-08-06 Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2 Bates, Timothy A. Weinstein, Jules B. Farley, Scotland E. Leier, Hans C. Messer, William B. Tafesse, Fikadu G. bioRxiv Article There is currently a lack of biological tools to study the replication cycle and pathogenesis of SARS-CoV-2, the etiological agent of COVID-19. Repurposing the existing tools, including antibodies of SARS-CoV, is an effective way to accelerate the development of therapeutics for COVID-19. Here, we extensively characterized antibodies of the SARS-CoV structural proteins for their cross-reactivity, experimental utility, and neutralization of SARS-CoV-2. We assessed a total of 10 antibodies (six for Spike, two for Membrane, and one for Nucleocapsid and Envelope viral protein). We evaluated the utility of these antibodies against SARS-CoV-2 in a variety of assays, including immunofluorescence, ELISA, biolayer interferometry, western blots, and micro-neutralization. Remarkably, a high proportion of the antibodies we tested showed cross-reactivity, indicating a potentially generalizable theme of cross-reactivity between SARS-CoV and SARS-CoV-2 antibodies. These antibodies should help facilitate further research into SARS-CoV-2 basic biology. Moreover, our study provides critical information about the propensity of SARS-CoV antibodies to cross-react with SARS-CoV-2 and highlights its relevance in defining the clinical significance of such antibodies to improve testing and guide the development of novel vaccines and therapeutics. Cold Spring Harbor Laboratory 2020-07-30 /pmc/articles/PMC7402058/ /pubmed/32766589 http://dx.doi.org/10.1101/2020.07.30.229377 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY-NC-ND 4.0 International license (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Article Bates, Timothy A. Weinstein, Jules B. Farley, Scotland E. Leier, Hans C. Messer, William B. Tafesse, Fikadu G. Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2 |
title | Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2 |
title_full | Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2 |
title_fullStr | Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2 |
title_full_unstemmed | Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2 |
title_short | Cross-reactivity of SARS-CoV structural protein antibodies against SARS-CoV-2 |
title_sort | cross-reactivity of sars-cov structural protein antibodies against sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402058/ https://www.ncbi.nlm.nih.gov/pubmed/32766589 http://dx.doi.org/10.1101/2020.07.30.229377 |
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