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Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles
The coronavirus disease 2019 (COVID-19) is still causing a wide range of infections and deaths due to the high variability of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Therefore, it is necessary to establish a reliable and convenient pseudovirus-based neutralization assay to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chinese Medical Association Publishing House. Published by Elsevier BV.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8721934/ https://www.ncbi.nlm.nih.gov/pubmed/35005601 http://dx.doi.org/10.1016/j.bsheal.2021.12.006 |
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author | Wang, Sheng Liu, Lizhen Wang, Can Wang, Ziqiang Duan, Xuhua Chen, Gang Zhou, Hu Shao, Hong |
author_facet | Wang, Sheng Liu, Lizhen Wang, Can Wang, Ziqiang Duan, Xuhua Chen, Gang Zhou, Hu Shao, Hong |
author_sort | Wang, Sheng |
collection | PubMed |
description | The coronavirus disease 2019 (COVID-19) is still causing a wide range of infections and deaths due to the high variability of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Therefore, it is necessary to establish a reliable and convenient pseudovirus-based neutralization assay to develop drug targeted variants of SARS-CoV-2. Based on the HIV-1 backbone, we generated a high titer luciferase (Luc)-expressing pseudovirus packaging system. Three dominant S mutant substitution pseudovirus were also established and identified compared to wide type in hACE2-overexpressing HEK-293T cells (293T-ACE2 cells). Compared to serine protease inhibitor camostat mesylate, the cysteine protease inhibitor E-64d could significantly block all SARS-CoV-2 mutant S pseudovirus infection in 293T-ACE2 cells. Furthermore, the neutralization ability of two antibodies targeted receptor-binding domain (RBD) of SARS-CoV-2 spike protein (S) was evaluated, which showed different inhibition dose–effect curves among four types of S pseudovirus. Overall, we developed a pseudovirus-based neutralization assay for SARS-CoV-2, which would be readily adapted to SARS-CoV-2 variants for evaluating antibodies. |
format | Online Article Text |
id | pubmed-8721934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Chinese Medical Association Publishing House. Published by Elsevier BV. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87219342022-01-03 Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles Wang, Sheng Liu, Lizhen Wang, Can Wang, Ziqiang Duan, Xuhua Chen, Gang Zhou, Hu Shao, Hong Biosaf Health Article The coronavirus disease 2019 (COVID-19) is still causing a wide range of infections and deaths due to the high variability of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Therefore, it is necessary to establish a reliable and convenient pseudovirus-based neutralization assay to develop drug targeted variants of SARS-CoV-2. Based on the HIV-1 backbone, we generated a high titer luciferase (Luc)-expressing pseudovirus packaging system. Three dominant S mutant substitution pseudovirus were also established and identified compared to wide type in hACE2-overexpressing HEK-293T cells (293T-ACE2 cells). Compared to serine protease inhibitor camostat mesylate, the cysteine protease inhibitor E-64d could significantly block all SARS-CoV-2 mutant S pseudovirus infection in 293T-ACE2 cells. Furthermore, the neutralization ability of two antibodies targeted receptor-binding domain (RBD) of SARS-CoV-2 spike protein (S) was evaluated, which showed different inhibition dose–effect curves among four types of S pseudovirus. Overall, we developed a pseudovirus-based neutralization assay for SARS-CoV-2, which would be readily adapted to SARS-CoV-2 variants for evaluating antibodies. Chinese Medical Association Publishing House. Published by Elsevier BV. 2022-02 2022-01-03 /pmc/articles/PMC8721934/ /pubmed/35005601 http://dx.doi.org/10.1016/j.bsheal.2021.12.006 Text en © 2022 Chinese Medical Association Publishing House. Published by Elsevier BV. 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 | Article Wang, Sheng Liu, Lizhen Wang, Can Wang, Ziqiang Duan, Xuhua Chen, Gang Zhou, Hu Shao, Hong Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles |
title | Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles |
title_full | Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles |
title_fullStr | Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles |
title_full_unstemmed | Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles |
title_short | Establishment of a pseudovirus neutralization assay based on SARS-CoV-2 S protein incorporated into lentiviral particles |
title_sort | establishment of a pseudovirus neutralization assay based on sars-cov-2 s protein incorporated into lentiviral particles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8721934/ https://www.ncbi.nlm.nih.gov/pubmed/35005601 http://dx.doi.org/10.1016/j.bsheal.2021.12.006 |
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