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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.
  • Wang S; Department of Biochemical Drugs and Biological Products, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
  • Liu L; NMPA Key Laboratory for Quality Control of Therapeutic Monoclonal Antibodies, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
  • Wang C; Department of Biochemical Drugs and Biological Products, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
  • Wang Z; NMPA Key Laboratory for Quality Control of Therapeutic Monoclonal Antibodies, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
  • Duan X; School of Pharmacy, Fudan University, Shanghai 201203, China.
  • Chen G; Department of Biochemical Drugs and Biological Products, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
  • Zhou H; NMPA Key Laboratory for Quality Control of Therapeutic Monoclonal Antibodies, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
  • Shao H; Department of Biochemical Drugs and Biological Products, Shanghai Institute for Food and Drug Control, Shanghai 201203, China.
Biosaf Health ; 4(1): 38-44, 2022 Feb.
Article in English | MEDLINE | ID: covidwho-1588181
ABSTRACT
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.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Topics: Variants Language: English Journal: Biosaf Health Year: 2022 Document Type: Article Affiliation country: J.bsheal.2021.12.006

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Topics: Variants Language: English Journal: Biosaf Health Year: 2022 Document Type: Article Affiliation country: J.bsheal.2021.12.006