High-Content Imaging-Based Assay for SARS-CoV-2-Neutralizing Antibodies

Author:

Rocha Vinícius Pinto Costa12ORCID,Machado Bruna Aparecida Souza1,Quadros Helenita Costa2ORCID,Fernandes Antônio Márcio Santana1,Fiuza Bianca Sampaio Dotto1ORCID,Meira Cássio Santana12,da Silva Vitória Torres Barbosa1,Evangelista Afrânio Ferreira1ORCID,Fonseca Larissa Moraes dos Santos12ORCID,Badaró Roberto José da Silva1ORCID,Soares Milena Botelho Pereira12

Affiliation:

1. Institute of Health Technology, National Industrial Learning Service—Integrated Manufacturing and Technology Campus, SENAI CIMATEC, Salvador 41650-010, Bahia, Brazil

2. Laboratory of Tissue Engineering and Immunopharmacology, Oswaldo Cruz Foundation, Gonçalo Moniz Institute—Fiocruz, Salvador 40296-710, Bahia, Brazil

Abstract

The COVID-19 pandemic and the consequent emergence of new SARS-CoV-2 variants of concern necessitates the determination of populational serum potency against the virus. Here, we standardized and validated an imaging-based method to quantify neutralizing antibodies against lentiviral particles expressing the spike glycoprotein (pseudovirus). This method was found to efficiently quantify viral titers based on ZsGreen-positive cells and detect changes in human serum neutralization capacity induced by vaccination with up to two doses of CoronaVac, Comirnaty, or Covishield vaccines. The imaging-based protocol was also used to quantify serum potency against pseudoviruses expressing spikes from Delta, Omicron BA.1.1.529, and BA.4/5. Our results revealed increases in serum potency after one and two doses of the vaccines evaluated and demonstrated that Delta and Omicron variants escape from antibody neutralization. The method presented herein represents a valuable tool for the screening of antibodies and small molecules capable of blocking viral entry and could be used to evaluate humoral immunity developed by different populations and for vaccine development.

Funder

National Research and Development Council

Ministry of Science, Technology, and Innovation of the Federal Government

Publisher

MDPI AG

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