| Literature DB >> 34342836 |
Marcelo S Conzentino1, Karl Forchhammer2, Emanuel M Souza3, Fábio O Pedrosa3, Meri B Nogueira4, Sônia M Raboni4, Fabiane G M Rego5, Dalila L Zanette6, Mateus N Aoki6, Jeanine M Nardin7, Bruna Fornazari7, Hugo M P Morales7, Paola A F Celedon8, Carla V P Lima8, Sibelle B Mattar8, Vanessa H Lin8, Luis G Morello6,8, Fabricio K Marchini6,8, Rodrigo A Reis1, Luciano F Huergo9.
Abstract
Serological assays are important tools to identify previous exposure to SARS-CoV-2, helping to track COVID-19 cases and determine the level of humoral response to SARS-CoV-2 infections and/or immunization to future vaccines. Here, the SARS-CoV-2 nucleocapsid protein was expressed in Escherichia coli and purified to homogeneity and high yield using a single chromatography step. The purified SARS-CoV-2 nucleocapsid protein was used to develop an indirect enzyme-linked immunosorbent assay for the identification of human SARS-CoV-2 seroconverts. The assay sensitivity and specificity were determined analyzing sera from 140 RT-qPCR-confirmed COVID-19 cases and 210 pre-pandemic controls. The assay operated with 90% sensitivity and 98% specificity; identical accuracies were obtained in head-to-head comparison with a commercial ELISA kit. Antigen-coated plates were stable for up to 3 months at 4 °C. The ELISA method described is ready for mass production and will be an additional tool to track COVID-19 cases.Entities:
Keywords: COVID-19; ELISA; Immunological test; Nucleocapsid protein; SARS-CoV-2
Year: 2021 PMID: 34342836 DOI: 10.1007/s42770-021-00556-6
Source DB: PubMed Journal: Braz J Microbiol ISSN: 1517-8382 Impact factor: 2.476