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Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion

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...

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Autores principales: Conzentino, Marcelo S., Forchhammer, Karl, Souza, Emanuel M., Pedrosa, Fábio O., Nogueira, Meri B., Raboni, Sônia M., Rego, Fabiane G. M., Zanette, Dalila L., Aoki, Mateus N., Nardin, Jeanine M., Fornazari, Bruna, Morales, Hugo M. P., Celedon, Paola A. F., Lima, Carla V. P., Mattar, Sibelle B., Lin, Vanessa H., Morello, Luis G., Marchini, Fabricio K., Reis, Rodrigo A., Huergo, Luciano F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329412/
https://www.ncbi.nlm.nih.gov/pubmed/34342836
http://dx.doi.org/10.1007/s42770-021-00556-6
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author Conzentino, Marcelo S.
Forchhammer, Karl
Souza, Emanuel M.
Pedrosa, Fábio O.
Nogueira, Meri B.
Raboni, Sônia M.
Rego, Fabiane G. M.
Zanette, Dalila L.
Aoki, Mateus N.
Nardin, Jeanine M.
Fornazari, Bruna
Morales, Hugo M. P.
Celedon, Paola A. F.
Lima, Carla V. P.
Mattar, Sibelle B.
Lin, Vanessa H.
Morello, Luis G.
Marchini, Fabricio K.
Reis, Rodrigo A.
Huergo, Luciano F.
author_facet Conzentino, Marcelo S.
Forchhammer, Karl
Souza, Emanuel M.
Pedrosa, Fábio O.
Nogueira, Meri B.
Raboni, Sônia M.
Rego, Fabiane G. M.
Zanette, Dalila L.
Aoki, Mateus N.
Nardin, Jeanine M.
Fornazari, Bruna
Morales, Hugo M. P.
Celedon, Paola A. F.
Lima, Carla V. P.
Mattar, Sibelle B.
Lin, Vanessa H.
Morello, Luis G.
Marchini, Fabricio K.
Reis, Rodrigo A.
Huergo, Luciano F.
author_sort Conzentino, Marcelo S.
collection PubMed
description 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.
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spelling pubmed-83294122021-08-03 Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion Conzentino, Marcelo S. Forchhammer, Karl Souza, Emanuel M. Pedrosa, Fábio O. Nogueira, Meri B. Raboni, Sônia M. Rego, Fabiane G. M. Zanette, Dalila L. Aoki, Mateus N. Nardin, Jeanine M. Fornazari, Bruna Morales, Hugo M. P. Celedon, Paola A. F. Lima, Carla V. P. Mattar, Sibelle B. Lin, Vanessa H. Morello, Luis G. Marchini, Fabricio K. Reis, Rodrigo A. Huergo, Luciano F. Braz J Microbiol Clinical Microbiology - Short Communication 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. Springer International Publishing 2021-08-03 /pmc/articles/PMC8329412/ /pubmed/34342836 http://dx.doi.org/10.1007/s42770-021-00556-6 Text en © Sociedade Brasileira de Microbiologia 2021
spellingShingle Clinical Microbiology - Short Communication
Conzentino, Marcelo S.
Forchhammer, Karl
Souza, Emanuel M.
Pedrosa, Fábio O.
Nogueira, Meri B.
Raboni, Sônia M.
Rego, Fabiane G. M.
Zanette, Dalila L.
Aoki, Mateus N.
Nardin, Jeanine M.
Fornazari, Bruna
Morales, Hugo M. P.
Celedon, Paola A. F.
Lima, Carla V. P.
Mattar, Sibelle B.
Lin, Vanessa H.
Morello, Luis G.
Marchini, Fabricio K.
Reis, Rodrigo A.
Huergo, Luciano F.
Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion
title Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion
title_full Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion
title_fullStr Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion
title_full_unstemmed Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion
title_short Antigen production and development of an indirect ELISA based on the nucleocapsid protein to detect human SARS-CoV-2 seroconversion
title_sort antigen production and development of an indirect elisa based on the nucleocapsid protein to detect human sars-cov-2 seroconversion
topic Clinical Microbiology - Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329412/
https://www.ncbi.nlm.nih.gov/pubmed/34342836
http://dx.doi.org/10.1007/s42770-021-00556-6
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