Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783732497608081408 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8329412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT conzentinomarcelos antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT forchhammerkarl antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT souzaemanuelm antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT pedrosafabioo antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT nogueiramerib antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT rabonisoniam antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT regofabianegm antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT zanettedalilal antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT aokimateusn antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT nardinjeaninem antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT fornazaribruna antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT moraleshugomp antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT celedonpaolaaf antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT limacarlavp antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT mattarsibelleb antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT linvanessah antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT morelloluisg antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT marchinifabriciok antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT reisrodrigoa antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion AT huergolucianof antigenproductionanddevelopmentofanindirectelisabasedonthenucleocapsidproteintodetecthumansarscov2seroconversion |