Nucleoprotein-based ELISA for detection of SARS-COV-2 IgG antibodies: Could an old assay be suitable for serodiagnosis of the new coronavirus?

•An in-house nucleoprotein-based ELISA SARS-CoV-2 IgG suitable for diagnosing COVID-19.•The nucleoprotein-based ELISA SARS-CoV-2 IgG is inexpensive and constitutes an alternative to current commercial tests.•SARS-CoV-2 IgG anti -nucleoprotein did not cross-react with serum samples from other respira...

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Veröffentlicht in:Journal of virological methods 2021-04, Vol.290, p.114064-114064, Article 114064
Hauptverfasser: Tozetto-Mendoza, Tania Regina, Kanunfre, Kelly Aparecida, Vilas-Boas, Lucy Santos, Sanchez Espinoza, Evelyn Patricia, Paião, Heuder Gustavo Oliveira, Rocha, Mussya Cisotto, de Paula, Anderson Vicente, de Oliveira, Maura Salaroli, Zampelli, Daniella Bosco, Vieira, José Mauro, Buss, Lewis, Costa, Silvia Figueiredo, Sabino, Ester Cerdeira, Witkin, Steven S., Okay, Thelma Suely, Mendes-Correa, Maria Cassia
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Sprache:eng
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Zusammenfassung:•An in-house nucleoprotein-based ELISA SARS-CoV-2 IgG suitable for diagnosing COVID-19.•The nucleoprotein-based ELISA SARS-CoV-2 IgG is inexpensive and constitutes an alternative to current commercial tests.•SARS-CoV-2 IgG anti -nucleoprotein did not cross-react with serum samples from other respiratory agents, dengue and zika. We evaluated the performance of a nucleoprotein-based enzyme-linked immunosorbent assay (ELISA) for detection of IgG antibodies to SARS-CoV-2. The ELISA was based on serum IgG reactivity to a 46-kDa protein derived from the recombinant SARS-CoV2 nucleoprotein. Assay sensitivity was assessed using serum samples from 134 COVID-19 confirmed cases obtained > 15 days after symptom onset. Specificity was determined by testing sera from 94 healthy controls. Cross-reactivity was evaluated with sera from 96 individuals with previous dengue or zika virus-confirmed infections, with 44 sera from individuals with confirmed infections to other respiratory viruses or with bacterial and fungal infections that cause pneumonia and with 40 sera negative for SARS-CoV-2 nucleoprotein by commercial ELISA kits. The majority of subjects were male and ≥ 60 years old. Assay sensitivity was 90.3 % (95 % confidence interval 84.1 %–94.2 %) and specificity was 97.9 % (92.6 %–99.4 %). There was no cross-reactivity with sera from individuals diagnosed with dengue, zika virus, influenza virus, rhinovirus, adenovirus, respiratory syncytial virus, seasonal coronavirus, Mycobacterium tuberculosis, Staphylococcus (S. aureus and coagulase-negative), Streptococcus pneumoniae, Klebsiella pneumoniae and the fungus Aspergillus fumigatus. The level of concordance of our test with results from commercial ELISA kits was 100 %. The nucleoprotein-based ELISA was specific for detection of IgG anti-nucleoprotein antibodies to SARS-CoV-2. It utilizes a frequently employed low expense assay protocol and is easier to perform than other currently available commercial SARS-CoV2 antibody detection tests.
ISSN:0166-0934
1879-0984
DOI:10.1016/j.jviromet.2021.114064