Performance of nucleocapsid and spike-based SARS-CoV-2 serologic assays

There is an urgent need for an accurate antibody test for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We have developed 3 ELISA methods, trimer spike IgA, trimer spike IgG, and nucleocapsid IgG, for detecting anti-SARS-CoV-2 antibodies. We evaluated their performance along with four commercial ELISAs, EDI™ Novel Coronavirus COVID-19 ELISA IgG and IgM, Euroimmun Anti-SARS-CoV-2 ELISA IgG and IgA, and one lateral flow assay, DPP® COVID-19 IgM/IgG System (Chembio). Both sensitivity and specificity were evaluated and the probable causes of false-positive reactions were determined. The assays were evaluated using 300 pre-epidemic samples and 100 PCR-confirmed COVID-19 samples. The sensitivities and specificities of the assays were as follows: 90%/100% (in-house trimer spike IgA), 90%/99.3% (in-house trimer spike IgG), 89%/98.3% (in-house nucleocapsid IgG), 73.7%/100% (EDI nucleocapsid IgM), 84.5%/95.1% (EDI nucleocapsid IgG), 95%/93.7% (Euroimmun S1 IgA), 82.8%/99.7% (Euroimmun S1 IgG), 82.0%/91.7% (Chembio nucleocapsid IgM), 92%/93.3% (Chembio nucleocapsid IgG). The presumed causes of false positive results from pre-epidemic samples in commercial and in-house assays were mixed. In some cases, assays lacked reproducibility. In other cases, reactivity was abrogated by competitive inhibition (spiking the sample with the same antigen that was used for coating ELISAs prior to performing the assay), suggesting positive reaction could be attributed to the presence of antibodies against these antigens. In other cases, reactivity was consistently detected but not abrogated by the spiking, suggesting positive reaction was not attributed to the presence of antibodies against these antigens. Overall, there was wide variability in assay performance using our samples, with in-house tests exhibiting the highest combined sensitivity and specificity. The causes of "false positivity" in pre-epidemic samples may be due to plasma antibodies apparently reacting with the corresponding antigen, or spurious reactivity may be directed against non-specific components in the assay system. Identification of these targets will be essential to improving assay performance.

Errataetall:

UpdateOf: medRxiv. 2020 Aug 07;:. - PMID 32793933

Media Type:

Electronic Article

Year of Publication:

2020

Publication:

2020

Contained In:

To Main Record - volume:15

Contained In:

PloS one - 15(2020), 11 vom: 02., Seite e0237828

Language:

English

Contributors:

Rikhtegaran Tehrani, Zahra [Author]
Saadat, Saman [Author]
Saleh, Ebtehal [Author]
Ouyang, Xin [Author]
Constantine, Niel [Author]
DeVico, Anthony L [Author]
Harris, Anthony D [Author]
Lewis, George K [Author]
Kottilil, Shyam [Author]
Sajadi, Mohammad M [Author]

Links:

Volltext

Keywords:

Antibodies, Viral
Immunoglobulin A
Immunoglobulin G
Immunoglobulin M
Journal Article
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Spike Glycoprotein, Coronavirus
Spike protein, SARS-CoV-2

Notes:

Date Completed 18.11.2020

Date Revised 16.02.2024

published: Electronic-eCollection

UpdateOf: medRxiv. 2020 Aug 07;:. - PMID 32793933

Citation Status MEDLINE

doi:

10.1371/journal.pone.0237828

funding:

Supporting institution / Project title:

PPN (Catalogue-ID):

NLM317054759