PLoS ONE (Jan 2023)

Standardization of in-house anti-IgG and IgA ELISAs for the detection of COVID-19.

  • Kamonthip Rungrojcharoenkit,
  • Rungarun Suthangkornkul,
  • Darunee Utennam,
  • Darunee Buddhari,
  • Soontorn Pinpaiboon,
  • Duangrat Mongkolsirichaikul,
  • Stefan Fernandez,
  • Anthony R Jones,
  • Thomas S Cotrone,
  • Taweewun Hunsawong

DOI
https://doi.org/10.1371/journal.pone.0287107
Journal volume & issue
Vol. 18, no. 6
p. e0287107

Abstract

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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 (COVID-19). RT-PCR detection of viral RNA represents the gold standard method for diagnosis of COVID-19. However, multiple diagnostic tests are needed for acute disease diagnosis and assessing immunity during the COVID-19 outbreak. Here, we developed in-house anti-RBD IgG and IgA enzyme-linked immunosorbent assays (ELISAs) using a well-defined serum sample panel for screening and identification of human SARS-CoV-2 infection. We found that our in-house anti-SARS-CoV-2 IgG ELISA displayed a 93.5% sensitivity and 98.8% specificity whereas our in-house anti-SARS-CoV-2 IgA ELISA provided assay sensitivity and specificity at 89.5% and 99.4%, respectively. The agreement kappa values of our in-house anti-SARS-CoV-2 IgG and IgA ELISA assays were deemed to be excellent and fair, respectively, when compared to RT-PCR and excellent for both assays when compared to Euroimmun anti-SARS-CoV-2 IgG and IgA ELISAs. These data indicate that our in-house anti-SARS-CoV-2 IgG and IgA ELISAs are compatible performing assays for the detection of SARS-CoV-2 infection.