Development of an in-house COVID-19 serology ELISA Test
Author | Chowdhury, Shazeda |
Author | Taleb, Sara |
Author | Elgamal, Mahmoud |
Author | Hassan, Nesyia |
Author | Nomikos, Michail |
Author | Hssain, Ali Ait |
Author | Zughaier, Susu M |
Available date | 2022-03-24T05:33:59Z |
Publication Date | 2021 |
Publication Name | Journal of Emergency Medicine, Trauma and Acute Care |
Resource | qscience |
Citation | Chowdhury S, Taleb S, Elgamal M, Hassan N, Nomikos M, Hssain AA, Zughaier SM. Development of an in-house COVID-19 serology ELISA Test, Journal of Emergency Medicine, Trauma & Acute Care, Qatar Health Care Conference 2021:7 http://dx.doi.org/10.5339/-jemtac.2021.qhc.7 |
ISSN | 1999-7094 |
Abstract | Background: COVID-19 pandemic created an unprecedented demand for reagents and diagnostic tools to confirm COVID-19 cases. Thus, the development of a robust in-house diagnostic test is considered of high importance. Within a few days after exposure, the human body produces specific antibodies that recognize the surface proteins of the invading SARS-CoV-2 virus 1 . Therefore, virus specific immunoglobulins are neutralizing antibodies and their appearance in the blood is a good sign of immunity 2 . The aim of this study was to develop an in-house COVID-19 serology ELISA test to quantify induced antibody responses. This test can help identify convalescent plasma donors with high antibody titers that can be used to treat other patients. Methods: Spike protein antigen is highly expressed in SARS-CoV-2 3 . Recombinant protein corresponding to the spike receptor-binding domain (RBD), which binds to specific antibodies circulating in COVID-19 patients' blood was used as the antigen in this colorimetric ELISA test. Briefly, a 96-microtiter well plate was coated with RBD protein, where serum dilutions were added. Antibody titers were detected using an anti-human IgG- peroxidase labelled antibody and the substrate o-phenylenediamine dihydrochloride; measured at optical density (OD) of 450 nm (Figure 1). Results: The in-house quantitative serology test was validated using serum samples collected from severe COVID-19 patients (n = 282) admitted to the intensive care unit at Hamad General Hospital. Serum samples from non-COVID-19 (n = 10) were used as a negative control. We detected high antibody titers in ~90% of COVID-19 sera. In contrast, no SARS-CoV-2 specific antibodies were detected in the serum of non-infected subjects (n = 6), pooled human serum collected before 2019, or Middle East Respiratory Syndrome (MERS) infected subjects (n = 3) confirming the specificity and the sensitivity of this in-house serology test. Conclusion: This in-house quantitative serology test is sensitive, specific, and inexpensive. The test can address the rising issue of COVID-19 supply chain globally and foster the capacity-building efforts envisioned by Qatar University. |
Language | en |
Publisher | Hamad bin Khalifa University Press (HBKU Press) |
Subject | COVID-19 SARS-CoV2 serology antibody titer ELISA |
Type | Article |
Issue Number | 2 |
Volume Number | 2021 |
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