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    Development of an in-house COVID-19 serology ELISA Test

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    jemtac.2021.qhc.7.pdf (310.1Kb)
    Date
    2021
    Author
    Chowdhury, Shazeda
    Taleb, Sara
    Elgamal, Mahmoud
    Hassan, Nesyia
    Nomikos, Michail
    Hssain, Ali Ait
    Zughaier, Susu M
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    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.
    URI
    https://doi.org/10.5339/jemtac.2021.qhc.7
    DOI/handle
    http://hdl.handle.net/10576/28965
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    • COVID-19 Research [‎848‎ items ]
    • Medicine Research [‎1739‎ items ]

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