Strategies That Facilitate Extraction-Free SARS-CoV-2 Nucleic Acid Amplification Tests |
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Authors: | David J. Delgado-Diaz Dhanasekaran Sakthivel Hanh H. T. Nguyen Khashayar Farrokzhad William Hopper Charles A. Narh Jack S. Richards |
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Affiliation: | 1.ZIP Diagnostics Pty Ltd., Collingwood, VIC 3066, Australia; (D.S.); (H.H.T.N.); (K.F.); (W.H.); (C.A.N.); (J.S.R.);2.Department of Medicine, University of Melbourne, Melbourne, VIC 3010, Australia;3.Department of Infectious Diseases, Monash University, Melbourne, VIC 3004, Australia |
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Abstract: | The COVID-19 pandemic has resulted in an unprecedented global demand for in vitro diagnostic reagents. Supply shortages and hoarding have impacted testing capacity which has led to inefficient COVID-19 case identification and transmission control, predominantly in developing countries. Traditionally, RNA extraction is a prerequisite for conducting SARS-CoV-2 nucleic acid amplification tests (NAAT); however, simplified methods of sample processing have been successful at bypassing typical nucleic acid extraction steps, enabling extraction-free SARS-CoV-2 NAAT workflows. These methods involve chemical and physical approaches that are inexpensive and easily accessible alternatives to overcome extraction kit supply shortages, while offering acceptable test performance. Here we provide an overview of three main sample preparation strategies that have been shown to facilitate extraction-free SARS-CoV-2 NAATs. |
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Keywords: | COVID-19 SARS-CoV-2 nucleic acid extraction diagnostics NAAT isothermal amplification RT-PCR |
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