As part of any plan to lift or ease the confinement restrictions that are in place in many different countries, there is an urgent need to increase the capacity of laboratory testing for SARS CoV-2. Detection of the viral genome through RT-qPCR is the golden standard for this test, however, the high demand of the materials and reagents needed to sample individuals, purify the viral RNA, and perform the RT-qPCR test has resulted in a worldwide shortage of several of these supplies. Here, we show that saliva samples treated with a lysis buffer can serve as a suitable source for viral RNA detection, that is cheaper and can be as efficient as the classical protocol that involves column purification of the viral RNA. In addition, it skips the need for swab sampling, decreases the risk of the healthcare personnel involved in this process, and accelerates the diagnostic procedure.
Collection : COVID-19 SARS-CoV-2 preprints from medRxiv and bioRxiv
