Saliva Sampling and Its Direct Lysis, an Excellent Option To Increase the Number of SARS-CoV-2 Diagnostic Tests in Settings with Supply Shortages.
Joaquín Moreno-ContrerasMarco A EspinozaCarlos Sandoval-JaimeMarco A Cantú-CuevasHéctor Barón-OlivaresOscar D Ortiz-OrozcoAsunción V Muñoz-RangelManuel Hernández-de la CruzCésar M Eroza-OsorioCarlos F AriasSusana LópezPublished in: Journal of clinical microbiology (2020)
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 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Detection of the viral genome through reverse transcription-quantitative PCR (RT-qPCR) is the gold standard for this virus; however, the high demand of the materials and reagents needed to sample individuals, purify the viral RNA, and perform the RT-qPCR has resulted in a worldwide shortage of several of these supplies. Here, we show that directly lysed saliva samples can serve as a suitable source for viral RNA detection that is less expensive and can be as efficient as the classical protocol, which involves column purification of the viral RNA. In addition, it bypasses the need for swab sampling, decreases the risk of the health care personnel involved in the testing process, and accelerates the diagnostic procedure.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- healthcare
- real time pcr
- randomized controlled trial
- loop mediated isothermal amplification
- high resolution
- dna methylation
- label free
- gene expression
- transcription factor
- liquid chromatography
- mass spectrometry
- genome wide
- coronavirus disease
- simultaneous determination
- silver nanoparticles
- sensitive detection