AI Article Synopsis

  • The rapid spread of SARS-CoV-2 highlighted the inadequate testing capabilities in many countries, with traditional RT-qPCR methods being expensive and time-intensive due to RNA extraction requirements.
  • A new quantitative nanofluidic assay using the BiomarkTM instrument allows for testing of 4608 samples in one run, with the capability to detect specific SARS-CoV-2 variants and other pathogens effectively.
  • The study evaluates inactivating lysis buffers that allow RNA extraction to be bypassed, suggesting that using optimized buffers with high-throughput PCR could significantly improve testing efficiency and speed.

Article Abstract

The emergence and quick spread of SARS-CoV-2 has pointed at a low capacity response for testing large populations in many countries, in line of material, technical and staff limitations. The traditional RT-qPCR diagnostic test remains the reference method and is by far the most widely used test. These assays are limited to a few probe sets, require large sample PCR reaction volumes, along with an expensive and time-consuming RNA extraction step. Here we describe a quantitative nanofluidic assay that overcomes some of these shortcomings, based on the BiomarkTM instrument from Fluidigm. This system offers the possibility of performing 4608 qPCR end-points in a single run, equivalent to 192 clinical samples combined with 12 pairs of primers/probe sets in duplicate, thus allowing the monitoring of SARS-CoV-2 including the detection of specific SARS-CoV-2 variants, as well as the detection other pathogens and/or host cellular responses (virus receptors, response markers, microRNAs). The 10 nL-range volume of BiomarkTM reactions is compatible with sensitive and reproducible reactions that can be easily and cost-effectively adapted to various RT-qPCR configurations and sets of primers/probe. Finally, we also evaluated the use of inactivating lysis buffers composed of various detergents in the presence or absence of proteinase K to assess the compatibility of these buffers with a direct reverse transcription enzymatic step and we propose several protocols, bypassing the need for RNA purification. We advocate that the combined utilization of an optimized processing buffer and a high-throughput real-time PCR device would contribute to improve the turn-around-time to deliver the test results to patients and increase the SARS-CoV-2 testing capacities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046349PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0243333PLOS

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