AI Article Synopsis

  • The developed testing methodology utilizes a reverse transcriptase loop-mediated amplification (RT-LAMP) assay in affordable glass capillaries to detect SARS-CoV-2 viral RNA quickly and effectively.
  • It features a simplified extraction process that can produce results in just over 30 minutes, requiring only 10 μl of reagents, which is significantly less than traditional testing methods.
  • This approach is compatible with existing laboratories and resources, making it ideal for use in resource-limited settings, thereby enhancing overall testing capacity and reducing supply chain demands.

Article Abstract

As the SARS-CoV-2 pandemic continues to spread, the necessity for rapid, easy diagnostic capabilities could never have been more crucial. With this aim in mind, we have developed a cost-effective and time-saving testing methodology/strategy that implements a sensitive reverse transcriptase loop-mediated amplification (RT-LAMP) assay within narrow, commercially available and cheap, glass capillaries for detection of the SARS-CoV-2 viral RNA. The methodology is compatible with widely used laboratory-based molecular testing protocols and currently available infrastructure. It employs a simple rapid extraction protocol that lyses the virus, releasing sufficient genetic material for amplification. This extracted viral RNA is then amplified using a SARS-CoV-2 RT-LAMP kit, at a constant temperature and the resulting amplified product produces a colour change which can be visually interpreted. This testing protocol, in conjunction with the RT-LAMP assay, has a sensitivity of ∼100 viral copies per reaction of a sample and provides results in a little over 30 min. As the assay is carried out in a water bath, commonly available within most testing laboratories, it eliminates the need for specialised instruments and associated skills. In addition, our testing pathway requires a significantly reduced quantity of reagents per test while providing comparable sensitivity and specificity to the RT-LAMP kit used in this study. While the conventional technique requires 25 μl of reagent, our test only utilises less than half the quantity (10 μl). Thus, with its minimalistic approach, this capillary-based assay could be a promising alternative to the conventional testing, owing to the fact that it can be performed in resource-limited settings, using readily available apparatus, and has the potential of increasing the overall testing capacity, while also reducing the burden on supply chains for mass testing.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406210PMC
http://dx.doi.org/10.1016/j.aca.2021.339002DOI Listing

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