Fersiynau electronig

Dangosydd eitem ddigidol (DOI)

  • Xinsheng Nan
    School of Healthcare Sciences, Cardiff University
  • Patrick Hardinge
    School of Healthcare Sciences, Cardiff University
  • Sven Hoehn
    School of Healthcare Sciences, Cardiff University
  • Shrinivas Nivrutti Dighe
    School of Healthcare Sciences, Cardiff University
  • John Ukeri
    School of Healthcare Sciences, Cardiff University
  • Darius F Pease
    School of Healthcare Sciences, Cardiff University
  • Joshua Griffin
    School of Healthcare Sciences, Cardiff University
  • Jessica I Warrington
    School of Healthcare Sciences, Cardiff University
  • Zack Saud
    School of Healthcare Sciences, Cardiff University
  • Emma Hottinger
    School of Healthcare Sciences, Cardiff University
  • Gordon Webster
    School of Healthcare Sciences, Cardiff University
  • Davey Jones
  • Peter Kille
    School of Healthcare Sciences, Cardiff University
  • Andrew Weightman
    School of Healthcare Sciences, Cardiff University
  • Richard Stanton
    School of Healthcare Sciences, Cardiff University
  • Oliver K Castell
    School of Healthcare Sciences, Cardiff University
  • James A H Murray
    School of Healthcare Sciences, Cardiff University
  • Tomasz P Jurkowski
    School of Healthcare Sciences, Cardiff University

The COVID-19 pandemic demonstrated the need for rapid molecular diagnostics. Vaccination programs can provide protection and facilitate the opening of society, but newly emergent and existing viral variants capable of evading the immune system endanger their efficacy. Effective surveillance for Variants of Concern (VOC) is therefore important. Rapid and specific molecular diagnostics can provide speed and coverage advantages compared to genomic sequencing alone, benefitting the public health response and facilitating VOC containment. Here we expand the recently developed SARS-CoV-2 CRISPR-Cas detection technology (SHERLOCK) to provide rapid and sensitive discrimination of SARS-CoV-2 VOCs that can be used at point of care, implemented in the pipelines of small or large testing facilities, and even determine the proportion of VOCs in pooled population-level wastewater samples. This technology complements sequencing efforts to allow facile and rapid identification of individuals infected with VOCs to help break infection chains. We show the optimisation of our VarLOCK assays (Variant-specific SHERLOCK) for multiple specific mutations in the S gene of SARS-CoV-2 and validation with samples from the Cardiff University Testing Service. We also show the applicability of VarLOCK to national wastewater surveillance of SARS-CoV-2 variants and the rapid adaptability of the technique for new and emerging VOCs.

Allweddeiriau

Iaith wreiddiolSaesneg
Rhif yr erthygl20832
CyfnodolynScientific Reports
Cyfrol13
Rhif y cyfnodolyn1
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - 27 Tach 2023
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