4.7 Article

Detection of Major SARS-CoV-2 Variants of Concern in ClinicalSamples via CRISPR-Cas12a-Mediated Mutation-Specific Assay

期刊

ACS SYNTHETIC BIOLOGY
卷 11, 期 5, 页码 1811-1823

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssynbio.1c00643

关键词

SARS-CoV-2; mutations; variants of concern; variant genotyping; CRISPR-Cas12a system

资金

  1. National Major Science and Technology Project of China [2018ZX10732-401-003-003]

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The CRISPR-Cas12a-based genotyping assay is highly sensitive and specific in detecting both the SARS-CoV-2 wild-type strain and major VOCs. It is a simple and rapid assay that can monitor and track the circulating SARS-CoV-2 variants and the dynamics of the coronavirus disease 2019 (COVID-19) pandemic and can be easily implemented in resource-limited settings.
Objectives: Emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants pose a great threat andburden to global public health. Here, we evaluated a clustered regularly interspaced short palindromic repeat-associated enzyme 12a(CRISPR-Cas12a)-based method for detecting major SARS-CoV-2 variants of concern (VOCs) in SARS-CoV-2 positive clinicalsamples.Methods: Allele-specific CRISPR RNAs (crRNAs) targeting the signature mutations in the spike protein of SARS-CoV-2 aredesigned. A total of 59 SARS-CoV-2 positive oropharyngeal swab specimens were used to evaluate the performance of the CRISPR-Cas12a-mediated assay to identify major SARS-CoV-2 VOCs.Results:Compared with Sanger sequencing, the eight allele-specificcrRNAs analyzed can specifically identify the corresponding mutations with a positive predictive value of 83.3-100% and a negativepredictive value of 85.7-100%. Our CRISPR-Cas12a-mediated assay distinguished wild-type and four major VOCs (Alpha, Beta,Delta, and Omicron) of SARS-CoV-2 with a sensitivity of 93.8-100.0% and a specificity of 100.0%. The two methods showed aconcordance of 98.3% (58/59) with a Kappa value of 0.956-1.000, while seven (11.9%) samples were found to be positive for extramutations by the CRISPR-based assay. Furthermore, neither virus titers nor the sequences adjacent to the signature mutations wereassociated with the variation offluorescence intensity detected or the false-positive reaction observed when testing clinical samples.In addition, there was no cross-reaction observed when detecting 33 SARS-CoV-2 negative clinical samples infected with commonrespiratory pathogens.Conclusions: The CRISPR-Cas12a-based genotyping assay is highly sensitive and specific when detecting boththe SARS-CoV-2 wild-type strain and major VOCs. It is a simple and rapid assay that can monitor and track the circulating SARS-CoV-2 variants and the dynamics of the coronavirus disease 2019 (COVID-19) pandemic and can be easily implemented inresource-limited settings

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