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Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2

The continuous emergence of new SARS-CoV-2 variants required rapid and reliable diagnostic methods for early detection and monitoring of the spread of the virus, especially in low-resource countries where whole genome sequencing is not available. We aimed to evaluate and compare the performance of t...

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Detalles Bibliográficos
Autores principales: Jallul, Mwada, Ibrahim, Khaled, Zaghdani, Ahmed, Abdusalam, Mohamed Musbah, Al Dwigen, Samira M, Atwair, Wafya S, Elbasir, Mohamed, Alhudiri, Inas, El Meshri, Salah Edin, Elzagheid, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467536/
https://www.ncbi.nlm.nih.gov/pubmed/36062935
http://dx.doi.org/10.1080/19932820.2022.2121252
Descripción
Sumario:The continuous emergence of new SARS-CoV-2 variants required rapid and reliable diagnostic methods for early detection and monitoring of the spread of the virus, especially in low-resource countries where whole genome sequencing is not available. We aimed to evaluate and compare the performance of two different RT-qPCR screening assays for the detection of B.1.617 lineage mutations. A total of 85 SARS-CoV-2 positive samples were collected between 9(th) August and 10 September 2021 and screened by two mutation-specific RT-qPCR assays for simultaneous detection of B.1.617.1 and B.1.617.2 lineage mutations. VIASURE Variant II PCR assay identified 2 Delta variant-specific mutations (L452R, and P681 R) in 80% of tested samples, while the PKamp™ Variant Detect™ assay was only able to detect one Delta variant specific mutation (L452R) in 75% of tested samples. This is the first report to show the Delta variant as the cause of the third wave in Libya. The use of multiplex RT-qPCR assays has allowed the identification of new variants for rapid screening. However, RT-qPCR results should be confirmed by whole genome sequencing of SARS-COV-2.