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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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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
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author 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
author_facet 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
author_sort Jallul, Mwada
collection PubMed
description 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.
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spelling pubmed-94675362022-09-13 Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2 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 Libyan J Med Original Article 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. Taylor & Francis 2022-09-05 /pmc/articles/PMC9467536/ /pubmed/36062935 http://dx.doi.org/10.1080/19932820.2022.2121252 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
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
Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2
title Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2
title_full Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2
title_fullStr Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2
title_full_unstemmed Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2
title_short Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2
title_sort variant-specific rt-qpcr for rapid screening of b.1.617 mutations in sars-cov-2
topic Original Article
url 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
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