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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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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. |
format | Online Article Text |
id | pubmed-9467536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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