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Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR
Since January 2021, the diffusion of the most propagated SARS-CoV-2 variants in France (UK variant 20I/501Y.V1 (lineage B.1.1.7), 20H/H501Y.V2 (lineage B.1.351) and 20J/H501Y.V3 (lineage P.1)) were urgently screened, needing a surveillance with an RT-PCR screening assay. In this study, we evaluated...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306735/ https://www.ncbi.nlm.nih.gov/pubmed/34359323 http://dx.doi.org/10.3390/diagnostics11071241 |
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author | Boudet, Agathe Stephan, Robin Bravo, Sophie Sasso, Milène Lavigne, Jean-Philippe |
author_facet | Boudet, Agathe Stephan, Robin Bravo, Sophie Sasso, Milène Lavigne, Jean-Philippe |
author_sort | Boudet, Agathe |
collection | PubMed |
description | Since January 2021, the diffusion of the most propagated SARS-CoV-2 variants in France (UK variant 20I/501Y.V1 (lineage B.1.1.7), 20H/H501Y.V2 (lineage B.1.351) and 20J/H501Y.V3 (lineage P.1)) were urgently screened, needing a surveillance with an RT-PCR screening assay. In this study, we evaluated one RT-PCR kit for this screening (ID SARS-CoV-2/UK/SA Variant Triplex(®), ID Solutions, Grabels, France) on 2207 nasopharyngeal samples that were positive for SARS-CoV-2. Using ID Solutions kit, 4.1% (92/2207) of samples were suspected to belonged to B.1.351 or P.1 variants. Next-generation sequencing that was performed on 67.4% (62/92) of these samples confirmed the presence of a B.1.351 variant in only 75.8% of the samples (47/62). Thirteen samples belonged to the UK variant (B.1.1.7), and two to A.27 with N501Y mutation. The thirteen with the UK variant presented one mutation in the S-gene, near the ΔH69/ΔV70 deletion (S71F or A67S), which impacted the detection of ΔH69/ΔV70 deletion. Using another screening kit (PKampVariantDetect SARS-CoV-2 RT-PCR combination 1 and 3(®) PerkinElmer, Waltham, MA, USA) on the misidentified samples, we observed that the two mutations, S71F or A67S, did not impact the detection of the UK variant. In conclusion, this study highlights the limitations of the screening strategy based on the detection of few mutations/deletions as well as it not being able to follow the virus evolution. |
format | Online Article Text |
id | pubmed-8306735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83067352021-07-25 Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR Boudet, Agathe Stephan, Robin Bravo, Sophie Sasso, Milène Lavigne, Jean-Philippe Diagnostics (Basel) Article Since January 2021, the diffusion of the most propagated SARS-CoV-2 variants in France (UK variant 20I/501Y.V1 (lineage B.1.1.7), 20H/H501Y.V2 (lineage B.1.351) and 20J/H501Y.V3 (lineage P.1)) were urgently screened, needing a surveillance with an RT-PCR screening assay. In this study, we evaluated one RT-PCR kit for this screening (ID SARS-CoV-2/UK/SA Variant Triplex(®), ID Solutions, Grabels, France) on 2207 nasopharyngeal samples that were positive for SARS-CoV-2. Using ID Solutions kit, 4.1% (92/2207) of samples were suspected to belonged to B.1.351 or P.1 variants. Next-generation sequencing that was performed on 67.4% (62/92) of these samples confirmed the presence of a B.1.351 variant in only 75.8% of the samples (47/62). Thirteen samples belonged to the UK variant (B.1.1.7), and two to A.27 with N501Y mutation. The thirteen with the UK variant presented one mutation in the S-gene, near the ΔH69/ΔV70 deletion (S71F or A67S), which impacted the detection of ΔH69/ΔV70 deletion. Using another screening kit (PKampVariantDetect SARS-CoV-2 RT-PCR combination 1 and 3(®) PerkinElmer, Waltham, MA, USA) on the misidentified samples, we observed that the two mutations, S71F or A67S, did not impact the detection of the UK variant. In conclusion, this study highlights the limitations of the screening strategy based on the detection of few mutations/deletions as well as it not being able to follow the virus evolution. MDPI 2021-07-12 /pmc/articles/PMC8306735/ /pubmed/34359323 http://dx.doi.org/10.3390/diagnostics11071241 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Boudet, Agathe Stephan, Robin Bravo, Sophie Sasso, Milène Lavigne, Jean-Philippe Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR |
title | Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR |
title_full | Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR |
title_fullStr | Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR |
title_full_unstemmed | Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR |
title_short | Limitation of Screening of Different Variants of SARS-CoV-2 by RT-PCR |
title_sort | limitation of screening of different variants of sars-cov-2 by rt-pcr |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306735/ https://www.ncbi.nlm.nih.gov/pubmed/34359323 http://dx.doi.org/10.3390/diagnostics11071241 |
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