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Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay
The circulation of certain SARS-CoV-2 variants may have a great impact on the epidemiological status of a geographical area; therefore, it is important that their presence is monitored. Currently, the gold standard method used to identify newly emerged variants is sequencing of either genes or whole...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226276/ https://www.ncbi.nlm.nih.gov/pubmed/37257757 http://dx.doi.org/10.1016/j.jviromet.2023.114759 |
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author | Eptaminitaki, Giasemi C. Parakatselaki, Maria-Eleni Petroulaki, Chara Marinopoulou, Dimitra Pitsikaki, Anthi Tseliou, Melpomeni Zafiropoulos, Alexandros Sourvinos, George |
author_facet | Eptaminitaki, Giasemi C. Parakatselaki, Maria-Eleni Petroulaki, Chara Marinopoulou, Dimitra Pitsikaki, Anthi Tseliou, Melpomeni Zafiropoulos, Alexandros Sourvinos, George |
author_sort | Eptaminitaki, Giasemi C. |
collection | PubMed |
description | The circulation of certain SARS-CoV-2 variants may have a great impact on the epidemiological status of a geographical area; therefore, it is important that their presence is monitored. Currently, the gold standard method used to identify newly emerged variants is sequencing of either genes or whole genomes. However, since this method is relatively expensive and has a long turnaround time, other rapid strategies should also be employed. The current study aimed to evaluate the performance of the Simplexa® SARS-CoV-2 Variants Direct assay, which is a RT-PCR that determines the variant present in a nasopharyngeal swab sample in approximately two hours. Totally, 527 positive samples for SARS-CoV-2 were analyzed from January until December 2022 and next-generation sequencing (NGS) was used as the reference method. The assay showed high sensitivity, ranging from 94.12 % to 100 %, depending on the variant. The assay also showed high specificity, reaching 100 % for Delta and BA.1 variants, and 99.74 % and 98.67 % for BA.2 and BA.4/BA.5 variants, respectively. Moreover, the assay was able to identify the correct variant category in the presence of any subvariant in the sample. We conclude that the assay can be used to facilitate faster monitoring of circulating SARS-CoV-2 variants, however sequencing cannot be completely replaced, since new variants always emerge, and constant updates are needed, so that the user is able to interpret the melting curve patterns. |
format | Online Article Text |
id | pubmed-10226276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102262762023-05-30 Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay Eptaminitaki, Giasemi C. Parakatselaki, Maria-Eleni Petroulaki, Chara Marinopoulou, Dimitra Pitsikaki, Anthi Tseliou, Melpomeni Zafiropoulos, Alexandros Sourvinos, George J Virol Methods Protocols The circulation of certain SARS-CoV-2 variants may have a great impact on the epidemiological status of a geographical area; therefore, it is important that their presence is monitored. Currently, the gold standard method used to identify newly emerged variants is sequencing of either genes or whole genomes. However, since this method is relatively expensive and has a long turnaround time, other rapid strategies should also be employed. The current study aimed to evaluate the performance of the Simplexa® SARS-CoV-2 Variants Direct assay, which is a RT-PCR that determines the variant present in a nasopharyngeal swab sample in approximately two hours. Totally, 527 positive samples for SARS-CoV-2 were analyzed from January until December 2022 and next-generation sequencing (NGS) was used as the reference method. The assay showed high sensitivity, ranging from 94.12 % to 100 %, depending on the variant. The assay also showed high specificity, reaching 100 % for Delta and BA.1 variants, and 99.74 % and 98.67 % for BA.2 and BA.4/BA.5 variants, respectively. Moreover, the assay was able to identify the correct variant category in the presence of any subvariant in the sample. We conclude that the assay can be used to facilitate faster monitoring of circulating SARS-CoV-2 variants, however sequencing cannot be completely replaced, since new variants always emerge, and constant updates are needed, so that the user is able to interpret the melting curve patterns. Elsevier B.V. 2023-09 2023-05-29 /pmc/articles/PMC10226276/ /pubmed/37257757 http://dx.doi.org/10.1016/j.jviromet.2023.114759 Text en © 2023 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Protocols Eptaminitaki, Giasemi C. Parakatselaki, Maria-Eleni Petroulaki, Chara Marinopoulou, Dimitra Pitsikaki, Anthi Tseliou, Melpomeni Zafiropoulos, Alexandros Sourvinos, George Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay |
title | Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay |
title_full | Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay |
title_fullStr | Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay |
title_full_unstemmed | Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay |
title_short | Rapid identification of SARS-CoV-2 variants: Validation of the simplexa SARS-CoV-2 variant direct assay |
title_sort | rapid identification of sars-cov-2 variants: validation of the simplexa sars-cov-2 variant direct assay |
topic | Protocols |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226276/ https://www.ncbi.nlm.nih.gov/pubmed/37257757 http://dx.doi.org/10.1016/j.jviromet.2023.114759 |
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