Cargando…

Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants

BACKGROUND: The recent emergence of new SARS CoV-2 variants (variants of concern, VOC) that spread rapidly and may lead to immune escape has emphasized the urgent need to monitor and control their spread. METHODS: We analyzed 2018 SARS-CoV-2 positive specimens collected between February 9 and March...

Descripción completa

Detalles Bibliográficos
Autores principales: Migueres, M., Lhomme, S., Trémeaux, P., Dimeglio, C., Ranger, N., Latour, J., Dubois, M., Nicot, F., Miedouge, M., Mansuy, J.M., Izopet, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411575/
https://www.ncbi.nlm.nih.gov/pubmed/34509927
http://dx.doi.org/10.1016/j.jcv.2021.104969
_version_ 1783747321256738816
author Migueres, M.
Lhomme, S.
Trémeaux, P.
Dimeglio, C.
Ranger, N.
Latour, J.
Dubois, M.
Nicot, F.
Miedouge, M.
Mansuy, J.M.
Izopet, J.
author_facet Migueres, M.
Lhomme, S.
Trémeaux, P.
Dimeglio, C.
Ranger, N.
Latour, J.
Dubois, M.
Nicot, F.
Miedouge, M.
Mansuy, J.M.
Izopet, J.
author_sort Migueres, M.
collection PubMed
description BACKGROUND: The recent emergence of new SARS CoV-2 variants (variants of concern, VOC) that spread rapidly and may lead to immune escape has emphasized the urgent need to monitor and control their spread. METHODS: We analyzed 2018 SARS-CoV-2 positive specimens collected between February 9 and March 22, 2021 using the Thermofisher® TaqPath™ COVID-19 CE-IVD RT-PCR kit (TaqPath) and the ID solutions® ID™ SARS-CoV-2/UK/SA Variant Triplex RT-PCR (ID triplex) assay to screen for VOCs. RESULTS: The ID triplex assay identified 62.8% of them as VOCs: 61.8% B.1.1.7 and 0.9% B.1.351/P.1. The agreement between the ID triplex results for B.1.1.7 and the TaqPath S gene target failure (SGTF)/ S gene target late detection (SGTL) profile for this variant agreed very well (k = 0.86). A low virus load was the main cause of discrepancies. Sequencing discordant results with both assays indicated that the TaqPath assay detected the B.1.1.7 lineage slightly better. Both assays suggested that the virus loads of B.1.1.7 variants were significantly higher than those of non-B.1.1.7 strains. Only 10/20 B1.351/P.1 strains detected with the ID triplex assay were confirmed by sequencing. CONCLUSIONS: We conclude that the SGTF/SGTL profiles identified using the TaqPath assay and ID triplex results are suitable for detecting the B.1.1.7 lineage. The ID triplex assay, which rapidly determines all three current VOCs simultaneously, could be a valuable tool for limiting virus spread by supporting contact-tracing and isolation.
format Online
Article
Text
id pubmed-8411575
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier B.V.
record_format MEDLINE/PubMed
spelling pubmed-84115752021-09-03 Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants Migueres, M. Lhomme, S. Trémeaux, P. Dimeglio, C. Ranger, N. Latour, J. Dubois, M. Nicot, F. Miedouge, M. Mansuy, J.M. Izopet, J. J Clin Virol Article BACKGROUND: The recent emergence of new SARS CoV-2 variants (variants of concern, VOC) that spread rapidly and may lead to immune escape has emphasized the urgent need to monitor and control their spread. METHODS: We analyzed 2018 SARS-CoV-2 positive specimens collected between February 9 and March 22, 2021 using the Thermofisher® TaqPath™ COVID-19 CE-IVD RT-PCR kit (TaqPath) and the ID solutions® ID™ SARS-CoV-2/UK/SA Variant Triplex RT-PCR (ID triplex) assay to screen for VOCs. RESULTS: The ID triplex assay identified 62.8% of them as VOCs: 61.8% B.1.1.7 and 0.9% B.1.351/P.1. The agreement between the ID triplex results for B.1.1.7 and the TaqPath S gene target failure (SGTF)/ S gene target late detection (SGTL) profile for this variant agreed very well (k = 0.86). A low virus load was the main cause of discrepancies. Sequencing discordant results with both assays indicated that the TaqPath assay detected the B.1.1.7 lineage slightly better. Both assays suggested that the virus loads of B.1.1.7 variants were significantly higher than those of non-B.1.1.7 strains. Only 10/20 B1.351/P.1 strains detected with the ID triplex assay were confirmed by sequencing. CONCLUSIONS: We conclude that the SGTF/SGTL profiles identified using the TaqPath assay and ID triplex results are suitable for detecting the B.1.1.7 lineage. The ID triplex assay, which rapidly determines all three current VOCs simultaneously, could be a valuable tool for limiting virus spread by supporting contact-tracing and isolation. Elsevier B.V. 2021-10 2021-09-02 /pmc/articles/PMC8411575/ /pubmed/34509927 http://dx.doi.org/10.1016/j.jcv.2021.104969 Text en © 2021 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 Article
Migueres, M.
Lhomme, S.
Trémeaux, P.
Dimeglio, C.
Ranger, N.
Latour, J.
Dubois, M.
Nicot, F.
Miedouge, M.
Mansuy, J.M.
Izopet, J.
Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants
title Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants
title_full Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants
title_fullStr Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants
title_full_unstemmed Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants
title_short Evaluation of two RT-PCR screening assays for identifying SARS-CoV-2 variants
title_sort evaluation of two rt-pcr screening assays for identifying sars-cov-2 variants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411575/
https://www.ncbi.nlm.nih.gov/pubmed/34509927
http://dx.doi.org/10.1016/j.jcv.2021.104969
work_keys_str_mv AT migueresm evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT lhommes evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT tremeauxp evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT dimeglioc evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT rangern evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT latourj evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT duboism evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT nicotf evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT miedougem evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT mansuyjm evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants
AT izopetj evaluationoftwortpcrscreeningassaysforidentifyingsarscov2variants