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Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays

BACKGROUND: Genomic surveillance efforts for SARS-CoV-2 are needed to understand the epidemiology of the COVID-19 pandemic. Viral variants may impact routine diagnostic testing, increase viral transmissibility, cause differences in disease severity, have decreased susceptibility to therapeutics, and...

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Autores principales: Borillo, Gwynngelle A., Kagan, Ron M., Marlowe, Elizabeth M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127862/
https://www.ncbi.nlm.nih.gov/pubmed/35619652
http://dx.doi.org/10.3389/fcimb.2022.894613
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author Borillo, Gwynngelle A.
Kagan, Ron M.
Marlowe, Elizabeth M.
author_facet Borillo, Gwynngelle A.
Kagan, Ron M.
Marlowe, Elizabeth M.
author_sort Borillo, Gwynngelle A.
collection PubMed
description BACKGROUND: Genomic surveillance efforts for SARS-CoV-2 are needed to understand the epidemiology of the COVID-19 pandemic. Viral variants may impact routine diagnostic testing, increase viral transmissibility, cause differences in disease severity, have decreased susceptibility to therapeutics, and/or confer the ability to evade host immunity. While viral whole-genome sequencing (WGS) has played a leading role in surveillance programs, many laboratories lack the expertise and resources for performing WGS. This study describes the performance of multiplexed real-time reverse transcription-PCR (RT-PCR) assays for identification of SARS-CoV-2 variants. METHODS: SARS-CoV-2 specimens were tested for spike-gene variants using a combination of allele-specific primer and allele-specific detection technology (PlexPrime(®) and PlexZyme(®)). Targeted detection of spike gene mutations by RT-PCR was compared to variant detection in positive specimens by WGS, including the recently emerged SARS-CoV-2 Omicron variant. RESULTS: A total of 398 SAR-CoV-2 RT-PCR positive and 39 negative specimens previously tested by WGS were re-tested by RT-PCR genotyping. PCR detection of spike gene mutations N501Y, E484K, and S982A correlated 100% with WGS for the 29 lineages represented, including Alpha (B.1.1.7), Beta (B.1.351), and Gamma (P.1). Incorporating the P681R spike gene mutation also allowed screening for the SARS-CoV-2 Delta variant (B.1.617.2 and AY sublineages). Further sampling of 664 specimens that were screened by WGS between June and August 2021 and then re-tested by RT-PCR showed strong agreement for Delta variant positivity: 34.5% for WGS vs 32.9% for RT-PCR in June; 100% vs 97.8% in August. In a blinded panel of 16 Omicron and 16 Delta specimens, results of RT-PCR were 100% concordant with WGS results. CONCLUSIONS: These data demonstrate that multiplexed real-time RT-PCR genotyping has strong agreement with WGS and may provide additional SARS-CoV-2 variant screening capabilities when WGS is unavailable or cost-prohibitive. RT-PCR genotyping assays may also supplement existing sequencing efforts while providing rapid results at or near the time of diagnosis to help guide patient management.
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spelling pubmed-91278622022-05-25 Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays Borillo, Gwynngelle A. Kagan, Ron M. Marlowe, Elizabeth M. Front Cell Infect Microbiol Cellular and Infection Microbiology BACKGROUND: Genomic surveillance efforts for SARS-CoV-2 are needed to understand the epidemiology of the COVID-19 pandemic. Viral variants may impact routine diagnostic testing, increase viral transmissibility, cause differences in disease severity, have decreased susceptibility to therapeutics, and/or confer the ability to evade host immunity. While viral whole-genome sequencing (WGS) has played a leading role in surveillance programs, many laboratories lack the expertise and resources for performing WGS. This study describes the performance of multiplexed real-time reverse transcription-PCR (RT-PCR) assays for identification of SARS-CoV-2 variants. METHODS: SARS-CoV-2 specimens were tested for spike-gene variants using a combination of allele-specific primer and allele-specific detection technology (PlexPrime(®) and PlexZyme(®)). Targeted detection of spike gene mutations by RT-PCR was compared to variant detection in positive specimens by WGS, including the recently emerged SARS-CoV-2 Omicron variant. RESULTS: A total of 398 SAR-CoV-2 RT-PCR positive and 39 negative specimens previously tested by WGS were re-tested by RT-PCR genotyping. PCR detection of spike gene mutations N501Y, E484K, and S982A correlated 100% with WGS for the 29 lineages represented, including Alpha (B.1.1.7), Beta (B.1.351), and Gamma (P.1). Incorporating the P681R spike gene mutation also allowed screening for the SARS-CoV-2 Delta variant (B.1.617.2 and AY sublineages). Further sampling of 664 specimens that were screened by WGS between June and August 2021 and then re-tested by RT-PCR showed strong agreement for Delta variant positivity: 34.5% for WGS vs 32.9% for RT-PCR in June; 100% vs 97.8% in August. In a blinded panel of 16 Omicron and 16 Delta specimens, results of RT-PCR were 100% concordant with WGS results. CONCLUSIONS: These data demonstrate that multiplexed real-time RT-PCR genotyping has strong agreement with WGS and may provide additional SARS-CoV-2 variant screening capabilities when WGS is unavailable or cost-prohibitive. RT-PCR genotyping assays may also supplement existing sequencing efforts while providing rapid results at or near the time of diagnosis to help guide patient management. Frontiers Media S.A. 2022-05-10 /pmc/articles/PMC9127862/ /pubmed/35619652 http://dx.doi.org/10.3389/fcimb.2022.894613 Text en Copyright © 2022 Borillo, Kagan and Marlowe https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Borillo, Gwynngelle A.
Kagan, Ron M.
Marlowe, Elizabeth M.
Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays
title Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays
title_full Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays
title_fullStr Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays
title_full_unstemmed Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays
title_short Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays
title_sort rapid and accurate identification of sars-cov-2 variants using real time pcr assays
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127862/
https://www.ncbi.nlm.nih.gov/pubmed/35619652
http://dx.doi.org/10.3389/fcimb.2022.894613
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