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Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples

The COVID-19 pandemic requires sensitive detection of the SARS-CoV-2 virus from samples to ensure accurate detection of infected patients, an essential component of effective national track and trace programs. Due to the scaling challenges of large sample numbers, sample pooling is an attractive sol...

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Autores principales: Jayakody, Harindi, Rowland, Daniel, Pereira, Clint, Blackwell, Rachel, Lasota, Tomasz, Laverick, Mark, Tisi, Laurence, Leese, Hannah S., Walsham, Alistair D. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965539/
https://www.ncbi.nlm.nih.gov/pubmed/35354857
http://dx.doi.org/10.1038/s41598-022-09254-1
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author Jayakody, Harindi
Rowland, Daniel
Pereira, Clint
Blackwell, Rachel
Lasota, Tomasz
Laverick, Mark
Tisi, Laurence
Leese, Hannah S.
Walsham, Alistair D. S.
author_facet Jayakody, Harindi
Rowland, Daniel
Pereira, Clint
Blackwell, Rachel
Lasota, Tomasz
Laverick, Mark
Tisi, Laurence
Leese, Hannah S.
Walsham, Alistair D. S.
author_sort Jayakody, Harindi
collection PubMed
description The COVID-19 pandemic requires sensitive detection of the SARS-CoV-2 virus from samples to ensure accurate detection of infected patients, an essential component of effective national track and trace programs. Due to the scaling challenges of large sample numbers, sample pooling is an attractive solution to reduce both extraction and amplification reagent costs, if high sensitivity can be maintained. We demonstrate that the Erba Molecular ErbaMDx SARS-CoV-2 RT-PCR Kit (EM kit) delivers high sensitivity, achieving analytical detection of 5 copies/reaction SARS-CoV-2 genomic RNA, and 200 copies/mL SARS-CoV-2 inactivated virus spiked into nasopharyngeal swab (NP) samples and extracted through workflow. Furthermore, the EM Kit demonstrates high sensitivity in both pooled (1 in 5) and non-pooled NP samples when compared to an FDA Emergency Use Authorization approved assay, following published FDA guidelines. These findings demonstrate that the EM Kit is suitable for sample pooling, with minimal impact on assay performance. As the COVID-19 pandemic progresses, high sensitivity assays such as the EM Kit will have an important role in ensuring high throughput and sensitive testing using pooled samples can be maintained, delivering the most cost-effective sample extraction and amplification option for national test and trace programs.
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spelling pubmed-89655392022-03-30 Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples Jayakody, Harindi Rowland, Daniel Pereira, Clint Blackwell, Rachel Lasota, Tomasz Laverick, Mark Tisi, Laurence Leese, Hannah S. Walsham, Alistair D. S. Sci Rep Article The COVID-19 pandemic requires sensitive detection of the SARS-CoV-2 virus from samples to ensure accurate detection of infected patients, an essential component of effective national track and trace programs. Due to the scaling challenges of large sample numbers, sample pooling is an attractive solution to reduce both extraction and amplification reagent costs, if high sensitivity can be maintained. We demonstrate that the Erba Molecular ErbaMDx SARS-CoV-2 RT-PCR Kit (EM kit) delivers high sensitivity, achieving analytical detection of 5 copies/reaction SARS-CoV-2 genomic RNA, and 200 copies/mL SARS-CoV-2 inactivated virus spiked into nasopharyngeal swab (NP) samples and extracted through workflow. Furthermore, the EM Kit demonstrates high sensitivity in both pooled (1 in 5) and non-pooled NP samples when compared to an FDA Emergency Use Authorization approved assay, following published FDA guidelines. These findings demonstrate that the EM Kit is suitable for sample pooling, with minimal impact on assay performance. As the COVID-19 pandemic progresses, high sensitivity assays such as the EM Kit will have an important role in ensuring high throughput and sensitive testing using pooled samples can be maintained, delivering the most cost-effective sample extraction and amplification option for national test and trace programs. Nature Publishing Group UK 2022-03-30 /pmc/articles/PMC8965539/ /pubmed/35354857 http://dx.doi.org/10.1038/s41598-022-09254-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jayakody, Harindi
Rowland, Daniel
Pereira, Clint
Blackwell, Rachel
Lasota, Tomasz
Laverick, Mark
Tisi, Laurence
Leese, Hannah S.
Walsham, Alistair D. S.
Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples
title Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples
title_full Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples
title_fullStr Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples
title_full_unstemmed Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples
title_short Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples
title_sort development of a high sensitivity rt-pcr assay for detection of sars-cov-2 in individual and pooled nasopharyngeal samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965539/
https://www.ncbi.nlm.nih.gov/pubmed/35354857
http://dx.doi.org/10.1038/s41598-022-09254-1
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