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Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing

Nucleic acid tests to detect the SARS-CoV-2 virus have been performed worldwide since the beginning of the COVID-19 pandemic. For the quality assessment of testing laboratories and the performance evaluation of molecular diagnosis products, reference materials (RMs) are required. In this work, we re...

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Autores principales: Lee, Sang-Soo, Kim, Seil, Yoo, Hee Min, Lee, Da-Hye, Bae, Young-Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711077/
https://www.ncbi.nlm.nih.gov/pubmed/34958396
http://dx.doi.org/10.1007/s00216-021-03846-y
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author Lee, Sang-Soo
Kim, Seil
Yoo, Hee Min
Lee, Da-Hye
Bae, Young-Kyung
author_facet Lee, Sang-Soo
Kim, Seil
Yoo, Hee Min
Lee, Da-Hye
Bae, Young-Kyung
author_sort Lee, Sang-Soo
collection PubMed
description Nucleic acid tests to detect the SARS-CoV-2 virus have been performed worldwide since the beginning of the COVID-19 pandemic. For the quality assessment of testing laboratories and the performance evaluation of molecular diagnosis products, reference materials (RMs) are required. In this work, we report the production of a lentiviral SARS-CoV-2 RM containing approximately 12 kilobases of its genome including common diagnostics targets such as RdRp, N, E, and S genes. The RM was measured with multiple assays using two different digital PCR platforms. To measure the homogeneity and stability of the lentiviral SARS-CoV-2 RM, reverse transcription droplet digital PCR (RT-ddPCR) was used with in-house duplex assays. The copy number concentration of each target gene in the extracted RNA solution was then converted to that of the RM solution. Their copy number values are measured to be from 1.5 × 10(5) to 2.0 × 10(5) copies/mL. The RM has a between-bottle homogeneity of 4.80–8.23% and is stable at 4 °C for 1 week and at −70 °C for 6 months. The lentiviral SARS-CoV-2 RM closely mimics real samples that undergo identical pre-analytical processes for SARS-CoV-2 molecular testing. By offering accurate reference values for the absolute copy number of viral target genes, the developed RM can be used to improve the reliability of SARS-CoV-2 molecular testing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-021-03846-y.
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spelling pubmed-87110772021-12-27 Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing Lee, Sang-Soo Kim, Seil Yoo, Hee Min Lee, Da-Hye Bae, Young-Kyung Anal Bioanal Chem Paper in Forefront Nucleic acid tests to detect the SARS-CoV-2 virus have been performed worldwide since the beginning of the COVID-19 pandemic. For the quality assessment of testing laboratories and the performance evaluation of molecular diagnosis products, reference materials (RMs) are required. In this work, we report the production of a lentiviral SARS-CoV-2 RM containing approximately 12 kilobases of its genome including common diagnostics targets such as RdRp, N, E, and S genes. The RM was measured with multiple assays using two different digital PCR platforms. To measure the homogeneity and stability of the lentiviral SARS-CoV-2 RM, reverse transcription droplet digital PCR (RT-ddPCR) was used with in-house duplex assays. The copy number concentration of each target gene in the extracted RNA solution was then converted to that of the RM solution. Their copy number values are measured to be from 1.5 × 10(5) to 2.0 × 10(5) copies/mL. The RM has a between-bottle homogeneity of 4.80–8.23% and is stable at 4 °C for 1 week and at −70 °C for 6 months. The lentiviral SARS-CoV-2 RM closely mimics real samples that undergo identical pre-analytical processes for SARS-CoV-2 molecular testing. By offering accurate reference values for the absolute copy number of viral target genes, the developed RM can be used to improve the reliability of SARS-CoV-2 molecular testing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-021-03846-y. Springer Berlin Heidelberg 2021-12-27 2022 /pmc/articles/PMC8711077/ /pubmed/34958396 http://dx.doi.org/10.1007/s00216-021-03846-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Paper in Forefront
Lee, Sang-Soo
Kim, Seil
Yoo, Hee Min
Lee, Da-Hye
Bae, Young-Kyung
Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing
title Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing
title_full Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing
title_fullStr Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing
title_full_unstemmed Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing
title_short Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing
title_sort development of sars-cov-2 packaged rna reference material for nucleic acid testing
topic Paper in Forefront
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711077/
https://www.ncbi.nlm.nih.gov/pubmed/34958396
http://dx.doi.org/10.1007/s00216-021-03846-y
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