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Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods

BACKGROUND: Reference materials are essential for the quality assurance of molecular detection methods. We developed and characterized synthetic norovirus GI and GII RNA reference materials. METHODS: Norovirus GI and GII RNA sequences including the ORF1–ORF2 junction region were designed based on 1,...

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Autores principales: Cho, Eun-Jung, Cha, Younggil, Lee, Su Kyung, Kim, Han-Sung, Kim, Jae-Seok, Lee, Eun Jin, Lee, Nuri, Hong, Ki Ho, Huh, Hee Jin, Cha, Young Joo, Kim, Hyun Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Laboratory Medicine 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467847/
https://www.ncbi.nlm.nih.gov/pubmed/36045055
http://dx.doi.org/10.3343/alm.2023.43.1.38
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author Cho, Eun-Jung
Cha, Younggil
Lee, Su Kyung
Kim, Han-Sung
Kim, Jae-Seok
Lee, Eun Jin
Lee, Nuri
Hong, Ki Ho
Huh, Hee Jin
Cha, Young Joo
Kim, Hyun Soo
author_facet Cho, Eun-Jung
Cha, Younggil
Lee, Su Kyung
Kim, Han-Sung
Kim, Jae-Seok
Lee, Eun Jin
Lee, Nuri
Hong, Ki Ho
Huh, Hee Jin
Cha, Young Joo
Kim, Hyun Soo
author_sort Cho, Eun-Jung
collection PubMed
description BACKGROUND: Reference materials are essential for the quality assurance of molecular detection methods. We developed and characterized synthetic norovirus GI and GII RNA reference materials. METHODS: Norovirus GI and GII RNA sequences including the ORF1–ORF2 junction region were designed based on 1,495 reported norovirus sequences and synthesized via plasmid preparation and in vitro transcription. The synthetic norovirus GI and GII RNAs were evaluated using six commercial norovirus detection kits used in Korea and subjected to homogeneity and stability analyses. A multicenter study involving five laboratories and using four commercial real-time PCR norovirus detection assays was conducted for synthetic norovirus RNA characterization and uncertainty measurements. RESULTS: The synthetic norovirus GI and GII RNAs were positively detected using the six commercial norovirus detection kits and were homogeneous and stable for one year when stored at –20°C or –70°C. All data from the five laboratories were within a range of 1.0 log copies/μL difference for each RNA, and the overall mean concentrations for norovirus GI and GII RNAs were 7.90 log copies/μL and 6.96 log copies/μL, respectively. CONCLUSIONS: The synthetic norovirus GI and GII RNAs are adequate for quality control based on commercial molecular detection reagents for noroviruses with high sequence variability. The synthetic RNAs can be used as reference materials in norovirus molecular detection methods.
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spelling pubmed-94678472022-12-26 Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods Cho, Eun-Jung Cha, Younggil Lee, Su Kyung Kim, Han-Sung Kim, Jae-Seok Lee, Eun Jin Lee, Nuri Hong, Ki Ho Huh, Hee Jin Cha, Young Joo Kim, Hyun Soo Ann Lab Med Original Article BACKGROUND: Reference materials are essential for the quality assurance of molecular detection methods. We developed and characterized synthetic norovirus GI and GII RNA reference materials. METHODS: Norovirus GI and GII RNA sequences including the ORF1–ORF2 junction region were designed based on 1,495 reported norovirus sequences and synthesized via plasmid preparation and in vitro transcription. The synthetic norovirus GI and GII RNAs were evaluated using six commercial norovirus detection kits used in Korea and subjected to homogeneity and stability analyses. A multicenter study involving five laboratories and using four commercial real-time PCR norovirus detection assays was conducted for synthetic norovirus RNA characterization and uncertainty measurements. RESULTS: The synthetic norovirus GI and GII RNAs were positively detected using the six commercial norovirus detection kits and were homogeneous and stable for one year when stored at –20°C or –70°C. All data from the five laboratories were within a range of 1.0 log copies/μL difference for each RNA, and the overall mean concentrations for norovirus GI and GII RNAs were 7.90 log copies/μL and 6.96 log copies/μL, respectively. CONCLUSIONS: The synthetic norovirus GI and GII RNAs are adequate for quality control based on commercial molecular detection reagents for noroviruses with high sequence variability. The synthetic RNAs can be used as reference materials in norovirus molecular detection methods. Korean Society for Laboratory Medicine 2023-01-01 2022-09-01 /pmc/articles/PMC9467847/ /pubmed/36045055 http://dx.doi.org/10.3343/alm.2023.43.1.38 Text en © Korean Society for Laboratory Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cho, Eun-Jung
Cha, Younggil
Lee, Su Kyung
Kim, Han-Sung
Kim, Jae-Seok
Lee, Eun Jin
Lee, Nuri
Hong, Ki Ho
Huh, Hee Jin
Cha, Young Joo
Kim, Hyun Soo
Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods
title Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods
title_full Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods
title_fullStr Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods
title_full_unstemmed Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods
title_short Development and Characterization of Synthetic Norovirus RNA for Use in Molecular Detection Methods
title_sort development and characterization of synthetic norovirus rna for use in molecular detection methods
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467847/
https://www.ncbi.nlm.nih.gov/pubmed/36045055
http://dx.doi.org/10.3343/alm.2023.43.1.38
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