Evidence map›Paper›PMID 36045055›Full record

ArticleAnnals of laboratory medicine2023

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

Eun-Jung Cho, Younggil Cha, Su Kyung Lee, Han-Sung Kim, Jae-Seok Kim, Eun Jin Lee, Nuri Lee, Ki Ho Hong, Hee Jin Huh, Young Joo Cha and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of laboratory medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Eun-Jung ChoDepartment of Laboratory Medicine, Hallym University College of Medicine, Chuncheon, Korea.ORCID 0000-0003-1907-9639
Younggil ChaMolecular Diagnostic R&D Center, Bioneer, Daejeon, Korea.ORCID 0000-0003-2671-9059
Su Kyung LeeDepartment of Laboratory Medicine, Hallym University College of Medicine, Chuncheon, Korea.ORCID 0000-0002-2536-413X
Han-Sung KimDepartment of Laboratory Medicine, Hallym University College of Medicine, Chuncheon, Korea.ORCID 0000-0002-5481-5390
Jae-Seok KimDepartment of Laboratory Medicine, Hallym University College of Medicine, Chuncheon, Korea.ORCID 0000-0001-6025-0341
Eun Jin LeeDepartment of Laboratory Medicine, Veterans Health Service Medical Center, Seoul, Korea.ORCID 0000-0002-4011-2782
Nuri LeeDepartment of Laboratory Medicine, Hallym University College of Medicine, Chuncheon, Korea.ORCID 0000-0001-7727-8279
Ki Ho HongDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0002-5700-9036
Hee Jin HuhDepartment of Laboratory Medicine, Dongguk University Ilsan Hospital, Ilsan, Korea.ORCID 0000-0001-6587-8568
Young Joo ChaCorporate R&D Center for Biological Standards and Control, Resources and Innovation Cooperative, Hanam, Korea.ORCID 0000-0001-7828-8401
Hyun Soo KimDepartment of Laboratory Medicine, Hallym University College of Medicine, Chuncheon, Korea.ORCID 0000-0002-7026-6715

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 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.

Indexed as

Caliciviridae InfectionsNorovirusGenotypeHumansReal-Time Polymerase Chain ReactionRepublic of KoreaRNA, ViralRNA, ViralCharacterizationMulticenter studyNorovirusesReference materialRNAUncertainty

Identifiers

PMID36045055
PMCPMC9467847

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