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Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2

BACKGROUND: We aimed to evaluate the analytical performance of five commercial RT‐PCR kits (Genekey, Daan, BioGerm, Liferiver, and Yaneng) commonly used in China, since such comparison data are lacking. METHODS: A total of 20 COVID‐19 confirmed patients and 30 negative nasopharyngeal swab specimens...

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Autores principales: Wang, Mengmeng, Chen, Dayang, Wu, Wei, Tang, Huamei, Kan, Lijuan, Zong, Zengyan, Dou, Xiaowen, Ji, Xiang, Xiong, Dan, Zhang, Xiuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645906/
https://www.ncbi.nlm.nih.gov/pubmed/33107116
http://dx.doi.org/10.1002/jcla.23643
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author Wang, Mengmeng
Chen, Dayang
Wu, Wei
Tang, Huamei
Kan, Lijuan
Zong, Zengyan
Dou, Xiaowen
Ji, Xiang
Xiong, Dan
Zhang, Xiuming
author_facet Wang, Mengmeng
Chen, Dayang
Wu, Wei
Tang, Huamei
Kan, Lijuan
Zong, Zengyan
Dou, Xiaowen
Ji, Xiang
Xiong, Dan
Zhang, Xiuming
author_sort Wang, Mengmeng
collection PubMed
description BACKGROUND: We aimed to evaluate the analytical performance of five commercial RT‐PCR kits (Genekey, Daan, BioGerm, Liferiver, and Yaneng) commonly used in China, since such comparison data are lacking. METHODS: A total of 20 COVID‐19 confirmed patients and 30 negative nasopharyngeal swab specimens were analyzed by five kits. The detection ability of five RT‐PCR kits was evaluated with 5 concentration gradients diluted by a single positive sample. The limit of detection was evaluated by N gene fragment solid standard. Two positive clinical specimens were used to evaluate the repeatability and imprecision. Finally, we used six human coronaviruses plasmid and four respiratory pathogens plasmid to check for cross‐reactivity. RESULTS: The positive detection rate was 100% for Genekey, Daan, and BioGerm,and 90% for Liferiver and Yaneng in 20 clinical SARS‐CoV‐2 infection. The coincidence rate of five kits in 10 negative samples was 100%. The detection rate of target genes for Daan, BioGerm, Liferiver, and Yaneng was 100% from Level 1 to Level 3. In Level 4, only Daan detection rate was 100%. In Level 5, five kits presented poor positive rate. The limit of detection declared by each manufacturer was verified. The repeatability for target genes was less than 5% and so did the total imprecision. There is no cross‐reactivity of five kits with six human coronaviruses and four respiratory pathogens for ORF1ab and N gene. CONCLUSIONS: Five RT‐PCR kits assessed in this study showed acceptable analytical performance characteristics and are useful tools for the routine diagnosis of SARS‐CoV‐2.
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spelling pubmed-76459062020-11-06 Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2 Wang, Mengmeng Chen, Dayang Wu, Wei Tang, Huamei Kan, Lijuan Zong, Zengyan Dou, Xiaowen Ji, Xiang Xiong, Dan Zhang, Xiuming J Clin Lab Anal Research Articles BACKGROUND: We aimed to evaluate the analytical performance of five commercial RT‐PCR kits (Genekey, Daan, BioGerm, Liferiver, and Yaneng) commonly used in China, since such comparison data are lacking. METHODS: A total of 20 COVID‐19 confirmed patients and 30 negative nasopharyngeal swab specimens were analyzed by five kits. The detection ability of five RT‐PCR kits was evaluated with 5 concentration gradients diluted by a single positive sample. The limit of detection was evaluated by N gene fragment solid standard. Two positive clinical specimens were used to evaluate the repeatability and imprecision. Finally, we used six human coronaviruses plasmid and four respiratory pathogens plasmid to check for cross‐reactivity. RESULTS: The positive detection rate was 100% for Genekey, Daan, and BioGerm,and 90% for Liferiver and Yaneng in 20 clinical SARS‐CoV‐2 infection. The coincidence rate of five kits in 10 negative samples was 100%. The detection rate of target genes for Daan, BioGerm, Liferiver, and Yaneng was 100% from Level 1 to Level 3. In Level 4, only Daan detection rate was 100%. In Level 5, five kits presented poor positive rate. The limit of detection declared by each manufacturer was verified. The repeatability for target genes was less than 5% and so did the total imprecision. There is no cross‐reactivity of five kits with six human coronaviruses and four respiratory pathogens for ORF1ab and N gene. CONCLUSIONS: Five RT‐PCR kits assessed in this study showed acceptable analytical performance characteristics and are useful tools for the routine diagnosis of SARS‐CoV‐2. John Wiley and Sons Inc. 2020-10-27 /pmc/articles/PMC7645906/ /pubmed/33107116 http://dx.doi.org/10.1002/jcla.23643 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Wang, Mengmeng
Chen, Dayang
Wu, Wei
Tang, Huamei
Kan, Lijuan
Zong, Zengyan
Dou, Xiaowen
Ji, Xiang
Xiong, Dan
Zhang, Xiuming
Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2
title Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2
title_full Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2
title_fullStr Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2
title_full_unstemmed Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2
title_short Analytical performance evaluation of five RT‐PCR kits for severe acute respiratory syndrome coronavirus 2
title_sort analytical performance evaluation of five rt‐pcr kits for severe acute respiratory syndrome coronavirus 2
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645906/
https://www.ncbi.nlm.nih.gov/pubmed/33107116
http://dx.doi.org/10.1002/jcla.23643
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