Perspective on SARS-CoV-2 Detection and Reference Materials

ZHAO Yujia; LIAO Tianyi; FAN Peilei; LIANG Liang; ZHAO Haibo; SHEN Zhengsheng

doi:10.12338/j.issn.2096-9015.2020.0375

Volume 66 Issue 1

Jan. 2022

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Article Navigation > Metrology Science and Technology > 2022 > 66(1): 3-8

ZHAO Yujia, LIAO Tianyi, FAN Peilei, LIANG Liang, ZHAO Haibo, SHEN Zhengsheng. Perspective on SARS-CoV-2 Detection and Reference Materials[J]. Metrology Science and Technology, 2022, 66(1): 3-8. doi: 10.12338/j.issn.2096-9015.2020.0375

Citation:

ZHAO Yujia, LIAO Tianyi, FAN Peilei, LIANG Liang, ZHAO Haibo, SHEN Zhengsheng. Perspective on SARS-CoV-2 Detection and Reference Materials[J]. Metrology Science and Technology, 2022, 66(1): 3-8. doi: 10.12338/j.issn.2096-9015.2020.0375

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Perspective on SARS-CoV-2 Detection and Reference Materials

doi: 10.12338/j.issn.2096-9015.2020.0375

1.
Beijing Institute of Metrology, Beijing 10029, China
2.
Pharmacy College, Tsinghua University, Beijing 100084, China
3.
Science College, Paris University, Paris 75006, France

Available Online: 2021-11-19
Publish Date: 2022-01-24

Abstract

Abstract

The novel coronavirus (SARS-CoV-2) has a strong ability to infect, which has caused the pandemic. It has seriously affected human health and life, social economy and development. Fast and accurate detection of the novel coronavirus is particularly important for the diagnosis, prevention, and control of the epidemic. Chinese CFDA has registered 22 nucleic acid detection kits, which can meet the needs of high-risk groups for large-scale screening and effectively guarantee the prevention and control of the epidemic. Meanwhile, the novel coronavirus reference material, as a measurement reference, developed by the National Institute of Metrology, China further guarantees the accuracy and traceability of test results. This article analyzes the data published by the State Food and Drug Administration and the National Standard Material Sharing Platform, and combines relevant domestic and international research results to systematically review the novel coronavirus detection methods, test kits and reference materials, hoping to shed light on diagnosis, prevention and control of the novel coronavirus and other infectious diseases.
- metrology,
- novel coronavirus,
- in vitro diagnosis,
- nucleic acid detection,
- reference materials

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References(24)

References

[1]	Zhou P, Yang X L, Wang X G, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin[J]. Nature, 2020, 579(7798): 270-273. doi: 10.1038/s41586-020-2012-7
[2]	Kannan S, Ali P S S, Sheeza A, et al. COVID-19 (Novel Coronavirus 2019)-recent trends[J]. European Review for Medical and Pharmacological Sciences, 2020, 24: 2006-2011.
[3]	Mustafa H, Kili S, Sara F. Coronaviruses and SARS-CoV-2[J]. Turkish Journal of Medical ences, 2020, 50: 1.
[4]	Watson J D, Crick F H. Molecular structure of nucleic acids: a structure for deoxyribose nucleic acid[J]. Nature, 1974, 248(5451): 765. doi: 10.1038/248765a0
[5]	Ciotti M, Angeletti S, Minieri M, et al. COVID-19 Outbreak: An Overview[J]. Chemotherapy, 2020, 64(5-6): 1-9.
[6]	Pai-dhungat J. Kary mullis-inventor of PCR[J]. J. Assoc. Physicians. India., 2019, 67(9): 96.
[7]	Kazuyuki M. PCR-based detection methods for single-nucleotide polymorphism or mutation: real-time pcr and its substantial contribution toward technological refinement[J]. Adv. Clin. Chem. 2017, 80: 45-72.
[8]	Beata K, Józef K, Karolina S, et al. Principles and applications of ligation mediated pcr methods for dna-based typing of microbial organisms[J]. Acta. Biochim. Pol. 2016, 63(1): 39-52.
[9]	Dahiya B, Mehta P K. Detection of potential biomarkers associated with outrageous diseases and environmental pollutants by nanoparticle-based immuno-PCR assays[J]. Anal. Biochem., 2019, 587: 113444. doi: 10.1016/j.ab.2019.113444
[10]	Kakizawa S. A multiplex-pcr method for diagnosis of ay-group phytoplasmas[J]. Methods Mol. Biol, 2019, 1875: 143-149.
[11]	Rajesh K, Sinha R P. Real-time immuno-PCR: an approach for detection of trace amounts of transgenic proteins[J]. Journal of Aoac Internationalm, 2014, 97(6): 1634-1637. doi: 10.5740/jaoacint.14-044
[12]	Nemeth A, Wurz A, Artim L, et al. Sensitive PCR analysis of animal tissue samples for fragments of endogenous and transgenic plant DNA[J]. Journal of Agricultural & Food Chemistry, 2004, 52(20): 6129.
[13]	Ehnert S, Linnemann C, Braun B, et al. One-step arms-pcr for the detection of snps-using the example of the padi4 gene[J]. Methods Protoc, 2019, 2(3): 63. doi: 10.3390/mps2030063
[14]	Romsos E L, Vallone P M. Rapid pcr of str markers: applications to human identification[J]. Forensic. Sci. Int. Genet, 2015, 18: 90-99. doi: 10.1016/j.fsigen.2015.04.008
[15]	张永卓, 王晶, 傅博强, 等. 2019新型冠状病毒的核酸检测[J]. 计量学报, 2020, 41(4): 393-398. doi: 10.3969/j.issn.1000-1158.2020.04.01
[16]	Wong Y P, Othman S, Lau Y L, et al. Loop-mediated isothermal amplification (LAMP): a versatile technique for detection of micro-organisms[J]. Journal of Applied Microbiology, 2018, 124(3): 626-643. doi: 10.1111/jam.13647
[17]	Notomi T, Okayama H, Masubuchi H, et al. Loop-mediated isothermal amplification of DNA[J]. Nucleic acid Res, 2000, 28(12): E63. doi: 10.1093/nar/28.12.e63
[18]	Mori Y, Nagamine K, Tomita N, et al. Detection of loop-mediated isothermal amplification reaction by turbidity derived from magnesium pyrophosphate formation[J]. Biochem Biophys Res Commun, 2001, 289(1): 150-154. doi: 10.1006/bbrc.2001.5921
[19]	Blomstrom A L, Hakhverdyan M, Reid S M, et al. A one-step reverse transcriptase loop-mediated isothermal amplification assay for simple and rapid detection of swine vesicular disease virus[J]. J Virol Methods, 2008, 147(1): 188-193. doi: 10.1016/j.jviromet.2007.08.023
[20]	Poon L L, Leung C S, Tashiro M, et al. Rapid detection of the severe acute respiratory syndrome (SARS) coronavirus by a loop-mediated isothermal amplification assay[J]. Clin Chem, 2004, 50(6): 1050-1052. doi: 10.1373/clinchem.2004.032011
[21]	Shiro F, Mizukami Y, Ishida A, et al. Real-time loop-mediated isothermal amplification for the CaMV-35S promoter as a screening method for genetically modified organisms[J]. Eur Food Res Technol, 2004, 218: 496-500. doi: 10.1007/s00217-003-0862-5
[22]	Alhassan A, Li Z, Poole C B, et al. Expanding the MDx toolbox for filarial diagnosis and surveillance[J]. Trends in Parasitology, 2015, 31(8): 391-400. doi: 10.1016/j.pt.2015.04.006
[23]	Yu L, Wu S, Hao X, et al. Rapid colorimetric detection of COVID-19 coronavirus using a reverse tran-scriptional loop-mediated isothermal amplification (RT-LAMP) diagnostic plat-form: iLACO[J]. medRxiv, 2020: 2020.02. 20.20025874.
[24]	Laura E L, Sarah N B, Elijah W, et al. Rapid detection of novel coronavirus/Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) by reverse transcription loop mediated isothermal amplification[J]. PLoS One. 2020, 15(6): e023468.