病毒学
核糖核酸
冠状病毒
病毒
核酸
生物
聚合酶链反应
逆转录聚合酶链式反应
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
噬菌体MS2
RNA提取
大流行
RNA病毒
2019年冠状病毒病(COVID-19)
外壳蛋白
基因
信使核糖核酸
疾病
传染病(医学专业)
医学
遗传学
病理
作者
Soo Khim Chan,Pinyi Du,Caroline Ignacio,Sanjay R. Mehta,Isabel G. Newton,Nicole F. Steinmetz
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-11-25
卷期号:15 (1): 1259-1272
被引量:54
标识
DOI:10.1021/acsnano.0c08430
摘要
Coronavirus disease 2019 (COVID-19) is a highly transmissible disease that has affected more than 90% of the countries worldwide. At least 17 million individuals have been infected, and some countries are still battling first or second waves of the pandemic. Nucleic acid tests, especially reverse transcription polymerase chain reaction (RT-PCR), have become the workhorse for early detection of COVID-19 infection. Positive controls for the molecular assays have been developed to validate each test and to provide high accuracy. However, most available positive controls require cold-chain distribution and cannot serve as full-process control. To overcome these shortcomings, we report the production of biomimetic virus-like particles (VLPs) as SARS-CoV-2 positive controls. A SARS-CoV-2 detection module for RT-PCR was encapsidated into VLPs from a bacteriophage and a plant virus. The chimeric VLPs were obtained either by in vivo reconstitution and coexpression of the target detection module and coat proteins or by in vitro assembly of purified detection module RNA sequences and coat proteins. These VLP-based positive controls mimic SARS-CoV-2 packaged ribonucleic acid (RNA) while being noninfectious. Most importantly, we demonstrated that the positive controls are scalable, stable, and can serve broadly as controls, from RNA extraction to PCR in clinical settings.
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