Department of Biochemistry and Metabolism, John Innes Centre, Norwich Research Park, Colney, NR4 7UH, UK.
Institute for Infection and Immunity, St. George's University of London, Cranmer Terrace, Tooting, London, SW17 0RE, UK.
J Virol Methods. 2022 Feb;300:114372. doi: 10.1016/j.jviromet.2021.114372. Epub 2021 Nov 24.
The current gold standard technique for SARS-CoV-2 diagnostics is hydrolysis probe-based RT-qPCR. Reliable testing requires reliable control reagents to monitor the efficiency of RNA extraction, reverse transcription and PCR amplification. Here we describe a custom RNA packaging system from the plant virus cowpea mosaic virus to produce virus-like particles that encapsidate specifically designed portions of the genome of SARS-CoV-2, the causative agent of COVID-19. These encapsidated mimics are highly stable particles which can be used either to spike patient swab samples for use as an in-tube extraction and reaction positive control in multiplex RT-qPCR, or alone as a side-by-side mock-positive control reagent. The selection of sequences in the packaged pseudogenomes ensures that these mimics are compatible with the most commonly used primer/probe combinations for SARS-CoV-2 diagnostics (including German Berlin Charité Hospital, American CDC, and Chinese CDC protocols). The plant transient expression system used to produce these encapsidated mimics is inherently low-cost, and sufficiently high-yielding that a single laboratory-scale preparation can provide enough positive control reagent for millions of tests.
目前用于 SARS-CoV-2 诊断的金标准技术是基于水解探针的 RT-qPCR。可靠的检测需要可靠的对照试剂来监测 RNA 提取、逆转录和 PCR 扩增的效率。在这里,我们描述了一种来自植物病毒豇豆花叶病毒的定制 RNA 包装系统,该系统可产生病毒样颗粒,这些颗粒可包裹 SARS-CoV-2(COVID-19 的致病因子)基因组的特定设计部分。这些包裹的模拟物是高度稳定的颗粒,可用于 spike 患者拭子样本,作为多重 RT-qPCR 中的管内提取和反应阳性对照,或单独用作侧面对照阳性对照试剂。包装假基因组中序列的选择确保了这些模拟物与最常用于 SARS-CoV-2 诊断的引物/探针组合兼容(包括德国柏林 Charité 医院、美国 CDC 和中国 CDC 方案)。用于生产这些包裹模拟物的植物瞬时表达系统成本低,产量高,单个实验室规模的制备就可以提供足够的阳性对照试剂用于数百万次检测。