Vaccine and Infectious Disease Organization, University of Saskatchewangrid.25152.31, Saskatoon, Saskatchewan, Canada.
Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewangrid.25152.31, Saskatoon, Saskatchewan, Canada.
J Virol. 2021 Aug 25;95(18):e0068721. doi: 10.1128/JVI.00687-21.
The emerging coronavirus disease 2019 (COVID-19) outbreak caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has rapidly spread worldwide, resulting in global public health emergencies and economic crises. In the present study, a noninfectious and biosafety level 2 (BSL2)-compatible SARS-CoV-2 replicon expressing a nano luciferase (nLuc) reporter was constructed in a bacterial artificial chromosomal (BAC) vector by reverse genetics. The nLuc reporter is highly sensitive, easily quantifiable, and high throughput adaptable. Upon transfecting the SARS-CoV-2 replicon BAC plasmid DNA into Vero E6 cells, we could detect high levels of nLuc reporter activity and viral RNA transcript, suggesting the replication of the replicon. The replicon replication was further demonstrated by the findings that deleting nonstructural protein 15 or mutating its catalytic sites significantly reduced replicon replication, whereas providing the nucleocapsid protein in enhanced replicon replication in a dose-dependent manner. Finally, we showed that remdesivir, a U.S. Food and Drug Administration-approved antiviral drug, significantly inhibited the replication of the replicon, providing proof of principle for the application of our replicon as a useful tool for developing antivirals. Taken together, this study established a sensitive and BSL2-compatible reporter system in a single BAC plasmid for investigating the functions of SARS-CoV-2 proteins in viral replication and evaluating antiviral compounds. This should contribute to the global effort to combat this deadly viral pathogen. The COVID-19 pandemic caused by SARS-CoV-2 is having a catastrophic impact on human lives. Combatting the pandemic requires effective vaccines and antiviral drugs. In the present study, we developed a SARS-CoV-2 replicon system with a sensitive and easily quantifiable reporter. Unlike studies involving infectious SARS-CoV-2 virus that must be performed in a biosafety level 3 (BSL3) facility, the replicon is noninfectious and thus can be safely used in BSL2 laboratories. The replicon will provide a valuable tool for testing antiviral drugs and studying SARS-CoV-2 biology.
新型冠状病毒病 2019(COVID-19)疫情是由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的,已迅速在全球范围内蔓延,导致全球公共卫生紧急情况和经济危机。在本研究中,通过反向遗传学在细菌人工染色体(BAC)载体中构建了表达纳米荧光素酶(nLuc)报告基因的非感染性和生物安全级别 2(BSL2)兼容的 SARS-CoV-2 复制子。nLuc 报告基因高度敏感,易于定量,并且可以高通量适应。将 SARS-CoV-2 复制子 BAC 质粒 DNA 转染到 Vero E6 细胞中后,我们可以检测到高水平的 nLuc 报告基因活性和病毒 RNA 转录,表明复制子的复制。通过发现删除非结构蛋白 15 或使其催化位点突变可显著降低复制子的复制,而以剂量依赖的方式提供核衣壳蛋白则可增强复制子的复制,进一步证明了复制子的复制。最后,我们表明,瑞德西韦是一种获得美国食品和药物管理局批准的抗病毒药物,可显著抑制复制子的复制,为应用我们的复制子作为开发抗病毒药物的有用工具提供了原理证明。综上所述,本研究在单个 BAC 质粒中建立了一种敏感且符合 BSL2 标准的报告系统,用于研究 SARS-CoV-2 蛋白在病毒复制中的功能,并评估抗病毒化合物。这将有助于全球抗击这种致命病毒病原体的努力。由 SARS-CoV-2 引起的 COVID-19 大流行对人类生命造成了灾难性的影响。抗击大流行需要有效的疫苗和抗病毒药物。在本研究中,我们开发了一种具有敏感且易于定量的报告基因的 SARS-CoV-2 复制子系统。与涉及必须在生物安全级别 3(BSL3)设施中进行的传染性 SARS-CoV-2 病毒的研究不同,该复制子是非传染性的,因此可以在 BSL2 实验室中安全使用。该复制子将为测试抗病毒药物和研究 SARS-CoV-2 生物学提供有价值的工具。