{"title":"In vitro Antiviral Activity of Remdesivir Against SARS-CoV-2 and its Variants","authors":"A. Nowakowska, Hanul Choi, Kihoon Park, Jinha Kim, Y. Jang, J. Chu, Y. B. Kim, H. Lee","doi":"10.4167/jbv.2022.52.4.149","DOIUrl":null,"url":null,"abstract":"The outbreak of COVID-19 has become a public health emergency of international concern;thus, it is important to not only develop drugs for treating COVID-19 but also develop a method for evaluating the therapeutic effect based on the characteristics of SARS-CoV-2 and its variants. To test the antiviral activity of a drug against COVID-19, in this study, we established and compared experimental conditions, such as the treatment time and mode of action (dose) of the therapeutic substance, and a test method to evaluate its effectiveness. We optimized an assay for testing antiviral activity by plaque reduction, tissue culture infectious dose 50, and quantitative RT-PCR. These methods were applied to test the antiviral efficacy of the therapeutic against SARS-CoV-2. Antiviral activity testing using in vitro assays against SARS-CoV-2 and its variants was assessed by measuring plaque-reducing or cytopathic effects in Vero-E6 cells. The in vitro assay was validated by evaluating the antiviral activity of remdesivir. Remdesivir reduced SARS-CoV-2 titer without detectable cytotoxicity and successfully inhibited viral replication in a dose-dependent manner. Therefore, we suggest this in vitro assay as an effective method for testing the antiviral activity for a potential repurposed drug against COVID-19 or rapid screening of therapeutic candidates. Copyright © 2022 Journal of Bacteriology and Virology.","PeriodicalId":39739,"journal":{"name":"Journal of Bacteriology and Virology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology and Virology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4167/jbv.2022.52.4.149","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 0
瑞德西韦对SARS-CoV-2及其变体的体外抗病毒活性研究
COVID-19疫情已成为国际关注的突发公共卫生事件,不仅要开发治疗COVID-19的药物,而且要根据SARS-CoV-2及其变体的特点,开发一种评估治疗效果的方法。为了检验药物对COVID-19的抗病毒活性,本研究建立并比较了治疗物质的治疗时间、作用方式(剂量)等实验条件,以及评价其有效性的试验方法。我们优化了一种通过菌斑减少、组织培养感染剂量50和定量RT-PCR检测抗病毒活性的方法。这些方法被用于测试治疗对SARS-CoV-2的抗病毒效果。通过测量Vero-E6细胞中的斑块减少或细胞病变效应,评估体外检测SARS-CoV-2及其变体的抗病毒活性。通过评价瑞德西韦的抗病毒活性,验证了体外实验的有效性。瑞德西韦降低了SARS-CoV-2滴度,但没有检测到细胞毒性,并以剂量依赖的方式成功抑制了病毒复制。因此,我们建议将这种体外实验作为一种有效的方法,用于测试针对COVID-19的潜在重新用途药物的抗病毒活性或快速筛选治疗候选药物。版权所有©2022细菌学与病毒学杂志。
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