Murray Jackelyn, Nogales Aitor, Martinez-Sobrido Luis, Martin David E, Sancilio Fred D, Tripp Ralph A
Department of Infectious Diseases, University of Georgia, Athens, GA 30602, USA.
Center for Animal Health Research, CISA-INIA-CSIC, 28130 Madrid, Spain.
Viruses. 2025 Feb 27;17(3):335. doi: 10.3390/v17030335.
It is essential to understand the molecular mechanisms of influenza antiviral therapeutics to evaluate their efficacy. Virus plaque assays are commonly used to assess the antiviral effects of drugs on virus replication; however, this method is labor-intensive and can present challenges. We avoided this method by using a replication-competent influenza A virus (IAV) expressing a reporter fluorescent gene fused to the non-structural protein 1 (NS1) gene. The reporter IAV was detectable in normal human bronchoepithelial (NHBE) infected cells and offered an improved method to determine the therapeutic efficacy of the antiviral drugs probenecid and oseltamivir compared to a standard plaque assay. This method provides an excellent means for evaluating therapeutic approaches against IAV.
了解流感抗病毒疗法的分子机制对于评估其疗效至关重要。病毒蚀斑测定法通常用于评估药物对病毒复制的抗病毒作用;然而,这种方法 labor-intensive 且可能存在挑战。我们通过使用表达与非结构蛋白1(NS1)基因融合的报告荧光基因的具有复制能力的甲型流感病毒(IAV)避免了这种方法。报告IAV在感染的正常人支气管上皮(NHBE)细胞中可检测到,与标准蚀斑测定法相比,它提供了一种改进的方法来确定抗病毒药物丙磺舒和奥司他韦的治疗效果。这种方法为评估针对IAV的治疗方法提供了一种极好的手段。 (注:原文中“labor-intensive”未翻译完整,应是“劳动密集型的”)