Nogales Aitor, Baker Steven F, Martínez-Sobrido Luis
Department of Microbiology and Immunology, University of Rochester, Rochester, NY, United States.
Department of Microbiology and Immunology, University of Rochester, Rochester, NY, United States.
Virology. 2015 Feb;476:206-216. doi: 10.1016/j.virol.2014.12.006. Epub 2014 Dec 30.
Like most animal viruses, studying influenza A in model systems requires secondary methodologies to identify infected cells. To circumvent this requirement, we describe the generation of replication-competent influenza A red fluorescent viruses. These influenza A viruses encode mCherry fused to the viral non-structural 1 (NS1) protein and display comparable growth kinetics to wild-type viruses in vitro. Infection of cells with influenza A mCherry viruses was neutralized with monoclonal antibodies and inhibited with antivirals to levels similar to wild-type virus. Influenza A mCherry viruses were also able to lethally infect mice, and strikingly, dose- and time-dependent kinetics of viral replication were monitored in whole excised mouse lungs using an in vivo imaging system (IVIS). By eliminating the need for secondary labeling of infected cells, influenza A mCherry viruses provide an ideal tool in the ongoing struggle to better characterize the virus and identify new therapeutics against influenza A viral infections.
与大多数动物病毒一样,在模型系统中研究甲型流感需要采用辅助方法来识别受感染细胞。为规避这一要求,我们描述了具有复制能力的甲型流感红色荧光病毒的产生。这些甲型流感病毒编码与病毒非结构蛋白1(NS1)融合的mCherry,并在体外显示出与野生型病毒相当的生长动力学。用单克隆抗体中和甲型流感mCherry病毒对细胞的感染,并用抗病毒药物将其抑制至与野生型病毒相似的水平。甲型流感mCherry病毒也能够致死性感染小鼠,而且引人注目的是,使用体内成像系统(IVIS)在完整切除的小鼠肺中监测到了病毒复制的剂量和时间依赖性动力学。通过消除对受感染细胞进行二次标记的需求,甲型流感mCherry病毒为在不断努力更好地表征该病毒并确定针对甲型流感病毒感染的新疗法的过程中提供了理想工具。