Howell Liam M, Newsome Timothy P
School of Life and Environmental Science, The University of Sydney, Camperdown, NSW, Australia.
Sydney Institute for Infectious Diseases, The University of Sydney, Camperdown, NSW, Australia.
Methods Mol Biol. 2025;2860:229-240. doi: 10.1007/978-1-0716-4160-6_15.
Here, we describe a robust and flexible method for analyzing the infection of single cells with a fluorescent-reporter virus, with real-time tracking of infected cells through microscopy. We subsequently generate quantitative data from the resulting time-lapse microscopy, and harness these data to generate biologically meaningful parameters at scale. Our methodology offers a practical solution for researchers seeking to understand the complexities and variability of virus-host interactions at a granular level.
在这里,我们描述了一种强大且灵活的方法,用于分析荧光报告病毒对单细胞的感染,并通过显微镜对受感染细胞进行实时追踪。我们随后从所得的延时显微镜图像中生成定量数据,并利用这些数据大规模生成具有生物学意义的参数。我们的方法为寻求在细粒度水平上理解病毒与宿主相互作用的复杂性和变异性的研究人员提供了一个切实可行的解决方案。