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Accounting for Space — Quantification of Cell-To-Cell Transmission Kinetics Using Virus Dynamics Models

机译:占空间-使用病毒动力学模型量化细胞间传递动力学

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摘要

Mathematical models based on ordinary differential equations (ODE) that describe the population dynamics of viruses and infected cells have been an essential tool to characterize and quantify viral infection dynamics. Although an important aspect of viral infection is the dynamics of viral spread, which includes transmission by cell-free virions and direct cell-to-cell transmission, models used so far ignored cell-to-cell transmission completely, or accounted for this process by simple mass-action kinetics between infected and uninfected cells. In this study, we show that the simple mass-action approach falls short when describing viral spread in a spatially-defined environment. Using simulated data, we present a model extension that allows correct quantification of cell-to-cell transmission dynamics within a monolayer of cells. By considering the decreasing proportion of cells that can contribute to cell-to-cell spread with progressing infection, our extension accounts for the transmission dynamics on a single cell level while still remaining applicable to standard population-based experimental measurements. While the ability to infer the proportion of cells infected by either of the transmission modes depends on the viral diffusion rate, the improved estimates obtained using our novel approach emphasize the need to correctly account for spatial aspects when analyzing viral spread.
机译:基于普通微分方程(ODE)的数学模型描述了病毒和受感染细胞的种群动态,已经成为表征和量化病毒感染动态的重要工具。尽管病毒感染的一个重要方面是病毒传播的动力学,其中包括无细胞病毒粒子的传播和直接细胞间的传播,但迄今为止使用的模型完全忽略了细胞间的传播,或者通过以下方式解释了这一过程:受感染和未感染细胞之间的简单质量作用动力学。在这项研究中,我们表明当描述在空间定义的环境中传播病毒时,简单的质量作用方法不足。使用模拟数据,我们提出了一种模型扩展,该模型扩展允许对单层细胞内的细胞间传输动力学进行正确定量。通过考虑随着感染的增加而可能导致细胞间扩散的细胞比例下降,我们的扩展考虑了单个细胞水平上的传播动态,同时仍然适用于基于标准人群的实验测量。虽然推断两种传播途径感染的细胞比例的能力取决于病毒的扩散速率,但使用我们的新方法获得的改进估计值强调了在分析病毒传播时需要正确考虑空间方面的需求。

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