Department of Chemistry & Biochemistry, Texas Christian University, Fort Worth, TX, USA.
Department of Physics & Astronomy, Texas Christian University, Fort Worth, TX, USA.
Virology. 2022 Oct;575:91-100. doi: 10.1016/j.virol.2022.08.016. Epub 2022 Sep 7.
Several viruses have the ability to form large multinucleated cells known as syncytia. Many properties of syncytia and the role they play in the evolution of a viral infection are not well understood. One basic question that has not yet been answered is how quickly syncytia form. We use a novel mathematical model of cell-cell fusion assays and apply it to experimental data from SARS-CoV-2 fusion assays to provide the first estimates of virus-mediated cell fusion rate. We find that for SARS-CoV2, the fusion rate is in the range of 6 × 10-12×10/h. We also use our model to compare fusion rates when the protease TMPRSS2 is overexpressed (2-4 times larger fusion rate), when the protease furin is removed (one third the original fusion rate), and when the spike protein is altered (1/10th the original fusion rate). The use of mathematical models allows us to provide additional quantitative information about syncytia formation.
几种病毒具有形成称为合胞体的多核巨细胞的能力。合胞体的许多特性及其在病毒感染进化中的作用尚不完全清楚。一个尚未回答的基本问题是合胞体形成的速度有多快。我们使用细胞融合分析的新的数学模型,并将其应用于来自 SARS-CoV-2 融合分析的实验数据,以首次提供病毒介导的细胞融合率的估计值。我们发现,对于 SARS-CoV2,融合率在 6×10-12×10/h 的范围内。我们还使用我们的模型比较了当蛋白酶 TMPRSS2 过表达(融合率增加 2-4 倍)、蛋白酶弗林被去除(原始融合率的三分之一)和 Spike 蛋白改变(原始融合率的十分之一)时的融合率。数学模型的使用使我们能够提供有关合胞体形成的更多定量信息。