Institute for Integrative Systems Biology (I2SysBio), Universitat de València-CSIC, Paterna, 46980 València, Spain.
Viruses. 2020 Mar 4;12(3):282. doi: 10.3390/v12030282.
The spread of viruses among cells and hosts often involves multi-virion structures. For instance, virions can form aggregates that allow for the co-delivery of multiple genome copies to the same cell from a single infectious unit. Previously, we showed that vesicular stomatitis virus (VSV), an enveloped, negative-strand RNA virus, undergoes strong aggregation in the presence of saliva from certain individuals. However, the molecular components responsible for such aggregation remain unknown. Here we show that saliva-driven aggregation is protein dependent, and we use comparative proteomics to analyze the protein content of strongly versus poorly aggregating saliva. Quantitative analysis of over 300 proteins led to the identification of 18 upregulated proteins in strongly aggregating saliva. One of these proteins, the fibrinogen gamma chain, was verified experimentally as a factor promoting VSV aggregation in a dose-dependent manner. This study hence identifies a protein responsible for saliva-driven VSV aggregation. Yet, the possible involvement of additional proteins or factors cannot be discarded.
病毒在细胞和宿主之间的传播通常涉及多病毒粒子结构。例如,病毒粒子可以形成聚集体,从而允许从单个感染单元将多个基因组拷贝共同递送到同一细胞。先前,我们表明,水疱性口炎病毒(VSV)是一种包膜的负链 RNA 病毒,在来自某些个体的唾液存在下会强烈聚集。然而,负责这种聚集的分子成分仍然未知。在这里,我们表明唾液驱动的聚集是依赖于蛋白质的,我们使用比较蛋白质组学来分析强聚集和弱聚集唾液的蛋白质含量。对 300 多种蛋白质的定量分析导致鉴定出强聚集唾液中 18 种上调的蛋白质。这些蛋白质之一,纤维蛋白原γ链,实验验证了其作为促进 VSV 聚集的因子以剂量依赖的方式发挥作用。因此,本研究确定了一种负责唾液驱动的 VSV 聚集的蛋白质。然而,不能排除其他蛋白质或因素的可能参与。