School of Biology, Centre for Biomolecular Sciences, BMS Building, North Haugh, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.
Section for Pathogen Research, Institute for Infection and Immunity, St George's, University of London, London SW17 0RE, UK.
J Gen Virol. 2023 Nov;104(11). doi: 10.1099/jgv.0.001916.
Parainfluenza virus type 5 (PIV5) can either have a persistent or a lytic phenotype in cultured cells. We have previously shown that the phenotype is determined by the phosphorylation status of the phosphoprotein (P). Single amino acid substitutions at critical residues, including a serine-to-phenylalanine substitution at position 157 on P, result in a switch between persistent and lytic phenotypes. Here, using PIV5 vectors expressing either mCherry or GFP with persistent or lytic phenotypes, we show that in co-infections the persistent phenotype is dominant. Thus, in contrast to the cell death observed with cells infected solely with the lytic variant, in co-infected cells persistence is immediately established and both lytic and persistent genotypes persist. Furthermore, 10-20 % of virus released from dually infected cells contains both genotypes, indicating that PIV5 particles can package more than one genome. Co-infected cells continue to maintain both genotypes/phenotypes during cell passage, as do individual colonies of cells derived from a culture of persistently infected cells. A refinement of our model on how the dynamics of virus selection may occur is presented.
副流感病毒 5 型(PIV5)在培养细胞中可以表现为持续感染或裂解感染两种表型。我们之前的研究表明,这种表型是由磷蛋白(P)的磷酸化状态决定的。在关键残基上的单个氨基酸取代,包括 P 上第 157 位丝氨酸到苯丙氨酸的取代,会导致持续感染和裂解感染表型之间的转换。在这里,我们使用表达持续感染或裂解感染表型的 mCherry 或 GFP 的 PIV5 载体,证明在共感染中,持续感染表型占主导地位。因此,与单独感染裂解变体的细胞中观察到的细胞死亡相反,在共感染的细胞中,持续感染立即建立,并且裂解和持续感染的基因型都持续存在。此外,从双重感染的细胞中释放的 10-20%的病毒含有两种基因型,表明 PIV5 颗粒可以包装不止一种基因组。在细胞传代过程中,共感染的细胞继续维持两种基因型/表型,来自持续感染细胞培养物的单个细胞集落也是如此。我们提出了一个关于病毒选择动力学如何发生的模型的改进。