Institute of Virology and Immunology IVI, Mittelhäusern, Switzerland.
Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
PLoS Pathog. 2024 Aug 26;20(8):e1012059. doi: 10.1371/journal.ppat.1012059. eCollection 2024 Aug.
Japanese encephalitis virus (JEV) is a zoonotic mosquito-transmitted Flavivirus circulating in birds and pigs. In humans, JEV can cause severe viral encephalitis with high mortality. Considering that vector-free direct virus transmission was observed in experimentally infected pigs, JEV introduction into an immunologically naïve pig population could result in a series of direct transmissions disrupting the alternating host cycling between vertebrates and mosquitoes. To assess the potential consequences of such a realistic scenario, we passaged JEV ten times in pigs. This resulted in higher in vivo viral replication, increased shedding, and stronger innate immune responses in pigs. Nevertheless, the viral tissue tropism remained similar, and frequency of direct transmission was not enhanced. Next generation sequencing showed single nucleotide deviations in 10% of the genome during passaging. In total, 25 point mutations were selected to reach a frequency of at least 35% in one of the passages. From these, six mutations resulted in amino acid changes located in the precursor of membrane, the envelope, the non-structural 3 and the non-structural 5 proteins. In a competition experiment with two lines of passaging, the mutation M374L in the envelope protein and N275D in the non-structural protein 5 showed a fitness advantage in pigs. Altogether, the interruption of the alternating host cycle of JEV caused a prominent selection of viral quasispecies as well as selection of de novo mutations associated with fitness gains in pigs, albeit without enhancing direct transmission frequency.
日本脑炎病毒(JEV)是一种通过蚊子传播的人畜共患黄病毒,在鸟类和猪中循环。在人类中,JEV 可引起严重的病毒性脑炎,死亡率很高。考虑到在实验感染的猪中观察到无媒介的直接病毒传播,JEV 引入免疫原性未成熟的猪群可能会导致一系列直接传播,破坏脊椎动物和蚊子之间交替宿主的循环。为了评估这种现实情景的潜在后果,我们在猪中进行了 JEV 的十次传代。这导致猪体内病毒复制增加,病毒脱落增加,先天免疫反应增强。然而,病毒组织嗜性仍然相似,直接传播的频率没有增加。下一代测序显示,在传代过程中基因组的 10%发生了单核苷酸偏差。总共选择了 25 个点突变,以在其中一个传代中至少达到 35%的频率。其中,6 个突变导致位于前膜、包膜、非结构蛋白 3 和非结构蛋白 5 中的氨基酸变化。在与两条传代线的竞争实验中,包膜蛋白中的 M374L 突变和非结构蛋白 5 中的 N275D 突变在猪中表现出适应性优势。总的来说,JEV 交替宿主循环的中断导致了病毒准种的显著选择,以及与猪适应性增益相关的新突变的选择,尽管没有增加直接传播的频率。