Junior Research Group Arenavirus Biology, Friedrich-Loeffler-Institut, Federal Research Institute of Animal Health, Greifswald-Isle of Riems, Germany.
Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
PLoS Pathog. 2020 Oct 12;16(10):e1008948. doi: 10.1371/journal.ppat.1008948. eCollection 2020 Oct.
Pathogenicity often differs dramatically among even closely related arenavirus species. For instance, Junín virus (JUNV), the causative agent of Argentine hemorrhagic fever (AHF), is closely related to Tacaribe virus (TCRV), which is normally avirulent in humans. While little is known about how host cell pathways are regulated in response to arenavirus infection, or how this contributes to virulence, these two viruses have been found to differ markedly in their ability to induce apoptosis. However, details of the mechanism(s) governing the apoptotic response to arenavirus infections are unknown. Here we confirm that TCRV-induced apoptosis is mitochondria-regulated, with associated canonical hallmarks of the intrinsic apoptotic pathway, and go on to identify the pro- and anti-apoptotic Bcl-2 factors responsible for regulating this process. In particular, levels of the pro-apoptotic BH3-only proteins Noxa and Puma, as well as their canonical transcription factor p53, were strongly increased. Interestingly, TCRV infection also led to the accumulation of the inactive phosphorylated form of another pro-apoptotic BH3-only protein, Bad (i.e. as phospho-Bad). Knockout of Noxa or Puma suppressed apoptosis in response to TCRV infection, whereas silencing of Bad increased apoptosis, confirming that these factors are key regulators of apoptosis induction in response to TCRV infection. Further, we found that while the highly pathogenic JUNV does not induce caspase activation, it still activated upstream pro-apoptotic factors, consistent with current models suggesting that JUNV evades apoptosis by interfering with caspase activation through a nucleoprotein-mediated decoy function. This new mechanistic insight into the role that individual BH3-only proteins and their regulation play in controlling apoptotic fate in arenavirus-infected cells provides an important experimental framework for future studies aimed at dissecting differences in the apoptotic responses between arenaviruses, their connection to other cell signaling events and ultimately the relationship of these processes to pathogenesis.
即使是密切相关的沙粒病毒属病毒,其致病性也有很大差异。例如,胡宁病毒(JUNV)是阿根廷出血热(AHF)的病原体,与通常对人类无毒性的塔卡里伯病毒(TCRV)密切相关。虽然人们对宿主细胞途径如何响应沙粒病毒感染进行调节以及这如何导致毒力差异知之甚少,但这两种病毒在诱导细胞凋亡的能力上有显著差异。然而,调节沙粒病毒感染后细胞凋亡的机制细节尚不清楚。在这里,我们证实 TCRV 诱导的细胞凋亡受线粒体调控,与内在凋亡途径的典型标志相关联,并进一步确定负责调节该过程的促凋亡和抗凋亡 Bcl-2 因子。特别是,促凋亡 BH3 仅蛋白 Noxa 和 Puma 及其典型转录因子 p53 的水平强烈增加。有趣的是,TCRV 感染还导致另一种促凋亡 BH3 仅蛋白 Bad(即磷酸化 Bad)的无活性磷酸化形式的积累。Noxa 或 Puma 的敲除抑制了 TCRV 感染后的细胞凋亡,而 Bad 的沉默增加了细胞凋亡,证实这些因子是 TCRV 感染后诱导细胞凋亡的关键调节因子。此外,我们发现,虽然高度致病性的 JUNV 不会诱导半胱天冬酶激活,但它仍然激活了上游促凋亡因子,这与当前的模型一致,即 JUNV 通过核蛋白介导的诱饵功能干扰半胱天冬酶激活来逃避凋亡。这一新的机制见解阐明了单个 BH3 仅蛋白及其调节在控制沙粒病毒感染细胞中的凋亡命运方面的作用,为未来旨在剖析沙粒病毒之间凋亡反应差异、它们与其他细胞信号事件的联系以及这些过程与发病机制的关系的研究提供了重要的实验框架。