Department of Molecular Microbiology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Department of Pathology and Immunology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
J Virol. 2019 Jan 17;93(3). doi: 10.1128/JVI.01400-18. Print 2019 Feb 1.
Orsay virus is the only known natural virus pathogen of , and its discovery has enabled virus-host interaction studies in this model organism. Host genes required for viral infection remain understudied. We previously established a forward genetic screen based on a virus-inducible green fluorescent protein transcriptional reporter to identify novel host factors essential for virus infection. Here, we report the essential role in Orsay virus infection of the dietary restriction-like () gene, which encodes a serine/threonine kinase similar to the mammalian MEKK3 kinase. Ablation of led to a >10,000-fold reduction in Orsay virus RNA levels, which could be rescued by ectopic expression of DRL-1. DRL-1 was dispensable for Orsay replication from an endogenous transgene replicon, suggesting that DRL-1 affects a prereplication stage of the Orsay life cycle. Thus, this study demonstrates the power of as a model to identify novel virus-host interactions essential for virus infection. The recent discovery of Orsay virus, the only known natural virus of , provides a unique opportunity to study virus-host interactions that mediate infection in a genetically tractable multicellular model organism. As viruses remain a global threat to human health, better insights into cellular components that enable virus infection and replication can ultimately lead to the development of new targets for antiviral therapeutics.
奥尔森病毒是唯一已知的能够感染 的天然病毒病原体,它的发现使我们能够在这个模式生物中研究病毒-宿主相互作用。宿主中用于病毒感染的基因仍然研究不足。我们之前建立了一个基于病毒诱导的绿色荧光蛋白转录报告基因的正向遗传筛选方法,以鉴定新的宿主因子对于病毒感染是必需的。在这里,我们报告了限制饮食样()基因在奥尔森病毒感染中的重要作用,该基因编码一种类似于哺乳动物 MEKK3 激酶的丝氨酸/苏氨酸激酶。DRL-1 的缺失导致奥尔森病毒 RNA 水平降低了 >10,000 倍,而通过异位表达 DRL-1 可以挽救。DRL-1 对于从内源性转基因复制子复制奥尔森病毒是可有可无的,这表明 DRL-1 影响奥尔森病毒生命周期的复制前阶段。因此,这项研究证明了作为一种模型识别新的病毒-宿主相互作用的强大功能,这些相互作用对于病毒感染是必需的。最近发现的奥尔森病毒是唯一已知的感染 的天然病毒,为研究在遗传上可操作的多细胞模式生物中介导感染的病毒-宿主相互作用提供了独特的机会。由于病毒仍然是对人类健康的全球性威胁,更好地了解使病毒感染和复制成为可能的细胞成分最终可以为抗病毒治疗药物的开发提供新的靶点。