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对尼帕病毒5'非翻译区功能的机制性见解揭示了一个抗病毒靶点。

Mechanistic insights into Nipah virus 5' UTR functionality reveal an antiviral target.

作者信息

Liu Lishi, Pan Chaohu, Chen Zhen, Zhang Fang, Guan Wuxiang, Zeng Aiping, Hao Haojie

机构信息

Center for Emerging Infectious Diseases, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, 430071, PR China.

Hubei Jiangxia Laboratory, Wuhan, Hubei, 430200, PR China.

出版信息

J Gen Virol. 2025 Aug;106(8). doi: 10.1099/jgv.0.002141.

Abstract

The highly pathogenic Nipah virus (NiV), a World Health Organization priority pathogen with pandemic potential, remains a critical public health threat due to its capacity to cause fatal encephalitis and respiratory disease. Despite its 1998 emergence, no approved therapeutics exist against NiV infection, underscoring the urgent need to identify genomic regulatory elements as antiviral targets. Our study focuses on the extended 5' UTRs characteristic of NiV transcripts, a distinctive genomic feature whose functional significance remained enigmatic. Comparative reporter assays showed these UTRs strongly inhibit downstream ORF translation through mechanisms distinct from internal ribosome entry site activity. Mutagenesis studies identified upstream ATG elements in multiple transcripts as critical regulators of translational efficiency, with the C 5' UTR exhibiting maximal suppression. A functional hotspot spanning within the C 5' UTR was mapped as the primary ribosomal initiation blockade, and ribosome leaky scanning was confirmed as the mechanism enabling dual-protein expression. Notably, therapeutic targeting of this regulatory element with antisense oligonucleotides significantly impaired viral replication. These findings provide fundamental insights into henipaviral translation regulation while identifying concrete antiviral targets, particularly the druggable C 5' UTR element, advancing efforts to combat this biosafety level 4 pathogen.

摘要

高致病性尼帕病毒(NiV)是世界卫生组织列为具有大流行潜力的重点病原体,因其能够引发致命性脑炎和呼吸道疾病,仍然是严重的公共卫生威胁。尽管该病毒于1998年首次出现,但目前尚无针对NiV感染的获批治疗方法,这凸显了将基因组调控元件确定为抗病毒靶点的迫切需求。我们的研究聚焦于NiV转录本特有的延伸5'非翻译区(UTR),这是一种独特的基因组特征,其功能意义一直成谜。比较报告基因检测显示,这些UTR通过不同于内部核糖体进入位点活性的机制强烈抑制下游开放阅读框(ORF)的翻译。诱变研究确定多个转录本中的上游ATG元件是翻译效率的关键调节因子,其中C 5' UTR表现出最大抑制作用。一个跨越C 5' UTR的功能热点被定位为主要的核糖体起始阻断位点,核糖体渗漏扫描被确认为实现双蛋白表达的机制。值得注意的是,用反义寡核苷酸对该调控元件进行治疗性靶向显著损害了病毒复制。这些发现为亨尼帕病毒的翻译调控提供了基本见解,同时确定了具体的抗病毒靶点,特别是可成药的C 5' UTR元件,推动了对抗这种生物安全4级病原体的努力。

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