Department of Chemistry, Faculty of Science, University of Colombo, Sri Lanka 00300.
Department of Biomedical Science, Faculty of Health Sciences, KIU Campus Sri Lanka 10120.
ACS Infect Dis. 2024 Jan 12;10(1):20-56. doi: 10.1021/acsinfecdis.3c00566. Epub 2023 Dec 18.
Flaviviruses such as dengue, Zika, and West Nile viruses are highly concerning pathogens that pose significant risks to public health. The NS1 protein is conserved among flaviviruses and is synthesized as a part of the flavivirus polyprotein. It plays a critical role in viral replication, disease progression, and immune evasion. Post-translational modifications influence NS1's stability, secretion, antigenicity, and interactions with host factors. NS1 protein forms extensive interactions with host cellular proteins allowing it to affect vital processes such as RNA processing, gene expression regulation, and cellular homeostasis, which in turn influence viral replication, disease pathogenesis, and immune responses. NS1 acts as an immune evasion factor by delaying complement-dependent lysis of infected cells and contributes to disease pathogenesis by inducing endothelial cell damage and vascular leakage and triggering autoimmune responses. Anti-NS1 antibodies have been shown to cross-react with host endothelial cells and platelets, causing autoimmune destruction that is hypothesized to contribute to disease pathogenesis. However, in contrast, immunization of animal models with the NS1 protein confers protection against lethal challenges from flaviviruses such as dengue and Zika viruses. Understanding the multifaceted roles of NS1 in flavivirus pathogenesis is crucial for effective disease management and control. Therefore, further research into NS1 biology, including its host protein interactions and additional roles in disease pathology, is imperative for the development of strategies and therapeutics to combat flavivirus infections successfully. This Review provides an in-depth exploration of the current available knowledge on the multifaceted roles of the NS1 protein in the pathogenesis of flaviviruses.
黄病毒(如登革热、寨卡和西尼罗河病毒)是高度关注的病原体,对公共卫生构成重大威胁。NS1 蛋白在黄病毒中保守,作为黄病毒多蛋白的一部分合成。它在病毒复制、疾病进展和免疫逃逸中发挥着关键作用。翻译后修饰影响 NS1 的稳定性、分泌、抗原性和与宿主因子的相互作用。NS1 蛋白与宿主细胞蛋白形成广泛的相互作用,使其能够影响 RNA 处理、基因表达调控和细胞内稳态等重要过程,从而影响病毒复制、疾病发病机制和免疫反应。NS1 通过延迟感染细胞的补体依赖性裂解而充当免疫逃逸因子,并通过诱导内皮细胞损伤和血管渗漏以及引发自身免疫反应而导致疾病发病机制。已显示抗 NS1 抗体与宿主内皮细胞和血小板发生交叉反应,导致自身免疫破坏,据推测这有助于疾病发病机制。然而,相反,用 NS1 蛋白对动物模型进行免疫接种可提供针对登革热和寨卡病毒等黄病毒的致命挑战的保护。了解 NS1 在黄病毒发病机制中的多方面作用对于有效管理和控制疾病至关重要。因此,进一步研究 NS1 的生物学特性,包括其与宿主蛋白的相互作用以及在疾病病理学中的其他作用,对于成功开发针对黄病毒感染的策略和治疗方法至关重要。本综述深入探讨了 NS1 蛋白在黄病毒发病机制中的多方面作用的现有知识。