Department of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, HI 96813, USA.
Molecular Biosciences and Bioengineering Graduate Program, College of Tropical Agriculture and Human Resources, University of Hawaii at Manoa, Honolulu, HI 96822, USA.
Viruses. 2024 Aug 16;16(8):1303. doi: 10.3390/v16081303.
West Nile virus (WNV) nonstructural protein 5 (NS5) possesses multiple enzymatic domains essential for viral RNA replication. During infection, NS5 predominantly localizes to unique replication organelles (ROs) at the rough endoplasmic reticulum (RER), known as vesicle packets (VPs) and convoluted membranes (CMs), with a portion of NS5 accumulating in the nucleus. NS5 is a soluble protein that must be in the VP, where its enzymatic activities are required for viral RNA synthesis. However, the mechanistic processes behind the recruitment of NS5 from the cytoplasm to the RER membrane remain unclear. Here, we utilize high-resolution confocal microscopy and sucrose density gradient ultracentrifugation to investigate whether the association of NS5 with other NS proteins contributes to its membrane recruitment and retention. We demonstrate that NS1 or NS3 partially influences the NS5 association with the membrane. We further demonstrate that processed NS5 is predominantly in the cytoplasm and nucleus, indicating that the processing of NS5 from the viral polyprotein does not contribute to its membrane localization. These observations suggest that other host or viral factors, such as the enwrapment of NS5 by the RO, may also be necessary for the complete membrane retention of NS5. Therefore, studies on the inhibitors that disrupt the membrane localization of WNV NS5 are warranted for antiviral drug development.
西尼罗河病毒(WNV)非结构蛋白 5(NS5)具有多个酶结构域,对于病毒 RNA 复制至关重要。在感染过程中,NS5 主要定位于内质网(RER)上独特的复制细胞器(RO),称为囊泡包(VP)和卷曲膜(CM),一部分 NS5 积累在核内。NS5 是一种可溶性蛋白,必须位于 VP 中,其酶活性对于病毒 RNA 合成是必需的。然而,NS5 从细胞质招募到 RER 膜的机制过程仍不清楚。在这里,我们利用高分辨率共聚焦显微镜和蔗糖密度梯度超速离心来研究 NS5 与其他 NS 蛋白的结合是否有助于其膜募集和保留。我们证明 NS1 或 NS3 部分影响 NS5 与膜的结合。我们进一步证明,加工后的 NS5 主要存在于细胞质和核内,表明 NS5 从病毒多蛋白中的加工并不有助于其膜定位。这些观察结果表明,其他宿主或病毒因素,如 RO 对 NS5 的包裹,也可能是 NS5 完全保留在膜上所必需的。因此,研究破坏 WNV NS5 膜定位的抑制剂对于抗病毒药物的开发是有必要的。