Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Epigenetics & Molecular Carcinogenesis, M.D. Anderson Cancer Center, University of Texas, Smithville, TX 78712, USA.
Viruses. 2021 Feb 12;13(2):288. doi: 10.3390/v13020288.
Filoviruses Ebola (EBOV) and Marburg (MARV) are devastating high-priority pathogens capable of causing explosive outbreaks with high human mortality rates. The matrix proteins of EBOV and MARV, as well as eVP40 and mVP40, respectively, are the key viral proteins that drive virus assembly and egress and can bud independently from cells in the form of virus-like particles (VLPs). The matrix proteins utilize proline-rich Late (L) domain motifs (e.g., PPxY) to hijack specific host proteins that contain WW domains, such as the HECT family E3 ligases, to facilitate the last step of virus-cell separation. We identified E3 ubiquitin ligase Smad Ubiquitin Regulatory Factor 2 (SMURF2) as a novel interactor with VP40 that positively regulates VP40 VLP release. Our results show that eVP40 and mVP40 interact with the three WW domains of SMURF2 via their PPxY motifs. We provide evidence that the eVP40-SMURF2 interaction is functional as the expression of SMURF2 positively regulates VLP egress, while siRNA knockdown of endogenous SMURF2 decreases VLP budding compared to controls. In sum, our identification of novel interactor SMURF2 adds to the growing list of identified host proteins that can regulate PPxY-mediated egress of VP40 VLPs. A more comprehensive understanding of the modular interplay between filovirus VP40 and host proteins may lead to the development of new therapies to combat these deadly infections.
丝状病毒埃博拉病毒 (EBOV) 和马尔堡病毒 (MARV) 是具有高破坏性的高优先级病原体,能够引发高死亡率的爆发性疫情。EBOV 和 MARV 的基质蛋白,以及分别的 eVP40 和 mVP40,是驱动病毒组装和出芽的关键病毒蛋白,可以独立于细胞以病毒样颗粒 (VLP) 的形式出芽。基质蛋白利用富含脯氨酸的晚期 (L) 结构域基序 (例如,PPxY) 劫持含有 WW 结构域的特定宿主蛋白,例如 HECT 家族 E3 连接酶,以促进病毒-细胞分离的最后一步。我们确定 E3 泛素连接酶 Smad 泛素调节因子 2 (SMURF2) 为与 VP40 相互作用的新型接头,可正向调节 VP40 VLP 的释放。我们的结果表明,eVP40 和 mVP40 通过其 PPxY 基序与 SMURF2 的三个 WW 结构域相互作用。我们提供的证据表明,eVP40-SMURF2 相互作用是功能性的,因为 SMURF2 的表达正向调节 VLP 出芽,而内源性 SMURF2 的 siRNA 敲低与对照相比会降低 VLP 出芽。总之,我们鉴定出的新型接头 SMURF2 增加了可调节 VP40 VLP 通过 PPxY 介导的出芽的鉴定宿主蛋白的数量。对丝状病毒 VP40 和宿主蛋白之间模块化相互作用的更全面了解可能会导致开发出针对这些致命感染的新疗法。