Thiruvaiyaru Aditya, Mattila Sari, Sadeghi Mohammadreza, Naumenko Krystyna, Merits Andres, Varjosalo Markku, Ahola Tero
Department of Microbiology, Faculty of Agriculture and Forestry, University of Helsinki, Helsinki, Finland.
Institute of Bioengineering, University of Tartu, Tartu, Estonia.
PLoS Pathog. 2025 Apr 7;21(4):e1013050. doi: 10.1371/journal.ppat.1013050. eCollection 2025 Apr.
All positive-strand RNA viruses replicate their genomes in association with modified intracellular membranes, inducing either membrane invaginations termed spherules, or double-membrane vesicles. Alphaviruses encode four non-structural proteins nsP1-nsP4, all of which are essential for RNA replication and spherule formation. To understand the host factors associated with the replication complex, we fused the efficient biotin ligase miniTurbo with Semliki Forest virus (SFV) nsP3, which is located on the cytoplasmic surface of the spherules. We characterized the proximal proteome of nsP3 in three cell lines, including cells unable to form stress granules, and identified >300 host proteins constituting the microenvironment of nsP3. These included all the nsPs, as well as several previously characterized nsP3 binding proteins. However, the majority of the identified interactors had no previously identified roles in alphavirus replication, including 39 of the top 50 interacting proteins. The most prominent biological processes involving the proximal proteins were nucleic acid metabolism, translational regulation, cytoskeletal rearrangement and membrane remodeling. siRNA silencing confirmed six novel proviral factors, USP10, AHNAK, eIF4G1, SH3GL1, XAB2 and ANKRD17, which are associated with distinct cellular functions. All of these except SH3GL1 were also important for the replication of chikungunya virus. We discovered that the small molecule 4E1RCat, which inhibits the interaction between the canonical translation initiation factors eIF4G and eIF4E, exhibits antiviral activity against SFV. Since the same molecule was previously found to inhibit coronaviruses, this suggest the possibility that translation initiation factors could be considered as targets for broadly acting antivirals.
所有正链RNA病毒都与修饰后的细胞内膜相关联来复制其基因组,从而诱导形成被称为小球体的膜内陷结构或双膜囊泡。甲病毒编码四种非结构蛋白nsP1 - nsP4,所有这些蛋白对于RNA复制和小球体形成都是必不可少的。为了了解与复制复合体相关的宿主因子,我们将高效生物素连接酶miniTurbo与位于小球体细胞质表面的辛德毕斯病毒(SFV)的nsP3融合。我们在三种细胞系中对nsP3的近端蛋白质组进行了表征,包括无法形成应激颗粒的细胞,并鉴定出构成nsP3微环境的300多种宿主蛋白。这些蛋白包括所有的nsP蛋白,以及几种先前已表征的nsP3结合蛋白。然而,大多数已鉴定的相互作用蛋白在甲病毒复制中以前没有被确定的作用,包括前50个相互作用蛋白中的39个。涉及近端蛋白的最突出的生物学过程是核酸代谢、翻译调控、细胞骨架重排和膜重塑。siRNA沉默证实了六个新的病毒前体因子,即USP10、AHNAK、eIF4G1、SH3GL1、XAB2和ANKRD17,它们与不同的细胞功能相关。除SH3GL1外,所有这些因子对基孔肯雅病毒的复制也很重要。我们发现小分子4E1RCat可抑制经典翻译起始因子eIF4G和eIF4E之间的相互作用,对SFV具有抗病毒活性。由于之前发现同一分子可抑制冠状病毒,这表明翻译起始因子有可能被视为广谱抗病毒药物的靶点。