Pieterse Lisa, McDonald Maranda, Abraham Rachy, Griffin Diane E
W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Department of Biochemistry and Molecular Biology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Viruses. 2024 Dec 14;16(12):1918. doi: 10.3390/v16121918.
Chikungunya virus (CHIKV) is an emerging, mosquito-borne arthritic alphavirus increasingly associated with severe neurological sequelae and long-term morbidity. However, there is limited understanding of the crucial host components involved in CHIKV replicase assembly complex formation, and thus virus replication and virulence-determining factors, within the central nervous system (CNS). Furthermore, the majority of CHIKV CNS studies focus on neuronal infection, even though astrocytes represent the main cerebral target. Heterogeneous ribonucleoprotein K (hnRNP K), an RNA-binding protein involved in RNA splicing, trafficking, and translation, is a regulatory component of alphavirus replicase assembly complexes, but has yet to be thoroughly studied in the context of CHIKV infection. We identified the hnRNP K CHIKV viral RNA (vRNA) binding site via sequence alignment and performed site-directed mutagenesis to generate a mutant, ΔhnRNPK-BS1, with disrupted hnRNPK-vRNA binding, as verified through RNA coimmunoprecipitation and RT-qPCR. CHIKV ΔhnRNPK-BS1 demonstrated hampered replication in both NSC-34 neuronal and C8-D1A astrocytic cultures. In astrocytes, disruption of the hnRNPK-vRNA interaction curtailed viral RNA transcription and shut down subgenomic RNA translation. Our study demonstrates that hnRNP K serves as a crucial RNA-binding host factor that regulates CHIKV replication through the modulation of subgenomic RNA translation.
基孔肯雅病毒(CHIKV)是一种新出现的、由蚊子传播的关节炎性甲病毒,越来越多地与严重的神经后遗症和长期发病相关。然而,对于中枢神经系统(CNS)中参与CHIKV复制酶组装复合体形成的关键宿主成分,以及因此对于病毒复制和毒力决定因素的了解有限。此外,尽管星形胶质细胞是主要的脑内靶点,但大多数CHIKV中枢神经系统研究都集中在神经元感染上。异质性核糖核蛋白K(hnRNP K)是一种参与RNA剪接、运输和翻译的RNA结合蛋白,是甲病毒复制酶组装复合体的一个调节成分,但在CHIKV感染的背景下尚未得到充分研究。我们通过序列比对确定了hnRNP K与CHIKV病毒RNA(vRNA)的结合位点,并进行了定点诱变以产生一个突变体ΔhnRNPK-BS1,其hnRNPK-vRNA结合被破坏,这通过RNA共免疫沉淀和RT-qPCR得到验证。CHIKV ΔhnRNPK-BS1在NSC-34神经元和C8-D1A星形胶质细胞培养物中的复制均受到阻碍。在星形胶质细胞中,hnRNPK-vRNA相互作用的破坏减少了病毒RNA转录并关闭了亚基因组RNA翻译。我们的研究表明,hnRNP K作为一种关键的RNA结合宿主因子,通过调节亚基因组RNA翻译来调控CHIKV复制。