Zhang Yahui, Ba Jianbo, Luan Jie, Qi Zhongtian, Liu Bin
Naval Medical Center, Naval Medical University, Shanghai, China.
Department of Cardiology, Shanghai East Hospital, Tongji University, Shanghai, China.
Front Microbiol. 2025 Apr 9;16:1565350. doi: 10.3389/fmicb.2025.1565350. eCollection 2025.
Each year, mosquito-borne orthoflaviviruses, including Zika virus, dengue virus, and the Japanese encephalitis virus, threaten the health of more than 400 million people worldwide. To date, knowledge about the pathogenic mechanisms underlying orthoflavivirus infection and the interactions of these viruses with host cells is limited. Mammalian target of rapamycin (mTOR) is pivotal for cell growth and metabolism. The downstream targets of mTOR regulate protein translation and cell autophagy to affect orthoflavivirus replication, and its upstream protein AKT performs similar functions. In this work, the mechanism underlying the relationship between the mTOR signaling pathway and orthoflavivirus infection was reviewed from three perspectives: orthoflavivirus structure and life cycle, mTOR structure and signaling pathway, and regulation of the mTOR signaling pathway during orthoflavivirus infection.
每年,包括寨卡病毒、登革病毒和日本脑炎病毒在内的蚊媒正黄病毒威胁着全球超过4亿人的健康。迄今为止,关于正黄病毒感染的致病机制以及这些病毒与宿主细胞相互作用的知识有限。哺乳动物雷帕霉素靶蛋白(mTOR)对细胞生长和代谢至关重要。mTOR的下游靶点调节蛋白质翻译和细胞自噬以影响正黄病毒复制,其上游蛋白AKT也发挥类似功能。在这项工作中,从三个方面综述了mTOR信号通路与正黄病毒感染之间关系的潜在机制:正黄病毒的结构与生命周期、mTOR的结构与信号通路以及正黄病毒感染期间mTOR信号通路的调控。