Yang Jinna, Huang Changbai, Feng Yao, He Junfang, Liu Yang, Zhang Ping, Liu Chao
Key Laboratory of Tropical Diseases Control, Sun Yat-sen University, Guangzhou, 510080, China; Department of Immunology and Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.
School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, 999077, China.
Virol Sin. 2025 Aug 5. doi: 10.1016/j.virs.2025.07.012.
Mosquito-borne flaviviruses, such as Zika virus (ZIKV) and dengue virus (DENV), cause diverse severe clinical manifestations including fever, rash, hepatitis, arthralgia, and congenital anomalies. Here, we identified a host factor, the adaptor protein complex 1 gamma 1 subunit (AP1G1), which plays an important role in both ZIKV and dengue virus 2 (DENV2) infections. We explored the role of AP1G1 in ZIKV and DENV2 infections using CRISPR/Cas9 gene editing technology and RNA interference (RNAi) techniques. Knockout or silencing of AP1G1 decreases the replication of ZIKV and DENV2 in multiple human cell lines. Intriguingly, depletion of AP1G1 results in a significant reduction in ZIKV at an early stage, but decreases DENV2 replication levels during the late stage, suggesting that AP1G1 plays distinct roles in the infection by ZIKV and DENV2. Furthermore, we determined that AP1G1 mediates ZIKV-endosomal membrane fusion through inhibitor experiments and fluorescence labeling assays. Mechanistically, we found that AP1G1 exerts its pro-viral effect through binding to the ZIKV envelope glycoprotein (E protein). This interaction promotes the fusion of viral and endosomal membranes, during which the ZIKV genomic RNAs are released from the endosome into the cytoplasm, a process that facilitates viral replication. However, for DENV2 infection, AP1G1 primarily affects its viral RNA replication stage, rather than the fusion of virus-endosomal membrane. Taken together, our work demonstrates that AP1G1 plays a pro-viral role in both ZIKV and DENV2 infections via distinct mechanisms, highlighting its potential as a therapeutic target for antiviral strategies.
蚊媒黄病毒,如寨卡病毒(ZIKV)和登革病毒(DENV),会引发多种严重的临床表现,包括发热、皮疹、肝炎、关节痛和先天性异常。在此,我们鉴定出一种宿主因子,即衔接蛋白复合体1γ1亚基(AP1G1),它在寨卡病毒和登革病毒2(DENV2)感染中均发挥重要作用。我们利用CRISPR/Cas9基因编辑技术和RNA干扰(RNAi)技术探究了AP1G1在寨卡病毒和DENV2感染中的作用。敲除或沉默AP1G1会降低寨卡病毒和DENV2在多种人类细胞系中的复制。有趣的是,AP1G1的缺失在早期会导致寨卡病毒显著减少,但在后期会降低DENV2的复制水平,这表明AP1G1在寨卡病毒和DENV2感染中发挥着不同的作用。此外,我们通过抑制剂实验和荧光标记分析确定AP1G1介导寨卡病毒与内体膜的融合。从机制上讲,我们发现AP1G1通过与寨卡病毒包膜糖蛋白(E蛋白)结合发挥其促病毒作用。这种相互作用促进病毒膜与内体膜的融合,在此过程中寨卡病毒基因组RNA从内体释放到细胞质中,这一过程有利于病毒复制。然而,对于DENV2感染,AP1G1主要影响其病毒RNA复制阶段,而非病毒与内体膜的融合。综上所述,我们的研究表明AP1G1通过不同机制在寨卡病毒和DENV2感染中发挥促病毒作用,突出了其作为抗病毒策略治疗靶点的潜力。