Chu J J H, Ng M L
Flavivirology Laboratory, Department of Microbiology, 5 Science Dr. 2, National University of Singapore, Singapore 117597, Singapore.
J Virol. 2004 Oct;78(19):10543-55. doi: 10.1128/JVI.78.19.10543-10555.2004.
The pathway of West Nile flavivirus early internalization events was mapped in detail in this study. Overexpression of dominant-negative mutants of Eps15 strongly inhibits West Nile virus (WNV) internalization, and pharmacological drugs that blocks clathrin also caused a marked reduction in virus entry but not caveola-dependent endocytosis inhibitory agent, filipin. Using immunocryoelectron microscopy, WNV particles were seen within clathrin-coated pits after 2 min postinfection. Double-labeling immunofluorescence assays and immunoelectron microscopy performed with anti-WNV envelope or capsid proteins and cellular markers (EEA1 and LAMP1) revealed the trafficking pathway of internalized virus particles from early endosomes to lysosomes and finally the uncoating of the virus particles. Disruption of host cell cytoskeleton (actin filaments and microtubules) with cytochalasin D and nocodazole showed significant reduction in virus infectivity. Actin filaments are shown to be essential during the initial penetration of the virus across the plasma membrane, whereas microtubules are involved in the trafficking of internalized virus from early endosomes to lysosomes for uncoating. Cells treated with lysosomotropic agents were largely resistant to infection, indicating that a low-pH-dependent step is required for WNV infection. In situ hybridization of DNA probes specific for viral RNA demonstrated the trafficking of uncoated viral RNA genomes to the endoplasmic reticulum.
本研究详细绘制了西尼罗河黄病毒早期内化事件的途径。Eps15显性负性突变体的过表达强烈抑制西尼罗河病毒(WNV)的内化,阻断网格蛋白的药物也显著降低病毒进入,但不影响小窝依赖的内吞抑制剂菲律宾菌素。利用免疫冷冻电镜,在感染后2分钟可见WNV颗粒位于网格蛋白包被小窝内。用抗WNV包膜或衣壳蛋白及细胞标志物(EEA1和LAMP1)进行的双标记免疫荧光测定和免疫电镜显示,内化病毒颗粒从早期内体到溶酶体的运输途径以及最终病毒颗粒的脱壳。用细胞松弛素D和诺考达唑破坏宿主细胞细胞骨架(肌动蛋白丝和微管)显示病毒感染性显著降低。肌动蛋白丝在病毒最初穿过质膜的过程中至关重要,而微管参与内化病毒从早期内体到溶酶体的运输以进行脱壳。用溶酶体促渗剂处理的细胞对感染有很大抗性,表明WNV感染需要一个低pH依赖步骤。对病毒RNA特异的DNA探针原位杂交显示未包被的病毒RNA基因组运输到内质网。