Mosso Clemente, Galván-Mendoza Ivan J, Ludert Juan Ernesto, del Angel Rosa M
Departamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, México City 07360, Mexico.
Virology. 2008 Aug 15;378(1):193-9. doi: 10.1016/j.virol.2008.05.012. Epub 2008 Jun 20.
The endocytic pathway followed by dengue virus to infect the mosquito cells C6/36 HT was analyzed. Using DIL-labeled virions and real-time imaging it was determined that viral entry into C6/36 HT takes approximately 5 to 7 min. Pretreatment of C6/36 HT cells with sucrose and bafilomycin A, but not filipin, inhibited dengue virus infection up to 80%. Furthermore, the overexpression of dominant-negative mutants of Eps15, a molecule required for the formation of clathrin-coated vesicles, reduced dengue infection up to 50%, indicating that dengue virus entry is through clathrin-mediated endocytosis and is pH-dependent. By double-immunofluorescence assays, DIL-labeled particles were colocalized with early endosomes at 5 min and with lysosomes mainly at 30 min post-infection. Finally, disruption of the microtubule and microfilaments by nocodazole and by cytochalasin D reduced viral infection by more than 80%. Taken together these results indicate that dengue virions enter into C6/36 HT cells by clathrin-mediated endocytosis, using the endosomal pathway from early endosomes to acidic lysosomes before viral RNA is released into the cytoplasm.
分析了登革病毒感染蚊虫细胞C6/36 HT所遵循的内吞途径。使用DIL标记的病毒粒子和实时成像技术确定,病毒进入C6/36 HT细胞大约需要5至7分钟。用蔗糖和巴弗洛霉素A预处理C6/36 HT细胞,而非菲律宾菌素,可将登革病毒感染抑制高达80%。此外,网格蛋白包被小泡形成所需分子Eps15的显性负突变体的过表达可将登革病毒感染降低高达50%,这表明登革病毒通过网格蛋白介导的内吞作用进入细胞,且依赖于pH值。通过双免疫荧光分析,DIL标记的颗粒在感染后5分钟与早期内体共定位,主要在感染后30分钟与溶酶体共定位。最后,诺考达唑和细胞松弛素D对微管和微丝的破坏使病毒感染减少了80%以上。综合这些结果表明,登革病毒粒子通过网格蛋白介导的内吞作用进入C6/36 HT细胞,在病毒RNA释放到细胞质之前,利用从早期内体到酸性溶酶体的内体途径。