Department of Medical Microbiology and Parasitology, Faculty of Medicine and Health Science, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
Department of Medical Laboratory Science, Faculty of Allied Health Science, College of Health Science, Bayero University Kano, PMB 3011 Kano State, Nigeria.
Viruses. 2019 Apr 9;11(4):335. doi: 10.3390/v11040335.
Recent evidence has demonstrated that dengue virus requires active filopodia formation for a successful infection. However, the cellular factor involved in the interaction has not been fully elucidated. We used a combination of virus overlay protein binding assay and LC-MS/MS, and identified annexin II as a dengue virus serotype 2 (DENV2) interacting protein on Vero cells, upon filopodia induction. Flow cytometry analysis showed annexin II on the Vero cells surface increased when DENV2 was added. The amount of annexin II in the plasma membrane fraction was reduced as the infection progressed. Antibody-mediated inhibition of infection and siRNA-mediated knockdown of annexin II expression significantly reduced DENV2 infection and production levels. Collectively, we demonstrated that annexin II is one of the host factor involved in DENV2 binding on Vero cells.
最近的证据表明,登革热病毒需要活跃的丝状伪足形成才能成功感染。然而,参与相互作用的细胞因子尚未完全阐明。我们使用病毒覆盖蛋白结合测定和 LC-MS/MS 的组合,在丝状伪足诱导时,在 Vero 细胞上鉴定出 annexin II 是登革热病毒血清型 2(DENV2)的相互作用蛋白。流式细胞术分析表明,当添加 DENV2 时,Vero 细胞表面的 annexin II 增加。随着感染的进展,质膜部分的 annexin II 量减少。抗体介导的感染抑制和 annexin II 表达的 siRNA 介导的敲低显著降低了 DENV2 的感染和产生水平。总的来说,我们证明 annexin II 是参与 DENV2 与 Vero 细胞结合的宿主因子之一。