Crucial role of the N-glycans on the viral E-envelope glycoprotein in DC-SIGN-mediated dengue virus infection

被引:36
作者
Alen, Marijke M. F. [1 ]
Dallmeier, Kai [1 ]
Balzarini, Jan [1 ]
Neyts, Johan [1 ]
Schols, Dominique [1 ]
机构
[1] Univ Louvain, Rega Inst Med Res, Lab Virol & Chemotherapy, B-3000 Louvain, Belgium
关键词
Dengue virus; DC-SIGN; Dendritic cells; Carbohydrate binding agent; N-glycan; Viral entry; HUMAN DENDRITIC CELLS; E-PROTEIN; IN-VITRO; GLYCOSYLATION; NONINTEGRIN; FEVER; BIOSYNTHESIS; REPLICATION; INHIBITION; RESOLUTION;
D O I
10.1016/j.antiviral.2012.10.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We generated in the mosquito cell line C6/36 a dengue virus (DENV) resistant to Hippeastrum hybrid agglutinin (HHA), a carbohydrate-binding agent (CBA). The genotype and phenotype were characterized of the HHA resistant (HHA(res)) DENV compared to the wild-type (WT) DENV. Sequencing the structural proteins of HHA(res) resulted in two mutations, N67D and T155I, indicating a deletion of both N-glycosylation sites on the viral envelope E-glycoprotein. The HHA(res) DENV could replicate in mammalian and mosquito cells that are lacking dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN) expression. In contrast, DC-SIGN expressing human cells namely monocyte-derived dendritic cells as well as DC-SIGN-transfected cells were no longer susceptible to HHA(res) DENV. This demonstrates a crucial role of the N-glycans in the E-glycoprotein in the infection of dendritic cells, which constitute primary target cells of DENV during viral pathogenesis in the human body. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:280 / 287
页数:8
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