Dengue virus strain DEN2 16681 utilizes a specific glycochain of syndecan-2 proteoglycan as a receptor

被引:40
作者
Okamoto, Kenta [1 ,2 ]
Kinoshita, Hitomi [1 ,2 ]
Parquet, Maria del Carmen [1 ,2 ]
Raekiansyah, Muhareva [1 ,2 ]
Kimura, Daisuke [2 ,3 ]
Yui, Katsuyuki [2 ,3 ]
Islam, Mohammed Alimul [4 ]
Hasebe, Futoshi [1 ,2 ]
Morita, Kouichi [1 ,2 ]
机构
[1] Nagasaki Univ, Dept Virol, Inst Trop Med, Nagasaki 852, Japan
[2] Global COE Program, Nagasaki, Japan
[3] Nagasaki Univ, Div Immunol, Dept Mol Microbiol & Immunol, Grad Sch Biomed Sci, Nagasaki 852, Japan
[4] Bangladesh Agr Univ, Dept Microbiol & Hyg, Fac Vet Sci, Mymensingh 2202, Bangladesh
基金
日本学术振兴会;
关键词
HEPARAN-SULFATE PROTEOGLYCANS; JAPANESE ENCEPHALITIS-VIRUS; HUMAN DENDRITIC CELLS; HUMAN-BONE-MARROW; ENVELOPE PROTEIN; MONONUCLEAR PHAGOCYTES; INDUCED HEMORRHAGE; MOUSE MODEL; INFECTION; BINDING;
D O I
10.1099/vir.0.037853-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Dengue virus (DENV) causes fever and severe haemorrhagic symptoms in humans. The DEN2 16681 strain, derived from a dengue haemorrhagic fever patient, has been widely used in studies related to DENV pathogenesis, such as mouse and non-human primate haemorrhagic models and human vascular endothelial-cell permeability. To clarify the entry mechanism of the 1 6681 strain, we characterized a novel cell receptor for this strain. Our two major findings were as follows: firstly, the SDC2 membrane protein was an effective DEN2 16681 receptor in a cloned K562 cell line. Secondly, a heparan sulfate (HS) glycochain (of four glycochains in SDC2) is the specific binding site of DENV and seems to be involved in tissue-culture adaptation. Our findings present an entry mechanism that could be implicated for DENV adaptation and HS-mediated DENV infection.
引用
收藏
页码:761 / 770
页数:10
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