Identification of the linear ligand epitope on classical swine fever virus that interacts with porcine kidney 15 cells

被引:0
|
作者
Mei, Yin [1 ]
Yue, Feng [2 ]
Ning, Hong-mei [1 ]
Zhou, Juan-juan [2 ]
Wang, Xuan-nian [2 ]
机构
[1] Henan Inst Sci & Technol, Coll Vet & Anim Sci, Xinxiang 453003, Henan, Peoples R China
[2] Xinxiang Univ, Coll Life Sci & Technol, Xinxiang 453003, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
ENVELOPE GLYCOPROTEIN E2; E-RNS; PROTEIN; REPLICATION; GROWTH; ENTRY; INFECTION; RECEPTORS; CULTURE; BINDING;
D O I
暂无
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Binding of the viral ligand to a specific receptor is the first step of virus entry into target cells. The envelope proteins Erns, E1, and E2 of classical swine fever virus (CSFV) are involved in the interaction with host cell receptors to mediate CSFV infection. The aim of this investigation was to identify epitopes that bind to porcine kidney (PK)-15 cells to prevent CSFV infection. Ten peptides representing Erns, E1, and E2 were synthesized. Immunohistochemical study showed that the SE24 peptide, which is derived from the E2 amino acid sequence, could effectively bind to PK-15 cells. Similarly, a flow cytometry assay demonstrated that SE24 binding to PK-15 cells could be blocked by CSFV. The binding of SE24 with PK-15 cells leads to decreased CSFV infection of PK-15 cells in a dose-dependent manner. These results suggest a potential new strategy for the prevention and control of CSFV infection that requires further investigation.
引用
收藏
页码:186 / 191
页数:6
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