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Identification of novel viral receptors with cell line expressing viral receptor-binding protein
被引:26
|作者:
Mei, Mei
[1
,2
]
Ye, Jianqiang
[1
,2
]
Qin, Aijian
[1
,2
,3
]
Wang, Lin
[1
,2
]
Hu, Xuming
[1
,2
]
Qian, Kun
[1
,2
,3
]
Shao, Hongxia
[1
,2
,3
]
机构:
[1] Yangzhou Univ, Key Lab Avian Prevent Med, Minist Educ, Yangzhou 225009, Jiangsu, Peoples R China
[2] Yangzhou Univ, Key Lab Jiangsu Prevent Vet Med, Yangzhou 225009, Jiangsu, Peoples R China
[3] Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
ANNEXIN-II;
SUBGROUP;
VIRUS;
ENTRY;
SARCOMA;
ANTIBODIES;
RESISTANT;
ENVELOPE;
TYPE-1;
D O I:
10.1038/srep07935
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The viral cell receptors and infection can be blocked by the expression of the viral receptor-binding protein. Thus, the viral cell receptor is an attractive target for anti-viral strategies, and the identification of viral cell receptor is critical for better understanding and controlling viral disease. As a model system for viral entry and anti-retroviral approaches, avian sarcoma/ leukosis virus (ASLV, including the A-J ten subgroups) has been studied intensively and many milestone discoveries have been achieved based on work with ASLV. Here, we used a DF1 cell line expressed viral receptor-binding protein to efficiently identify chicken Annexin A2 (chANXA2) as a novel receptor for retrovirus ALV-J (avian leukosis virus subgroup J). Our data demonstrate that antibodies or siRNA to chANXA2 significantly inhibited ALV-J infection and replication, and over-expression of chANXA2 permitted the entry of ALV-J into its non-permissible cells. Our findings have not only identified chANXA2 as a novel biomarker for anti-ALV-J, but also demonstrated that cell lines with the expression of viral receptor-binding protein could be as efficient tools for isolating functional receptors to identify novel anti-viral targets.
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页数:6
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