Penaeus monodon chitin-binding protein (PmCBP) is involved in white spot syndrome virus (WSSV) infection

被引:84
作者
Chen, Kuan-Yu [1 ]
Hsu, Tai-Ching [1 ,2 ]
Huang, Po-Yu [1 ]
Kang, Shih-Ting [3 ]
Lo, Chu-Fang [3 ]
Huang, Wei-Pang [3 ]
Chen, Li-Li [1 ]
机构
[1] Natl Taiwan Ocean Univ, Inst Marine Biol, Chilung 20224, Taiwan
[2] Chung Shan Med Univ, Dept Biomed Sci, Taichung 40201, Taiwan
[3] Natl Taiwan Univ, Inst Zool, Taipei 10617, Taiwan
关键词
White spot syndrome virus (WSSV); Envelope protein; VP53A; Penaeus monodon chitin-binding protein (PmCBP); In vivo neutralization; DC-SIGN; GENOME SEQUENCE; SHRIMP; CELLS; IDENTIFICATION; GLYCOPROTEINS; PATHOGENESIS; RECOGNITION; INTERACT; LECTINS;
D O I
10.1016/j.fsi.2009.06.018
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
White spot syndrome virus (WSSV) can cause the most serious viral disease of shrimp and has a wide host range among crustaceans. Although researches show a lot about its genome and structure, information concerning the mechanism of how WSSV infects' cells is lacking. In this study, some experiments were applied to confirm the biological meaning of the protein-protein interaction between WSSV envelope protein, VP53A, and Penaeus monodon chitin-binding protein (PmCBP). Immunofluorescent study indicated that PmCBP is located on the cell surface of host cells. PmCBP amounts of about 34 kDa can be detected in both P. monodon and Litopenaeus vannamei tissues by Western blotting. In the in vivo neutralization experiment, both rVP53A and rPmCBP that were produced by Esherichia coli can promote resp. a 40% and 20% survival rate of the shrimp which were challenged by WSSV. Furthermore, a yeast-two-hybrid result revealed that PmCBP could interact with at least 11 WSSV envelope proteins. Those findings suggest that PmCBP may be involved in WSSV infection. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:460 / 465
页数:6
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