Identification and characterization of a late gene encoded by grouper iridovirus 2L (GIV-2L)

被引:2
作者
Lin, H-Y [1 ,2 ]
Cheng, C-F [1 ]
Chiou, P. P. [3 ]
Liou, C-J [4 ,5 ]
Yiu, J-C [2 ]
Lai, Y-S [1 ]
机构
[1] Natl Ilan Univ, Dept Biotechnol & Anim Sci, Yilan 26047, Taiwan
[2] Natl Ilan Univ, Dept Hort, Yilan 26047, Taiwan
[3] Acad Sinica, Inst Cellular & Organism Biol, Taipei 115, Taiwan
[4] Chang Gung Univ Sci & Technol, Dept Nursing, Taoyuan, Taiwan
[5] Chang Gung Univ Sci & Technol, Res Ctr Ind Human Ecol, Taoyuan, Taiwan
关键词
grouper iridovirus; grouper iridovirus 2L; immunofluorescence; monoclonal antibodies; EPINEPHELUS-AWOARA TEMMINCK; SPOT SYNDROME VIRUS; NERVOUS NECROSIS VIRUS; MONOCLONAL-ANTIBODY; CELL-LINES; YELLOW GROUPER; FAMILY IRIDOVIRIDAE; ENVELOPE PROTEIN; SCHLEGEL; INFECTION;
D O I
10.1111/jfd.12302
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Grouper iridovirus (GIV) belongs to the Ranavirus genus and is one of the most important viral pathogens in grouper, particularly at the fry and fingerling stages. In this study, we identified and characterized the GIV-2L gene, which encodes a protein of unknown function. GIV-2L is 1242bp in length, with a predicted protein mass of 46.2kDa. It displayed significant identity only with members of the Ranavirus and Iridovirus genera. We produced mouse monoclonal antibodies against the GIV-2L protein by immunizing mice with GIV-2L-His-tag recombinant protein. By inhibiting de novo protein and DNA synthesis in GIV-infected cells, we showed that GIV-2L was a late gene during the viral replication. Finally, immunofluorescence microscopy revealed that GIV-2L protein accumulated in both the nucleus and cytoplasm of infected cells. These results offer important insights into the pathogenesis of GIV.
引用
收藏
页码:881 / 890
页数:10
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