Global Landscape of Structural Proteins of Infectious Spleen and Kidney Necrosis Virus

被引:46
|
作者
Dong, Chuan-Fu [1 ]
Xiong, Xiao-Peng [1 ]
Shuang, Fan [1 ]
Weng, Shao-Ping [1 ]
Zhang, Jing [1 ]
Zhang, Ye [1 ]
Luo, Yong-Wen [1 ]
He, Jian-Guo [1 ,2 ]
机构
[1] Sun Yat Sen Zhongshan Univ, Sch Life Sci, State Key Lab Biocontrol, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Zhongshan Univ, Key Lab Aquat Prod Safety, Minist Educ, Sch Marine Sci, Guangzhou 510275, Guangdong, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金; 中国博士后科学基金;
关键词
SPOT SYNDROME VIRUS; SINGAPORE GROUPER IRIDOVIRUS; RED-SEA BREAM; PROTEOMIC ANALYSIS; ENVELOPE PROTEIN; PHYLOGENETIC ANALYSIS; MAJOR ENVELOPE; DISEASE VIRUS; CELL-LINE; IN-VITRO;
D O I
10.1128/JVI.01444-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Infectious spleen and kidney necrosis virus (ISKNV), the type species of the genus Megalocytivirus in the family Iridoviridae, causes severe damage to mandarin fish cultures in China. Little is known about the proteins of ISKNV virions. In this study, a total of 38 ISKNV virion-associated proteins were identified by four different workflows with systematic and comprehensive proteomic approaches. Among the 38 identified proteins, 21 proteins were identified by the gel-based workflows (one-dimensional [1-D] and two-dimensional [2-D] gel electrophoresis). Fifteen proteins were identified by 1-D gel electrophoresis, and 16 proteins were identified by 2-D gel electrophoresis, with 10 proteins identified by both methods. Another 17 proteins were identified only by liquid chromatography (LC)-based workflows (LC-matrix-assisted laser desorption ionization [MALDI] and linear trap quadrupole [LTQ]-Orbitrap). Among these 17 LC-identified proteins, 5 proteins were identified uniquely by the LC-MALDI workflow, whereas another 6 proteins were identified only by the LTQ-Orbitrap workflow. These results underscore the importance of incorporation of multiple approaches in identification of viral proteins. Based on viral genomic sequence, genes encoding these 38 viral proteins were cloned and expressed in vitro. Antibodies were produced against these 38 proteins to confirm the ISKNV structural proteins by Western blotting. Of the newly identified proteins, ORF 056L and ORF 118L were identified and confirmed as two novel viral envelope proteins by Western blotting and immunoelectron microscopy (IEM). The ISKNV proteome reported here is currently the only characterized megalocytivirus proteome. The systematic and comprehensive identification of ISKNV structural proteins and their localizations in this study will facilitate future studies of the ISKNV assembly process and infection mechanism.
引用
收藏
页码:2869 / 2877
页数:9
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