Identification of the structural proteins of VP1 and VP2 of a novel mud crab dicistrovirus

被引:16
作者
Zhang, Rui [1 ]
He, Jianguo [1 ]
Su, Hongjun [1 ]
Dong, Chuanfu [1 ]
Guo, Zhixun [1 ]
Ou, Yujie [1 ]
Deng, Xiexiong [1 ]
Weng, Shaoping [1 ]
机构
[1] Sun Yat Sen Zhongshan Univ, Sch Life Sci, State Key Lab Biocontrol, Guangzhou 510275, Guangdong, Peoples R China
关键词
Mud crab dicistrovirus (MCDV); Structural protein; Monoclonal antibodies (MAbs); SPOT SYNDROME VIRUS; PICORNA-LIKE VIRUS; TAURA-SYNDROME-VIRUS; COMPLETE GENOME SEQUENCE; CRICKET-PARALYSIS-VIRUS; ENVELOPE PROTEIN; CAPSID PROTEINS; NUCLEOTIDE-SEQUENCE; SCYLLA-SERRATA; IRES ELEMENTS;
D O I
10.1016/j.jviromet.2010.09.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mud crab dicistrovirus (MCDV), a newly identified single-stranded positive RNA virus, is an important pathogen that causes serious economic losses to mud crab aquaculture. In this study, MCDV was purified, and three structural proteins of MCDV were separated by SDS-PAGE. The N-terminal 15 amino acids were sequenced and aligned with the main structural proteins of other dicistrovirus. The three structural proteins were named VP1, VP2 and VP3. Monoclonal antibodies (MAbs) against the two main structural proteins, VP1 and VP2, were prepared, and the two structural proteins were then identified using these MAbs. The results of Western blot analyses demonstrated that five MAbs recognised VP1 and two recognised VP2. The results of immunogold transmission electron microscopy (IEM) revealed that the epitopes of the two structural proteins recognised by the MAbs were located at the outer surface of the virions, which suggested that the two structural proteins are MCDV capsid proteins. The identification of the two structural proteins of MCDV is useful for studying their functions, as well as the mechanism of infection and the pathogenesis of MCDV. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:323 / 328
页数:6
相关论文
共 63 条
[21]  
Fushimi H, 2000, UJNR TECH REP, V28, P9
[22]   Analysis of the complete genome sequence of acute bee paralysis virus shows that it belongs to the novel group of insect-infecting RNA viruses [J].
Govan, VA ;
Leat, N ;
Allsopp, M ;
Davison, S .
VIROLOGY, 2000, 277 (02) :457-463
[23]   Development of an RT-PCR detection method for mud crab reovirus [J].
Guo, Zhi-Xun ;
Weng, Shao-Ping ;
Li, Guang ;
Chan, Siu-Ming ;
He, Jian-Guo .
JOURNAL OF VIROLOGICAL METHODS, 2008, 151 (02) :237-241
[24]   Genome sequence and molecular characterization of Homalodisca coagulata virus-1, a novel virus discovered in the glassy-winged sharpshooter (Hemiptera: Cicadellidae) [J].
Hunnicutt, Laura E. ;
Hunter, Wayne B. ;
Cave, Ronald D. ;
Powell, Charles A. ;
Mozoruk, Jerry J. .
VIROLOGY, 2006, 350 (01) :67-78
[25]   Divergent IRES elements in invertebrates [J].
Jan, Eric .
VIRUS RESEARCH, 2006, 119 (01) :16-28
[26]   The novel genome organization of the insect picorna-like virus Drosophila C virus suggests this virus belongs to a previously undescribed virus family [J].
Johnson, KN ;
Christian, PD .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :191-203
[27]   Spatial variation in burrow morphology of the mud shore crab Helograpsus haswellianus (Brachyura, Grapsidae) in South Australian saltmarshes [J].
Katrak, G. ;
Dittmann, S. ;
Seuront, L. .
MARINE AND FRESHWATER RESEARCH, 2008, 59 (10) :902-911
[28]  
Keenan C P., 1999, Proceedings of an international scientific forum held in Darwin, Australia, 21-24 April 1997, ACIAR Proceedings, P9
[29]  
Keenan Clive P., 1999, ACIAR Proceedings, V78, P48
[30]   CONTINUOUS CULTURES OF FUSED CELLS SECRETING ANTIBODY OF PREDEFINED SPECIFICITY [J].
KOHLER, G ;
MILSTEIN, C .
NATURE, 1975, 256 (5517) :495-497