Isolation of a Ranavirus-type grouper iridovirus in mainland China and comparison of its pathogenicity with that of a Megalocytivirus-type grouper iridovirus

被引:18
作者
Ma, Hongling [1 ]
Peng, Chao [1 ]
Su, Youlu [1 ]
Feng, Juan [1 ]
Guo, Zhixun [1 ]
机构
[1] Chinese Acad Fishery Sci, South China Sea Fisheries Res Inst, Key Lab Aquat Prod Proc,Minist Agr, South China Sea Resource Exploitat & Protect Coll, Guangzhou 510300, Guangdong, Peoples R China
关键词
Grouper iridovirus; Ronoyints; Megalocytivirus; Pathogenicity; EPINEPHELUS-AWOARA TEMMINCK; COMPLETE GENOME SEQUENCE; MAJOR CAPSID PROTEIN; CROMILEPTES-ALTIVELIS; INFECTIOUS SPLEEN; SPOTTED GROUPER; GENUS RANAVIRUS; NECROSIS VIRUS; ENLARGED CELLS; FISH;
D O I
10.1016/j.aquaculture.2016.05.032
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Megalocytivirus- and Ranavirus-type grouper iridoviruses (GIV-M and GIV-R, respectively) are causative agents in cultured groupers. GIV-R is recoded in the grouper industry in Chinese Taiwan and Singapore but rarely found in other regions or countries, including mainland China. In this study, a novel GIV-R, designated as GIV-R-SY1301, was isolated and identified from diseased juvenile hybrid groupers (tiger grouper Epinephelus fuscoguttatus female x giant grouper Epinephehis lanceolatus male) in Sanya, Hainan Island of China through PCR detection, cell culture, and transmission electron microscopy observation. Multiple alignment analysis based on the full-length major capsid protein (MCP) genes (1392 bp) showed that twenty-three and four nucleotide substitutions were observed among GIV-R-SY1301 and two early GIV-R isolates from Taiwan and Singapore, respectively. At the protein level, there are one or two amino acid substitutions in MCP among these isolates. Artificial challenge with GIV-R-SY1301 and a GIV-M isolate (OSGIV-HN11) indicated that both OSGIV-NH11 and GIV-R-SY1301 were highly virulent to infected tiger groupers. Cumulative mortalities of 97.5% (39/40) and 85% (34/40) were obtained in OSGIV-HN11- and GIV-R-SY1301-challenged fish, respectively. Histopathological analysis showed numerous abnormally enlarged cells in OSGIV-HN11-infected grouper spleen and kidney tissues but not in GIV-R-SY1301-infected grouper tissues. Abnormally enlarged cells in infected fish tissues could be a notable histopathological marker to distinguish GIV-M infection from GIV-R infection. Taken together, this study is the first to isolate and characterize GIV-R iridovirus in mainland China. GIV-R would be an alarming agent to grouper industry in mainland China, as well as GIV-M has been influencing. Statements of relevance: 1. First isolation and characterization of a Ranavirus-type grouper iridovirus in mainland China; 2. Comparative pathogenicity of Runavints- and Megulocylivirus-type GIV was firstly studied; both Runavirus- and Megalocytivirus-type GIV showed highly virulent to infected tiger groupers under artificial infection of the same viral dosages. By contrast, GIV-M showed a higher virulence than GIV-R, but the latter showed a more rapid lethality; 3. The differential histopathology caused by GIV-R and GIV-M was also studied. Abnormally enlarged cells in infected fish tissues could be a notable histopathological marker to distinguish GIV-M infection from GIV-R infection. All these findings contributed important information for grouper aquaculture worldwide. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:145 / 151
页数:7
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