Sivasankar P, John K Riji, George M Rosalind, Mageshkumar P, Manzoor M Mohamed, Jeyaseelan M J Prince
Department of Fish Pathology and Health Management, Fisheries College and Research Institute, Tamil Nadu Fisheries University, Thoothukudi, 628008 India.
Virusdisease. 2017 Dec;28(4):373-382. doi: 10.1007/s13337-017-0408-2. Epub 2017 Nov 14.
A viral agent implicated in the mortality of marine ornamental "Similar Damselfish" ( Allen, 1991) was isolated and characterized. The virus grew well in marine and freshwater fish cell lines from seabass and snakehead. The virus was sensitive to chloroform, acidic pH (3.0) and heat treatment at 56 °C. Biochemical characterisation indicated that the virus had double stranded DNA genome. Transmission electron microscopic analysis of ultrathin sections of infected cell pellets showed iridovirus-like icosahedral virus particles of 120-130 nm. Purified virus had six structural protein bands that ranged from of 44 to 132 kDa. PCR analysis confirmed the presence of viral DNA in infected cell cultures and sequence analysis of the major capsid protein gene showed an identity of 99.82% to that of largemouth bass virus. Serum neutralization studies involving the viral agent and koi ranavirus (KIRV) indicated partial homogeneity between the two isolates. Experimental infection of seabass () and similar damselfish () fingerlings with the similar damselfish virus showed cumulative mortalities of 68.75 and 93.33%. The biophysical and biochemical properties of the viral agent isolated, serological characteristics, size of major capsid proteins and the sequence similarity of the MCP gene proved that the virus belongs to the genus of the family . Ability of the virus to grow in marine and freshwater fish cell lines and its pathogenicity to one of the cultivable marine fish shows the wide host range of the virus. This is the first report of ranavirus induced mortality in marine fish in India.
一种与海洋观赏“似雀鲷”(艾伦,1991年)死亡有关的病毒病原体被分离并鉴定。该病毒在来自海鲈和乌鳢的海水和淡水鱼类细胞系中生长良好。该病毒对氯仿、酸性pH值(3.0)和56°C热处理敏感。生化鉴定表明该病毒具有双链DNA基因组。对感染细胞沉淀超薄切片的透射电子显微镜分析显示,病毒粒子呈120 - 130纳米的虹彩病毒样二十面体。纯化病毒有六条结构蛋白带,分子量在44至132千道尔顿之间。PCR分析证实感染细胞培养物中存在病毒DNA,主要衣壳蛋白基因的序列分析显示与大口黑鲈病毒的同源性为99.82%。涉及该病毒病原体和锦鲤蛙病毒(KIRV)的血清中和研究表明这两种分离株之间存在部分同源性。用似雀鲷病毒对海鲈和似雀鲷幼鱼进行实验感染,累积死亡率分别为68.75%和93.33%。分离出的病毒病原体的生物物理和生化特性、血清学特征、主要衣壳蛋白大小以及MCP基因的序列相似性证明该病毒属于蛙病毒科蛙病毒属。该病毒在海水和淡水鱼类细胞系中生长的能力及其对一种可养殖海水鱼的致病性表明该病毒具有广泛的宿主范围。这是印度首次关于蛙病毒导致海水鱼死亡的报告。