Juvenile turbot Scophthalmus maximus that became sick during an outbreak of disease at mariculture facilities at Go-Chang, Korea, in 2003, were examined to identify the cause of the disease. The fish had pale body color, an enlarged abdomen, protruding eyes, an enlarged spleen and kidney, and pale gills and/or liver. Histopathogical examination revealed basophilic enlarged cells in the kidney, spleen, gills, heart, stomach, intestine, liver, pancreas and skin. Hexagonal viral particles with a diameter of 136 to 159 nm were observed in the enlarged cells. A specific 1299 bp fragment of the major capsid protein (MCP) gene of the turbot iridovirus (TBIV) was amplified by PCR. Sequence homology was greater than 93.76% between the MCP gene in TBIV and the same gene in 5 viruses in the tentatively proposed genus Tropivirus (family Iridoviridae): red sea bream iridovirus, sea bass iridovirus, grouper sleepy disease iridovirus, African lampeye iridovirus and dwarf gourami iridovirus. These results suggest that the virus detected from turbot is similar to the proposed genus Tropivirus.
KEY WORDS: Turbot · Scophthalmus maximus · Iridovirus · RSIV · MCP · Tropivirus
Resale or republication not permitted without written consent of the publisherDis Aquat Org 64: [175][176][177][178][179][180] 2005 Korea. Juvenile turbot (mean weight 9.0 ± 1.9 g, mean length 7.9 ± 0.5 cm) began to show signs of disease in June 2003. Affected fish were lethargic and had a reduced appetite, pale body color, enlarged abdomen and protruding eyes. The key internal characteristics of the diseased fish were an extremely enlarged spleen and kidney, and pale gills and/or liver (Fig. 1).The fish farmers misdiagnosed the disease as hirame rhabdovirus (HRV) disease or viral hemorrhagic septicemia (VHS) disease, and increased the water temperature from 17-18°C to 20-23°C in an attempt to control the disease. The mortality increased rapidly when the water temperature was increased. Total mortality was about 50 to 70%. After sampling some of the diseased turbot, the remaining fish were killed, and all facilities were disinfected with sodium hypochlorite.Histology. The kidney, spleen, gills, heart, stomach, intestine, liver, pancreas, skin, eye and brain were removed from diseased fish and immediately fixed in 10% neutral buffered formalin (NBF). After fixation, standard histological procedures were used for tissue dehydration and paraffin embedding. Tissue sections were stained with haematoxylin and eosin (H&E).Electron microscopy. The spleens were fixed in 2.5% glutaraldehyde in 0.1 M phosphate buffer (pH 7.2) at 4°C. After several rinses with 0.1 M phosphate buffer, each sample was post-fixed with 1% OsO 4 for 1 h. Subsequently, the tissue was dehydrated in an ethanol series and embedded in Epon 812. Ultra thin sections were prepared using an RMC-MTX ultramicrotome (SIMS). Sections were stained with lead citrate and uranyl acetate. Stained grids were observed under a Hitachi-7000 electron microscope. DNA extraction. In preliminary investigati...