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Propagation of yellow grouper nervous necrosis virus (YGNNV) in a new nodavirus‐susceptible cell line from yellow grouper, Epinephelus awoara (Temminck & Schlegel), brain tissue
Author(s) -
Lai YS,
Murali S,
Chiu HC,
Ju HY,
Lin YS,
Chen SC,
Guo IC,
Fang K,
Chang CY
Publication year - 2001
Publication title -
journal of fish diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.819
H-Index - 85
eISSN - 1365-2761
pISSN - 0140-7775
DOI - 10.1046/j.1365-2761.2001.00303.x
Subject(s) - grouper , biology , virus , virology , cell culture , epinephelus , necrosis , microbiology and biotechnology , fishery , fish <actinopterygii> , genetics
A nodavirus was isolated from diseased yellow grouper, Epinephelus awoara , larvae cultured in southern Taiwan. The histopathology and RT–PCR results confirmed that it was a fish nodavirus; its coat protein gene sequence was similar to that of red spotted grouper nervous necrosis virus (RGNNV) and it is named yellow grouper nervous necrosis virus (YGNNV). A new nodavirus‐susceptible cell line, grouper brain (GB) was established and characterized from the brain tissue of yellow grouper. The GB cells multiplied well in Leibovitz’s L‐15 medium supplemented with 10% foetal bovine serum at temperatures between 24 and 32 °C, and have been subcultured more than 80 times, becoming a continuous cell line. The GB cell line consists of fibroblast‐like cells and some epithelioid cells. The cell line yielded titres of YGNNV up to 10 8.5 TCID 50 mL –1 . The GB cells effectively replicated the virus at 28 °C, which could be purified to homogeneity by caesium chloride gradient centrifugation. Electron microscopy studies showed that purified virus particles were 25–30 nm in diameter. The cytoplasm of infected cells was filled with aggregates of virus particles. These results indicate that the GB cell line is a significant tool for the study of fish nodaviruses.