Abstract
A virus isolated from the internal organs of a moribund corn snake (Elaphe guttata) replicated in reptilian cell cultures (IgH-2, TH-1 cells) between 10 and 30°C. Highest infectivity titers of 105.5 TCID50/ml were obtained in IgH-2 cells at 25°C. Infected IgH-2 cells showed the development of three morphologically different intranuclear inclusion bodies. During viral assembly the particles formed typical crystalline aggregates in the nucleus. About 64 h after infection progressive desintegration of the nuclear membrane was evident and virus particles were released into the cytoplasm. Different fish cell lines (CLC, CHSE-214, BF-2, PG, RTG-2) were not capable of propagating the virus. The DNA containing agent proved to be stable at pH 3, more or less at pH 12 and to treatment with chloroform, but it was rapidly inactivated at 56°C. Electron microscopy revealed nonenveloped icosahedral particles with a diameter of 65–70 nm.