Journal of Okayama Medical Association
Published by Okayama Medical Association

Full-text articles are available 3 years after publication.


Hiraki, Kiyoshi
Ota, Zensuke
Suzuki, Shinya
Takahashi, Kenji
Muguruma, Masahito
The ultrastructure and developmental process of Japanese B encephalitis virus were studied by electron microscopy in porcine kidney stable (PS) cells infected with the Mukai strain of Japanese B encephalitis virus. The virus and PS cells were kindly supplied by Dr. Y. Kanda Inoue at the Virus Institue of Kyoto University. PS cells were cultivated in bottles containing 10% calf serum and 0.5% lactalbumin hydrolyzate in Earle's balanced solution. Titration of cellassociated virus was estimated by cytopathic effect. At various intervals following infection, the cells were fixed in buffered 1% osmium tetroxide solution, embedded in methacrylates and cut on a Leitz ultramicrotome. After sections were stained in saturated uranyl acetate solution, they were observed in the Hitachi type HU ll electron microscope. Japanese B encephalitis virus particles were hexagonal in thin sections and approximately 40 mμ in the longest diameter, composed of the outer membrane, 30Å in thickness, viroplasm, 30Å in thickness and an electron-dense nucleoid, 25 mμ in diameter, After the virus particles developed in the process of budding on the wall of the cytoplasmic vacuole, they were densely packed in the vacuole usually in random arrangement and occasionally in crystalline arrays. The vacuole containing the virus particles gradually migrated to the cell surface and liberted the particles to the exterior of the cell through a narrow canaliculus which was formed between the vacuole and cell surface.