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Sequential Passages of Human Rotavirus in MA‐104 Cells
Author(s) -
Urasawa Tomoko,
Urasawa Shozo,
Taniguchi Koki
Publication year - 1981
Publication title -
microbiology and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 70
eISSN - 1348-0421
pISSN - 0385-5600
DOI - 10.1111/j.1348-0421.1981.tb00109.x
Subject(s) - rotavirus , biology , feces , virology , reoviridae , antigenicity , virus , microbiology and biotechnology , trypsin , agar , cell culture , virus quantification , neutralization , antigen , bacteria , immunology , biochemistry , genetics , enzyme
Abstract Starting with a small amount of diarrheal feces containing human rotavirus (HRV), we succeeded in propagation of the virus using the roller culture technique with MA‐104 cells. Furthermore, we made a successful adaptation of HRV to a stationary culture and developed a plaque assay for the cell culture‐adapted viruses. The 3 culture‐adapted virus isolates, KU, YO, and 44 produced plaques (about 0.5–1.0 mm in diameter) under the overlay medium consisting of 0.6% purified agar, 3 μg of acetyl trypsin/ml and 50 μg of DEAE‐dex‐tran/ml. Subsequent plaque purification resulted in the formation of clear, larger plaques. It was shown from the results of cross neutralization tests using the fluorescent focus reduction method that the three culture‐adapted HRV isolates were clearly different antigenically from bovine rotavirus (NCDV) and, further, that a noticeable difference in antigenicity also existed among the HRV isolates.