Key result
Interferon treatment differentially affected the replication of leukemia, encephalomyocarditis, and vesicular stomatitis viruses across three murine cell lines.
Interferon exhibits differential antiviral effects and enzyme induction profiles depending on the specific virus and murine cell line.
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Differential interferon effects across murine viruses and cells caution against uniform antiviral assumptions; leaves open virus-specific mechanisms for targeted study.
Infectious leukemia virus production by two chronically infected NIH/MOL lines was strongly inhibited by interferon treatment of the cells. The corresponding degree of inhibition in JLSV-11 cells was much lower. Multiplication of encephalomyocarditis virus in all three cell lines was barely affected by interferon treatment. Replication of vesicular stomatitis virus, on the other hand, was highly sensitive to interferon in the JLSV-11 line and in one NIH/MOL line but was practically insensitive in the other NIH/MOL line. Anticellular actions of interferon were more pronounced in the JLSV-11 line than in the others. In response to interferon treatment, 2',5'-oligoadenylate synthetase activity was induced to a high level in JLSV-11 cells and to lower levels in the NIH/MOL lines. We failed to detect any 2',5'-oligoadenylate-dependent endonuclease activity in extracts of these cells. Double-stranded RNA-dependent protein kinase activity was present in extracts of interferon-treated NIH/MOL cells, but it was barely detectable in extracts of interferon-treated JLSV-11 cells. The above studies demonstrated that interferon could differentially affect the replication of three different viruses in three different cell lines, including two seemingly identical NIH/MOL lines, and that certain tentative conclusions can be drawn regarding the roles of different interferon-inducible enzyme markers in the different antiviral actions of interferons.
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Sen et al. (1983) studied Viral infection in murine cell lines. Interferon was evaluated on Viral replication and enzyme marker induction. Interferon treatment differentially affected the replication of leukemia, encephalomyocarditis, and vesicular stomatitis viruses across three murine cell lines.
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