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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 26 (1969), S. 105-117 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of actinomycin D on the replication of CAM strain of influenza A1 virus was studied in the human conjunctival cell line, clone 1-5C-4. Actinomycin D in a concentration of 0.5 mcg/ml suppressed the virus yield to less than l/1000th of that from the uninhibited culture. When the addition of actinomycin D was delayed, the resistance of the production of virus and viral components to actinomycin D developed progressively in the order of the soluble antigen, hemagglutinin, and the infective virus. The synthesis of virus-specific RNA was demonstrable by the incorporation of tritiated uridine when actinomycin D was added to the culture at 6 hours after infection, but not when it was added at 1 hour after infection. These findings indicated that actinomycin D illhibits influenza virus replication because it inhibits the synthesis of virusspecific RNA and that, however, it does not directly block virus-specific RNA synthesisper se but exerts the inhibitory effect on some event(s) preceding virus-specific RNA synthesis. In FL cells, in which CAM virus undergoes an abortive multiplication cycle, virus-specific RNA was synthesized in the same period after infection and in a similar quantity as in clone 1-5C-4 cells in which complete multiplication occurs.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1831
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A wide variety of influenza A viruses, comprising human, equine, porcine, and avian strains, grew productively in an established line of canine kidney cells (MDCK) under an overlay medium containing trypsin, and formed well-defined plaques regardless of their prior passage history. Plaquing efficiency was comparable to the efficiency of infection in fertile eggs via allantoic route. MDCK cells have also been successfully employed for the primary isolation of influenza A virus from throat washings of patients. Parallel titration of several clinical specimens showed that the inoculation into MDCK cells followed by incubation in the presence of trypsin was an isolation procedure as sensitive as the amniotic inoculation into fertile eggs.
    Type of Medium: Electronic Resource
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