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From the Department of Bacteriology and Immunology, Harvard Medical School, Boston, Massachusetts
Abstract
The formation of noninfectious, cell-associated viral hemagglutinins in Krebs 2 ascites tumor cells inoculated with large amounts of influenza virus, PR8 strain, was accompanied by high titered complement-fixing soluble antigen. This antigen appeared 1 to 2 hr before the hemagglutinin, was less affected by adverse conditions, and could be found in cells with a dilute input of virus which was insufficient for hemagglutinin formation.
Comparison to other influenza systems in deembryonated eggs and HeLa cells revealed no significant quantitative differences in the production of the intracellular hemagglutinin and S antigen, irrespective of whether complete or incomplete virus was being formed.
The formation of hemagglutinin could be preferentially inhibited by dilution of the virus input, by 0.1% glutamine, by low concentration (0.005 to 0.01%) of (NH4)2HPO4, or by a 15-min delay in addition of higher concentrations of ammonium salts.
Proflavine had no effect in this system.
Footnotes
1 These studies were supported by Research Grant C-3762 from the U. S. Public Health Service and by funds from the Eugene Higgins Trust.
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