Infect Immun. 1972 October; 6(4): 501-507
Copyright © 1972 American Society for Microbiology. All Rights Reserved.
Enhanced Growth of a Murine Coronavirus in Transformed Mouse Cells
Lawrence S. Sturman1 and
Kenneth K. Takemoto2
1 Virus Laboratory, Division of Laboratories and Research, New York State Department of Health, Albany, New York 12201
2 Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20014
ABSTRACT
Plaque formation by A59 virus, a murine coronavirus, was facilitated in AL/N and Balb mouse cells transformed by polyoma virus, simian virus 40, murine sarcoma virus, or mammary tumor virus. In these virus-transformed cells, A59 virus plaques were larger, they appeared earlier, and plaquing efficiencies were higher than in normal, untransformed cells. "Spontaneously" transformed AL/N cells behaved similarly to untransformed cells, whereas "spontaneously" transformed Balb cells resembled virus-transformed cell hosts. Both untransformed and transformed AL/N and Balb cells were permissive hosts for A59 virus. However, multiplication of A59 virus was enhanced at least fivefold in the virus-transformed AL/N cell hosts. Larger differences (100-fold or greater) in A59 virus production were obtained during the first cycle of infection in Balb cells at low multiplicities and in AL/N cells after multiple cycles of virus growth. In virus-transformed and "spontaneously" transformed Balb cells, A59 virus induced extensive syncytia formation.
Infect Immun. 1972 October; 6(4): 501-507
Copyright © 1972 American Society for Microbiology. All Rights Reserved.
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Copyright © 1972 by the American Society for Microbiology. All rights reserved.