Abstract
Specific cellular and host tropism is a characteristic property of many viruses mediated by the interaction of viral attachment proteins with components of the plasma membrane of the cell. We have studied the binding of virus to cells quantitatively by using type 3 reovirus labeled with 125I and GH4C1 pituitary cells in culture. Binding was rapid at both 4 degrees and 15 degrees C and was stable over a 9-h period. Unlabeled virus inhibited binding of the labeled virus in a dose-dependent manner. Scatchard analysis revealed 4,200 viral binding sites/cell with an apparent affinity of 1.2 X 10(-11) M. Also, binding of type 3 reovirus was inhibited by antibodies directed against the viral hemagglutinin and partially inhibited by type 2 reovirus, but was unaffected by type 1 reovirus or a variety of other ligands that bind to receptors on GH4C1 cells. These data indicate that reovirus binds to a high affinity, specific receptor on target cells, which may control its tropism and ultimate disease expression.
MeSH Terms
Animals
Antibodies, Monoclonal/physiology
Antibodies, Viral/physiology
Binding, Competitive
Cell Line
Hemagglutinins, Viral/immunology
Kinetics
Mammalian orthoreovirus 3/immunology,metabolism
Mice
Rats
Receptors, Virus/analysis
Reoviridae Infections/immunology,microbiology
Chemicals
Antibodies, Monoclonal
Antibodies, Viral
Hemagglutinins, Viral
Receptors, Virus
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Maratos-Flier E
Kahn C R
Spriggs D R
Fields B N
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