Fv-1 restriction of endogenous feline C-type RD114 virus genome phenotypically mixed with ecotropic murine leukemia viruses
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Japanese Journal of Cancer Research : Gann
|August 1, 1990
Abstract:
Endogenous feline leukemia RD114 virus genome rendered capable of infecting mouse cells by phenotypic mixing with an ecotropic murine leukemia virus (MuLV) exhibited the Fv-1 restriction pattern of the ecotropic murine virus. However, RD114 genomes phenotypically mixed with ecotropic MuLV showed one-hit dose-response kinetics, even when titrated with murine cells with the restricted Fv-1 phenotype.
Insights
Phenotypic mixing allowed feline leukemia virus (RD114) to infect mouse cells, adopting the murine leukemia virus (MuLV) Fv-1 restriction pattern. Despite this, RD114/MuLV mixtures showed one-hit kinetics, even in restricted mouse cells.
Area of Science:
- Virology
- Genetics
- Molecular Biology
Background:
- Endogenous feline leukemia virus RD114 can infect mouse cells through phenotypic mixing with ecotropic murine leukemia virus (MuLV).
- The Fv-1 gene in mice restricts the replication of certain MuLV strains.
Purpose of the Study:
- To investigate the Fv-1 restriction pattern and dose-response kinetics of feline leukemia virus RD114 genomes when phenotypically mixed with ecotropic MuLV in mouse cells.
Main Methods:
- Phenotypic mixing of RD114 virus with ecotropic MuLV.
- Infection of mouse cells with the mixed virus.
- Titration of the mixed virus on mouse cells with known Fv-1 restriction phenotypes.
- Analysis of dose-response kinetics.
Main Results:
- The phenotypically mixed RD114/MuLV exhibited the Fv-1 restriction pattern of the ecotropic MuLV.
- Despite the Fv-1 restriction, the mixed RD114 genomes showed one-hit dose-response kinetics when titrated on restricted murine cells.
Conclusions:
- Phenotypic mixing can confer a specific host range and restriction pattern to a virus genome.
- One-hit dose-response kinetics suggest a single-hit mechanism for infection, irrespective of the Fv-1 restriction status in this specific mixed-virus system.