Abstract
Visna and progressive pneumonia virus (PPV), two antigenically related, non-oncogenic "slow viruses" which have ribonucleic acid (RNA)-dependent deoxyribonucleic acid (DNA) polymerase activity, were examined for their ability to transform cells. Murine cells which had been exposed to either visna or PPV developed foci of altered, spindle-shaped cells 3 to 4 weeks after infection. Visna and PPV transformed lines were established from these cultures. There was no evidence that other oncogenic DNA or RNA viruses were involved in the observed transformation. Visna or PPV could be "rescued" from all transformed lines by co-cultivation with normal sheep testis cells. "Rescued" virus was identified as visna or PPV, and they retained the capacity to transform mouse cells. These experiments may have important implications in the understanding of both viral carcinogenesis and "slow" viral infections.
MeSH Terms
Animals
Cell Line
Cell Transformation, Neoplastic
Complement Fixation Tests
Culture Techniques
Fluorescent Antibody Technique
Immune Sera
Lung
Male
Mice
Prions/isolation & purification,pathogenicity
Pulmonary Adenomatosis, Ovine
RNA Viruses/isolation & purification,pathogenicity
Rats
Sheep
Testis
Virus Cultivation
Viruses, Unclassified/isolation & purification,pathogenicity
Chemicals
Immune Sera
Prions
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Takemoto K K
Stone L B
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