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J Gen Virol 65 (1984), 2237-2248; DOI 10.1099/0022-1317-65-12-2237
© 1984 Society for General Microbiology

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Oncogenic Retrovirus from Spontaneous Murine Osteomas. I. Isolation and Biological Characterization

Jörg Schmidt1, Volker Erfle1, Finn Skou Pedersen2, Heike Rohmer1, H. Schetters3, Karl-Horst Marquart1 and Arne Luz1

1 Abteilung für Pathologie, Gesellschaft für Strahlen und Umweltforschung (GSF), D-8042 Neuherberg, Federal Republic of Germany
2 Department of Molecular Biology, University of Aarhus, DK-8000 Aarhus C, Denmark
and3 Medizinisch Poliklinik der Universität München, Pettenkoferstrasse 8a, D-8000 München 2, Federal Republic of Germany

Spontaneous osteomas in strain 101 mice, a strain which has a high incidence of benign bone tumours, harbour numerous C-type virus-like particles with pleomorphic characteristics. A cell-free extract from osteomas from two mice induced bone tumours, together with osteopetrosis and lymphomas, in newborn mice of the low incidence NMRI strain after a latent period of 12 to 15 months. When C3H embryo fibroblasts were infected with the osteoma extract, the resulting cell line produced virus (OA MuLVC) with a high titre. OA MuLVC was cloned by serial endpoint dilution and NIH 3T3 cells were productively infected. The resulting virus was named OA MuLVN. OA MuLVC and OA MuLVN also induced bone tumours, osteopetrosis and lymphomas 12 to 15 months after injection into newborn NMRI mice. The isolated virus showed typical characteristics of the murine retrovirus group. Fv-1 host range restriction assays classified the viruses as N-ecotropic and XC-positive. Tryptic p30 peptide analysis and RNase T1 fingerprint analysis of OA MuLVC and OA MuLVN indicated that OA MuLVC contains an Akv-like virus as well as additional components, whereas OA MuLVN is closely related to Akv, but not identical to it. Serological analysis of the envelope proteins using monoclonal antibodies also showed the virus to be similar, but not identical, to Akv virus.

Keywords: C-type retrovirus, osteoma, osteopetrosis, lymphoma

Received 2 April 1984; accepted 10 September 1984.


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