Bovine polyomavirus, a cell-transforming virus with tumorigenic potential

1 Department of Virology, University of Amsterdam, Academic Medical Centre, Meibergdreef 15, 1105 AZ Amsterdam and 2 National Institute of Public Health and Environmental Protection, P.O. Box 1, 3720 BA Bilthoven, The Netherlands The early region of bovine polyomavirus (BPyV) was tested for its cell...

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Veröffentlicht in:Journal of general virology 1992-11, Vol.73 (11), p.2871-2878
Hauptverfasser: Schuurman, Rob, van Strien, Ans, van Steenis, Bert, van der Noordaa, Jan, Sol, Cees
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Sprache:eng
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Zusammenfassung:1 Department of Virology, University of Amsterdam, Academic Medical Centre, Meibergdreef 15, 1105 AZ Amsterdam and 2 National Institute of Public Health and Environmental Protection, P.O. Box 1, 3720 BA Bilthoven, The Netherlands The early region of bovine polyomavirus (BPyV) was tested for its cell transformation potential employing an assay of dense focus formation. Dense foci of morphologically transformed cells were observed upon transfection of primary rodent cells with a plasmid construct encoding the complete early region of BPyV under the transcriptional control of the long terminal repeat of Rous sarcoma virus. No transformation of primary rodent cells was observed upon transfection of these cells with a plasmid encoding the complete early region of BPyV under the control of its own transcriptional regulatory sequences. In BPyV-transformed cells, the viral sequences had become integrated into the cellular genome, and expression of large T antigen could be detected in a high percentage of cells. The transformed cells were demonstrated to be capable of anchorage-independent growth and to be oncogenic in immunocompromised newborn rats. Therefore BPyV should be considered as a potentially tumorigenic polyomavirus. Since many commercial batches of calf serum have been shown to be contaminated with BPyV, our observations may have implications for the use of calf serum in cell culture. Received 13 March 1992; accepted 22 June 1992.
ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-73-11-2871