J Gen Virol
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Published online ahead of print on 4 March 2009 as doi:10.1099/vir.0.007500-0
Journal of General Virology 2009;90:1035.

A more recent version of this article appeared on April 1, 2009 J Gen Virol (2009), DOI 10.1099/vir.0.007500-0
© 2009 Society for General Microbiology

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Transmission of scrapie and sheep-passaged BSE prions to transgenic mice expressing elk prion protein

Gültekin Tamgüney1, Michael W. Miller2, Kurt Giles1, Azucena Lemus1, Stephen J. DeArmond1 and Stanley B. Prusiner1,3

1 University of California San Francisco;
2 Wildlife Research Center

3 E-mail: stanley{at}ind.ucsf.edu

Chronic wasting disease (CWD) is a transmissible, fatal prion disease of cervids and is largely confined to North America. The origin of CWD continues to pose a conundrum: does the disease arise spontaneously or result from some other naturally occurring reservoir? To address whether prions from sheep might be able to cause disease in cervids, we inoculated mice expressing the elk prion protein (PrP) transgene with two scrapie prion isolates. The SSBP/1 scrapie isolate transmitted disease to Tg(ElkPrP) mice with a median incubation time of ~270 days but a second isolate failed to produce neurologic dysfunction in these mice. Although prions from cattle with bovine spongiform encephalopathy (BSE) did not transmit to the Tg(ElkPrP) mice, they did transmit after being passaged through sheep. In Tg(ElkPrP) mice, the sheep-passaged BSE prions exhibited an incubation time of ~300 days. SSBP/1 prions produced abundant deposits of the disease-causing PrP isoform, denoted PrPSc, in the cerebellum and pons of Tg(ElkPrP) mice while PrPSc accumulation in Tg mice inoculated with sheep-passaged BSE prions was confined to the deep cerebellar nuclei, habenula and the brainstem. The susceptibility of 'cervidized' mice to 'ovinized' prions raises the question about why CWD has not been reported in other parts of the world where cervids and scrapie-infected sheep coexist.

Received 23 September 2008; accepted 22 December 2008.





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