J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Originally published as JGV in Press, 10.1099/vir.0.007500-0 on March 4, 2009 J Gen Virol 90 (2009), 1035-1047; DOI 10.1099/vir.0.007500-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary figures and tables
Right arrow All Versions of this Article:
vir.0.007500-0v1
90/4/1035    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tamgüney, G.
Right arrow Articles by Prusiner, S. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tamgüney, G.
Right arrow Articles by Prusiner, S. B.
Agricola
Right arrow Articles by Tamgüney, G.
Right arrow Articles by Prusiner, S. B.

Transmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein

Gültekin Tamgüney1,2, Michael W. Miller3, Kurt Giles1,2, Azucena Lemus4, David V. Glidden5, Stephen J. DeArmond1,4 and Stanley B. Prusiner1,2

1 Institute for Neurodegenerative Diseases, University of California, San Francisco, CA 94143-0518, USA
2 Department of Neurology, University of California, San Francisco, CA, USA
3 Colorado Division of Wildlife, Wildlife Research Center, Fort Collins, CO, USA
4 Department of Pathology, University of California, San Francisco, CA, USA
5 Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA

Correspondence
Stanley B. Prusiner
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 [Tg(ElkPrP) mice] 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 neurological 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 approximately 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, whereas 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.

Supplementary figures and tables are available with the online version of this paper.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2009 by the Society for General Microbiology.