| Literature DB >> 25510416 |
Hervé Cassard1, Juan-Maria Torres2, Caroline Lacroux1, Jean-Yves Douet1, Sylvie L Benestad3, Frédéric Lantier4, Séverine Lugan1, Isabelle Lantier4, Pierrette Costes1, Naima Aron1, Fabienne Reine5, Laetitia Herzog5, Juan-Carlos Espinosa2, Vincent Beringue5, Olivier Andréoletti1.
Abstract
Although Bovine Spongiform Encephalopathy (BSE) is the cause of variant Creutzfeldt Jakob disease (vCJD) in humans, the zoonotic potential of scrapie prions remains unknown. Mice genetically engineered to overexpress the human prion protein (tgHu) have emerged as highly relevant models for gauging the capacity of prions to transmit to humans. These models can propagate human prions without any apparent transmission barrier and have been used used to confirm the zoonotic ability of BSE. Here we show that a panel of sheep scrapie prions transmit to several tgHu mice models with an efficiency comparable to that of cattle BSE. The serial transmission of different scrapie isolates in these mice led to the propagation of prions that are phenotypically identical to those causing sporadic CJD (sCJD) in humans. These results demonstrate that scrapie prions have a zoonotic potential and raise new questions about the possible link between animal and human prions.Entities:
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Year: 2014 PMID: 25510416 DOI: 10.1038/ncomms6821
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919