| Literature DB >> 12456643 |
Emmanuel A Asante1, Jacqueline M Linehan, Melanie Desbruslais, Susan Joiner, Ian Gowland, Andrew L Wood, Julie Welch, Andrew F Hill, Sarah E Lloyd, Jonathan D F Wadsworth, John Collinge.
Abstract
Variant Creutzfeldt-Jakob disease (vCJD) has been recognized to date only in individuals homozygous for methionine at PRNP codon 129. Here we show that transgenic mice expressing human PrP methionine 129, inoculated with either bovine spongiform encephalopathy (BSE) or variant CJD prions, may develop the neuropathological and molecular phenotype of vCJD, consistent with these diseases being caused by the same prion strain. Surprisingly, however, BSE transmission to these transgenic mice, in addition to producing a vCJD-like phenotype, can also result in a distinct molecular phenotype that is indistinguishable from that of sporadic CJD with PrP(Sc) type 2. These data suggest that more than one BSE-derived prion strain might infect humans; it is therefore possible that some patients with a phenotype consistent with sporadic CJD may have a disease arising from BSE exposure.Entities:
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Year: 2002 PMID: 12456643 PMCID: PMC136957 DOI: 10.1093/emboj/cdf653
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598