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- W2017092523 abstract "Bovine spongiform encephalopathy (BSE) may have transmitted to sheep through feed and pose a risk to human health. Sheep BSE cannot be clinically distinguished from scrapie, and conventional strain typing would be impractical on a significant scale. As human prion strains can be distinguished by differences in prion protein (PrPSc) conformation and glycosylation we have applied PrPSc typing to sheep. We found multiple Western blot patterns of PrPSc in scrapie, consistent with the known scrapie strain diversity in sheep. Sheep passaged BSE showed a PrPSc banding pattern similar to BSE passaged in other species [Collinge, J., Sidle, K.C.L., Meads, J., Ironside, J. and Hill, A.F., Nature, 383 (1996) 685–690], both in terms of fragment size following proteinase K cleavage and abundance of diglycosylated PrP. However, none of the historical or contemporary scrapie cases studied had a PrPSc type identical to sheep BSE. While more extensive studies, including sheep of all PrP genotypes, will be required to fully evaluate these findings, these results suggest that large scale screening of sheep for BSE may be possible." @default.
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- W2017092523 date "1998-10-01" @default.
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- W2017092523 title "Molecular screening of sheep for bovine spongiform encephalopathy" @default.
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- W2017092523 doi "https://doi.org/10.1016/s0304-3940(98)00736-8" @default.
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