Journal of General Virology · 1994 · 438 citations · 22 references
Veterinary MedicineInfectious DiseasesPathobiologyGenetic EpidemiologyInfectious Disease PathologyPrion DiseasesAnimal Prion DiseasesNeuropathology Of Prion DiseaseSheep Infectious DiseasesAllelic EffectsDisease Incidence PatternsGenotype Data AnalysisNatural Disease ProcessesNon-allelic InteractionPrion Disease Phenotype CorrelationScrapie NeuropathologySpongiform Degeneration
Man and sheep are the two species in which spongiform encephalopathies occur naturally, and in which there are recognized genetic components that predispose an individual person or sheep to clinical disease. In both species mutations/polymorphisms in the PrP gene have been linked to the incidence of natural disease, but only in sheep is it possible to investigate by deliberate exposure to infection whether these polymorphisms are directly correlated with survival time. Cheviot sheep of different PrP genotypes were challenged with one of two isolates of scrapie or an isolate of bovine spongiform encephalopathy and the survival time and incidence of disease were monitored. Genotype analysis showed that dimorphisms in codons 136 and 171 of the ovine PrP gene correlated with control of disease incidence and modulation of incubation time. Crucially, the functional effects of these domains of PrP were shown to alternate depending on the isolate of infecting agent.
22
Mice devoid of PrP are resistant to scrapie
Hansruedi Büeler, Adriano Aguzzi, Andreas W. Sailer et al. · Cell · 1993 · 2.1K citations · Full text
A cellular gene encodes scrapie PrP 27-30 protein
Bruno Oesch, David Westaway, Monika Wälchli et al. · Cell · 1985 · 1.5K citations
Veterinary Medicine, Molecular Biology, Molecular Genetics +13
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease
Mark S. Palmer, Aidan J. Dryden, John T. Hughes et al. · Nature · 1991 · 897 citations
Life Sciences, Genetics, Neurology +13