Abstract
Transmissible spongiform encephalopathies (TSEs) are neurodegenerative diseases that are caused by prions and affect humans and many animal species. It is now widely accepted that the infectious agent that causes TSEs is PrP(Sc), an aggregated moiety of the host-derived membrane glycolipoprotein PrP(C). Although PrP(C) is encoded by the host genome, prions themselves encipher many phenotypic TSE variants, known as prion strains. Prion strains are TSE isolates that, after inoculation into distinct hosts, cause disease with consistent characteristics, such as incubation period, distinct patterns of PrP(Sc) distribution and spongiosis and relative severity of the spongiform changes in the brain. The existence of such strains poses a fascinating challenge to prion research.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Amino Acid Sequence
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Animals
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Brain / metabolism
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Brain / pathology*
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Conserved Sequence
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Creutzfeldt-Jakob Syndrome / etiology
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Creutzfeldt-Jakob Syndrome / metabolism
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Creutzfeldt-Jakob Syndrome / pathology
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Disease Transmission, Infectious
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Forecasting
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Genetic Variation
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Glycosylation
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Humans
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Incidence
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Models, Biological
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Molecular Sequence Data
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PrPSc Proteins / chemistry
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PrPSc Proteins / genetics
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PrPSc Proteins / isolation & purification
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PrPSc Proteins / metabolism
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PrPSc Proteins / pathogenicity*
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PrPSc Proteins / toxicity*
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Prion Diseases / classification
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Prion Diseases / epidemiology
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Prion Diseases / etiology
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Prion Diseases / pathology
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Prion Diseases / transmission
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Prion Diseases / veterinary
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Prions / chemistry
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Prions / genetics*
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Prions / metabolism
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Prions / pathogenicity*
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Prions / toxicity*
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Protein Sorting Signals
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Protein Structure, Secondary
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Scrapie / pathology
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Scrapie / transmission
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Species Specificity
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Tissue Distribution
Substances
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PrPSc Proteins
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Prions
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Protein Sorting Signals