scrapie /scra·pie/ (skra´pe) a prion disease occurring in sheep and goats, characterized by severe pruritus, debility, and muscular incoordination, ending in death.
scrapie
scra·pie (skr  p , skr p)n. A usually fatal infectious disease of sheep and goats, marked by chronic itching, loss of muscular coordination, and progressive deterioration of the central nervous system, thought to be caused by a prion. |
scrapie
[skrā′pē]
the first of the prion diseases to be recognized, occurring in sheep and goats and characterized by severe pruritus, muscular incoordination, and increasing debility ending in death.
Scrapie
A prion-induced infection, which causes fatal neurologic degeneration in sheep and goats, who scrape themselves on rocks and other surrogate back-scratchers; the scrapie agents are transmissible spongiform encephalopathy agents, which integrate themselves into the cell membrane, possibly as replicable glycoproteins
scrapie
an infectious, fatal, chronic disease of sheep and goats with clinical signs of pruritus, abnormalities of gait, recumbency and a long illness of about 6 months. A transmissible spongiform encephalopathy. The incubation period is at least 2 years. Susceptibility to scrapie is genetically determined and control programs are developed to select scrapie resistant sheep.
scrapie agent
scrapie is caused by an agent that acts like a virus but does not have the physical characteristics of one. Despite intensive study the true nature of the scrapie agent has not been defined; it is not a conventional virus or a viroid and current studies suggest that it may be a small-molecular-weight, 'self-replicating' basic protein for which the term prion has been proposed. The scrapie agent is of interest beyond its role as a rare pathogen for sheep in that it is a prototype of a new class of infectious agents responsible for a number of slow degenerative central nervous system diseases of humans and other animal species. See scrapie, prion, bovine spongiform encephalopathy, feline spongiform encephalopathy.
scrapie-associated fibrils
characteristic proteinaceous fibrils in the neurons of sheep with scrapie; the fibrils consist of membrane glycoprotein the DNA of which exists in the patient's brain cells. The glycoprotein accumulates because horizontally acquired scrapie agent induces transcription of the related host chromosomal gene and converts it to a polymerized proteinase-resistant fibrillar form.
scrapie eradication programs
most countries with scrapie have established scrapie eradication or scrapie monitoring schemes based on genotyping. According to the 2003 EU-Directive 2003/100/EC every member state has to establish a breeding program based on scrapie resistance.
scrapie eyelid test
the presence of the scrapie agent in lymphoid tissue allows its detection in the lymphoid tissue of the third eyelid in live sheep. This is in contrast to the BSE agent in cattle which does not occur in lymphoid tissue and for which there is no ante mortem test.
scrapie genotyping
susceptibility to scrapie is associated with polymorphisms in the ovine prion protein (PrP) gene at codons 136, 154 and 171. Genotyping can establish resistant sheep and genotype testing for susceptibility to scrapie is a key element of the scrapie eradication program.
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