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Bovine Spongiform Encephalopathy (view source)
Revision as of 14:36, 6 June 2011
, 14:36, 6 June 2011no edit summary
Also known as: '''''BSE — Bovine Spongiform Encephalopathy''''', '''''TSE — Transmissible Spongiform Encephalopathy'''''', '''''Mad Cow Disease''''', '''''Prion — proteinaceous infectious particle''''', '''''Scrapie — a transmissble prion affecting sheep that causes non-febrile neurological disease'''''
Also known as: '''''BSE — Bovine Spongiform Encephalopathy''''', '''''TSE — Transmissible Spongiform Encephalopathy'''''', '''''Mad Cow Disease''''', '''''Prion — proteinaceous infectious particle''''', '''''Scrapie — a transmissble prion affecting sheep that causes non-febrile neurological disease'''''
==Introduction==
==Introduction==
Bovine spongiform encephalopathy (BSE) is a prion –associated transmissible spongiform encephalopathy (TSE) which causes a non-febrile neurological disorder affecting adult cattle. It has occurred as a result of the exposure of cattle to animal and ruminant-derived protein feeds e.g. meat-and-bone meal (MBM) containing the scrapie-like agent. As the disease progresses histological changes show bilateral symmetrical vacuolation in the grey matter of the brain, gliosis and hypertrophy of astrocytes, neuronal degeneration and cerebral amyloidosis. There is no evidence to support the horizontal transmission of BSE under natural circumstances but there is evidence supporting vertical transmission <ref name="Wilesmith 1997">Wilesmith, J.W., Ryan, J.B.M., 1997. Absence of BSE in the offspring of pedigree suckler cows affected by BSE in Great Britain. Veterinary Record, 141(10):250-251; 5 ref..</ref>., <ref name="Donnelly 1998">Donnelly ,C.A., 1998. Maternal transmission of BSE: interpretation of the data on the offspring of BSE-affected pedigree suckler cows. Veterinary Record, 142(21):579-580; 9 ref..</ref>,
Transmissible Spongiform Encephalopathies (TSEs) are neurological diseases that have been found in humans, cattle, sheep and other mammals (e.g. cats, goats, deer, antelope). The agent of disease is believed to be an abnormal prion protein (or is prion associated). An abnormal prion is a protein with an abnormal folding structure when compared to the naturally occurring prion found in nervous and lymphoreticular tissues. Various abbreviations are in use to refer to this: Prion Protein (PrP); Abnormal Prion Protein (PrP<sup>ab</sup>); Resistant Prion Protein (PrP<sup>res</sup>); Scrapie Prion Protein PrP<sup>sc</sup>) and others.
==Signalment==
==Signalment==
==Clinical Signs==
==Clinical Signs==
==Control==
==Control==
==Refereneces==
==Refereneces==
[[Category:Transmissible_Spongiform_Encephalopathies]]
[[Category:Transmissible_Spongiform_Encephalopathies]]
[[Category:To_Do_-_Jaimie Meagor]]
[[Category:To_Do_-_Jaimie Meagor]]