BSE in cattle, scrapie in sheep and Creutzfeldt-Jakob disease (CJD) in huma
ns are members of a family of fatal neurodegenerative diseases called Trans
missible Spongiform Encephalopathies (TSEs) or Prion diseases. They are cha
racterised by a long pre-clinical incubation period and a variable length c
linical course determined by the strain of agent and the species of host. T
hey are invariably fatal. The link between BSE in cattle and a variant form
of CJD (vCJD) has focused attention on the controls in place to minimise t
he spread of these agents both within the animal population and to humans.
Here the strategies for reducing the transmission of these agents are discu
ssed and the potential for successful eradication of these animal diseases
considered.