Transmissible mink encephalopathy
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Transmissible mink encephalopathy (TME) is a rare sporadic disease that affects the central nervous system of ranch-raised adult mink. It is a transmissible spongiform encephalopathy, caused by proteins called prions.[1]
This illness has a minimum incubation period of 7 months with a maximum of 12 months. This disease results in mortality of adult animals.[2]
Clinical signs of TME include behavioural changes such as confusion, loss of cleanliness, and aimless circling. An affected animal shows signs of weight loss, might develop matted fur, hindquarter ataxia, and its tail arched over its back. Seizures may very rarely occur. Near-death stages include the animal showing signs of drowsiness and unresponsiveness.
Early clinical signs of TME are often subtle, and can include difficulty eating and swallowing as well as changes in typical grooming behavior. Affected mink may soil their nests or scatter feces within their habitats. As the condition progresses, affected animals may become hyperexcitable and develop the tendency to bite compulsively. Other signs of the condition include incoordination, circling, jaw clenching, and self-mutilation. Once clinical signs of TME appear, the condition only progresses to fatality, with death typically occurring within 2–8 weeks.[2]
Diagnosis
Currently, no tests are available to detect signs of this illness in live animals. However, veterinary pathologists can confirm this illness by microscopic examination of the brain tissue in animals suspected to have died of this disease, where they expect to detect areas of distinct sponge-like formations, or by the identification of the prion protein in these tissue samples.
