Prions

Prions are abnormal proteins that are believed to be responsible for several rare, degenerative brain disorders in animals and humans. These disorders, known as transmissible spongiform encephalopathies (TSEs), include mad cow disease in cows, scrapie in sheep, and Creutzfeldt-Jakob disease (CJD) in humans.

Prions are unusual in that they are infectious agents that do not contain nucleic acid, the genetic material found in all living organisms. Instead, they are thought to be composed solely of proteins. Prions are believed to cause TSEs by altering the shape and function of normal proteins in the brain. This leads to the accumulation of abnormal, proteinaceous aggregates in the brain, which can cause damage to brain tissue and lead to the symptoms of TSEs.

Prions are difficult to detect and eliminate, and there is currently no cure for TSEs. However, research into the biology of prions and TSEs is ongoing, and scientists are working to develop treatments and prevention strategies for these disorders.

TSEs are characterized by the accumulation of abnormal, proteinaceous aggregates in the brain, which can cause damage to brain tissue and lead to the symptoms of the disease.

Here are some examples of TSEs caused by prions:

Creutzfeldt-Jakob disease (CJD): CJD is a rare, degenerative brain disorder that affects humans. It is characterized by a rapid decline in mental function, personality changes, and involuntary movements. CJD is caused by abnormal prion proteins that accumulate in the brain.
Mad cow disease (bovine spongiform encephalopathy, BSE): BSE is a TSE that affects cows. It is characterized by abnormal behavior, difficulty standing and walking, and a loss of body weight. BSE is caused by abnormal prion proteins that accumulate in the brain.
Scrapie: Scrapie is a TSE that affects sheep. It is characterized by abnormal behavior, difficulty standing and walking, and a loss of body weight. Scrapie is caused by abnormal prion proteins that accumulate in the brain.
Chronic wasting disease (CWD): CWD is a TSE that affects deer, elk, and moose. It is characterized by abnormal behavior, difficulty standing and walking, and a loss of body weight. CWD is caused by abnormal prion proteins that accumulate in the brain.
Kuru: Kuru is a TSE that affects humans and is found primarily in the Fore people of Papua New Guinea. It is characterized by tremors, difficulty speaking and swallowing, and a loss of muscle control. Kuru is thought to be transmitted through the consumption of infected human brain tissue.

Overall, TSEs caused by prions are rare but serious diseases that can lead to significant brain damage and death. There is currently no cure for TSEs, and research into these diseases is ongoing.