Bovine Spongiform Encephalopathy

Bovine Spongiform Encephalopathy (BSE) BSE is a disease that contaminates the brain seen in dairy cattle. Because there is no known cure, we kill many cows every year. Humans are known as Creutzfeld's disease - Jakob disease. It may be infected with a disease called scrapie. There is no known cure for infectious spongiform encephalopathy including CJD. To prevent this disease, please check the beef before entering America. Without antibodies, the microscope is the only way to confirm that cattle are infected.

The term BSE is short but it represents bovine spongiform encephalopathy with a long name. "Cattle" means that the disease affects the cow, "sponge" means that the brains of the diseased cow looks like a sponge under the microscope. Mad cow disease is often called "mad cow disease." Most scientists believe that mad cow disease is caused by a protein called a prion protein. Normal prion proteins become harmful abnormal prion proteins for reasons that are not well understood. The sick cow's body does not even know that there is an abnormal prion. I do not know where it is, the bull's body can not resist disease.

CWD is a contagious spongiform encephalopathy and belongs to the same type of disease as bovine spongiform encephalopathy (BSE - commonly referred to as "mad cow disease"). These diseases are caused by prion, which is an infectious protein. These diseases affect the brain and spinal cord, causing symptoms such as weakness, discordance, abnormal behavior. How CWD is transmitted from animals to animals is not fully understood, but it is transmitted by direct contact between animals or when an animal eats soil contaminated with saliva or feces of infected animals It is conceivable. It shows the path from Moose to Moose.

Infectious agents composed of prion viruses and proteins are unique in that they are associated with certain forms of neurodegenerative diseases. Bovine spongiform encephalopathy (BSE, or "mad cow disease") is a bovine prion disease associated with human mutant Creutzfeldt-Jakob disease (vCJD). Consumption of cattle products, including certain hazardous substances such as brain tissue, is the most likely route for prions to spread to humans. Natural toxins include mycotoxins, marine organism toxins, toxins from cyanoglucosides, poison mushrooms, and the like. Staple foods such as corn and cereal may contain high levels of mycotoxins such as aflatoxin and ochratoxin produced by grain molds. Long-term exposure can affect the immune system and normal development and can cause cancer