In the study of micro-biology, there are several kinds of pathogens that can be observed in the

Creutzfeldt-Jakob Disease: It happens when a prion protein misfolds itself, thus causing a “domino effect” which unfolds itself causing a malfunction.

Proteinaceous Infectious Particles, commonly known as Prions, are extremely rare misfolds of the protein PrPc, which cause fatally neurodegenerative diseases, and are theorized to be infectious only by the protein itself (U.S National Library of Medicine, 1998). This “protein-only theory” is still heavily debated today, as some scientists deny the theory, and there isn’t a significant amount of evidence on each side to qualify the theory or disprove it (Soto, C. 2011). The base “Prion” protein is encoded in the gene PRNP, while being non-infectious. Prions are most commonly found in human prion diseases, but they can also be in other animals in the form of Mad Cow Disease and Chronic Wasting Disease, classified as Bovine Spongiform Encephalopathies

Humans have to deal with many different diseases and the ones most disliked are the ones with no cures. Like cancer, transmissible spongiform encephalopathies have no cure, but they are more rare. These diseases are prion diseases which cause the brain to deteriorate. Prions are proteins that sometimes behave like viruses, which mean that they should have some form of nucleic acid, but since they don’t, they cause abnormalities. The nervous system contains many normal prions, but when an abnormal prion comes along, it transforms all the normal prions into abnormal ones. Bovine spongiform encephalopathy is found in cattle, but it can be transmitted to humans.

Mad cow disease is to serious and deadly that it is not worth the risk of eating beef from a feedlot. Michael Pollan stated, "Mad cow is a brain disease that is always fatal. It is spread by eating the brains of infected animals" (56). Clearly mad cow disease will kill anyone that gets infected so it is not worth the risk to eat CAFO beef. In addition, "Ground-up cattle brains were put into cattle feed and some of those cows got mad cow disease. Human beings who ate infected beef also got the disease..." (Pollan and Chevat 56). This shows how completely unnatural CAFOs are and why people should not eat or buy CAFO meat. It also illustrates just how dangerous mad cow disease is; that people should be cautious by boycotting CAFO beef. However, an author for the Los Angeles Times, Paul Roberts said, “there has never been a confirmed case of mad cow disease connected with anyone eating U.S. beef" (Rodgers). Evidently getting mad cow disease in the U.S. is unlikely. Pollan retaliated by saying "Then people in England began dying of a sickness called mad cow disease" (55-56). This shows that although people have not eaten infected beef in the U.S. they have in other places. Therefore if people want to stay safe then they should not eat the beef produced in CAFOs so that they do not get mad cow

     Mad Cow Disease, scientifically referred to as (BSE) Bovine Spongiform Encephalopathy, is a disease that affects those humans who eat the meat from infected cows. Mad Cow Disease is one of several fatal brain diseases called (TSE) Transmissible Spongiform Encephalopathy. (USDA) There was evidence of a new illness resembling the sheep disease scrapie. It was technically named BSE but quickly acquired the mad cow tag because of the way infected cattle behave. (CNN) In 1997, there was an award given to Stanley Prusiner, for concluding that a distorted protein called a prion was responsible for Mad Cow Disease, noted the long incubation period made it difficult to distinguish (Bryant).

In bovine spongiform encephalopathy (BSE), the disease is caused by the misfolding of proteins that cause proteins and peptides to develop a fibrillary structure. The PrPc is a correctly folded prion and the misfolded form is called PrPSc. BSE occurs when the normal PrPc come into contact with the toxic PrPSc and the normal prion takes on the shape of the PrPSc. The normal chaperones are unable to convert the PrPSc back to the normal form. The PrPSc now takes on the role of chaperone and the conversion of PrPc prions continue over and over. PrPSc, now being hydrophobic avoids the water of the inner cell and begin to accumulate and form plaques along the neuronal cell membranes. The aggregation of the prions on the cell membrane eventually lead to cell death which produces the sponge-like appearance in the brain of cattle infected with BSE (Thompson, 2014).

Although mad-cow disease is always fatal, it is not really much of a worry in the United States. There have only been four cases of mad-cow disease ever recorded in the United States. In every case, the United States Department of Agriculture has intervened and recalled tons of beef, 10,400 lbs. in the first case to be exact, in order to insure that the meat did not reach the plates of United States citizens.

Encephalitis literally means an inflammation of the brain, but it usually refers to brain inflammation caused by a virus. It may also be called “acute viral encephalitis or aseptic encephalitis';. Encephalitis is an infectious disease of the Central Nervous System characterized by pathologic changes in both the gray and white matter of the spinal cord and brain. It may be due to specific disease entity such as rabies or an arthropod-borne virus (arbovirus), or it may occur as a sequela of influenza, measles, German measles, chicken pox, herpes virus infection, small pox, vaccinia, or other diseases. The specific viruses involved may vary. Exposure can also occur through insect bites, food or drink, or skin

Abnormal changes happen in the brain, and it appears as a sponge-like holes and gaps, causing deterioration in the areas of the brain. This can turn into spongiform degeneration that results in the progressive neurological and neuromuscular symptoms that are associated with CJD. This disorder is a result from a mutation in the gene that regulates the production of the human protein or direct transmission with abnormal protein in infected brain tissue. Scientist believe that there is a transmissible agent that is responsible for causing CJD. This is a slow virus, since it can take many years from exposure to the appearance of

What is Mad Cow Disease? Mad Cow Disease "is a normally extremely rare neurological disorder that affects the central nervous system of an animal and a human. The disease infested brain of the animal or human is slowly, progressively, and severely damaged. It has been categorized as a disease, which falls into the category of a disease known as Spongiform Encephalopathy. Having Bovine Spongiform Encephalopathy is an over-dramatized way of specifying that one has diseased brain tissue which is; spongy, porous, and no

The aggregation of prion proteins and their transmissibility from one cell to another has been shown to be evident (Cushman et al.; Goedert et al. 2010), therefore strongly suggesting that these events may play a role in pathogenesis for many diseases, including both AD and PD. While none of these diseases is infectious in an identical way as

Chronic Wasting Disease (CWD) is a fatal neurodegenerative transmissible spongiform encephalopathy (TSE ) found in some white tailed deer. CWD is associated with diseases such as Mad-Cow disease, Scrapie, and Creutzfeldt–Jakob disease. With well supported evidence it is hypothesized that CWD originated from Scrapie. The causation of CWD is an abnormal form of PrPcwd prion. This prion is a naturally occurring protein found in mammals. Prions lack genome and are highly resistant to degradation. Chronic Wasting Disease can be transmitted by direct contact between the animals and/or on resources such as salt licks.

Mad Cow Disease Bovine spongiform encephalophathy ( BSE), which is mainly known as mad cow disease has infected the society and has put the lives of individuals at risk. This was very frightening to the people that ate meat during that time. The terrified people would not even want to eat hamburgers at MacDonald, steak at restaurant and much more. What also alarmed the people was the fact that there was a possibility of getting the human form of mad cow disease. This was called variant Creutzfeldt-Jakob disease (vCJD) which is through tainted blood, but this was only a theory which

Prions are a type of protein found naturally in the brain and other regions of the central nervous system. The diseases associated with

Creutzfeldt-Jakob’s Disease affects one person in every million people per year worldwide. In the United States, there are about three-hundred cases per year, making Creutzfeldt-Jakob’s Disease a rare disease. However, once the brain is affected, this degenerative, debilitating disease progresses rapidly. The particles responsible for this rare, fatal disease are called prions. Prions are protienaceous infectious particles formed when normal proteins misfold and clump together, which causes the brain to be filled with tiny holes resembling a sponge.