1. Creutzfelt-Jacob Disease (CJD)
A transmissible spongiform encephalopathy or “prion disease”

2. CJD and TSEs
Creutzfelt-Jacob disease (CJD) is one of a small group of disease classified as transmissible spongiform encephalopathies (TSEs)
The leading hypothesis is that TSEs are not transmitted by microbes or viruses, but are spread by specific misshaped proteins, given the name prion proteins

3. CJD and TSEs
At present, only 6 human man diseases are thought to be caused by prion proteins: Creutzfelt-Jacob disease, new variant CJD (vCJD), Gertmann-Straussler-Scheinker syndrome, fatal familial insomnia, kuru, and possibly Alpers' disease.

4. CJD and TSEs
There are up to 25 prion diseases that have been identified in animals, including scrapie (sheep), bovine spongiform encephalopathy (cattle), and chronic wasting disease (deer & elk).

5. History of CJD and prion diseases
5th Century BC:
Hippocrates described disease with symptoms similar to TSE that was occurring in sheep and cattle
4th and 5th Century AD:
Similar disease was recorded by the Roman Renatus
1755:
Great Britain’s House of Commons discussed the epidemic of scrapie in sheep
1759 :
There were unsupported claims scrapie might be contagious

6. History of CJD and prion diseases
Early 20th Century:
Despite earlier failures in attempting to show transmission of scrapie, it was finally proven through the intraocular injection of infected nervous tissue from diseased sheep, to healthy sheep, which then developed the disease.
First instance showing transmissibility of TSEs.
1921:
The first described case of disease that became known at Creutzfeldt-Jakob disease
1950s and 60s
The disease kuru was described and was shown to be transmitted via cannibalism.
Scrapie-Iike lesions were found the brains of kuru victims.
Kuru and CJD shown to be transmissable to chimpanzees.

7. History of CJD and prion diseases
1980s: Stanley Prusiner put forth the hypothesis that that a protein was responsible for the transfer of the disease
1988 : Neuropathology, bovine spongiform encephalopathy (BSE), AKA mad cow disease was described in cows
Late 1980s the prevalence of BSE in British cattle caused concerns that BSE might be transferable to humans. BSE believed to result from scrapie jumping species to cows
1990s: a new disease similar to CJD and kuru called “new variant CJD” was found in humans who had been exposed to BSE infected cattle or their products.

8. Case Study: Patient had a surgical procedure in 1971, at age 38.
Determined to be the most likely source of the infection, after CJD diagnosis
Occurred before prion hypothesis or before it was believed the infectious agent was resistant to sterilization techniques
Long incubation period
The malformed prion protein induces refolding of normal proteins like itself
Slow process at first (exponential growth)
Much longer replication times than microbes
It takes time to build up the levels of mis-folded prion protein in neural tissue
CJD first suspected 1.5 months after first consulting physicians (11 weeks after first symptoms)
CJD diagnosis at 2 months
Diagnostic Tests
Electroencephalograph
Cerebrospinal fluid analysis for protein
MRI of the brain

9. Case Study: Final stages of disease progression (months 5 &6)
Profound dementia
Loss of speech, nearly complete inability to move
Treatment focused on comfort measures, symptom management, sedation, and prevention of opportunistic infections in hospital
Death, age 68, occurred 25 weeks after first seeking medical help for symptoms (31 weeks after first signs and symptoms)
Cause of death was pneumonia due to inability to clear lungs
Infection of others?
Because of knowledge of CJT being passed by prions, appropriate precautions were taken clinically and post mortem, so it is unlikely that others were infected after the acute stage of the disease. Transmissibility is believed to be low during incubation period. The patient was not a blood or tissue donor before or after onset of symptoms, which would have been been a risk for transmission.

10. Etiologic Agent & Pathophysiology
The infectious agent in Creutzfeldt-Jacob disease (CJD) is a mis-folded protein. This malformed protein has fewer alpha-helices and more beta-sheets than the normal protein.
Exposure to the malformed prion protein, can induce correctly folded proteins of the same type, to re-fold into the mutant form of the protein.

11. Etiologic Agent & Pathophysiology

12. Etiologic Agent & Pathophysiology
The disease state results from build-up of the malformed protein in neural tissues which kills neural cells.
Incubation period can range from months to decades.
The death of the nerve cells and glial cells is the cause of all signs and symptoms of CJD and other TSE diseases.
Most instances of CJD are sporadic, occur in people with no known risk factors or gene mutations – ‘unknown source ‘
Some cases of CJD are transmitted by exposure to prion-contaminated instruments, tissues, serum, hormones, etc, from individuals with CJD - ‘known or suspected source’

13. The Leading Hypothesis
Protein-only hypothesis
The protein is believed to be the sole infectious agent.
It induces its own replication by causing conformational (folding) changes in normal proteins

14. The 2 Competing Hypotheses
Multi-component hypotheses
Proposes prion protein is the infectious agent for the disease
Also proposes that more than just the mutated prion protein is required – cofactors also
Cofactors may include lipids and nucleic acids (but no genomic information contributes to the disease)
Cofactors may form part of the prion or serve as catalysts for the refolding of normal proteins
Viral hypothesis
Postulates that an infectious virus causes the disease
Support for this hypothesis is waning
Mostly a holdover of the long-held belief that a virus must be responsible for this type of disease

15. Related Human Prion Diseases
There are 2 inherited human prion diseases, fatal familial insomnia and Gertmann-Straussler-Scheinker syndrome. These diseases are caused by the inheritance of mutations in the PRNP gene from a parent. The mutation results in a prion protein being made which folds incorrectly without exposure to malformed proteins.
There are believed to be cases of the hereditary TSEs that resulted from random point mutations in the PRNP gene, rather than being present in the genes of a parent.
The human disease new variant CJD (vCJD) is caused by exposure to cows (or their products) that were infected with the prion disease bovine spongiform encephalopathy (BSE) commonly known as mad cow disease.

16. Pathology Human prion disease share 4 characteristics:
1 spongiform changes in brain tissues – lesions leave holes in tissue making it appear spongy
Neuronal loss – death of neuron cells
Astrocytosis – death of glial cells
Amyloid plaque formation – some features are found in animal prion diseases

17. Clinical Signs and Symptoms of CJD
Personality changes
Psychiatric problems (depression)
Lack of coordination and control
Ataxia
Involuntary jerky movements
Unusual sensations
Insomnia
Confusion
Memory problems
Final stages of the disease:
Dementia
Loss of ability to speak
Loss of ability to move
Eventual death

18. “Virulence Factors”
While not true virulence factors as we see in microbial diseases, there are several characteristics of all prion diseases which facilitate their transmission.
Long incubation periods (months to decades)
No signs or symptoms during incubation
So far, no way of detecting the mutated prion protein in living individuals
Examinations of brain tissue after death is only sure way to confirm CJD and other TSEs
Research is working on promising technology which may solve this

19. “Virulence Factors”
Documented Zoonotic infection of animal TSE diseases to humans
Scrapie may be the origin of BSE
BSE is the causative prion for new variant CJD
Chronic wasting disease (deer & elk) is being watched closely to see if it jumps to humans. Hunter are given advise to reduce any risk from game animals they harvest
Prion proteins are highly stable – very resistant to usual sterilization procedures
Boiling, autoclave, cooking and other heat sterilization methods don’t denature the prion protein
Irradiation dose not denature the prion protein
Special proteases, bleach, acid baths followed by autoclaving seem effective
We don’t know how long mutated prion proteins persist on surfaces or in contaminated tissues.
Some TSE may be transmissible thru aerosols (tiny droplets)

20. Modes of Transmission
CJD is mostly a sporadic disease. No mode of transmission is proven to account for common form of the disease.
New variant CJD (nvCJD)is believed to occur in humans as a result of exposure to bovine spongiform encephalopathy
A hereditary form of CJD (fCJD) occurs as a result of an inherited defective gene that promotes the misfolding of the prion protein with no exposure to malformed proteins
Exposure or consumption of tissues from animals with any TSE is considered a risk factor
Nervous tissue (brain and spinal cord) have highest concentration of prion proteins

21. Diagnostic Procedures
Electroencephalograph
Cerebrospinal fluid analysis for protein
MRI of the brain
Brain Biopsy
Autopsy, post mortem

22. Prevention Measures
Feeding of rendered mammal proteins to mammals in human food chain (sheep, goats, cows, farmed deer, elk, etc) has been banned in most developed countries
Brain and spinal cord are separated from carcass early in butchering process
Hunters in CWD affected areas are advised to bone out meat and avoid contact of meat with any nervous tissue.
Elimination of cannibalistic funerary practices in New Guinea contributed to the end of kuru epidemic

23. Treatment of CJD No known cure, therapy or vaccine for TSE diseases
Treatment of the disease is primarily limited to treatment of symptoms and palliative care
Study of kuru suggests there may have been resistance factors in some individuals in the population
Active research in all avenues of treatment is ongoing

24. Prevalence of CJD
102 cases in Oregon ( ): an avg. of 5.7 per year)
About 1 case per million people, per year, in the US of the common (sporadic) form of CJD
About 1 case per million people, per year, world wide

25. Why is this an important disease to study?
CJD and all other known prion diseases are fatal
Evidence suggests that prion diseases can jump species
Humans have contact with most of these species
BSE is still occasionally discovered – we eat lots of beef
Because of long incubation period, epidemics could become wide spread, before signs of disease start appearing
The Prion hypothesis was one of the most significant and controversial biological proposals in the modern era of biology

26. References:
Articles, books: Belay, E. (1999). Transmissible spongiform encephelopathies in humans. Annual Review of Microbiology, 53, Retrieved from Cowan, M., & Bunn, J. (2013). Microbiology fundamentals: A clinical approach. (pp ). New York: McGraw-Hill. Webpages: CJD (creutzfeldt-jakob disease, classic). (n.d.). Retrieved from Creutzfeldt–jakob disease. (n.d.). Retrieved from Oregon Health Authorty. (2009, Sept 28). Oregon reprted deaths fromm creutzfeldt-jacob disease, present. Retrieved from Prion. (n.d.). Retrieved from Prion diseases. (n.d.). Retrieved from Transmissible spongiform encephalopathy. (n.d.). Retrieved from vCJD (variant creutzfeldt-jakob disease). (n.d.). Retrieved from

27. Photos, Illustrations:
Deyo, S., & Deyo, H. (Producer). (2001). CJD USA map. [Print Photo]. Retrieved from
(n.d.). Major regions of the human brain affected by tse. [Web Graphic]. Retrieved from
(n.d.). Normal to abnormal protein. [Web Graphic]. Retrieved from
(n.d.). Plaques from creutzfeldt–jakob disease in the brain.. [Web Photo]. Retrieved from
(n.d.). Prion theory. [Web Photo]. Retrieved from
(n.d.). Prion graphic, mayo foundation. [Web Graphic]. Retrieved from
(n.d.). Prions, image 1 and image 2. [Web Graphic]. Retrieved from
(n.d.). Deer with chronic wasting disease (cwd). [Web Photo]. Retrieved from
(n.d.). sheep. [Web Photo]. Retrieved from
(n.d.). madcow2. [Web Photo]. Retrieved from

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