Prion Diseases Flashcards

0
Q

What are the similarities and dissimilarities between Alzheimer’s and prion diseases?

A

Prion: rapid onset (6-12months), amyloids make vacuolation, dementia
Alzheimer’s: slow onset, shaking, dementia, amyloids make fibers

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1
Q

What is the risk of contracting prion disease after exposure to deer with chronic wasting disease?

A

Some humans may be resistant to CWD

Could not induce it in macaques which are closest to humans

5 cases were reported

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2
Q

What are the causes of prion diseases?

A

PrPc is normal and converts it to PrPsc which is a beta sheet protein and it forms amyloids

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3
Q

What is the mechanism and pathology of prion diseases?

A

PRP protein converting others into PrPsc form

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4
Q

What are possible tests for prion diseases?

A
Do by ruling out
EEG - sharp wave complexes
LP - meningitis
CT - tumor
CSF - elevation of protein 14-3-3
MRI - hockey stick test, high intensity in putamen and caudate or Pulvinar thalamic nucleus
Biochem - western of PrPsc following digestion
DNA seq - PRNP gene 
Brain biopsy - spongiform change
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5
Q

What does CBC and cultures show with prion diseases?

A

No organisms and normal CBC

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6
Q

What do you see on a brain autopsy with prion diseases?

A

Minimal inflammation

Formation of plaques

Spongiform encephalopathy

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7
Q

What can prions survive?

A
30min of boiling
60 days freezing
Chemicals
UV
Smaller than a virus
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8
Q

What does PrP normally do?

A

Glycoprotein expressed in cell growth and maintenance

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9
Q

What are amyloids and how can you detect and treat them?

A

Fibrous protein deposits

Initiate unfolded protein response and increased vacuolation

Possiblly treat with Congo Red

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10
Q

What does Congo red do?

A

Bind to amyloids

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11
Q

What are the ways of transmission of prion diseases?

A
  • canniblism
  • cow meat
  • hormones, skin, surgical instruments, and corneal transplants from infected people or cadavers
  • mutations in the PRNP gene
  • unknown
  • no evidence for vertical transmission
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12
Q

What is Gerstmann-Strausslee-scheinker syndrome?

A

Familial fatal insomnia

Inherited for of mutant of PRNP gene resulting in PrPsc
Begins in adulthood and death within 3 years

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13
Q

What is the variant of PRNP that causes vCJD?

A

Codon 129 of PRNP

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14
Q

Where does PrPsc go?

A

Gut –> spleen –> lymph nodes –> peripheral nerves –> brain

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15
Q

What are TSEs?

A

Transmissible spongiform encephalopathies

Prion diseases

16
Q

What is the presentation of CJD

A

Variant - 28, 13-14months,

Classic - 68, 4-5 months

17
Q

What are horizontal transmission routs of chronic wasting diseases?

A

Urine, feces, ground water, saliva, lab processing plants