Prions Flashcards

1
Q

are prions dead or alive

A

good question

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2
Q

what is the chain of infection

A

infectious agent
reservoir
portal of exit
mode of transmission
portal of entry
susceptible host

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3
Q

what is an example of a prion disease

A

transmissible spongiform encephalopathies

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4
Q

describe transmissible spongiform encephalopathies

A

they can pass from one individual to another. spongiform is the appearance the infection causes in the brain, which appears spongy under the microscope.

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5
Q

what is transmissible spongiform encephalopathy

A

a fatal neurological disease with no known cure that occurs due to the accumulation within the central nervous system of insoluble aggregates of a cell membrane protein called prion protein

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6
Q

what is the name prion derived from

A

proteinaceous infection particle

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7
Q

what are the types of transmissible spongiform encephalopathies

A

classic CJD (sporadic)
kuru
scrapie

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8
Q

what does scrapie affect

A

sheep

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9
Q

what are the features of prions

A
  • devoid of nucleic acid
  • due to accumulation of an abnormal form of a natural protein
  • as such, there is no immune response
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10
Q

are there prions in a healthy body

A

yes, we have normal prion proteins that reside on the exterior surface of the cell membrane that have a believed role in relation to intercellular communication

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11
Q

how are prion diseases unique

A

there are infectious agent forms like from contaminated blood, which could be genetic sporadic

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12
Q

how common are genetic sporadic prion diseases

A

one in a million across the globe

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13
Q

what causes the spongiform appearance of the brain

A

accumulation of a form of the prion protein that is difficult to degrade and accumulate over time to cause the spongiform appearance

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14
Q

why is there no immune response to prion diseases

A

they are a form of a normal protein

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15
Q

what are some prion inactivation agents

A

steam sterilisation of chemical disinfectant

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16
Q

how do prion proteins reproduce

A

prion protein is proposed to be produced from the prion protien gene and is translated to prion protein cellular, which could encounter an abnormal form of prion protein, which can alter the shape of the normal cell protein to convert it to another abnormal prion protein.

17
Q

describe the biomechanics of prion protein production

A

the inital change from one abnormal prion protein to many is slow, but once you have achieved the transformation there is more rapid aggregation of the prion proteins to give a more spongiform appearance in the human brain tissue

18
Q

what are the types of human CJD

A

sporadic
familial
iatrogenic

19
Q

what is sCJD

A

sporadic CJD

20
Q

what is fCJD

A

familial CJD

21
Q

what is iCJD

A

iatrogenic CJD

22
Q

how can iCJD be transmitted

A

by surgical instruments contaminated hormones and gradts.

23
Q

what is kuru a form of

A

iatrogenic CJD

24
Q

how is kuru iatrogenic CJD transmitted

A

generation to generation by cannibalistic rituals

25
Q

how is variant CJD transmitted

A

consumption of contaminated food material from bovine spongiform encephalopathy

26
Q

how many cattle had to be killed as a result of BSE

A

5 million

27
Q

at what age does normal CJD occur

A

60 to 70

28
Q

at what age does variant CJD occur

A

a much younger age in comparison to variant

29
Q

how does the tissue infectivity of sporadic CJD compare to variant CJD

A

vCJD can spread outside of the central nervous system and affect the appendix, tonsils and spleen

30
Q

what areas of the central nervous system are affected by CJD

A
  • brain
  • spinal cord
  • cranial and spinal ganglia
  • optic nerve
  • retina
31
Q

does CJD in any form have a large effect on blood or other tissues

A

no

32
Q

how many years have passed since the arrival of a new clinical case of CJD

A

four years

33
Q

which tissues in the oral cavity have been affected by forms of CJD

A

gingival
pulpal
saliva
tongue tissue

34
Q

why is CJD clinically relevent in dentistry

A

can have an impact on the oral cavity as this is a fast way for the infection to reach the brain

35
Q

which ganglion in the face can be affected by human CJD

A

the trigeminal ganglion that branches to supply the teeth and lip

36
Q

why is abnormal prion protein such an issue in the dental setting

A

hard to clean from surgical instruments, can survive steam sterilisation. the incubation period can be decades long and carriage can be asymptomatic

37
Q

which dental instruments can be connected with abnormal prion protein

A

dental instruments like matrix bands and endodontic files had residual blood and tissue after cleaning and sterilisation, which could be a risk of transmission despite being sterilised

38
Q

are dental procedures high risk procedures for transmission of CJD

A

no, so the standard infection control precautions and cleaning can be used to treat people safely in our own dental practice

39
Q
A