MICROBIOLOGY PPT LECTURE NOTES | Karya Tulis Ilmiah
Prion
Similar to Viruses Atypical
Agents
Small
Filterable
Need host cells
No machinery for energy generation of
protein synthesis
Different from viruses
No dectectable virions in infected tissues
No detectable virions in purified infectious
material
If nucleic acid is present, very small
Very resistant
Resistant to or only
1.
2.
3.
4.
5.
partially inactivated
by
Formaldehyde
Ethanol
Glutaraldehyde
Ultraviolet and ionizi
ng irradiation
Non-ionic detergents
1.
2.
Inactivated by
Autoclaving
5%sodium
hypochlorite
3. Sodium hydroxide
4. Proteases, urea,
other protein
denaturants
Pathogensis
Kuru
CJD(Creutzfeldt Jakob disease)
GSS(Gerstmann Straussler-Scheinker syndrom
e)
FFI(Fetal familial insomnia)
Scrapie(sheep and goats)
Bovine spongiform encephalopathy
Transmissible mink encephalopathy
Chronic wasting disease of mule deer
Simplified model for prion disease.
How can this model explain the sporadic, acquired or
inherited form of the disease?
Why are there differences in prion dise
ases?
Similar to Viruses Atypical
Agents
Small
Filterable
Need host cells
No machinery for energy generation of
protein synthesis
Different from viruses
No dectectable virions in infected tissues
No detectable virions in purified infectious
material
If nucleic acid is present, very small
Very resistant
Resistant to or only
1.
2.
3.
4.
5.
partially inactivated
by
Formaldehyde
Ethanol
Glutaraldehyde
Ultraviolet and ionizi
ng irradiation
Non-ionic detergents
1.
2.
Inactivated by
Autoclaving
5%sodium
hypochlorite
3. Sodium hydroxide
4. Proteases, urea,
other protein
denaturants
Pathogensis
Kuru
CJD(Creutzfeldt Jakob disease)
GSS(Gerstmann Straussler-Scheinker syndrom
e)
FFI(Fetal familial insomnia)
Scrapie(sheep and goats)
Bovine spongiform encephalopathy
Transmissible mink encephalopathy
Chronic wasting disease of mule deer
Simplified model for prion disease.
How can this model explain the sporadic, acquired or
inherited form of the disease?
Why are there differences in prion dise
ases?