A General Model of Prion Strains and Their Pathogenicity
Prions are lethal mammalian pathogens composed of aggregated conformational isomers of a host-encoded glycoprotein and which appear to lack nucleic acids. Their unique biology, allied with the public-health risks posed by prion zoonoses such as bovine spongiform encephalopathy, has focused much attention on the molecular basis of prion propagation and the “species barrier” that controls cross-species transmission. Both are intimately linked to understanding how multiple prion “strains” are encoded by a protein-only agent. The underlying mechanisms are clearly of much wider importance, and analogous protein-based inheritance mechanisms are recognized in yeast and fungi. Recent advances suggest that prions themselves are not directly neurotoxic, but rather their propagation involves production of toxic species, which may be uncoupled from infectivity.
A General Model of Prion Strains and Their Pathogenicity
Science 2007 318: 930-936
Related:
- Variant Creutzfeldt-Jacob disease (vCJD) update
- Prions, Proteasomes, and Mad Cows
- New forms of bovine spongiform encephalopathy
- Prions and Alzheimers disease
Tags: Biology, Health, Medicine, Microbiology, Prions, Science
dear doctors,
prion diseases ,however many there may be, all result in death,not a good prognosis. since i read in voice of freedom, that, prions are released in urine into the soil and our water supplies, i am making an assumption that the entire world is already infected. whos counting?
thank you, stephany