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Prions are infectious agents composed exclusively of a single sialoglycoprotein called PrP 27-30. They contain no nucleic acid. PrP 27-30 has a mass of 27,000 - 30,000 daltons and is composed of 145 amino acids with glycosylation at or near amino acids 181 and 197. The carboxy terminus contains a phosphatidylinositol glycolipid whose components are ethanolamine, phosphate, myo-inositol and stearic acid. This protein polymerizes into rods possessing the ultrastructural and histochemical characteristics of amyloid. Amyloid is a generic term referring to any optically homogenous, waxy, translucent glycoprotein; it is deposited intercellularly and/or intracellularly in many human diseases such as:

  • Alzheimer's disease
  • Creutzfeldt-Jakob disease
  • Down's syndrome
  • Fatal familial insomnia
  • Gerstmann-Straussler syndrome
  • Kuru Leprosy

Viroids are infectious agents composed exclusively of a single piece of circular single stranded RNA which has some double-stranded regions.

  • Because of their simplified structures both prions and viroids are sometimes called subviral particles. Viroids mainly cause plant diseases but have recently been reported to cause a human disease.

    Catalytic RNAs are those that have the intrinsic ability to break and form covalent bonds; Viroids are catalytic RNA's (ribozymes) that cleave RNA to produce fragments containing a 5'-hydroxyl and a 2', 3'-cyclic phosphate.

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Viruses and prions are examples of non-living pathogens. Viruses require host cells to replicate, while prions are misfolded proteins that can cause disease by inducing other proteins to misfold.


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Both are missing some key characteristics of life - prions more so than viruses. The most prominent feature that is missing is the ability to reproduce without a host. Viruses can't reproduce without a host cell and prions can't propagate without a normal protein that is transformed into a prion.


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