Transmissions to Mice Indicate That 'New Variant' CJD Is Caused by the BSE Agent

Nature. 1997 Oct 2;389(6650):498-501. doi: 10.1038/39057.

Abstract

There are many strains of the agents that cause transmissible spongiform encephalopathies (TSEs) or 'prion' diseases. These strains are distinguishable by their disease characteristics in experimentally infected animals, in particular the incubation periods and neuropathology they produce in panels of inbred mouse strains. We have shown that the strain of agent from cattle affected by bovine spongiform encephalopathy (BSE) produces a characteristic pattern of disease in mice that is retained after experimental passage through a variety of intermediate species. This BSE 'signature' has also been identified in transmissions to mice of TSEs of domestic cats and two exotic species of ruminant, providing the first direct evidence for the accidental spread of a TSE between species. Twenty cases of a clinically and pathologically atypical form of Creutzfeldt-Jakob disease (CJD), referred to as 'new variant' CJD (vCJD), have been recognized in unusually young people in the United Kingdom, and a further case has been reported in France. This has raised serious concerns that BSE may have spread to humans, putatively by dietary exposure. Here we report the interim results of transmissions of sporadic CJD and vCJD to mice. Our data provide strong evidence that the same agent strain is involved in both BSE and vCJD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / pathology
  • Cats
  • Cattle
  • Creutzfeldt-Jakob Syndrome / etiology*
  • Creutzfeldt-Jakob Syndrome / pathology
  • Creutzfeldt-Jakob Syndrome / transmission
  • Encephalopathy, Bovine Spongiform / etiology*
  • Encephalopathy, Bovine Spongiform / pathology
  • Encephalopathy, Bovine Spongiform / transmission
  • Glycosylation
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Prion Diseases / etiology
  • Prion Diseases / pathology
  • Prion Diseases / transmission
  • Prions* / chemistry
  • Prions* / pathogenicity
  • Species Specificity
  • Time Factors

Substances

  • Prions