Literature DB >> 6358899

Scrapie-associated fibrils in Creutzfeldt-Jakob disease.

P A Merz, R A Somerville, H M Wisniewski, L Manuelidis, E E Manuelidis.   

Abstract

Scrapie of sheep, and Creutzfeldt-Jakob disease (CJD) of man belong to a group of transmissible encephalopathies which have been successfully transmitted to a variety of hosts. In susceptible hosts, these diseases are characterized by progressive degeneration of the central nervous system leading inevitably to death. The agents responsible for these diseases have not yet been identified, but they exhibit similar physicochemical characteristics. Abnormal fibrils designated 'scrapie associated fibrils' (SAF) have been observed in synaptosomal preparations of scrapie infected brain. They have never been observed in various types of control animals. We report here that SAF are present in CJD brain fractions in the experimentally transmitted disease as well as in a few naturally occurring human cases of CJD. SAF are also present in spleen extracts of animals experimentally infected with scrapie or CJD. This close association of SAF with these two diseases and two different tissues (brain and spleen) known to contain titres of infectivity, suggest that the SAF are: (1) a unique pathological response to the disease or (2) the infectious agent of these diseases.

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Year:  1983        PMID: 6358899     DOI: 10.1038/306474a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  46 in total

1.  A specific RFLP type associated with the occurrence of sheep scrapie in Japan.

Authors:  Y Muramatsu; K Tanaka; M Horiuchi; N Ishiguro; M Shinagawa; T Matsui; T Onodera
Journal:  Arch Virol       Date:  1992       Impact factor: 2.574

2.  PrP amyloid plaques in Creutzfeldt-Jakob disease of short duration: immunohistochemical studies of 5 cases from Poland.

Authors:  P P Liberski; H Kwiecinski; M Barcikowska; B Mirecka; J Kulczycki; E Kida; P Brown; D C Gajdusek
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

3.  N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state.

Authors:  B Caughey; G J Raymond; D Ernst; R E Race
Journal:  J Virol       Date:  1991-12       Impact factor: 5.103

4.  Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis.

Authors:  M P McKinley; R K Meyer; L Kenaga; F Rahbar; R Cotter; A Serban; S B Prusiner
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

5.  Characterization of major peptides in Creutzfeldt-Jakob disease and scrapie.

Authors:  T Sklaviadis; L Manuelidis; E E Manuelidis
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

6.  Bovine spongiform encephalopathy.

Authors:  P B Little; J Thorsen
Journal:  Can Vet J       Date:  1989-09       Impact factor: 1.008

7.  Scrapie: Report of an outbreak and brief review.

Authors:  L Petrie; B Heath; D Harold
Journal:  Can Vet J       Date:  1989-04       Impact factor: 1.008

8.  A 54-kDa normal cellular protein may be the precursor of the scrapie agent protease-resistant protein.

Authors:  P E Bendheim; D C Bolton
Journal:  Proc Natl Acad Sci U S A       Date:  1986-04       Impact factor: 11.205

9.  Immunological comparison of scrapie-associated fibrils isolated from animals infected with four different scrapie strains.

Authors:  R J Kascsak; R Rubenstein; P A Merz; R I Carp; N K Robakis; H M Wisniewski; H Diringer
Journal:  J Virol       Date:  1986-09       Impact factor: 5.103

10.  A new method to classify amyloid fibril proteins.

Authors:  T Kitamoto; J Tateishi; K Hikita; H Nagara; I Takeshita
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

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