Literature DB >> 2872607

Scrapie: how much do we really understand?

R H Kimberlin.   

Abstract

Biological studies have produced convincing evidence for different scrapie strains, some of which undergo mutation. This argues strongly in favour of the infectious scrapie agent having a genome. The length of incubation period is influenced by the strain of agent but is also under strict host control. In mice, this control is exerted by a gene called Sinc which affects the overall rate of agent replication in the CNS. After peripheral infection, invasion of the CNS from lymphoreticular sites of agent replication is a key step in pathogenesis. Evidence from one scrapie model indicates spread of infection along autonomic nerves to the thoracic spinal cord and then to other parts of the CNS. Other studies have shown that infection can spread in neurons. There are close relationships between the presence of replicating agent and the development of vacuolation, and also of cerebral amyloid when it occurs. We can, therefore, begin to understand the patterns of lesion development in the brain in terms of the targeting of infection and its replication at certain sites. Structures known as SAF (Scrapie Associated Fibrils) have been discovered in extracts of scrapie brain (but not uninfected brain) and a glycoprotein (PrP 27-30: SAF protein) is a major constituent of purified SAF. The glycoprotein is coded by a single gene which is present in several species and expressed in uninfected brain. The normal protein seems to be modified in scrapie infected brain so that it accumulates as SAF. The modified protein may also be deposited as extracellular amyloid because there appear to be common epitopes between SAF and scrapie amyloid. The biochemical nature of the scrapie agent remains in doubt and the association between infectivity and purified SAF may arise fortuitously from the fact that scrapie agent is 'sticky'.

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Year:  1986        PMID: 2872607     DOI: 10.1111/j.1365-2990.1986.tb00046.x

Source DB:  PubMed          Journal:  Neuropathol Appl Neurobiol        ISSN: 0305-1846            Impact factor:   8.090


  12 in total

Review 1.  The search for scrapie agent nucleic acid.

Authors:  J M Aiken; R F Marsh
Journal:  Microbiol Rev       Date:  1990-09

2.  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

3.  Immunological analysis of host and agent effects on Creutzfeldt-Jakob disease and scrapie prion proteins.

Authors:  J M Bockman; D T Kingsbury
Journal:  J Virol       Date:  1988-09       Impact factor: 5.103

4.  The extended cell panel assay characterizes the relationship of prion strains RML, 79A, and 139A and reveals conversion of 139A to 79A-like prions in cell culture.

Authors:  Anja M Oelschlegel; Mohammad Fallahi; Shannon Ortiz-Umpierre; Charles Weissmann
Journal:  J Virol       Date:  2012-02-29       Impact factor: 5.103

5.  Measurement of the concentration of amphotericin B in brain tissue of scrapie-infected hamsters with a simple and sensitive method.

Authors:  P Casaccia; A Ladogana; Y G Xi; L Ingrosso; M Pocchiari; M C Silvestrini; A Cittadini
Journal:  Antimicrob Agents Chemother       Date:  1991-07       Impact factor: 5.191

Review 6.  On the biology of prions.

Authors:  S B Prusiner; R Gabizon; M P McKinley
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

7.  A case of Creutzfeldt-Jakob disease related to familial retinitis pigmentosa patients.

Authors:  E Mitrovà
Journal:  Eur J Epidemiol       Date:  1988-03       Impact factor: 8.082

8.  Comparison of spongiform lesions in experimental scrapie and rabies in skunks.

Authors:  A Bundza; K M Charlton
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

9.  Generating Bona Fide Mammalian Prions with Internal Deletions.

Authors:  Carola Munoz-Montesino; Christina Sizun; Mohammed Moudjou; Laetitia Herzog; Fabienne Reine; Jérôme Chapuis; Danica Ciric; Angelique Igel-Egalon; Hubert Laude; Vincent Béringue; Human Rezaei; Michel Dron
Journal:  J Virol       Date:  2016-07-11       Impact factor: 5.103

10.  Impaired axonal transport in motor neurons correlates with clinical prion disease.

Authors:  Vladimir Ermolayev; Toni Cathomen; Julia Merk; Mike Friedrich; Wolfgang Härtig; Gregory S Harms; Michael A Klein; Eckhard Flechsig
Journal:  PLoS Pathog       Date:  2009-08-21       Impact factor: 6.823

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