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PMID: 11432823 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Scrapie strains maintain biological phenotypes on propagation in a cell line in culture.

The EMBO journal ·Vol. 20 ·No. 13 ·2001-07-02 ·Pages 3351-8

Birkett CR, Hennion RM, Bembridge DA, Clarke MC, Chree A, Bruce ME, Bostock CJ

Abstract

Bovine spongiform encephalopathy (BSE) and its human equivalent, variant Creutzfeldt-Jakob disease (vCJD), are caused by the same strain of infectious agent, which is similar to, but distinct from, >20 strains of their sheep scrapie homologue. A better understanding of the molecular strain determinants could be obtained from cells in monoculture than from whole animal studies where different cell targeting is commonly a strain-related feature. Although a few cell types can be infected with different strains, the phenotypes of the emergent strains have not been studied. We have cured the scrapie-infected, clonal SMB cell line with pentosan sulfate, stably re-infected it with a different strain of scrapie and shown that biological properties and prion protein profiles characteristic of each original strain are propagated faithfully in this single non-neuronal cell type. These findings attest to the fact that scrapie strain determinants are stable and host-independent in isolated cells.

MeSH Terms
Animals Brain/metabolism Cattle Cell Line Creutzfeldt-Jakob Syndrome/etiology Encephalopathy, Bovine Spongiform/etiology Humans Mice Phenotype PrPSc Proteins/biosynthesis,genetics Protein Isoforms/biosynthesis,genetics,physiology Scrapie/etiology,physiopathology
Chemicals
PrPSc Proteins Protein Isoforms
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Birkett C R
Institute for Animal Health, Compton Laboratory, Compton, Newbury, RG20 7NN, UK. chris.birkett@bbsrc.ac.uk
Hennion R M
Bembridge D A
Clarke M C
Chree A
Bruce M E
Bostock C J
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
2001-07-02
Pages
3351-8
Language
English
Region
England
NLM ID
8208664
PMCID
PMC125505
Subset
IM
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