Literature DB >> 96212

Evidence that the transmission of one source of scrapie agent to hamsters involves separation of agent strains from a mixture.

R H Kimberlin, C A Walker.   

Abstract

A previous paper (Kimberlin & Walker, 1977) described an experimental model of scrapie in hamsters in which the incubation period decreased progressively over the first 4 passages before becoming stable at the 5th and subsequent passes. Studies have been made of some of the agent strains present in brains taken from the 2nd, 3rd, 4th and 6th hamster passes. The results indicate the presence of at least two strains of agent at the 3rd passage level. One of these (431K) is highly pathogenic for mice and the other (263K) has an extremely low pathogenicity for mice. However only one of these strains (263K) is present in hamster brain after the 6th serial passage. It is suggested that the 'adaptation' of scrapie to hamsters may involve the selection, from a mixture, of a single strain which is highly pathogenic for hamsters. The possibility of modification of the properties of agent strains on passage discussed.

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Year:  1978        PMID: 96212     DOI: 10.1099/0022-1317-39-3-487

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  90 in total

1.  Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein.

Authors:  C Wong; L W Xiong; M Horiuchi; L Raymond; K Wehrly; B Chesebro; B Caughey
Journal:  EMBO J       Date:  2001-02-01       Impact factor: 11.598

2.  Species-independent inhibition of abnormal prion protein (PrP) formation by a peptide containing a conserved PrP sequence.

Authors:  J Chabry; S A Priola; K Wehrly; J Nishio; J Hope; B Chesebro
Journal:  J Virol       Date:  1999-08       Impact factor: 5.103

3.  Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.

Authors:  A J Raeber; R E Race; S Brandner; S A Priola; A Sailer; R A Bessen; L Mucke; J Manson; A Aguzzi; M B Oldstone; C Weissmann; B Chesebro
Journal:  EMBO J       Date:  1997-10-15       Impact factor: 11.598

4.  Changes in prion replication environment cause prion strain mutation.

Authors:  Nuria Gonzalez-Montalban; Young Jin Lee; Natallia Makarava; Regina Savtchenko; Ilia V Baskakov
Journal:  FASEB J       Date:  2013-05-31       Impact factor: 5.191

Review 5.  Prion liposomes.

Authors:  R Gabizon; S B Prusiner
Journal:  Biochem J       Date:  1990-02-15       Impact factor: 3.857

6.  Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy.

Authors:  J C Bartz; R A Bessen; D McKenzie; R F Marsh; J M Aiken
Journal:  J Virol       Date:  2000-06       Impact factor: 5.103

7.  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

8.  Prion formation, but not clearance, is supported by protein misfolding cyclic amplification.

Authors:  Ronald A Shikiya; Thomas E Eckland; Alan J Young; Jason C Bartz
Journal:  Prion       Date:  2014       Impact factor: 3.931

9.  Prion interference is due to a reduction in strain-specific PrPSc levels.

Authors:  Jason C Bartz; Michelle L Kramer; Meghan H Sheehan; Jessica A L Hutter; Jacob I Ayers; Richard A Bessen; Anthony E Kincaid
Journal:  J Virol       Date:  2006-11-01       Impact factor: 5.103

10.  Biological and biochemical characterization of sheep scrapie in Japan.

Authors:  Motohiro Horiuchi; Takuya Nemoto; Naotaka Ishiguro; Hidefumi Furuoka; Shirou Mohri; Morikazu Shinagawa
Journal:  J Clin Microbiol       Date:  2002-09       Impact factor: 5.948

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