Literature DB >> 1167887

Comparison of scrapie and transmissible mink encephalopathy in hamsters. I. Biochemical studies of brain during development of disease.

R H Kimberlin, R F Marsh.   

Abstract

A series of 15 different biochemical measurements were made on brains taken at stages throughout the development of scrapie and of transmissible mink encephalopathy in hamsters. With both diseases biochemical abnormalities were found only after the development of early histologic lesions, when animals showed clinical signs of disease. Changes were recorded in body weight, in the activities of six glycosidases, and the rates of incorporation of DNA and of glycoprotein precursors. The profiles of changes in hamster brain were almost indistinguishable,qualitatively and quantitatively, in the two diseases, an observation suggesting a close similarity in the way both disease-producing agents interact with this particular host species, . However, there were some major differences between the profile of changes in hamster scrapie and that previously observed in mouse scrapie. Thus it would appear that many of the well-characterized abnormalities of mouse scrapie are not fundamentally involved in the development of disease but represent mainly secondary changes.

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Year:  1975        PMID: 1167887     DOI: 10.1093/infdis/131.2.97

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  9 in total

1.  Temporal distribution of transmissible mink encephalopathy virus in mink inoculated subcutaneously.

Authors:  W J Hadlow; R E Race; R C Kennedy
Journal:  J Virol       Date:  1987-10       Impact factor: 5.103

2.  Characterization of nucleic acids in membrane vesicles from scrapie-infected hamster brain.

Authors:  C Dees; B C McMillan; W F Wade; T L German; R F Marsh
Journal:  J Virol       Date:  1985-07       Impact factor: 5.103

3.  Microglial cell line established from prion protein-overexpressing mice is susceptible to various murine prion strains.

Authors:  Yoshifumi Iwamaru; Takato Takenouchi; Kazumasa Ogihara; Megumi Hoshino; Masuhiro Takata; Morikazu Imamura; Yuichi Tagawa; Hiroko Hayashi-Kato; Yuko Ushiki-Kaku; Yoshihisa Shimizu; Hiroyuki Okada; Morikazu Shinagawa; Hiroshi Kitani; Takashi Yokoyama
Journal:  J Virol       Date:  2006-11-22       Impact factor: 5.103

Review 4.  Prion strains: shining new light on old concepts.

Authors:  Alyssa J Block; Jason C Bartz
Journal:  Cell Tissue Res       Date:  2022-07-07       Impact factor: 5.249

5.  Membrane-free scrapie activity.

Authors:  T G Malone; R F Marsh; R P Hanson; J S Semancik
Journal:  J Virol       Date:  1978-03       Impact factor: 5.103

6.  Experimental scrapie in golden Syrian hamsters: temporal comparison of in vitro cell-fusing activity with brain infectivity and histopathological changes.

Authors:  M C Moreau-Dubois; P Brown; R G Rohwer; C L Masters; M Franko; D C Gajdusek
Journal:  Infect Immun       Date:  1982-07       Impact factor: 3.441

7.  Transmission of chronic wasting disease identifies a prion strain causing cachexia and heart infection in hamsters.

Authors:  Richard A Bessen; Cameron J Robinson; Davis M Seelig; Christopher P Watschke; Diana Lowe; Harold Shearin; Scott Martinka; Alex M Babcock
Journal:  PLoS One       Date:  2011-12-12       Impact factor: 3.240

Review 8.  Prion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?

Authors:  Diane L Ritchie; Marcelo A Barria
Journal:  Biomolecules       Date:  2021-02-02

9.  Resistance of bovine spongiform encephalopathy (BSE) prions to inactivation.

Authors:  Kurt Giles; David V Glidden; Robyn Beckwith; Rose Seoanes; David Peretz; Stephen J DeArmond; Stanley B Prusiner
Journal:  PLoS Pathog       Date:  2008-11-14       Impact factor: 6.823

  9 in total

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