Literature DB >> 14522852

TSE strain variation.

Moira E Bruce1.   

Abstract

Studies in mice have revealed considerable strain variation in the agents causing transmissible spongiform encephalopathies (TSEs). TSE strains interact with genetic factors in the host (in particular PrP genotype) to influence characteristics of the disease such as incubation period and neuropathology. TSE strains can retain their identity after propagation in different host species or PrP genotypes, showing that these agents carry their own strain-specific information. It is not known whether this information resides in specific self-perpetuating modifications of PrP, or whether a separate informational molecule is required. Strain typing in mice can be used to explore links between TSEs occurring naturally in different species. Such studies have demonstrated that the strain causing BSE in cattle has also infected domestic cats and exotic ungulates. Most importantly, the BSE strain has also been isolated from patients with variant CJD. In contrast, different TSE strains are associated with sporadic CJD and sheep scrapie.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14522852     DOI: 10.1093/bmb/66.1.99

Source DB:  PubMed          Journal:  Br Med Bull        ISSN: 0007-1420            Impact factor:   4.291


  108 in total

1.  Lower specific infectivity of protease-resistant prion protein generated in cell-free reactions.

Authors:  Mikael Klingeborn; Brent Race; Kimberly D Meade-White; Bruce Chesebro
Journal:  Proc Natl Acad Sci U S A       Date:  2011-11-07       Impact factor: 11.205

Review 2.  Prions on the move.

Authors:  Charles Weissmann; Jiali Li; Sukhvir P Mahal; Shawn Browning
Journal:  EMBO Rep       Date:  2011-10-28       Impact factor: 8.807

3.  The charge structure of helix 1 in the prion protein regulates conversion to pathogenic PrPSc.

Authors:  Eric M Norstrom; James A Mastrianni
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

4.  Diversity in prion protein oligomerization pathways results from domain expansion as revealed by hydrogen/deuterium exchange and disulfide linkage.

Authors:  Frederic Eghiaian; Thorsten Daubenfeld; Yann Quenet; Marieke van Audenhaege; Anne-Pascale Bouin; Guillaume van der Rest; Jeanne Grosclaude; Human Rezaei
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-18       Impact factor: 11.205

5.  Cell-specific susceptibility to prion strains is a property of the intact cell.

Authors:  Maria E Herva; Charles Weissman
Journal:  Prion       Date:  2012-05-11       Impact factor: 3.931

6.  Most, but not all, yeast strains in the deletion library contain the [PIN(+)] prion.

Authors:  Anita L Manogaran; Viviana M Fajardo; Robert J D Reid; Rodney Rothstein; Susan W Liebman
Journal:  Yeast       Date:  2010-03       Impact factor: 3.239

7.  Prion strain-dependent differences in conversion of mutant prion proteins in cell culture.

Authors:  Ryuichiro Atarashi; Valerie L Sim; Noriyuki Nishida; Byron Caughey; Shigeru Katamine
Journal:  J Virol       Date:  2006-08       Impact factor: 5.103

8.  Cell-free propagation of prion strains.

Authors:  Joaquín Castilla; Rodrigo Morales; Paula Saá; Marcelo Barria; Pierluigi Gambetti; Claudio Soto
Journal:  EMBO J       Date:  2008-09-18       Impact factor: 11.598

9.  Prion propagation and toxicity occur in vitro with two-phase kinetics specific to strain and neuronal type.

Authors:  Samia Hannaoui; Layal Maatouk; Nicolas Privat; Etienne Levavasseur; Baptiste A Faucheux; Stéphane Haïk
Journal:  J Virol       Date:  2012-12-19       Impact factor: 5.103

Review 10.  The role of amyloidogenic protein oligomerization in neurodegenerative disease.

Authors:  Gregor P Lotz; Justin Legleiter
Journal:  J Mol Med (Berl)       Date:  2013-03-27       Impact factor: 4.599

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.