Literature DB >> 10640408

Inactivation of transmissible degenerative encephalopathy agents: A review.

D M Taylor1.   

Abstract

The unconventional agents that cause transmissible degenerative encephalopathies, such as bovine spongiform encephalopathy, scrapie, and Creutzfeldt-Jakob disease (CJD), are relatively resistant to inactivation by standard decontamination procedures. The only methods that appear to be completely effective under worst-case conditions are strong sodium hypochlorite solutions or hot solutions of sodium hydroxide. Other procedures that result in significant degrees of inactivation are described. The infectivity levels in histologically-fixed tissue can be reduced substantially by treatment with concentrated formic acid without adversely affecting the microscopic quality of the tissue. Copyright 2000 Harcourt Publishers Ltd.

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Year:  2000        PMID: 10640408     DOI: 10.1053/tvjl.1999.0406

Source DB:  PubMed          Journal:  Vet J        ISSN: 1090-0233            Impact factor:   2.688


  58 in total

1.  Enzymatic digestion of chronic wasting disease prions bound to soil.

Authors:  Samuel E Saunders; Jason C Bartz; Kurt C Vercauteren; Shannon L Bartelt-Hunt
Journal:  Environ Sci Technol       Date:  2010-06-01       Impact factor: 9.028

2.  Conformational stability of Syrian hamster prion protein PrP(90-231).

Authors:  Megan Grabenauer; Thomas Wyttenbach; Narinder Sanghera; Susan E Slade; Teresa J T Pinheiro; James H Scrivens; Michael T Bowers
Journal:  J Am Chem Soc       Date:  2010-07-07       Impact factor: 15.419

3.  [Variant Creutzfeldt-Jakob disease. Epidemiology, detection, diagnosis and prevention with special reference to minimizing risk of iatrogenic transmission by medical products, especially surgical instruments. Report of the Variant Creutzfeldt-Jakob Disease Task Force on this topic].

Authors: 
Journal:  HNO       Date:  2002-04       Impact factor: 1.284

4.  [Decontamination and sterilization of surgical instruments in suspected Creutzfeldt-Jakob disease. Are we converting to the recommendations by the Robert Koch Institute?].

Authors:  A Tropitzsch; H P Zenner
Journal:  HNO       Date:  2004-10       Impact factor: 1.284

5.  Osseous regeneration in the presence of oxidized cellulose and collagen.

Authors:  G J Dias; P V Peplow; F Teixeira
Journal:  J Mater Sci Mater Med       Date:  2003-09       Impact factor: 3.896

6.  Inactivation of template-directed misfolding of infectious prion protein by ozone.

Authors:  Ning Ding; Norman F Neumann; Luke M Price; Shannon L Braithwaite; Aru Balachandran; Miodrag Belosevic; Mohamed Gamal El-Din
Journal:  Appl Environ Microbiol       Date:  2011-12-02       Impact factor: 4.792

7.  Infrared microspectroscopy: a multiple-screening platform for investigating single-cell biochemical perturbations upon prion infection.

Authors:  Alessandro Didonna; Lisa Vaccari; Alpan Bek; Giuseppe Legname
Journal:  ACS Chem Neurosci       Date:  2011-01-11       Impact factor: 4.418

8.  Evidence for degradation of abnormal prion protein in tissues from sheep with scrapie during composting.

Authors:  Hongsheng Huang; J Lloyd Spencer; Andrei Soutyrine; Jeiwen Guan; Jasmine Rendulich; Aru Balachandran
Journal:  Can J Vet Res       Date:  2007-01       Impact factor: 1.310

9.  Adsorption and decontamination of α-synuclein from medically and environmentally-relevant surfaces.

Authors:  Hanh T M Phan; Jason C Bartz; Jacob Ayers; Benoit I Giasson; Mathias Schubert; Keith B Rodenhausen; Negin Kananizadeh; Yusong Li; Shannon L Bartelt-Hunt
Journal:  Colloids Surf B Biointerfaces       Date:  2018-03-09       Impact factor: 5.268

10.  Lipopolysaccharide induced conversion of recombinant prion protein.

Authors:  Fozia Saleem; Trent C Bjorndahl; Carol L Ladner; Rolando Perez-Pineiro; Burim N Ametaj; David S Wishart
Journal:  Prion       Date:  2014-05-12       Impact factor: 3.931

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