Literature DB >> 16763054

Prion infectivity in variant Creutzfeldt-Jakob disease rectum.

J D F Wadsworth1, S Joiner, K Fox, J M Linehan, M Desbruslais, S Brandner, E A Asante, J Collinge.   

Abstract

BACKGROUND: Disease-related prion protein (PrP(Sc)) is readily detectable in lymphoreticular tissues in variant Creutzfeldt-Jakob disease (vCJD), but not in other forms of human prion disease. This distinctive pathogenesis, with the unknown population prevalence of asymptomatic vCJD infection, has led to significant concerns that secondary transmission of vCJD prions will occur through a wide range of surgical procedures. To date PrP(Sc):prion infectivity ratios have not been determined in vCJD, and it is unknown whether vCJD prions are similar to experimental rodent prions, where PrP(Sc) concentration typically reflects infectious prion titre. AIM: To investigate prion infectivity in vCJD tissue containing barely detectable levels of PrP(Sc).
METHODS: Transgenic mice expressing only human PrP (Tg(HuPrP129M(+/+)Prnp(o/o))-35 and Tg(HuPrP129M(+/+)Prnp(o/o))-45 mice) were inoculated with brain or rectal tissue from a previously characterised patient with vCJD. These tissues contain the maximum and minimum levels of detectable PrP(Sc) that have been observed in vCJD.
RESULTS: Efficient transmission of prion infection was observed in transgenic mice inoculated with vCJD rectal tissue containing PrP(Sc) at a concentration of 10(4.7)-fold lower than that in vCJD brain.
CONCLUSIONS: These data confirm the potential risks for secondary transmission of vCJD prions via gastrointestinal procedures and support the use of PrP(Sc) as a quantitative marker of prion infectivity in vCJD tissues.

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Year:  2006        PMID: 16763054      PMCID: PMC1856674          DOI: 10.1136/gut.2006.091637

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  33 in total

Review 1.  Laboratory diagnosis of variant Creutzfeldt-Jakob disease.

Authors:  J W Ironside; M W Head; J E Bell; L McCardle; R G Will
Journal:  Histopathology       Date:  2000-07       Impact factor: 5.087

2.  Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues.

Authors:  M E Bruce; I McConnell; R G Will; J W Ironside
Journal:  Lancet       Date:  2001-07-21       Impact factor: 79.321

Review 3.  Variant Creutzfeldt-Jakob disease (vCJD) and gastrointestinal endoscopy.

Authors:  A T Axon; U Beilenhoff; M G Bramble; S Ghosh; A Kruse; G E McDonnell; C Neumann; J F Rey; K Spencer
Journal:  Endoscopy       Date:  2001-12       Impact factor: 10.093

Review 4.  Creutzfeldt-Jakob disease: implications for gastroenterology.

Authors:  M G Bramble; J W Ironside
Journal:  Gut       Date:  2002-06       Impact factor: 23.059

5.  High levels of disease related prion protein in the ileum in variant Creutzfeldt-Jakob disease.

Authors:  S Joiner; J M Linehan; S Brandner; J D F Wadsworth; J Collinge
Journal:  Gut       Date:  2005-10       Impact factor: 23.059

6.  An enzyme-detergent method for effective prion decontamination of surgical steel.

Authors:  Graham S Jackson; Edward McKintosh; Eckhard Flechsig; Kanella Prodromidou; Petra Hirsch; Jackie Linehan; Sebastian Brandner; Anthony R Clarke; Charles Weissmann; John Collinge
Journal:  J Gen Virol       Date:  2005-03       Impact factor: 3.891

7.  Transmission of scrapie by steel-surface-bound prions.

Authors:  E Flechsig; I Hegyi; M Enari; P Schwarz; J Collinge; C Weissmann
Journal:  Mol Med       Date:  2001-10       Impact factor: 6.354

8.  Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay.

Authors:  J D Wadsworth; S Joiner; A F Hill; T A Campbell; M Desbruslais; P J Luthert; J Collinge
Journal:  Lancet       Date:  2001-07-21       Impact factor: 79.321

9.  Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

Authors:  E Flechsig; D Shmerling; I Hegyi; A J Raeber; M Fischer; A Cozzio; C von Mering; A Aguzzi; C Weissmann
Journal:  Neuron       Date:  2000-08       Impact factor: 17.173

Review 10.  Prion diseases of humans and animals: their causes and molecular basis.

Authors:  J Collinge
Journal:  Annu Rev Neurosci       Date:  2001       Impact factor: 12.449

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  11 in total

1.  A non-invasive screen for infectivity in transmissible spongiform encephalopathies.

Authors:  D G Glover; B J Pollard; L González; S Sisó; D Kennedy; M Jeffrey
Journal:  Gut       Date:  2007-09       Impact factor: 23.059

2.  Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice.

Authors:  Jonathan D F Wadsworth; Susan Joiner; Jacqueline M Linehan; Melanie Desbruslais; Katie Fox; Sharon Cooper; Sabrina Cronier; Emmanuel A Asante; Simon Mead; Sebastian Brandner; Andrew F Hill; John Collinge
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-03       Impact factor: 11.205

Review 3.  vCJD and the gut: implications for endoscopy.

Authors:  M W Head; J W Ironside
Journal:  Gut       Date:  2007-01       Impact factor: 23.059

4.  A standardized comparison of commercially available prion decontamination reagents using the Standard Steel-Binding Assay.

Authors:  Julie Ann Edgeworth; Anita Sicilia; Jackie Linehan; Sebastian Brandner; Graham S Jackson; John Collinge
Journal:  J Gen Virol       Date:  2010-11-17       Impact factor: 3.891

Review 5.  Molecular pathology of human prion disease.

Authors:  Jonathan D F Wadsworth; John Collinge
Journal:  Acta Neuropathol       Date:  2010-08-08       Impact factor: 17.088

6.  Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein.

Authors:  Malin K Sandberg; Huda Al-Doujaily; Christina J Sigurdson; Markus Glatzel; Catherine O'Malley; Caroline Powell; Emmanuel A Asante; Jacqueline M Linehan; Sebastian Brandner; Jonathan D F Wadsworth; John Collinge
Journal:  J Gen Virol       Date:  2010-07-07       Impact factor: 3.891

7.  Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein.

Authors:  Susan Joiner; Emmanuel A Asante; Jacqueline M Linehan; Lara Brock; Sebastian Brandner; Susan J Bellworthy; Marion M Simmons; James Hope; John Collinge; Jonathan D F Wadsworth
Journal:  J Neurol Sci       Date:  2017-12-29       Impact factor: 3.181

8.  Bioassay studies support the potential for iatrogenic transmission of variant Creutzfeldt Jakob Disease through dental procedures.

Authors:  Elizabeth Kirby; Joanne Dickinson; Matthew Vassey; Mike Dennis; Mark Cornwall; Neil McLeod; Andrew Smith; Philip D Marsh; James T Walker; J Mark Sutton; Neil D H Raven
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

9.  Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD.

Authors:  Vincent Béringue; Annick Le Dur; Philippe Tixador; Fabienne Reine; Laurence Lepourry; Armand Perret-Liaudet; Stéphane Haïk; Jean-Luc Vilotte; Michel Fontés; Hubert Laude
Journal:  PLoS One       Date:  2008-01-09       Impact factor: 3.240

10.  Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease.

Authors:  Sebastian Brandner; Jerome Whitfield; Ken Boone; Anderson Puwa; Catherine O'Malley; Jacqueline M Linehan; Susan Joiner; Francesco Scaravilli; Ian Calder; Michael P Alpers; Jonathan D F Wadsworth; John Collinge
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2008-11-27       Impact factor: 6.237

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