Pre‐symptomatic detection of prions by cyclic amplification of protein misfolding
- 25 December 2004
- journal article
- Published by Wiley in FEBS Letters
- Vol. 579 (3), 638-642
- https://doi.org/10.1016/j.febslet.2004.12.035
Abstract
Transmissible spongiform encephalopathies (TSEs) are neurodegenerative disorders affecting humans and animals. At present, it is not possible to recognize individuals incubating the disease before the clinical symptoms appear. We investigated the effectiveness of the "Protein Misfolding Cyclic Amplification" (PMCA) technology to detect the protease-resistance disease-associated prion protein (PrP(res)) in pre-symptomatic stages. PMCA allowed detection of PrP(res) in the brain of pre-symptomatic hamsters, enabling a clear identification of infected animals as early as two weeks after inoculation. Furthermore, PMCA was able to amplify minute quantities of PrP(res) from a variety of experimental and natural TSEs. Finally, PMCA allowed the demonstration of PrP(res) in an experimentally infected cow 32 month post-inoculation, that did not show clinical signs and was negative by standard Western blot analysis. Our findings indicate that PMCA may be useful for the development of an ultra-sensitive diagnostic test to minimize the risk of further propagation of TSEs.Keywords
This publication has 29 references indexed in Scilit:
- Diagnosing prion diseases: needs, challenges and hopesNature Reviews Microbiology, 2004
- Curcumin has potent anti‐amyloidogenic effects for Alzheimer's β‐amyloid fibrils in vitroJournal of Neuroscience Research, 2004
- RNA molecules stimulate prion protein conversionNature, 2003
- In Vitro Amplification of Protease-Resistant Prion Protein Requires Free Sulfhydryl GroupsBiochemistry, 2003
- Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic miceNature Biotechnology, 2002
- Rapid test for the preclinical postmortem diagnosis of BSE in central nervous system tissueVeterinary Record, 2001
- Sensitive detection of pathological prion protein by cyclic amplification of protein misfoldingNature, 2001
- Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsAnnals of Neurology, 1999
- Strain-dependent Differences in β-Sheet Conformations of Abnormal Prion ProteinJournal of Biological Chemistry, 1998
- Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion DiversityScience, 1996