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Rapid End-point Quantitation of Prion Seeding Activity with Sensitivity Comparable to Bioassays

Overview
Journal PLoS Pathog
Specialty Microbiology
Date 2010 Dec 15
PMID 21152012
Citations 289
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Abstract

A major problem for the effective diagnosis and management of prion diseases is the lack of rapid high-throughput assays to measure low levels of prions. Such measurements have typically required prolonged bioassays in animals. Highly sensitive, but generally non-quantitative, prion detection methods have been developed based on prions' ability to seed the conversion of normally soluble protease-sensitive forms of prion protein to protease-resistant and/or amyloid fibrillar forms. Here we describe an approach for estimating the relative amount of prions using a new prion seeding assay called real-time quaking induced conversion assay (RT-QuIC). The underlying reaction blends aspects of the previously described quaking-induced conversion (QuIC) and amyloid seeding assay (ASA) methods and involves prion-seeded conversion of the alpha helix-rich form of bacterially expressed recombinant PrP(C) to a beta sheet-rich amyloid fibrillar form. The RT-QuIC is as sensitive as the animal bioassay, but can be accomplished in 2 days or less. Analogous to end-point dilution animal bioassays, this approach involves testing of serial dilutions of samples and statistically estimating the seeding dose (SD) giving positive responses in 50% of replicate reactions (SD(50)). Brain tissue from 263K scrapie-affected hamsters gave SD(50) values of 10(11)-10(12)/g, making the RT-QuIC similar in sensitivity to end-point dilution bioassays. Analysis of bioassay-positive nasal lavages from hamsters affected with transmissible mink encephalopathy gave SD(50) values of 10(3.5)-10(5.7)/ml, showing that nasal cavities release substantial prion infectivity that can be rapidly detected. Cerebral spinal fluid from 263K scrapie-affected hamsters contained prion SD(50) values of 10(2.0)-10(2.9)/ml. RT-QuIC assay also discriminated deer chronic wasting disease and sheep scrapie brain samples from normal control samples. In principle, end-point dilution quantitation can be applied to many types of prion and amyloid seeding assays. End point dilution RT-QuIC provides a sensitive, rapid, quantitative, and high throughput assay of prion seeding activity.

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References
1.
Kocisko D, Come J, Priola S, Chesebro B, Raymond G, Lansbury P . Cell-free formation of protease-resistant prion protein. Nature. 1994; 370(6489):471-4. DOI: 10.1038/370471a0. View

2.
Vascellari M, Nonno R, Mutinelli F, Bigolaro M, Di Bari M, Melchiotti E . PrPSc in salivary glands of scrapie-affected sheep. J Virol. 2007; 81(9):4872-6. PMC: 1900156. DOI: 10.1128/JVI.02148-06. View

3.
Konold T, Moore S, Bellworthy S, Simmons H . Evidence of scrapie transmission via milk. BMC Vet Res. 2008; 4:14. PMC: 2374774. DOI: 10.1186/1746-6148-4-14. View

4.
Saa P, Castilla J, Soto C . Presymptomatic detection of prions in blood. Science. 2006; 313(5783):92-4. DOI: 10.1126/science.1129051. View

5.
Thorne L, Terry L . In vitro amplification of PrPSc derived from the brain and blood of sheep infected with scrapie. J Gen Virol. 2008; 89(Pt 12):3177-3184. DOI: 10.1099/vir.0.2008/004226-0. View