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Updated: Apr 25, 2026

Clinical Examination Protocol to Detect Atypical and Classical Scrapie in Sheep
Published on: January 19, 2014
White blood cell-based detection of asymptomatic scrapie infection by ex vivo assays
Sophie Halliez1, Emilie Jaumain1, Alvina Huor2
1INRA (Institut National de la Recherche Agronomique), UR892, Virologie Immunologie Moléculaires, Jouy-en-Josas, France.
Abstract:
Prion transmission can occur by blood transfusion in human variant Creutzfeldt-Jakob disease and in experimental animal models, including sheep. Screening of blood and its derivatives for the presence of prions became therefore a major public health issue. As infectious titer in blood is reportedly low, highly sensitive and robust methods are required to detect prions in blood and blood derived products. The objectives of this study were to compare different methods--in vitro, ex vivo and in vivo assays--to detect prion infectivity in cells prepared from blood samples obtained from scrapie infected sheep at different time points of the disease. Protein misfolding cyclic amplification (PMCA) and bioassays in transgenic mice expressing the ovine prion protein were the most efficient methods to identify infected animals at any time of the disease (asymptomatic to terminally-ill stages). However scrapie cell and cerebellar organotypic slice culture assays designed to replicate ovine prions in culture also allowed detection of prion infectivity in blood cells from asymptomatic sheep. These findings confirm that white blood cells are appropriate targets for preclinical detection and introduce ex vivo tools to detect blood infectivity during the asymptomatic stage of the disease.
Insights
Detecting prions in blood is crucial for public health. This study found that protein misfolding cyclic amplification (PMCA) and cell-based assays can detect prion infectivity in sheep blood, even in asymptomatic animals.
Area of Science:
- Veterinary Medicine
- Neuroscience
- Infectious Diseases
Background:
- Prion diseases, like variant Creutzfeldt-Jakob disease (vCJD) and scrapie in sheep, can be transmitted via blood transfusion.
- Sensitive diagnostic methods are needed to screen blood and blood products for prions due to low infectious titers.
Purpose of the Study:
- To compare various in vitro, ex vivo, and in vivo methods for detecting prion infectivity in blood cells from scrapie-infected sheep.
- To assess the efficacy of these methods at different disease stages, including pre-symptomatic phases.
Main Methods:
- Protein Misfolding Cyclic Amplification (PMCA) assay.
- Bioassays using transgenic mice expressing ovine prion protein.
- Scrapie cell-based and organotypic slice culture assays.
Main Results:
- Protein misfolding cyclic amplification (PMCA) and transgenic mouse bioassays were highly effective in detecting prions across all disease stages.
- Scrapie cell-based and organotypic slice culture assays successfully detected prion infectivity in blood cells from asymptomatic sheep.
Conclusions:
- White blood cells are suitable targets for preclinical prion detection.
- Ex vivo cell culture assays offer potential for detecting blood infectivity during the asymptomatic stage of prion disease.

