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Content archived on 2024-06-16

Understanding prion strains and species barriers and devising novel diagnostic approaches

Objective

The existence of stable strains of prions, differing in incubation times, clinical features, and neuroanatomical PrPSc deposition, is disquieting. The structural and biological features which encode strains and determine their disease phenotype are obscure. Some strains, including BSE, easily traverse species barriers causing serious concerns in the EU. Promiscuous strains present a public health threat if they propagate through the food chain, while remaining either undetected or misidentified. These dangers are illustrated by the atypical cases of scrapie which have appeared throughout the EU, including in sheep hitherto considered genetically resistant, and by the identification of BSE in a goat in France. As yet there are no diagnostic procedures to identify TSE strains, except in some rare cases. We propose studying fundamental and applied aspects of prions strains and their relationship to the species barrier, and to use the knowledge generated to initiate diagnostic methodologies to detect strains and predict their epidemiological behaviour. We have assembled a powerful consortium of partners with proven experimental and industrial achievements. We will (i) systematically examine the properties of field strains and their species barriers when propagated (ii) examine strain-dependent biochemical and biophysical properties of PrPSc (iii) apply novel cryoelectron tomographical techniques to determine the 3-D structure (at 4 nm resolution) of PrPSc in various strains in neuronal (stem) cells (iv) study strain-specific features of prion infection in cultured cells, including their uptake receptors, (v) characterize strain dependent cytopathogenic mechanisms in infected cells. We will prepare novel diagnostic and research reagents such as a) possibly strain specific, PrP monoclonal antibodies, b) a goat PrP transgenic mouse, and c) novel ovine, caprine and bovine neuronal stem cells susceptible to prion infection.

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Keywords

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Topic(s)

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Call for proposal

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FP6-2004-FOOD-3-B
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Funding Scheme

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STREP - Specific Targeted Research Project

Coordinator

THE HEBREW UNIVERSITY OF JERUSALEM
EU contribution
No data
Address
The Authority for Research and Development, Edmond J. Safra Campus, Givat Ram
JERUSALEM
Israel

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Total cost

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Participants (10)

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