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The TeSeE PrP171 screen test has been successfully evaluated at various laboratories involved in sheep genotyping. The assay performance was assessed in comparison to the animal's "true genotype" given by the method currently in use in the laboratory. The test demonstrated very good correlation with PCR methods.
Data modeling has clearly shown that, when associated with a well-considered breeding strategy, the test enables breeders to progressively increase the proportion of the most resistant animals and to protect their flocks from all forms of prion-associated diseases (BSE, scrapie, etc.).
The denatured PrP protein is first captured with an antibody (3B5) coated on the surface of the wells in the ELISA microplate.
The secondary antibody (2A11) is specifically directed against position 171 of the PrP protein. It detects samples bearing a "Q" (Glutamine) or an "H" (Histidine) amino acid at this position, but does not detect those with an "R" (Arginine) amino acid.
Samples with a "Q" at position 171 of the PrP will then give a high signal while samples with an "R" at position 171 of the PrP will give a very low background signal. The test will give increasing signals for all possible allele combinations, making it possible to easily distinguish between sheep resistant to prions and those susceptible to them.
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