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Vet Pathol 40:164-174 (2003)
© 2003 American College of Veterinary Pathologists

Accumulation of Pathogenic Prion Protein (PrPSc) in Nervous and Lymphoid Tissues of Sheep with Subclinical Scrapie

C. Ersdal, M. J. Ulvund, S. L. Benestad and M. A. Tranulis

Departments of Sheep and Goat Research, Sandnes, Norway (CE, MJU, MAT 1) and Morphology, Genetics, and Aquatic Biology, Oslo, Norway (CE), The Norwegian School of Veterinary Science; and Department of Pathology, National Veterinary Institute, Oslo, Norway (SLB)

All sheep older than 1 year of age from a flock of the Rygja breed in which clinical scrapie was detected for the first time in two animals (4%) were examined for accumulation of pathogenic prion protein (PrPSc) by immunohistochemistry in the obex, the cerebellum, and the medial retrophayngeal lymph node. In addition, six lambs, 2–3 months old, all offspring of PrPSc-positive dams, were examined for PrPSc in the ileal Peyers' patch (IPP), the distal jejunal lymph node, the spleen, and the medial retropharyngeal lymph node (RPLN). In this flock, 35% (17/48) of the adult sheep showed accumulation of PrPSc, an eightfold increase compared with clinical disease. All positives carried susceptible PrP genotypes. Three sheep had deposits of PrPSc in the RPLN and not in the brain, suggesting that this organ, easily accessible at slaughter, is suitable for screening purposes. Two 7-year-old clinically healthy homozygous V136Q171 ewes showed sparse immunostaining in the central nervous system and may have been infected as adults. Further, two littermates, 86-days-old, showed PrPSc in the IPP. Interestingly, one of these lambs had the intermediate susceptible PrP genotype, VA136QR171. In addition to early immunolabeling in the dorsal motor nucleus of the vagal nerve, a few of the sheep had early involvement of the cerebellum. In fact, a 2-year-old sheep had sparse deposits of PrPSc in the cerebellum only. Because experimental bovine spongiform encephalopathy (BSE) in sheep seems to behave in a similar manner as natural scrapie, these results, particularly regarding spread of infectivity, may have implications for the handling of BSE should it be diagnosed in sheep.


Key words: Brain; immunohistochemistry; lymphoid tissue; PrPSc; sheep; subclinical scrapie.

Request reprints from Dr. M. J. Ulvund, Department of Sheep and Goat Research, The Norwegian School of Veterinary Science, Kyrkjevegen 332/334, N-4325 Sandnes (Norway). E-mail: martha.ulvund{at}veths.no.


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