Characterization of a US Sheep Scrapie Isolate with Short Incubation Time

Author:

Hamir A. N.1,Richt J. A.1,Kunkle R. A.1,Greenlee J. J.1,Bulgin M. S.2,Gregori L.3,Rohwer R. G.3

Affiliation:

1. National Animal Disease Center, ARS, USDA, Ames, IA

2. Department of Animal and Veterinary Science, University of Idaho, Caldwell, ID

3. Laboratory of Molecular Neurovirology, VA Medical Center, Baltimore, MD

Abstract

Scrapie is a naturally occurring fatal neurodegenerative disease of sheep and goats. Susceptibility to the disease is partly dependent upon the genetic makeup of the host. In a previous study it was shown that sheep intracerebrally inoculated with US scrapie inoculum (No. 13–7) developed terminal disease within an average of 19 months. We have since produced an inoculum, No. x124 from pooled brains of US-origin sheep scrapie, that results in incubations nearly threefold shorter. The present study documents clinicopathologic findings and the distribution of abnormal prion proteins (PrPSc) by immunohistochemical (IHC) and Western blot (WB) techniques, in tissues of sheep inoculated with No. x124. All inoculated sheep developed clinical disease and were euthanatized within an average of 7.7 months postinoculation (MPI). Sheep that had valine/valine or alamine/valine at codon 136 of prion protein ( PRNP) gene developed the disease faster and were euthanatized at an average of 4.3 and 5.6 MPI, respectively. Also, the inoculum was able to induce disease in a short time (7 MPI) in a sheep that was relatively resistant (QR at codon 171) to scrapie. This indicates that inoculum No. x124 appears to induce scrapie in shorter time than inoculum No. 13–7, especially in sheep homozygous or heterozygous for valine at codon 136.

Publisher

SAGE Publications

Subject

General Veterinary

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