newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes

Scrapie in small ruminants belongs to transmissible spongiform encephalopathies (TSEs), or prion diseases, a family of fatal neurodegenerative disorders that affect humans and animals and can transmit within and between species by ingestion or inoculation. Conversion of the host-encoded prion protei...

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Published in:Proceedings of the National Academy of Sciences - PNAS Vol. 102; no. 44; pp. 16031 - 16036
Main Authors: Le Dur, A, Beringue, V, Andreoletti, O, Reine, F, Lai, T.L, Baron, T, Bratberg, B, Vilotte, J.L, Sarradin, P, Benestad, S.L
Format: Journal Article
Language:English
Published: United States National Academy of Sciences 01-11-2005
National Acad Sciences
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Summary:Scrapie in small ruminants belongs to transmissible spongiform encephalopathies (TSEs), or prion diseases, a family of fatal neurodegenerative disorders that affect humans and animals and can transmit within and between species by ingestion or inoculation. Conversion of the host-encoded prion protein (PrP), normal cellular PrP (PrP(c)), into a misfolded form, abnormal PrP (PrP(Sc)), plays a key role in TSE transmission and pathogenesis. The intensified surveillance of scrapie in the European Union, together with the improvement of PrP(Sc) detection techniques, has led to the discovery of a growing number of so-called atypical scrapie cases. These include clinical Nor98 cases first identified in Norwegian sheep on the basis of unusual pathological and PrP(Sc) molecular features and "cases" that produced discordant responses in the rapid tests currently applied to the large-scale random screening of slaughtered or fallen animals. Worryingly, a substantial proportion of such cases involved sheep with PrP genotypes known until now to confer natural resistance to conventional scrapie. Here we report that both Nor98 and discordant cases, including three sheep homozygous for the resistant PrP(ARR) allele (A136R154R171), efficiently transmitted the disease to transgenic mice expressing ovine PrP, and that they shared unique biological and biochemical features upon propagation in mice. These observations support the view that a truly infectious TSE agent, unrecognized until recently, infects sheep and goat flocks and may have important implications in terms of scrapie control and public health.
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A.L.D. and V.B. contributed equally to this work.
Author contributions: H.L. designed research; A.L.D., V.B., O.A., F.R., T.L.L., J.-L.V., and H.L. performed research; T.B., B.B., P.S., and S.L.B. contributed new reagents/analytic tools; V.B., O.A., and H.L. analyzed data; and H.L. wrote the paper.
Conflict of interest statement: No conflicts declared.
To whom correspondence should be addressed. E-mail: laude@jouy.inra.fr.
This paper was submitted directly (Track II) to the PNAS office.
Edited by Stanley B. Prusiner, University of California, San Francisco, CA
Abbreviations: TSE, transmissible spongiform encephalopathy; PrP, prion protein; PrPSc, abnormal PrP; PrPres, protease-resistant PrP; PK, proteinase K; BSE, bovine spongiform encephalopathy.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0502296102