Folio Bioscience, clinical sample procurement  Sign up for PNAS Online eTocs
Link: Info for AuthorsLink: Editorial BoardLink: AboutLink: SubscribeLink: AdvertiseLink: ContactLink: Sitemap Link: PNAS Home
Proceedings of the National Academy of Sciences
Link: Current Issue "" Link: Archives "" Link: Online Submission ""  Link: Advanced Search

Published online on October 20, 2005, 10.1073/pnas.0502296102

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a colleague
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Le Dur, A.
Right arrow Articles by Laude, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Le Dur, A.
Right arrow Articles by Laude, H.
Right arrowPubmed/NCBI databases
*Gene*GEO Profiles
*HomoloGene*UniGene
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg  
What's this?

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

( sheep prion | transgenic mice )

Annick Le Dur *{dagger}, Vincent Béringue *{dagger}, Olivier Andréoletti {ddagger}, Fabienne Reine *, Thanh Lan Laï *, Thierry Baron {sect}, Bjørn Bratberg ¶, Jean-Luc Vilotte ||, Pierre Sarradin **, Sylvie L. Benestad ¶, and Hubert Laude *{dagger}{dagger}

*Virologie Immunologie Moléculaires and ||Génétique Biochimique et Cytogénétique, Institut National de la Recherche Agronomique, 78350 Jouy-en-Josas, France; {ddagger}Unité Mixte de Recherche, Institut National de la Recherche Agronomique-Ecole Nationale Vétérinaire de Toulouse, Interactions Hôte Agent Pathogène, 31066 Toulouse, France; {sect}Agence Française de Sécurité Sanitaire des Aliments, Unité Agents Transmissibles Non Conventionnels, 69364 Lyon, France; **Pathologie Infectieuse et Immunologie, Institut National de la Recherche Agronomique, 37380 Nouzilly, France; and Department of Pathology, National Veterinary Institute, 0033 Oslo, Norway

Edited by Stanley B. Prusiner, University of California, San Francisco, CA, and approved September 12, 2005 (received for review March 21, 2005)

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 (PrPc), into a misfolded form, abnormal PrP (PrPSc), plays a key role in TSE transmission and pathogenesis. The intensified surveillance of scrapie in the European Union, together with the improvement of PrPSc 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 PrPSc 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 PrPARR 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.


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.

{dagger}A.L.D. and V.B. contributed equally to this work.

{dagger}{dagger}To whom correspondence should be addressed.

Hubert Laude, E-mail: laude{at}jouy.inra.fr

www.pnas.org/cgi/doi/10.1073/pnas.0502296102
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg    What's this?


This article has been cited by other articles in HighWire Press-hosted journals:


Home page
Vet Rec.Home page
M. P. Dagleish, S. M. Rodger, M. M. Simmons, J. Finlayson, D. Buxton, and F. Chianini
Atypical scrapie in a sheep in Scotland
Vet Rec., April 19, 2008; 162(16): 518 - 519.
[Full Text] [PDF]


Home page
NeurologyHome page
P. Brown
Transmissible spongiform encephalopathy in the 21st century: Neuroscience for the clinical neurologist
Neurology, February 26, 2008; 70(9): 713 - 722.
[Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. M. Barron, S. L. Campbell, D. King, A. Bellon, K. E. Chapman, R. A. Williamson, and J. C. Manson
High Titers of Transmissible Spongiform Encephalopathy Infectivity Associated with Extremely Low Levels of PrPSc in Vivo
J. Biol. Chem., December 7, 2007; 282(49): 35878 - 35886.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
D. M. Green, V. J. del Rio Vilas, C. P. D. Birch, J. Johnson, I. Z. Kiss, N. D. McCarthy, and R. R. Kao
Demographic risk factors for classical and atypical scrapie in Great Britain
J. Gen. Virol., December 1, 2007; 88(12): 3486 - 3492.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
A. M. Thackray, L. Hopkins, M. A. Klein, and R. Bujdoso
Mouse-Adapted Ovine Scrapie Prion Strains Are Characterized by Different Conformers of PrPSc
J. Virol., November 15, 2007; 81(22): 12119 - 12127.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
S. Paquet, N. Daude, M.-P. Courageot, J. Chapuis, H. Laude, and D. Vilette
PrPc Does Not Mediate Internalization of PrPSc but Is Required at an Early Stage for De Novo Prion Infection of Rov Cells
J. Virol., October 1, 2007; 81(19): 10786 - 10791.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
J. P. Owen, H. C. Rees, B. C. Maddison, L. A. Terry, L. Thorne, R. Jackman, G. C. Whitelam, and K. C. Gough
Molecular Profiling of Ovine Prion Diseases by Using Thermolysin-Resistant PrPSc and Endogenous C2 PrP Fragments
J. Virol., October 1, 2007; 81(19): 10532 - 10539.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
V. Beringue, O. Andreoletti, A. Le Dur, R. Essalmani, J.-L. Vilotte, C. Lacroux, F. Reine, L. Herzog, A.-G. Biacabe, T. Baron, et al.
A Bovine Prion Acquires an Epidemic Bovine Spongiform Encephalopathy Strain-Like Phenotype on Interspecies Transmission
J. Neurosci., June 27, 2007; 27(26): 6965 - 6971.
[Abstract] [Full Text] [PDF]


Home page
J ANIM SCIHome page
S. Hesketh, J. Sassoon, R. Knight, J. Hopkins, and D. R. Brown
Elevated manganese levels in blood and central nervous system occur before onset of clinical signs in scrapie and bovine spongiform encephalopathy
J Anim Sci, June 1, 2007; 85(6): 1596 - 1609.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
G. Lalatta-Costerbosa, M. Mazzoni, P. Clavenzani, G. Di Guardo, G. Mazzuoli, G. Marruchella, L. De Grossi, U. Agrimi, and R. Chiocchetti
Nitric Oxide Synthase Immunoreactivity and NADPH-d Histochemistry in the Enteric Nervous System of Sarda Breed Sheep With Different PrP Genotypes in Whole-mount and Cryostat Preparations
J. Histochem. Cytochem., April 1, 2007; 55(4): 387 - 401.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
F. Corbiere, F. Barillet, O. Andreoletti, F. Fidelle, N. Laphitz-Bordet, F. Schelcher, and P. Joly
Advanced survival models for risk-factor analysis in scrapie
J. Gen. Virol., February 1, 2007; 88(2): 696 - 705.
[Abstract] [Full Text] [PDF]


Home page
jvdiHome page
T. Seuberlich, C. Botteron, S. L. Benestad, H. Brunisholz, R. Wyss, U. Kihm, H. Schwermer, M. Friess, A. Nicolier, D. Heim, et al.
Atypical scrapie in a swiss goat and implications for transmissible spongiform encephalopathy surveillance
J Vet Diagn Invest, January 1, 2007; 19(1): 2 - 8.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
A. Gretzschel, A. Buschmann, J. Langeveld, and M. H. Groschup
Immunological characterization of abnormal prion protein from atypical scrapie cases in sheep using a panel of monoclonal antibodies
J. Gen. Virol., December 1, 2006; 87(12): 3715 - 3722.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
N. Picard-Hagen, V. Gayrard, C. Viguie, M. Moudjou, C. Imbs, and P.-L. Toutain
Prion protein in the cerebrospinal fluid of healthy and naturally scrapie-affected sheep
J. Gen. Virol., December 1, 2006; 87(12): 3723 - 3727.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
C. Cordier, A. Bencsik, S. Philippe, D. Betemps, F. Ronzon, D. Calavas, C. Crozet, and T. Baron
Transmission and characterization of bovine spongiform encephalopathy sources in two ovine transgenic mouse lines (TgOvPrP4 and TgOvPrP59)
J. Gen. Virol., December 1, 2006; 87(12): 3763 - 3771.
[Abstract] [Full Text] [PDF]