J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 87 (2006), 251-254; DOI 10.1099/vir.0.81277-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
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 Download to citation manager
Right arrow reprints & permissions
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 Thomzig, A.
Right arrow Articles by Beekes, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Thomzig, A.
Right arrow Articles by Beekes, M.
Agricola
Right arrow Articles by Thomzig, A.
Right arrow Articles by Beekes, M.
© 2006 Society for General Microbiology

Short Communication

Pathological prion protein in muscles of hamsters and mice infected with rodent-adapted BSE or vCJD

Achim Thomzig1,{dagger}, Franco Cardone2,{dagger}, Dominique Krüger1, Maurizio Pocchiari2, Paul Brown3 and Michael Beekes1

1 Robert Koch-Institut (P24 – Transmissible Spongiform Encephalopathies), Nordufer 20, 13353 Berlin, Germany
2 Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
3 7815 Exeter Road, Bethesda, MD 20814, USA

Correspondence
Michael Beekes
BeekesM{at}rki.de

Recently, pathological prion protein (PrPTSE) was detected in muscle from sheep infected with scrapie, the archetype of transmissible spongiform encephalopathies (TSEs). This finding has highlighted the question of whether mammalian muscle may potentially also provide a reservoir for TSE agents related to bovine spongiform encephalopathy (BSE) and variant Creutzfeldt–Jakob Disease (vCJD). Here, results are reported from studies in hamsters and mice that provide direct experimental evidence, for the first time, of BSE- and vCJD-associated PrPTSE deposition in muscles. Our findings emphasize the need for further assessment of possible public-health risks from TSE involvement of skeletal muscle.

{dagger}These authors contributed equally to this work.




This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
F. Cardone, A. Thomzig, W. Schulz-Schaeffer, A. Valanzano, M. Sbriccoli, H. Abdel-Haq, S. Graziano, S. Pritzkow, M. Puopolo, P. Brown, et al.
PrPTSE in muscle-associated lymphatic tissue during the preclinical stage of mice infected orally with bovine spongiform encephalopathy
J. Gen. Virol., October 1, 2009; 90(10): 2563 - 2568.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
J. E. Jewell, J. Brown, T. Kreeger, and E. S. Williams
Prion protein in cardiac muscle of elk (Cervus elaphus nelsoni) and white-tailed deer (Odocoileus virginianus) infected with chronic wasting disease.
J. Gen. Virol., November 1, 2006; 87(Pt 11): 3443 - 3450.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2006 by the Society for General Microbiology.