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PMID: 11904434 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Prions in skeletal muscle.

Bosque PJ, Ryou C, Telling G, Peretz D, Legname G, DeArmond SJ, Prusiner SB

Abstract

Considerable evidence argues that consumption of beef products from cattle infected with bovine spongiform encephalopathy (BSE) prions causes new variant Creutzfeldt-Jakob disease. In an effort to prevent new variant Creutzfeldt-Jakob disease, certain "specified offals," including neural and lymphatic tissues, thought to contain high titers of prions have been excluded from foods destined for human consumption [Phillips, N. A., Bridgeman, J. & Ferguson-Smith, M. (2000) in The BSE Inquiry (Stationery Office, London), Vol. 6, pp. 413-451]. Here we report that mouse skeletal muscle can propagate prions and accumulate substantial titers of these pathogens. We found both high prion titers and the disease-causing isoform of the prion protein (PrP(Sc)) in the skeletal muscle of wild-type mice inoculated with either the Me7 or Rocky Mountain Laboratory strain of murine prions. Particular muscles accumulated distinct levels of PrP(Sc), with the highest levels observed in muscle from the hind limb. To determine whether prions are produced or merely accumulate intramuscularly, we established transgenic mice expressing either mouse or Syrian hamster PrP exclusively in muscle. Inoculating these mice intramuscularly with prions resulted in the formation of high titers of nascent prions in muscle. In contrast, inoculating mice in which PrP expression was targeted to hepatocytes resulted in low prion titers. Our data demonstrate that factors in addition to the amount of PrP expressed determine the tropism of prions for certain tissues. That some muscles are intrinsically capable of accumulating substantial titers of prions is of particular concern. Because significant dietary exposure to prions might occur through the consumption of meat, even if it is largely free of neural and lymphatic tissue, a comprehensive effort to map the distribution of prions in the muscle of infected livestock is needed. Furthermore, muscle may provide a readily biopsied tissue from which to diagnose prion disease in asymptomatic animals and even humans.

MeSH Terms
Actins/genetics Animals Chickens Cricetinae Diet Endopeptidases/metabolism Food Contamination Hepatocytes/metabolism Injections, Intramuscular Meat Mesocricetus Mice Mice, Transgenic Muscle, Skeletal/metabolism,pathology Organ Specificity PrPSc Proteins/biosynthesis,genetics,metabolism Prion Diseases/etiology,genetics,metabolism,pathology Prions/administration & dosage,biosynthesis,genetics,metabolism Time Factors Transgenes/genetics
Chemicals
Actins PrPSc Proteins Prions Endopeptidases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Bosque Patrick J
Institute for Neurodegenerative Diseases, Department of Neurology, University of California, San Francisco, CA 94143, USA.
Ryou Chongsuk
Telling Glenn
Peretz David
Legname Giuseppe
DeArmond Stephen J
Prusiner Stanley B
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
2002-03-19
Pages
3812-7
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC122606
Subset
IM
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