Species-barrier-independent prion replication in apparently resistant species

被引:244
作者
Hill, AF
Joiner, S
Linehan, J
Desbruslais, M
Lantos, PL
Collinge, J [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med St Marys, MRC, Prion Unit, London W2 1PG, England
[2] Univ London Imperial Coll Sci Technol & Med, Sch Med St Marys, Dept Neurogenet, London W2 1PG, England
[3] Inst Psychiat, Dept Neuropathol, London SE5 8AF, England
基金
英国惠康基金;
关键词
D O I
10.1073/pnas.97.18.10248
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transmission of prions between mammalian species is thought to be limited by a "species barrier," which depends on differences in the primary structure of prion proteins in the infecting inoculum and the host, Here we demonstrate that a strain of hamster prions thought to be nonpathogenic for conventional mice leads to prion replication to high levels in such mice but without causing clinical disease. Prions pathogenic in both mice and hamsters are produced. These results demonstrate the existence of subclinical forms of prion infection with important public health implications, both with respect to iatrogenic transmission from apparently healthy humans and dietary exposure to cattle and other species exposed to bovine spongiform encephalopathy prions, Current definitions of the species barrier, which have been based on clinical endpoints, need to be fundamentally reassessed.
引用
收藏
页码:10248 / 10253
页数:6
相关论文
共 42 条
[31]  
Pattison I.H., 1965, SLOW LATENT TEMPERAT, P249
[32]   NOVEL PROTEINACEOUS INFECTIOUS PARTICLES CAUSE SCRAPIE [J].
PRUSINER, SB .
SCIENCE, 1982, 216 (4542) :136-144
[33]   TRANSGENETIC STUDIES IMPLICATE INTERACTIONS BETWEEN HOMOLOGOUS PRP ISOFORMS IN SCRAPIE PRION REPLICATION [J].
PRUSINER, SB ;
SCOTT, M ;
FOSTER, D ;
PAN, KM ;
GROTH, D ;
MIRENDA, C ;
TORCHIA, M ;
YANG, SL ;
SERBAN, D ;
CARLSON, GA ;
HOPPE, PC ;
WESTAWAY, D ;
DEARMOND, SJ .
CELL, 1990, 63 (04) :673-686
[34]   MOLECULAR-PROPERTIES, PARTIAL-PURIFICATION, AND ASSAY BY INCUBATION PERIOD MEASUREMENTS OF THE HAMSTER SCRAPIE AGENT [J].
PRUSINER, SB ;
GROTH, DF ;
COCHRAN, SP ;
MASIARZ, FR ;
MCKINLEY, MP ;
MARTINEZ, HM .
BIOCHEMISTRY, 1980, 19 (21) :4883-4891
[35]   Scrapie infectivity found in resistant species [J].
Race, R ;
Chesebro, B .
NATURE, 1998, 392 (6678) :770-770
[36]  
REED L. J., 1938, AMER JOUR HYG, V27, P493
[37]   Eight prion strains have PrPSc molecules with different conformations [J].
Safar, J ;
Wille, H ;
Itrri, V ;
Groth, D ;
Serban, H ;
Torchia, M ;
Cohen, FE ;
Prusiner, SB .
NATURE MEDICINE, 1998, 4 (10) :1157-1165
[38]   NO PROPAGATION OF PRIONS IN MICE DEVOID OF PRP [J].
SAILER, A ;
BUELER, H ;
FISCHER, M ;
AGUZZI, A ;
WEISSMANN, C .
CELL, 1994, 77 (07) :967-968
[39]   TRANSGENIC MICE EXPRESSING HAMSTER PRION PROTEIN PRODUCE SPECIES-SPECIFIC SCRAPIE INFECTIVITY AND AMYLOID PLAQUES [J].
SCOTT, M ;
FOSTER, D ;
MIRENDA, C ;
SERBAN, D ;
COUFAL, F ;
WALCHLI, M ;
TORCHIA, M ;
GROTH, D ;
CARLSON, G ;
DEARMOND, SJ ;
WESTAWAY, D ;
PRUSINER, SB .
CELL, 1989, 59 (05) :847-857
[40]   RAPID DETECTION OF CREUTZFELDT-JAKOB DISEASE AND SCRAPIE PRION PROTEINS [J].
SERBAN, D ;
TARABOULOS, A ;
DEARMOND, SJ ;
PRUSINER, SB .
NEUROLOGY, 1990, 40 (01) :110-117