Transmission of bovine spongiform encephalopathy

被引:0
作者
Espinosa, Juan Carlos [1 ]
Morales, Monica [1 ]
Herva, Maria Eugenia [1 ]
Torres, Juan Maria [1 ]
机构
[1] Ctr Invest & Sanidad Anim, INIA, E-28130 Madrid, Spain
关键词
bovine spongiform encephalopathy; BSE propagation; BSE transmission; prion strain; PrPSc; spongiform encephalopathy; transmissible spongiform encephalopathy; variant Creutzfeldt-Jakob disease;
D O I
10.2217/17460794.1.3.393
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bovine spongiform encephalopathy (BSE) is one of several diseases known collectively as transmissible spongiform encephalopathies (TSE) and caused by prions, which are nonconventional infectious agents. The risk of human infection by exposure to a TSE agent is generally considered to be low, because of the species barrier. However, the prions causing BSE in cattle are able to cross the species barrier easily. The appearance of variant Creutzfeldt-Jakob disease (vCJD) offer human exposure to BSE prions has highlighted the possible impacts of this infection on human health, Today, a major concern is that the number of BSE cases in many European countries, including the emerging eastern European countries of the EU, is growing. A further concern now emerging is the possibility that BSE could spread to other livestock species, such as sheep or goats. This paper provides an overview of BSE transmission and its potential implications for public health.
引用
收藏
页码:393 / 402
页数:10
相关论文
共 89 条
[1]   Mammalian prion biology: One century of evolving concepts [J].
Aguzzi, A ;
Polymenidou, M .
CELL, 2004, 116 (02) :313-327
[2]   PrPSc accumulation in placentas of ewes exposed to natural scrapie:: influence of foetal PrP genotype and effect on ewe-to-lamb transmission [J].
Andréoletti, O ;
Lacroux, C ;
Chabert, A ;
Monnereau, L ;
Tabouret, G ;
Lantier, F ;
Berthon, P ;
Eychenne, F ;
Lafond-Benestad, S ;
Elsen, JM ;
Schelcher, F .
JOURNAL OF GENERAL VIROLOGY, 2002, 83 :2607-2616
[3]   BSE priors propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein [J].
Asante, EA ;
Linehan, JM ;
Desbruslais, M ;
Joiner, S ;
Gowland, I ;
Wood, AL ;
Welch, J ;
Hill, AF ;
Lloyd, SE ;
Wadsworth, JDF ;
Collinge, J .
EMBO JOURNAL, 2002, 21 (23) :6358-6366
[4]   Prion diseases and the immune system [J].
Aucouturier, P ;
Carp, RI ;
Carnaud, C ;
Wisniewski, T .
CLINICAL IMMUNOLOGY, 2000, 96 (02) :79-85
[5]   Infected splenic dendritic cells are sufficient for prion transmission to the CNS in mouse scrapie [J].
Aucouturier, P ;
Geissmann, F ;
Damotte, D ;
Saborio, GP ;
Meeker, HC ;
Kascsak, R ;
Kascsak, R ;
Carp, RI ;
Wisniewski, T .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (05) :703-708
[6]   Rapid prion neuroinvasion following tongue infection [J].
Bartz, JC ;
Kincaid, AE ;
Bessen, RA .
JOURNAL OF VIROLOGY, 2003, 77 (01) :583-591
[7]   Cerebral targeting indicates vagal spread of infection in hamsters fed with scrapie [J].
Beekes, M ;
McBride, PA ;
Baldauf, E .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :601-607
[8]   Distinct molecular phenotypes in bovine prion diseases [J].
Biacabe, AG ;
Laplanche, JL ;
Ryder, S ;
Baron, T .
EMBO REPORTS, 2004, 5 (01) :110-114
[9]   Natural and experimental oral infection of nonhuman primates by bovine spongiform encephalopathy agents [J].
Bons, N ;
Mestre-Frances, N ;
Belli, P ;
Cathala, F ;
Gajdusek, DC ;
Brown, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :4046-4051
[10]   Prions in skeletal muscle [J].
Bosque, PJ ;
Ryou, C ;
Telling, G ;
Peretz, D ;
Legname, G ;
DeArmond, SJ ;
Prusiner, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) :3812-3817