Atypical BSE in Germany - Proof of transmissibility and biochemical characterization

被引:119
作者
Buschmann, A.
Gretzschel, A.
Biacabe, A. -G.
Schiebel, K.
Corona, C.
Hoffmann, C.
Eiden, M.
Baron, T.
Casalone, C.
Groschup, Martin H.
机构
[1] FLI, Inst Novel & Emerging Infect Dis, D-17493 Greifswald, Germany
[2] AFSSA Lyon, Unite ATNC, Lyon, France
[3] Univ Erlangen Nurnberg, Inst Biochem, Erlangen, Germany
[4] CEA, Inst Zooprofilatt Turino, Turin, Italy
关键词
BSE; cattle; PrPSc; biochemical differentiation;
D O I
10.1016/j.vetmic.2006.06.016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Intensive active surveillance has uncovered two atypical German BSE cases in older cattle which resemble the two different atypical BSE phenotypes that have recently been described in France (designated H-type) and Italy (designated L-type or BASE). The H-type is characterized by a significantly higher molecular size, but a conventional glycopattern of the proteinase K treated abnormal prion protein (PrPSc), while the L-type PrPSc has only a slightly lower molecular size and a distinctly different glycopattern. In this paper we describe the successful transmission of both German atypical BSE cases to transgenic mice overexpressing bovine PrPC. Upon challenge with the L-type, these mice developed BSE after a substantially shorter incubation period than any classical BSE transmission using these mice to date. In contrast, the incubation period was distinctly prolonged when these mice were challenged with the H-type. PrPSc accumulated in the brains of these mice were of the same atypical BSE type that had been used for the transmission. These atypical cases suggest the possible existence of sporadic BSE cases in bovines. It is thus feasible that the BSE epidemic in the UK could have also been initiated by an intraspecies transmission from a sporadic BSE case. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 116
页数:14
相关论文
共 35 条
[1]  
Baron T, 2006, LANCET, V367, P297, DOI 10.1016/S0140-6736(06)68060-4
[2]   Distinct molecular phenotypes in bovine prion diseases [J].
Biacabe, AG ;
Laplanche, JL ;
Ryder, S ;
Baron, T .
EMBO REPORTS, 2004, 5 (01) :110-114
[3]  
Bruce M, 1996, TRANSMISSIBLE SUBACUTE SPONGIFORM ENCEPHALOPATHIES: PRION DISEASES, P259
[4]   Highly bovine spongiform encephalopathy-sensitive transgenic mice confirm the essential restriction of infectivity to the nervous system in clinically diseased cattle [J].
Buschmann, A ;
Groschup, MH .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (05) :934-942
[5]   Identification of a second bovine amyloidotic spongiform encephalopathy: Molecular similarities with sporadic Creutzfeldt-Jakob disease [J].
Casalone, C ;
Zanusso, G ;
Acutis, P ;
Ferrari, S ;
Capucci, L ;
Tagliavini, F ;
Monaco, S ;
Caramelli, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :3065-3070
[6]   The origin of bovine spongiform encephalopathy: the human prion disease hypothesis [J].
Colchester, ACF ;
Colchester, NTH .
LANCET, 2005, 366 (9488) :856-861
[7]   Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD [J].
Collinge, J ;
Sidle, KCL ;
Meads, J ;
Ironside, J ;
Hill, AF .
NATURE, 1996, 383 (6602) :685-690
[8]  
DEBOSSCHERE H, 2004, J APPL RES VET MED, V2, P52
[9]  
Eddy RG, 1995, VET REC, V137, P648
[10]   Strain typing of German transmissible spongiform encephalopathies field cases in small ruminants by biochemical methods [J].
Gretzschel, A ;
Buschmann, A ;
Eiden, M ;
Ziegler, U ;
Lühken, G ;
Erhardt, G ;
Groschup, MH .
JOURNAL OF VETERINARY MEDICINE SERIES B-INFECTIOUS DISEASES AND VETERINARY PUBLIC HEALTH, 2005, 52 (02) :55-63