Recombinant canarypox virus vaccine co-expressing genes encoding the VP2 and VP5 outer capsid proteins of bluetongue virus induces high level protection in sheep

被引:77
作者
Boone, Josh D.
Balasuriya, Udeni B.
Karaca, Kemal
Audonnet, Jean-Christophe
Yao, Jiansheng
He, Ling
Nordgren, Robert
Monaco, Federica
Savini, Giovanni
Gardner, Ian A.
MacLachlan, N. James [1 ]
机构
[1] Univ Calif Davis, Sch Vet Med, Equine Viral Dis Lab, Dept Pathol Microbiol & Immunol, Davis, CA 95616 USA
[2] Merital Ltd, Athens, GA 30601 USA
[3] Merial SAS, Biol Discovery Res, F-69007 Lyon, France
[4] Sanofi Pasteur, Toronto, ON, Canada
[5] Ist Zooprofilatt Sperimentale Abruzzo & Molise G, I-64100 Teramo, Italy
[6] Univ Calif Davis, Sch Vet Med, Dept Med & Epidemiol, Davis, CA 95616 USA
关键词
bluetongue; canarypox virus; vaccine; sheep;
D O I
10.1016/j.vaccine.2006.08.025
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We describe the development and preliminary characterization of a recombinant canarypox virus vectored vaccine for protective immunization of ruminants against bluetongue virus (BTV) infection. Sheep (n = 6) immunized with recombinant canarypox virus vector (BTV-CP) co-expressing synthetic genes encoding the two outer capsid proteins (VP2 and VP5) of BTV serotype 17 (BTV-17) developed high titers (40-160) of virus-specific neutralizing antibodies and were resistant to challenge with a field strain of BTV-17. In contrast, sheep (11 = 5) immunized with a commercial recombinant canarypox virus vector expressing the E and preM genes of West Nile virus were seronegative to BTV and developed pyrexia, lymphopenia, and extended, high-titered viremias following challenge exposure to the field strain of BTV-17. These data confirm that the BTV-CP vaccine may be useful for the protective immunization of ruminants against bluetongue, and it may avoid the problems inherent to live-attenuated (LA) BTV vaccines. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:672 / 678
页数:7
相关论文
共 43 条
[21]   Differentiation between field and vaccine strain of bluetongue virus serotype 16 [J].
Monaco, F. ;
Camma, C. ;
Serini, S. ;
Savini, G. .
VETERINARY MICROBIOLOGY, 2006, 116 (1-3) :45-52
[22]   Vaccines for bluetongue [J].
Murray, PK ;
Eaton, BT .
AUSTRALIAN VETERINARY JOURNAL, 1996, 73 (06) :207-210
[23]  
Ostlund EN, 2001, EMERG INFECT DIS, V7, P665
[24]  
Panagiotatos DE, 2004, VETER ITAL SER, V40, P61
[25]  
Patta C, 2004, Vet Ital, V40, P601
[26]  
PICCINI A, 1987, METHOD ENZYMOL, V153, P545
[27]   VP2-segment sequence analysis of some isolates of bluetongue virus recovered in the Mediterranean basin during the 1998-2003 outbreak [J].
Potgieter, AC ;
Monaco, F ;
Mangana, O ;
Nomikou, K ;
Yadin, H ;
Savini, G .
JOURNAL OF VETERINARY MEDICINE SERIES B-INFECTIOUS DISEASES AND VETERINARY PUBLIC HEALTH, 2005, 52 (09) :372-379
[28]   Efficacy of a canarypox virus-vectored vaccine against feline leukaemia [J].
Poulet, H ;
Brunet, S ;
Boularand, C ;
Guiot, AL ;
Leroy, V ;
Tartaglia, J ;
Minke, J ;
Audonnet, JC ;
Desmettre, P .
VETERINARY RECORD, 2003, 153 (05) :141-145
[29]   Climate change and the recent emergence of bluetongue in Europe [J].
Purse, BV ;
Mellor, PS ;
Rogers, DJ ;
Samuel, AR ;
Mertens, PPC ;
Baylis, M .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (02) :171-181
[30]   COMPARISON OF VIROLOGIC AND SEROLOGIC RESPONSES OF LAMBS AND CALVES INFECTED WITH BLUETONGUE VIRUS SEROTYPE-10 [J].
RICHARDS, RG ;
MACLACHLAN, NJ ;
HEIDNER, HW ;
FULLER, FJ .
VETERINARY MICROBIOLOGY, 1988, 18 (3-4) :233-242