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
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