Evaluation of novel recombinant porcine circovirus type 2d (PCV2d) vaccine in pigs naturally infected with PCV2d

被引:21
作者
Kim, Kiju [1 ,2 ]
Hahn, Tae-Wook [1 ,2 ]
机构
[1] Kangwon Natl Univ, Coll Vet Med, Chunchon 24341, South Korea
[2] Kangwon Natl Univ, Inst Vet Sci, Chunchon 24341, South Korea
关键词
Porcine circovirus type 2 (PCV2); Capsid protein; PCV2d vaccine; Recombinant baculovirus; Virus-like particle (VLP); PROTECTIVE IMMUNITY; NONPATHOGENIC PCV1; TRANSMISSION; CHALLENGE; PMWS; DNA; PATHOGENESIS; ANTIBODIES; BACKBONE; SUBTYPES;
D O I
10.1016/j.vaccine.2020.12.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: The pathogenic porcine circovirus type 2 (PCV2) causes significant economic losses in pig production. Emergence of the PCV2d genotype has been linked with PCV2-associated disease (PCVAD) outbreaks. However, no study has been conducted efficacy of an experimental PCV2d-based subunit vaccine in pigs. Therefore, PCV2b- and PCV2d-based capsid (CP) proteins were generated using a baculovirus (Bac) expression system, and we evaluated the protective immune responses in a commercial pig farm where predominant PCV2d is circulating. Methods: Eighteen 3-week-old pigs with maternal antibodies were randomly divided into four groups, and were immunized with purified Bac-2dCP, mixed 1:1 ratio with purified Bac-2bCP and Bac-2dCP (Bac-mCP), a commercial PCV2a-based subunit vaccine (VAC) or phosphate-buffered saline (PBS) as controls. Results: The Bac-2dCP and Bac-mCP groups had significantly higher PCV2b- or PCV2d-specific IgG and neutralizing antibody without interference by maternal antibody compared to control group in pigs naturally infected with PCV2d. Interestingly, not only serum IL-4 level was significantly increased in the Bac-2dCP group, but also PCV2d viremia level was significantly reduced than the control group. Conclusions: The recombinant Bac-2dCP subunit vaccine is a good candidate for the effective reduction against PCV2d infection. (C) 2020 The Author(s). Published by Elsevier Ltd.
引用
收藏
页码:529 / 535
页数:7
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