首页> 外文期刊>Veterinary Microbiology >Oral vaccination with attenuated Salmonella enterica serovar Typhimurium expressing Cap protein of PCV2 and its immunogenicity in mouse and swine models
【24h】

Oral vaccination with attenuated Salmonella enterica serovar Typhimurium expressing Cap protein of PCV2 and its immunogenicity in mouse and swine models

机译:表达减毒小肠沙门氏菌表达鼠伤寒沙门氏菌PCV2 Cap蛋白的疫苗及其在小鼠和猪模型中的免疫原性

获取原文
获取原文并翻译 | 示例
           

摘要

Attenuated Salmonella enterica serovar Typhimurium (S. typhimurium) was selected as a transgenic vehicle for the development of oral vaccines against Porcine circovirus type 2 (PCV2). The Cap-encoding gene of PCV2 was amplified by PCR and cloned into expression vector pYA3341. The recombinant plasmid pYA3341-Cap was transformed into attenuated S. typhimurium X4550. BALB/c mice were inoculated orally with various doses of attenuated S. typhimurium X4550/pYA3341-Cap. The bacterium was safe to mice at dose of 2 x 10(9) cfu and eventually eliminated in the spleen and mesenteric lymph nodes at 4 weeks post-immunization. The flow cytometry analysis showed that the percentage of CD4(+) T cells and CD4(+)/CD8(+) ratio were increased significantly in mice immunized with attenuated S. typhimurium X4550/pYA3341-Cap. Vaccine tests in swine showed that the oral immunization with attenuated S. typhimurium X4550/pYA3341-Cap could elicit significantly higher Cap antibody titers in the treated swine than the control groups. Virus neutralization test showed that serum from the swine treated with attenuated S. typhimurium X4550/pYA3341-Cap had significant levels of neutralization activities. The swine lymphocyte proliferative responses indicated that attenuated S. typhimurium X4550/pYA3341-Cap could induce obvious cellular immune response. An in vivo challenge study showed the swine treated with attenuated S. typhimurium X4550/pYA3341-Cap had significantly lower PCV2-associated lesions and PCV2 viremia than the control groups. The results indicated that attenuated S. typhimurium X4550/pYA3341-Cap can be a potential vaccine against PCV2 infections. (C) 2012 Elsevier B.V. All rights reserved.
机译:选择减毒的肠炎沙门氏菌鼠伤寒沙门氏菌(S. typhimurium)作为转基因载体,用于开发抗2型猪圆环病毒(PCV2)的口服疫苗。通过PCR扩增PCV2的Cap编码基因,并将其克隆到表达载体pYA3341中。重组质粒pYA3341-Cap被转化入减毒鼠伤寒沙门氏菌X4550。用不同剂量的减毒鼠伤寒沙门氏菌X4550 / pYA3341-Cap口服BALB / c小鼠。该细菌对小鼠安全,剂量为2 x 10(9)cfu,并在免疫后4周最终在脾脏和肠系膜淋巴结中消除。流式细胞仪分析表明,用减毒鼠伤寒沙门氏菌X4550 / pYA3341-Cap免疫的小鼠中CD4(+)T细胞百分比和CD4(+)/ CD8(+)比显着增加。猪中的疫苗试验表明,用减毒鼠伤寒沙门氏菌X4550 / pYA3341-Cap进行的口服免疫接种可以使治疗后的猪的Cap抗体滴度明显高于对照组。病毒中和试验表明,用减毒鼠伤寒沙门氏菌X4550 / pYA3341-Cap处理的猪血清具有显着水平的中和活性。猪淋巴细胞增殖反应表明减毒鼠伤寒沙门氏菌X4550 / pYA3341-Cap可以诱导明显的细胞免疫反应。一项体内攻击研究表明,用减毒鼠伤寒沙门氏菌X4550 / pYA3341-Cap处理的猪的PCV2相关病变和PCV2病毒血症明显低于对照组。结果表明减毒鼠伤寒沙门氏菌X4550 / pYA3341-Cap可能是针对PCV2感染的潜在疫苗。 (C)2012 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号