Li Gang, Xie Fang, Li Jianjun, Liu Jiao, Li Dapeng, Zhang Yanhe, Langford Paul R, Li Yanwen, Liu Siguo, Wang Chunlai
State Key Laboratory of Veterinary Biotechnology, Division of Bacterial Diseases, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Section of Paediatrics, Department of Medicine, Imperial College London, St. Mary's Campus, London, United Kingdom.
J Proteomics. 2017 Jun 23;163:111-117. doi: 10.1016/j.jprot.2017.05.014. Epub 2017 May 17.
Haemophilus parasuis is the aetiological agent of Glässer's disease, which is responsible for cases of fibrinous polyserositis, polyarthritis and meningitis. No vaccine is known that provides cross-protection against all serovars. The identification of novel immunoprotective antigens would undoubtedly contribute to the development of efficient subunit vaccines. In the present study, an immunoproteomic approach was used to analyze secreted proteins of H. parasuis and six proteins with high immunogenicity were identified. Five of them were successfully expressed, and their immunogenicity and protective efficacy were assessed in a mouse challenge model. All five proteins elicited strong humoral antibody and cellular immune responses in mice. They all effectively reduced the growth of H. parasuis in mouse organs and conferred different levels of protection (40-80%) against challenge. IgG subtype analysis revealed that the five proteins induce a bias toward a Th1-type immune response, and a significant increase was observed in the cytokine levels of IL-2, IFN-γ and Th2-specific IL-4 in the culture supernatants of splenocytes isolated from immunized mice. The results suggest that both Th1 and Th2 responses are involved in mediating protection. These data suggest that the five proteins could be potential subunit vaccine candidates for use to prevent H. parasuis infection.
Haemophilus parasuis can cause huge financial loss in the swine industry worldwide. There are still no vaccines which can provide cross-protection against all serovars. To address this need, we applied an immunoproteomic approach involving 2-DE, MALDI-TOF/TOF MS and Western-blot to identify the secreted proteins which may be able to provide immunoprotection to this disease. We identified six immunogenic proteins, and the immunogenicity and protective efficacy were validated. This result provides a foundation for developing novel subunit vaccines against Haemophilus parasuis.
副猪嗜血杆菌是格拉泽氏病的病原体,可导致纤维素性多浆膜炎、多关节炎和脑膜炎病例。目前尚无已知疫苗能对所有血清型提供交叉保护。鉴定新的免疫保护性抗原无疑将有助于开发高效的亚单位疫苗。在本研究中,采用免疫蛋白质组学方法分析副猪嗜血杆菌的分泌蛋白,鉴定出6种具有高免疫原性的蛋白。其中5种成功表达,并在小鼠攻毒模型中评估了它们的免疫原性和保护效果。所有5种蛋白均在小鼠中引发了强烈的体液抗体和细胞免疫反应。它们都有效地减少了副猪嗜血杆菌在小鼠器官中的生长,并对攻毒提供了不同程度(40%-80%)的保护。IgG亚型分析表明,这5种蛋白诱导了偏向Th1型免疫反应的倾向,并且在从免疫小鼠分离的脾细胞培养上清液中,IL-2、IFN-γ和Th2特异性IL-4的细胞因子水平显著升高。结果表明,Th1和Th2反应均参与介导保护作用。这些数据表明,这5种蛋白可能是用于预防副猪嗜血杆菌感染的潜在亚单位疫苗候选物。
副猪嗜血杆菌可在全球养猪业中造成巨大经济损失。目前仍没有能对所有血清型提供交叉保护的疫苗。为满足这一需求,我们应用了一种涉及二维电泳、基质辅助激光解吸电离飞行时间串联质谱和蛋白质免疫印迹的免疫蛋白质组学方法,以鉴定可能能够为该病提供免疫保护的分泌蛋白。我们鉴定出6种免疫原性蛋白,并验证了其免疫原性和保护效果。这一结果为开发针对副猪嗜血杆菌的新型亚单位疫苗奠定了基础。