Suppr超能文献

减毒胸膜肺炎放线杆菌双缺失突变体S-8∆clpP/apxIIC可抵御同源或异源菌株的攻击。

Attenuated Actinobacillus pleuropneumoniae double-deletion mutant S-8∆clpP/apxIIC confers protection against homologous or heterologous strain challenge.

作者信息

Xie Fang, Li Gang, Zhou Long, Zhang Yanhe, Cui Ning, Liu Siguo, Wang Chunlai

机构信息

State Key Laboratory of Veterinary Biotechnology, Division of Bacterial Diseases, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, Heilongjiang, People's Republic of China.

出版信息

BMC Vet Res. 2017 Jan 6;13(1):14. doi: 10.1186/s12917-016-0928-9.

Abstract

BACKGROUND

Actinobacillus pleuropneumoniae is the etiological agent of porcine pleuropneumonia, which leads to large economic losses to the swine industry worldwide. In this study, S-8△clpP△apxIIC, a double-deletion mutant of A. pleuropneumoniae was constructed, and its safety and protective efficacy were evaluated in pigs.

RESULTS

The S-8△clpP△apxIIC mutant exhibited attenuated virulence in a murine (BALB/c) model, and caused no detrimental effects on pigs even at a dose of up to 1.0 × 10 CFU. Furthermore, the S-8△clpP△apxIIC mutant was able to induce a strong immune response in pigs, which included high levels of IgG1 and IgG2, stimulated gamma interferon (IFN-γ), interleukin 12 (IL-12), and interleukin 4 (IL-4) production, and conferred effective protection against the lethal challenge with A. pleuropneumoniae serovars 7 or 5a. The pigs in the S-8△clpP△apxIIC immunized groups have no lesions and reduced bacterial loads in the lung tissue after challenge.

CONCLUSIONS

The data obtained in this study suggest that the S-8△clpP△apxIIC mutant can serve as a highly immunogenic and potential live attenuated vaccine candidate against A. pleuropneumoniae infection.

摘要

背景

胸膜肺炎放线杆菌是猪胸膜肺炎的病原体,给全球养猪业造成巨大经济损失。在本研究中,构建了胸膜肺炎放线杆菌的双缺失突变株S-8△clpP△apxIIC,并在猪体内评估了其安全性和保护效力。

结果

S-8△clpP△apxIIC突变株在小鼠(BALB/c)模型中表现出毒力减弱,即使在高达1.0×10⁹CFU的剂量下对猪也无有害影响。此外,S-8△clpP△apxIIC突变株能够在猪体内诱导强烈的免疫反应,包括高水平的IgG1和IgG2,刺激γ干扰素(IFN-γ)、白细胞介素12(IL-12)和白细胞介素4(IL-4)的产生,并对胸膜肺炎放线杆菌血清型7或5a的致死性攻击提供有效保护。S-8△clpP△apxIIC免疫组的猪在攻毒后肺组织无病变且细菌载量降低。

结论

本研究获得的数据表明,S-8△clpP△apxIIC突变株可作为一种高免疫原性且有潜力的抗胸膜肺炎放线杆菌感染的减毒活疫苗候选株。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验