首页> 外文期刊>BMC Veterinary Research >Protective immunity induced by Eimeria common antigen 14–3-3 against Eimeria tenella, Eimeria acervulina and Eimeria maxima
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Protective immunity induced by Eimeria common antigen 14–3-3 against Eimeria tenella, Eimeria acervulina and Eimeria maxima

机译:艾美球虫共有抗原14-3-3诱导的针对艾美球虫,小球艾美球虫和极大艾美球虫的保护性免疫

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Avian coccidiosis is often caused by co-infection with several species of Eimeria worldwide. Developing a multivalent vaccine with an antigen common to multiple Eimeria species is a promising strategy for controlling clinical common co-infection of Eimeria. In the previous study, 14–3-3 was identified as one of the immunogenic common antigen in E. tenella, E. acervulina and E. maxima. The aim of the present study was to evaluate the immunogenicity and protective efficacy of Ea14–3-3 in the form of DNA vaccine against infection with three species of Eimeria both individually and simultaneously. After vaccination with pVAX-Ea14–3-3, the Ea14–3-3 gene was transcribed and expressed in the injected muscles. Vaccination with pVAX-Ea14–3-3 significantly increased the proportion of CD4+ and CD8+ T lymphocytes and produced a strong IgY response in immunized chickens. Similarly, pVAX-Ea14–3-3 stimulated the chicken’s splenocytes to produce high levels of Th1-type (IFN-γ, IL-2) and Th2-type (IL-4) cytokines. The vaccine-induced immune response was responsible to increase weight gain, decreased the oocyst output, and alleviated enteric lesions significantly in immunized chickens as compared to control group, in addition to induce moderate anti-coccidial index (ACI). These results indicate that Ea14–3-3 is highly immunogenic and capable to induce significant immune responses. Furthermore, Ea14–3-3 antigen can provide effective protection against infection with Eimeria tenella, Eimeria acervulina, Eimeria maxima both individually and in combination with three Eimeria species. Significant outcomes of our study provide an effective candidate antigen for developing a multivalent Eimeria vaccine against mixed infection with various Eimeria species under natural conditions.
机译:禽球虫病通常是由全球范围内与几种艾美球虫共同感染引起的。用多种艾美球虫属种共有的抗原开发多价疫苗是控制艾美球虫临床常见共感染的一种有前途的策略。在先前的研究中,14–3-3被鉴定为大肠杆菌中的免疫原性常见抗原之一,而小肠埃希菌和大肠埃希菌也是如此。本研究的目的是评估针对DNA疫苗形式的Ea14-3-3的免疫原性和保护功效,以分别或同时抵抗三种艾美球虫感染。用pVAX-Ea14-3-3疫苗接种后,Ea14-3-3基因被转录并在注射的肌肉中表达。用pVAX-Ea14-3-3进行疫苗接种可显着增加CD4 +和CD8 + T淋巴细胞的比例,并在免疫鸡中产生强烈的IgY反应。同样,pVAX-Ea14-3-3刺激鸡的脾细胞产生高水平的Th1型(IFN-γ,IL-2)和Th2型(IL-4)细胞因子。与对照组相比,疫苗免疫的鸡与对照组相比,疫苗诱导的免疫反应还可以增加体重,降低卵囊产量并显着减轻肠道损害。这些结果表明,Ea14-3-3具有高度的免疫原性,能够诱导明显的免疫反应。此外,Ea14-3-3抗原可单独或与三种艾美尔球虫结合提供有效的保护,以防感染艾美尔球虫,小叶艾美尔球虫,最大艾美尔球虫。我们研究的重要成果为开发针对自然条件下多种艾美球虫混合感染的多价艾美球虫疫苗提供了有效的候选抗原。

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