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首页> 外文期刊>Veterinary Parasitology >Prolonging and enhancing the protective efficacy of the EtMIC3-C-MAR against eimeria tenella through delivered by attenuated salmonella typhimurium
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Prolonging and enhancing the protective efficacy of the EtMIC3-C-MAR against eimeria tenella through delivered by attenuated salmonella typhimurium

机译:延长并增强ETMIC3-C-MAR对eimeria tenella通过减毒的沙门氏菌伤寒伤寒菌递送的保护效果

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The microneme adhesive repeats (MAR) of Eimeria tenella microneme protein 3 (EtMIC3) are associated with binding to and invasion of host cells. Adhesion and invasion-related proteins or domains are often strongly immunogenic, immune responses mounted against these factors that play a key role in blocking invasion. In the present study, an oral live vaccine consisting of attenuated Salmonella typhimurium X4550 carrying two MAR domains fragment (St-X4550-MAR) was constructed and its protective efficacies were evaluated. The results showed that St-X4550-MAR was more immunogenic and conferred a higher degree of protection than recombinant MAR polypeptide as reflected by increased body weight, decreased oocyst shedding and lesion scores, increased serum IgG and cecal sIgA antibody production, and increasing levels of interferon-y and interleukin10. Thus, MAR domains are highly immunogenic and St-X4550-MAR had moderate activity against E. tenella infection by stimulating humoral, mucosal and cellular immunity. Chickens immunized with our constructed live vaccine provided considerable protections as early as at 10 d post-immunization (ACI: 155.17), and maintained higher protection levels at 20 d post-immunization (ACI: 173.66), and at 30 d post-immunization (ACI: 162.4). While the protective efficacy of chickens immunized with the recombinant MAR peptides showed a decreased trend as the post immunization time prolonging. Thus, using live-attenuated S. typhimurium X4550 as a vaccine expression and delivery system can significantly improve the protective efficacy and duration of protective immunity of MAR of EtMIC3.
机译:eimeria tenella microneme蛋白3(Etmic3)的微型粘合剂重复(MAR)与宿主细胞的结合和侵袭有关。粘附和侵袭性相关的蛋白质或域通常是强烈的免疫原性的,免疫应答安装在阻断侵袭中起关键作用的这些因素。在本研究中,构建了由携带两个MAR域片段的减毒沙门氏菌X4550组成的口腔活疫苗(ST-X4550-MAR),并评估其保护效率。结果表明,ST-X4550-MAR更具免疫原性,并且比重组MS多肽赋予更高程度的保护,如因体重增加,卵囊脱落和病变分数降低,血清IgG和肠系SIGA抗体产生增加,以及增加水平干扰素-Y和白细胞介素10。因此,通过刺激体液,粘膜和细胞免疫力,MAR结构域具有高度免疫原性和ST-X4550-MAR对E. Tenella感染的激活。用我们构建的活疫苗免疫的鸡,早在免疫后的10 d(ACI:155.17)中提供了相当大的保护,并在免疫后的20 d处保持更高的保护水平(ACI:173.66),并在免疫后30℃( ACI:162.4)。虽然用重组Mar肽免疫鸡免疫的保护效果显示出作为后免疫时间延长的趋势降低。因此,使用活病毒的S. Typhimurium X4550作为疫苗表达和输送系统可以显着提高Etmic3 Mar的保护性免疫的保护效率和持续时间。

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