Codon optimization of voraxin α sequence enhances the immunogenicity of a recombinant vaccine against Hyalomma anatolicum infestation in rabbits

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY
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Abstract

Research has shown that voraxin α derived from male ticks stimulates blood feeding to engorge in female ticks. Whereas, the oviposition rate, egg weight, and body weight of female ticks were reduced in animals vaccinated with recombinant (r-) voraxin α. These data suggest a potential role of r-voraxin α as a functional anti-tick antigen in Rhipicephalus appendiculatus and Amblyomma hebraeum tick infestation. This study investigated the immunogenicity of r-voraxin α protein from Hyalomma anatolicum (H. anatolicum) tick as an anti-tick vaccine in rabbits. The H. anatolicum voraxin α sequence was optimized according to the codon usage in E. coli before being sub-cloned into pQE30. The gene sequence of the voraxin α was synthesized, verified by DNA sequencing, cloned in a pQE30 vector, and transformed into E. coli. Then, the expression of the r-voraxin α protein was confirmed by SDS-PAGE and Western blot analysis. Subsequently, three rabbits were immunized with the r-voraxin α as the vaccinated group, whereas three rabbits without injection were considered the control group. The result indicated the success of cloning of codon-optimized H. anatolicum voraxin α gene. Moreover, the expression of the r-voraxin α protein (approximately 18 kDa) in the bacterial expression system was confirmed by SDS-PAGE and Western blot analysis. The results of this study showed that the mortality rate in vaccine recipients increased compared to the control group (P < 0.01). Also, the egg weight, oviposition rate, and engorgement weight of female ticks fed from vaccinated animals were significantly reduced compared to the control group (P < 0.01). The results confirmed that the codon-optimized H. anatolicum voraxin α gene expressed in the bacterial expression system could be a suitable anti-tick vaccine against H. anatolicum tick infestation.

优化伏拉菌素α序列的密码子可增强重组疫苗的免疫原性,以预防家兔疟原虫感染
研究表明,从雄蜱中提取的伏拉克辛 α 能刺激雌蜱吸血。这些数据表明,在 Rhipicephalus appendiculatus 和 Amblyomma hebraeum 的蜱虫感染中,r-voraxin α 作为一种功能性抗蜱抗原具有潜在的作用。本研究调查了锐蜱r-voraxin α蛋白作为兔抗蜱疫苗的免疫原性。根据大肠杆菌中密码子的使用情况,对H. anatolicum voraxin α序列进行了优化,然后将其子克隆到pQE30中。合成出 voraxin α 的基因序列,经 DNA 测序验证后克隆到 pQE30 载体中,并转化到大肠杆菌中。然后,通过 SDS-PAGE 和 Western 印迹分析确认了 r-voraxin α 蛋白的表达。随后,用 r-voraxin α 对 3 只兔子进行免疫接种,作为接种组,而 3 只兔子未注射 r-voraxin α 作为对照组。结果表明,经过密码子优化的锐毒花斑癣菌花斑素α基因克隆成功。此外,SDS-PAGE 和 Western 印迹分析证实了 r-voraxin α 蛋白(约 18 kDa)在细菌表达系统中的表达。研究结果表明,与对照组相比,疫苗接种者的死亡率有所上升(P < 0.01)。此外,与对照组相比,疫苗接种动物喂养的雌性蜱的卵重、排卵率和吞食重量均显著降低(P <0.01)。结果证实,在细菌表达系统中表达的经过密码子优化的锐蝽oraxin α基因可作为一种合适的抗锐蝽蜱虫害疫苗。
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来源期刊
CiteScore
3.40
自引率
5.60%
发文量
79
审稿时长
70 days
期刊介绍: The journal reports basic, comparative and clinical immunology as they pertain to the animal species designated here: livestock, poultry, and fish species that are major food animals and companion animals such as cats, dogs, horses and camels, and wildlife species that act as reservoirs for food, companion or human infectious diseases, or as models for human disease. Rodent models of infectious diseases that are of importance in the animal species indicated above,when the disease requires a level of containment that is not readily available for larger animal experimentation (ABSL3), will be considered. Papers on rabbits, lizards, guinea pigs, badgers, armadillos, elephants, antelope, and buffalo will be reviewed if the research advances our fundamental understanding of immunology, or if they act as a reservoir of infectious disease for the primary animal species designated above, or for humans. Manuscripts employing other species will be reviewed if justified as fitting into the categories above. The following topics are appropriate: biology of cells and mechanisms of the immune system, immunochemistry, immunodeficiencies, immunodiagnosis, immunogenetics, immunopathology, immunology of infectious disease and tumors, immunoprophylaxis including vaccine development and delivery, immunological aspects of pregnancy including passive immunity, autoimmuity, neuroimmunology, and transplanatation immunology. Manuscripts that describe new genes and development of tools such as monoclonal antibodies are also of interest when part of a larger biological study. Studies employing extracts or constituents (plant extracts, feed additives or microbiome) must be sufficiently defined to be reproduced in other laboratories and also provide evidence for possible mechanisms and not simply show an effect on the immune system.
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