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首页> 外文期刊>Vaccine >DNA vaccination based on pyolysin co-immunized with IL-1 beta enhances host antibacterial immunity against Trueperella pyogenes infection
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DNA vaccination based on pyolysin co-immunized with IL-1 beta enhances host antibacterial immunity against Trueperella pyogenes infection

机译:基于与IL-1β共同免疫的溶血素的DNA疫苗接种增强了宿主对化脓性脓单胞菌感染的抗菌免疫力

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Trueperella pyogenes is a commensal and opportunistic pathogen normally causes mastitis, liver abscesses and pneumonia of economically important livestock. To date, no specific control measure was reported to prevent T. pyogenes infections. In this study, we first constructed a recombinant plasmid pVAX1-PLO based on the main virulent factor pyolysin gene as DNA vaccine against T. pyogenes infection. Subsequently, transient expression of pVAX1-PLO and pcDNA3.1/V5-flL-1 beta were identified in Human embryonic kidney cells (HEK293T) by immunofluorescence assay. Humoral and cellular immune responses were evaluated in mice to compare the immunogenicity between different immunized groups. The results showed that the successful expression of PLO or flL-1 beta protein was detected by confocal microscopy for cells transfected with plasmid pVAX1-PLO and/or pcDNA3.1/V5-flL-1 beta. The mice immunized with pVAX1-PLO elicited a higher titer of PLO-specific antibody than the control group. The levels of IFN-gamma and IL-2 were significantly increased in the pVAX1-PLO immunized mice, while the expression level of IL-4 was slightly increased but not significant. These findings suggested that the DNA vaccine pVAX1-PLO can primarily induce Th1 immune response. The residual Colony-Forming Units (CFUs) from the liver and peritonea fluid were decreased obviously in the pVAX1-PLO treated mice compared with the control. Importantly, co-immunization with pcDNA3.1/V5-flL-1 beta and pVAX1-PLO could enhance host humoral and cellular immune responses and significantly protect mouse from T. pyogenes infection. In conclusion, our study provides a promising strategy against T. pyogenes infections and implies the potential clinical application of combined DNA vaccines in diseases control. (C) 2016 Elsevier Ltd. All rights reserved.
机译:化脓小球藻是一种常见的机会病原体,通常会引起经济上重要的牲畜的乳腺炎,肝脓肿和肺炎。迄今为止,尚无报道报告采取特定的控制措施来预防化脓性支原体感染。在这项研究中,我们首先基于主要的毒性因子pyyolysin基因构建了重组质粒pVAX1-PLO,作为针对化脓性链球菌感染的DNA疫苗。随后,通过免疫荧光测定在人胚胎肾细胞(HEK293T)中鉴定了pVAX1-PLO和pcDNA3.1 / V5-flL-1 beta的瞬时表达。在小鼠中评估体液和细胞免疫应答,以比较不同免疫组之间的免疫原性。结果表明,通过共聚焦显微镜检测了用质粒pVAX1-PLO和/或pcDNA3.1 /V5-flL-1β转染的细胞的PLO或fIL-1β蛋白的成功表达。用pVAX1-PLO免疫的小鼠引起的PLO特异性抗体滴度高于对照组。在pVAX1-PLO免疫的小鼠中,IFN-γ和IL-2的水平显着升高,而IL-4的表达水平略有升高,但不显着。这些发现表明DNA疫苗pVAX1-PLO可以主要诱导Th1免疫应答。与对照组相比,pVAX1-PLO处理的小鼠肝脏和腹膜液中残留的菌落形成单位(CFU)明显减少。重要的是,与pcDNA3.1 / V5-flL-1 beta和pVAX1-PLO共同免疫可增强宿主的体液和细胞免疫反应,并显着保护小鼠免受化脓性链球菌感染。总之,我们的研究为化脓性链球菌感染提供了一种有希望的策略,并暗示了组合DNA疫苗在疾病控制中的潜在临床应用。 (C)2016 Elsevier Ltd.保留所有权利。

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