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鱼类迟缓爱德华氏菌低氧应答蛋白 1 重组疫苗对大口黑鲈的保护效力。

The protective efficacy of recombinant hypoxic response protein 1 of Nocardia seriolae in largemouth bass (Micropterus salmoides).

机构信息

Department of Veterinary Medicine, College of Veterinary Medicine, National Pingtung University of Science and Technology, No. 1 Shuefu Road, Neipu, Pingtung 91201, Taiwan.

Department of Veterinary Medicine, College of Veterinary Medicine, National Pingtung University of Science and Technology, No. 1 Shuefu Road, Neipu, Pingtung 91201, Taiwan; Southern Taiwan Fish Disease Centre, National Pingtung University of Science and Technology, No. 1 Shuefu Road, Neipu, Pingtung 91201, Taiwan.

出版信息

Vaccine. 2020 Mar 23;38(14):2925-2936. doi: 10.1016/j.vaccine.2020.02.062. Epub 2020 Feb 27.

Abstract

Nocardia seriolae has become one of the major pathogens affecting the aquaculture industry and causes Nocardiosis, a highly devastating disease of marine and freshwater fish that leads to severe economic losses. Therefore, research efforts towards developing efficacious vaccines to control this disease are of high importance. In this study, the hypoxic response protein 1 (HRP1) cloned into pET32a vector was expressed, and produced in Escherichia coli strain BL21 (DE3). The antigenicity of purified recombinant TRX-tagged HRP (rHRP1) was analysed by western blotting using largemouth bass anti-N. seriolae sera. The results showed that largemouth bass anti-N. seriolae sera could specifically detect a 33 kDa rHRP1 protein. Further, the vaccine efficacy of rHRP1 was evaluated in a largemouth bass fish model by calculating the relative percent survival (RPS). rHRP1 incurred an RPS of 73.33% as compared to the control group. Immunological analysis showed that rHRP1 could produce significantly higher serum concentrations of anti-N. seriolae antibodies and serum lysozyme activity as compared to the control groups. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) analysis showed that rHRP1 significantly enhanced the expression of immune-related genes, such as IL-12p40, IL-8, IL-1β, TNFα, IFNγ, NKEF, MHCIα, MHCIIα, CD4-1, CD8α, IgM, NF-κβ, STAT3, IRF4, RORα, and CCL20. These results indicate that rHRP1 may be a promising vaccine candidate against nocardiosis.

摘要

海洋鱼类诺卡氏菌已成为影响水产养殖业的主要病原体之一,引发诺卡氏病,这是一种对海水和淡水鱼类具有高度破坏性的疾病,导致严重的经济损失。因此,开发有效疫苗来控制这种疾病的研究工作非常重要。在本研究中,将克隆到 pET32a 载体中的低氧反应蛋白 1(HRP1)在大肠杆菌 BL21(DE3)菌株中表达和生产。使用大口黑鲈抗海洋鱼类诺卡氏菌血清通过 Western blot 分析纯化的重组 TRX 标记 HRP(rHRP1)的抗原性。结果表明,大口黑鲈抗海洋鱼类诺卡氏菌血清可以特异性检测到 33 kDa 的 rHRP1 蛋白。此外,通过计算相对存活率(RPS),在大口黑鲈鱼模型中评估了 rHRP1 的疫苗效力。与对照组相比,rHRP1 的 RPS 为 73.33%。免疫分析表明,与对照组相比,rHRP1 可以产生明显更高浓度的抗海洋鱼类诺卡氏菌抗体和血清溶菌酶活性。定量逆转录聚合酶链反应(qRT-PCR)分析表明,rHRP1 显著增强了免疫相关基因的表达,如 IL-12p40、IL-8、IL-1β、TNFα、IFNγ、NKEF、MHCIα、MHCIIα、CD4-1、CD8α、IgM、NF-κβ、STAT3、IRF4、RORα 和 CCL20。这些结果表明,rHRP1 可能是一种有前途的抗诺卡氏病疫苗候选物。

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