Department of Infectious Diseases & Immunology, College of Veterinary Medicine, University of Florida, Gainesville, FL, United States.
Front Immunol. 2022 Jan 25;12:802760. doi: 10.3389/fimmu.2021.802760. eCollection 2021.
We have successfully designed and constructed a RAEV vector system with regulated-delayed attenuation attributes that synthesizes (Ich) protective antigen IAG52B to enable vaccination of fish susceptible to edwardsiellosis and white spot disease. The first feature of this vaccine delivery system is an strain carrying genomic deletions of . AsdA is an enzyme necessary for the synthesis of diaminopimelic acid (DAP), which is an essential component of the peptidoglycan layer of the cell wall of Gram-negative bacteria. mutant strains have obligate growth requirements for DAP in the medium or a plasmid vector with the wild-type gene enabling synthesis of DAP. This balanced-lethal plasmid vector-host system in enables as a second feature the synthesis of recombinant antigens to induce protective immunity against fish pathogens. Recombinant protective antigen IAG52B from the fish pathogen was synthesized by RAEV strains harboring the AsdA plasmid pG8R8029. The third feature of this vaccine strain is a regulated-delayed attenuation phenotype that is based on the replacement of an arabinose-regulated P cassette for the promoters of the and genes of such that the expression of these genes is dependent on arabinose provided during growth. Thus, following colonization, the Fur and Crp proteins stop being synthesized due to the lack of arabinose and attenuation is progressively achieved to prevent generation of diseases symptoms. Our vaccine strain χ16022 with the genotype Δ ΔP::TT P ΔP::TT P contains the AsdA plasmid, pG8R8029, which encodes the IAG52B antigen. Vaccine strain χ16022(pG8R8029) is attenuated and induces systemic and mucosal IgM titer against and Ich in zebrafish. In addition, transcript levels of , , and were significantly increased in different tissues of vaccinated zebrafish compared to unimmunized fish. Zebrafish vaccinated with χ16022(pG8R8029) showed 60% survival upon intracoelomic (i.c.) challenge with a lethal dose of virulent strain J118. Our RAEV system could be used as a generalized vaccine-vector system to protect teleost fish against multiple bacterial, viral and parasitic infectious diseases.
我们成功设计并构建了一个具有调节延迟衰减特性的 RAEV 载体系统,该系统合成了(Ich)保护性抗原 IAG52B,以实现对易患爱德华氏菌病和白点病的鱼类的疫苗接种。该疫苗传递系统的第一个特征是携带基因组缺失的 菌株。AsdA 是合成二氨基庚二酸(DAP)所必需的酶,DAP 是革兰氏阴性细菌细胞壁肽聚糖层的一个组成部分。ΔAsdA 突变菌株在培养基中或携带野生型 基因的质粒载体中对 DAP 有严格的生长要求,使 DAP 得以合成。在 中,这种平衡致死质粒载体-宿主系统作为第二个特征,能够合成重组抗原,诱导鱼类病原体的保护性免疫。来自鱼类病原体 的重组保护性抗原 IAG52B 由携带 AsdA 质粒 pG8R8029 的 RAEV 菌株合成。该疫苗株的第三个特征是一种调节延迟衰减表型,它基于阿拉伯糖调节的 P 盒替换为 的 和 基因的启动子,使得这些基因的表达依赖于生长过程中提供的阿拉伯糖。因此,定植后,由于缺乏阿拉伯糖,Fur 和 Crp 蛋白停止合成,衰减逐渐实现,以防止疾病症状的产生。我们的疫苗株 χ16022 基因型为 Δ ΔP::TT P ΔP::TT P 含有 AsdA 质粒 pG8R8029,该质粒编码 IAG52B 抗原。疫苗株 χ16022(pG8R8029)是衰减的,能诱导系统和黏膜 IgM 效价对斑马鱼的 和 Ich。此外,与未免疫的鱼相比,接种疫苗的斑马鱼不同组织中的 、 、 和 的转录水平显著增加。用 χ16022(pG8R8029)接种的斑马鱼在腹腔内(i.c.)用致死剂量的毒力菌株 J118 攻毒后,存活率为 60%。我们的 RAEV 系统可以作为一种通用的疫苗载体系统,保护硬骨鱼类免受多种细菌性、病毒性和寄生虫性传染病的侵害。