Harry K. Dupree Stuttgart National Aquaculture Research Center, Agricultural Research Service, United States Department of Agriculture, Stuttgart, AR, United States.
Front Immunol. 2019 Jun 6;10:1175. doi: 10.3389/fimmu.2019.01175. eCollection 2019.
causes substantial losses among cultured finfish species. The Gram-negative bacterium is an opportunistic pathogen that manifests as biofilms on the host's mucosal surfaces as the disease progresses. We previously demonstrated that the dominant mucosal IgM antibody response to is to the chaperone protein DnaK that is found in the extracellular fraction. To establish the efficacy of using recombinant protein technology to develop a new vaccine against columnaris disease, we are reporting on two consecutive years of vaccine trials using a recombinant DnaK protein (rDnaK). In year one, three groups of channel catfish ( = 300) were immunized by bath immersion with a live attenuated isolate, rDnaK or sham immunized. After 6 weeks, an laboratory challenge showed a significant increase in survival (>30%) in both the live attenuated and rDnaK vaccines when compared to the non-immunized control. A rDnaK-specific ELISA revealed significant levels of mucosal IgM antibodies in the skin of catfish immunized with rDnaK at 4- and 6-weeks post immunization. In the second year, three groups of channel catfish ( = 300) were bath immunized with rDnaK alone or with rDnaK after a brief osmotic shock or sham immunized. After 6 weeks a laboratory challenge with was conducted and showed a significant increase in survival in the rDnaK (> 25%) and in rDnaK with osmotic shock (>35%) groups when compared to the non-immunized control. The rDnaK-specific ELISA demonstrated significant levels of mucosal IgM antibodies in the skin of catfish groups immunized with rDnaK at 4- and 6-weeks post immunization. To further understand the processes which have conferred immune protection in the rDnaK group, we conducted RNA sequencing of skin samples from the non-immunized ( = 6) and rDnaK treated channel catfish at 1-week ( = 6) and 6 weeks ( = 6) post immunization. Significantly altered gene expression was identified and results will be discussed. Work to further enhance the catfish immune response to rDnaK is underway as this protein remains a promising candidate for additional optimization and experimental trials in a production setting.
该革兰氏阴性菌是一种机会性病原体,随着疾病的发展,会在宿主的黏膜表面形成生物膜。我们之前的研究表明,对 的主要黏膜 IgM 抗体反应是针对存在于细胞外部分的伴侣蛋白 DnaK。为了确定利用重组蛋白技术开发柱状病新疫苗的功效,我们报告了使用重组 DnaK 蛋白(rDnaK)进行的连续两年疫苗试验。在第一年,三组斑点叉尾鮰( = 300)通过浸浴免疫接种用减毒 分离株、rDnaK 或假免疫接种。6 周后,实验室挑战显示,与未免疫对照相比,活减毒疫苗和 rDnaK 疫苗的存活率显著提高(>30%)。rDnaK 特异性 ELISA 显示,rDnaK 免疫接种的斑点叉尾鮰皮肤在免疫后 4-6 周时产生了显著水平的黏膜 IgM 抗体。在第二年,三组斑点叉尾鮰( = 300)通过浸浴免疫接种 rDnaK 单独或在短暂渗透休克后与 rDnaK 一起免疫接种,然后进行 rDnaK 的实验室挑战。6 周后,与未免疫对照相比,rDnaK(>25%)和 rDnaK 与渗透休克(>35%)组的存活率显著增加。rDnaK 特异性 ELISA 显示,rDnaK 免疫接种的斑点叉尾鮰皮肤在免疫后 4-6 周时产生了显著水平的黏膜 IgM 抗体。为了进一步了解 rDnaK 组赋予免疫保护的过程,我们对未免疫( = 6)和 rDnaK 处理的斑点叉尾鮰皮肤样本进行了 RNA 测序,分别在免疫后 1 周( = 6)和 6 周( = 6)。鉴定出显著改变的基因表达,结果将进行讨论。正在努力进一步增强斑点叉尾鮰对 rDnaK 的免疫反应,因为该蛋白仍然是在生产环境中进行进一步优化和实验试验的有前途的候选物。