Xu Guojing, Cao Lili, Chen Xiuli, Guo Fangfang, Jiang Yan, Li Xiangyue, Xu Haiqiang, Zang Jinliang, Wang Junpeng, Qin Yuguang
Shandong Provincial Key Laboratory of Freshwater Genetics and Breeding, Shandong Freshwater Fisheries Research Institute, Ji'nan, 250013, People's Republic of China.
Binzhou Marine Development Research Institute, Binzhou, People's Republic of China.
Sci Rep. 2025 Apr 1;15(1):11055. doi: 10.1038/s41598-025-95374-3.
This research was intended to investigate the kinetics of polymeric immunoglobulin receptor (pIgR) and its ligand immunoglobulins (Ig) in snakehead (Channa argus) through different vaccine delivery methods. First, we employed Oxford Nanopore Technologies (ONT) sequencing technology to acquire the snakehead fish's complete transcriptome, and the full coding sequence (CDS) of pIgR was identified and isolated through transcriptome sequencing named ChpIgR. The CDS sequence spanned 1251 base pairs, translating into a protein that consists of 416 amino acids and has a molecular weight of around 45.80 kDa. The ChpIgR had a pair of immunoglobulin-like domains in addition to a transmembrane region and an intracellular region. Furthermore, a polyclonal antibody targeting the snakehead recombinant ChpIgR was constructed. ChpIgR and IgM responses were analyzed after immunization with Aeromonas hydrophila. Although ChpIgR and IgM displayed a comparable transcription level, ChpIgR exhibited a more rapid increase and reached its peak earlier than IgM. Both vaccinated groups experienced an elevation in ChpIgR mRNA levels in the gill and spleen. On the other hand, the bath immersion group manifested that the skin, gills, and intestines had an elevated IgM mRNA expression, whereas the intraperitoneal vaccination group reported that the spleen and head kidney possessed a greater expression. The ELISA results indicated that the IgM and ChpIgR levels reached their highest peak more rapidly in the skin and gill mucus in the bathing group, whereas they reached a greater peak in intestinal mucus in the injection group. The outcomes indicated that both bath and intraperitoneal vaccinations increased ChpIgR and secretory Ig levels in mucus and bile, shedding light on the function of pIgR in immune response and laying the foundation for future studies on pIgR-linked immune defenses in teleosts.
本研究旨在通过不同的疫苗递送方法,研究乌鳢(Channa argus)中聚合免疫球蛋白受体(pIgR)及其配体免疫球蛋白(Ig)的动力学。首先,我们采用牛津纳米孔技术(ONT)测序技术获取乌鳢的完整转录组,并通过转录组测序鉴定和分离出pIgR的全长编码序列(CDS),命名为ChpIgR。CDS序列跨度为1251个碱基对,翻译成一种由416个氨基酸组成、分子量约为45.80 kDa的蛋白质。ChpIgR除了具有一个跨膜区域和一个细胞内区域外,还有一对免疫球蛋白样结构域。此外,构建了一种靶向乌鳢重组ChpIgR的多克隆抗体。在用嗜水气单胞菌免疫后,分析了ChpIgR和IgM的反应。虽然ChpIgR和IgM显示出相当的转录水平,但ChpIgR的增加更为迅速,并且比IgM更早达到峰值。两个接种组的鳃和脾脏中ChpIgR mRNA水平均有所升高。另一方面,浸浴组显示皮肤、鳃和肠道中IgM mRNA表达升高,而腹腔接种组报告脾脏和头肾中表达更高。ELISA结果表明,浸浴组的皮肤和鳃黏液中IgM和ChpIgR水平更快达到最高峰,而注射组在肠道黏液中达到更高峰值。结果表明,浸浴和腹腔接种均增加了黏液和胆汁中ChpIgR和分泌型Ig的水平,揭示了pIgR在免疫反应中的功能,为今后研究硬骨鱼中与pIgR相关的免疫防御奠定了基础。