Cheng Chu-Fan, Chuang Hsiang-Chieh, Lai Yu-Shen
Department of Biotechnology and Animal Science, National Ilan University, Yilan 26047, Taiwan.
Department of Aquaculture, National Kaohsiung University of Science and Technology, Kaohsiung 81157, Taiwan.
Virus Res. 2025 Aug 25;360:199625. doi: 10.1016/j.virusres.2025.199625.
Grouper iridovirus (GIV) is regarded as a prominent viral pathogen of grouper, particularly during the larval and juvenile stages. The aim of this study was to comprehensively characterize the GIV-120L gene during viral infection. The results of sequence analysis suggest that GIV-120L is a 1,470 bp gene encoding a Ranavirus-specific viral protein. Recombinant GIV-120L protein was purified using a nickel-affinity column, and its molecular weight was found to be 59.1 kDa. To obtain antibodies against GIV, mice were immunized with recombinant GIV-120L protein, the spleen was harvested 8 weeks later, and hybridoma testing was performed using Sp2/0 myeloma cells. Polyclonal and monoclonal antibodies against GIV-120L were obtained. To characterize GIV-120L gene expression, grouper kidney (GK) cells were infected with GIV using cycloheximide (CHX) and cytosine arabinoside (AraC). GIV-120L transcripts and protein were found at 12-30 h post infection (hpi) and 18-30 hpi, respectively. In addition, inhibition with CHX and AraC confirmed that GIV-120L was a late gene. Immunofluorescence staining using the antibodies produced in the study confirmed that GIV-120L protein is expressed at viral assembly sites at 24 hpi. The findings of this study provide functional characterization of the GIV-120L viral gene, enhance understanding of GIV assembly, and offer insights for GIV diagnostic applications.
石斑鱼虹彩病毒(GIV)被认为是石斑鱼的一种主要病毒病原体,尤其是在幼体和成鱼阶段。本研究的目的是全面表征病毒感染过程中的GIV - 120L基因。序列分析结果表明,GIV - 120L是一个1470 bp的基因,编码一种蛙病毒属特异性病毒蛋白。使用镍亲和柱纯化重组GIV - 120L蛋白,发现其分子量为59.1 kDa。为了获得抗GIV的抗体,用重组GIV - 120L蛋白免疫小鼠,8周后采集脾脏,并使用Sp2/0骨髓瘤细胞进行杂交瘤检测。获得了抗GIV - 120L的多克隆和单克隆抗体。为了表征GIV - 120L基因的表达,用环己酰亚胺(CHX)和阿糖胞苷(AraC)感染石斑鱼肾脏(GK)细胞。分别在感染后12 - 30小时(hpi)和18 - 30小时(hpi)发现GIV - 120L转录本和蛋白。此外,用CHX和AraC抑制证实GIV - 120L是一个晚期基因。使用本研究中产生的抗体进行免疫荧光染色证实,GIV - 120L蛋白在感染后24小时在病毒装配位点表达。本研究结果提供了GIV - 120L病毒基因的功能表征,增强了对GIV装配的理解,并为GIV诊断应用提供了见解。