Sohn Min-Young, Kim Ju-Won, Kang Gyoungsik, Woo Won-Sik, Kim Kyung-Ho, Son Ha-Jeong, Park Jong-Won, Kim Do-Hyung, Park Chan-Il
Department of Marine Biology & Aquaculture, College of Marine Science, Gyeongsang National University, 455, Tongyeong, 650-160, Republic of Korea.
Biotechnology Research Division, National Institute of Fisheries Science, Busan, 46083, Republic of Korea.
Dev Comp Immunol. 2023 Dec;149:105054. doi: 10.1016/j.dci.2023.105054. Epub 2023 Sep 9.
In this study, the starry flounder L1 cell adhesion molecule (L1CAM) sequence was obtained using next-generation sequencing, and the integrity of the sequence was verified by cloning and sequencing. First, the amino acid sequence was predicted using the cDNA sequence, and the gene was then identified through multiple sequence alignment analysis with related sequences and phylogenetic analysis. Thus, homogeneity was confirmed. The expression level of PsL1CAM (Platichthys stellatus L1CAM) mRNA in healthy starry flounder was detected in all tissues used in the experiment, and tissue- and gene-specific expression levels were confirmed. In addition, as a result of mRNA expression analysis after artificial infection with viral hemorrhagic septicemia virus (VHSV) and Streptococcus parauberis PH0710, significant expression changes and characteristics were confirmed following infection with VHSV and S. parauberis PH0710. After artificial infection with VHSV, the expression level of PsL1CAM mRNA was significantly upregulated in almost all major tissues of the starry flounder, whereas it was significantly downregulated in mucosal-associated lymphoid tissues, such as the gills and intestine. Infection with S. parauberis PH0710 significantly upregulated the expression of PsL1CAM mRNA in almost all major tissues of the starry flounder, whereas it was significantly downregulated in the heart after infection. Our results indicate that PsL1CAM may be involved in the host immune response to starry flounders.
在本研究中,利用新一代测序技术获得了星斑川鲽L1细胞粘附分子(L1CAM)序列,并通过克隆和测序验证了序列的完整性。首先,利用cDNA序列预测氨基酸序列,然后通过与相关序列的多序列比对分析和系统发育分析鉴定该基因。由此确认了同源性。在实验所用的所有组织中检测了健康星斑川鲽中PsL1CAM(星斑川鲽L1CAM)mRNA的表达水平,并确认了组织特异性和基因特异性表达水平。此外,对感染病毒性出血性败血症病毒(VHSV)和副乳房链球菌PH0710后的mRNA表达进行分析,结果显示,感染VHSV和副乳房链球菌PH0710后,出现了显著的表达变化和特征。人工感染VHSV后,星斑川鲽几乎所有主要组织中PsL1CAM mRNA的表达水平均显著上调,而在鳃和肠道等黏膜相关淋巴组织中则显著下调。感染副乳房链球菌PH0710后,星斑川鲽几乎所有主要组织中PsL1CAM mRNA的表达均显著上调,而感染后心脏中的表达则显著下调。我们的结果表明,PsL1CAM可能参与星斑川鲽的宿主免疫反应。