Institute of Marine Biology, National Taiwan Ocean University, Keelung, Taiwan, ROC; Center of Excellence for the Oceans, National Taiwan Ocean University, Keelung, Taiwan, ROC.
Institute of Marine Biology, National Taiwan Ocean University, Keelung, Taiwan, ROC.
Dev Comp Immunol. 2019 Aug;97:1-10. doi: 10.1016/j.dci.2019.03.006. Epub 2019 Mar 20.
In this study, we describe 19 different CC chemokine genes from the orange-spotted grouper, Epinephelus coioides, identified by the analysis of the spleen transcriptome. Multiple sequence alignment of the 19 CC chemokines showed that although two genes, EcSCYA115 and EcSCYA117, shared 80% amino acid similarity (72% identity), the majority exhibited low similarity to each other. Phylogenetic analysis divided the 19 CC chemokines into six major groups. Tissue distribution analysis by RT-PCR showed that most of these chemokines were ubiquitously expressed in the 9 examined tissues, whereas some exhibited tissue-preferential expression patterns. For example, EcSCYA103 was preferentially expressed in fin and gill; EcSCYA109 in head kidney and spleen; EcSCYA114 in fin, gill, and liver; and EcSCYA119 in fin and stomach. Quantitative RT-PCR showed that after challenge with grouper iridovirus (GIV), four of the 19 CC chemokine genes, EcSYCA102, EcSYCA103, EcSYCA116, and EcSYCA118, were highly induced in the spleen. The expression of these four genes could also be upregulated by LPS and poly (I:C) challenges, suggesting that these four genes might be involved in immune response against invading pathogens.
在这项研究中,我们通过分析脾脏转录组,从卵形鲷(Epinephelus coioides)中鉴定了 19 种不同的 C 型趋化因子基因。对这 19 种 C 型趋化因子的多重序列比对表明,尽管两个基因 EcSCYA115 和 EcSCYA117 具有 80%的氨基酸相似性(72%的同一性),但大多数基因彼此之间的相似性较低。系统进化分析将这 19 种 C 型趋化因子分为六个主要组。通过 RT-PCR 的组织分布分析表明,这些趋化因子中的大多数在 9 种检测组织中广泛表达,而有些则表现出组织偏好表达模式。例如,EcSCYA103 在鳍和鳃中优先表达;EcSCYA109 在头肾和脾脏中优先表达;EcSCYA114 在鳍、鳃和肝脏中优先表达;而 EcSCYA119 在鳍和胃中优先表达。定量 RT-PCR 显示,在卵形鲷虹彩病毒(GIV)感染后,19 种 C 型趋化因子基因中的 4 种(EcSYCA102、EcSYCA103、EcSYCA116 和 EcSYCA118)在脾脏中高度诱导。这四个基因的表达也可以被 LPS 和 poly(I:C)的挑战上调,这表明这四个基因可能参与了对入侵病原体的免疫反应。