College of Life Science, Liaoning Normal University, Dalian, 116081, China.
Key Laboratory of Environment Controlled Aquaculture (KLECA), Ministry of Education, 52 Heishijiao Street, Dalian, 116023, China.
Mar Biotechnol (NY). 2023 Apr;25(2):291-313. doi: 10.1007/s10126-023-10205-8. Epub 2023 Apr 11.
Takifugu rubripes is important commercially fish species in China and it is under serious threat from white spot disease (cyptocaryoniasis), which leads to heavy economic losses. In this study, we used proteomics and phosphoproteomic analysis to identify differentially abundant proteins in the spleen of T. rubripes infected with the Cryptocaryon irritans. We identified 5,307 proteins and 6,644 phosphorylated sites on 2,815 phosphoproteins using high-throughput proteomics analysis of the spleen of T. rubripes based on 26,421 unique peptides and 5,013 modified peptides, respectively. The 5,307 quantified host proteins, 40 were upregulated and 43 were downregulated in the infection group compared to the control group. Among the 2815 phosphoproteins, 44/120 were upregulated/downregulated, and 62/151 were upregulated/downregulated in the 6644 quantified phosphosites. Using the combination of Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses, screening for significantly different phosphoproteins, motif analysis and protein-protein interaction analysis, we ultimately identified three phosphorylated proteins (G-protein-signaling modulator 1-like, zinc finger protein 850-like, and histone H1-like) and three phosphorylated protein kinases (serine/threonine-protein kinase homolog isoform X2, mitogen-activated protein kinase 5-like, and protein kinase C theta type) as potential biomarkers for T. rubripes immune responses. We then screened the phosphorylation sites of these biomarker proteins for further verification. Based on our results, we speculate that phosphorylation modification of the phosphorylation sites is involved in the immunity of T. rubripes against C. irritans.
红鳍东方鲀是中国重要的商业鱼类,但其受到白点病(刺激隐核虫病)的严重威胁,导致了巨大的经济损失。在这项研究中,我们使用蛋白质组学和磷酸化蛋白质组学分析来鉴定感染刺激隐核虫的红鳍东方鲀脾脏中的差异丰度蛋白。我们使用高通量蛋白质组学分析方法,基于 26421 个独特肽段和 5013 个修饰肽段,分别鉴定了红鳍东方鲀脾脏中的 5307 种蛋白质和 6644 个磷酸化位点。在感染组与对照组相比,5307 种定量宿主蛋白中,有 40 种上调,43 种下调。在 2815 个磷酸化蛋白中,有 44/120 个上调/下调,6644 个定量磷酸化位点中有 62/151 个上调/下调。通过基因本体和京都基因与基因组百科全书分析的组合、显著差异磷酸化蛋白的筛选、基序分析和蛋白质-蛋白质相互作用分析,我们最终鉴定了三个磷酸化蛋白(G 蛋白信号调节因子 1 样、锌指蛋白 850 样和组蛋白 H1 样)和三个磷酸化蛋白激酶(丝氨酸/苏氨酸蛋白激酶同源异构体 X2、有丝分裂原激活蛋白激酶 5 样和蛋白激酶 C 型 theta 同工酶),它们可能是红鳍东方鲀免疫反应的生物标志物。然后,我们筛选了这些生物标志物蛋白的磷酸化位点进行进一步验证。根据我们的结果,我们推测磷酸化修饰磷酸化位点参与了红鳍东方鲀对刺激隐核虫的免疫反应。