College of Fisheries, Henan Normal University, Xinxiang 453007, Henan, China; Department of Biological Sciences, Clemson University, Clemson, SC 29634, USA; Observation and Research Station on Water Ecosystem in Danjiangkou Reservoir of Henan Province, Nanyang 474450, China.
Key Laboratory of Exploration and Utilization of Aquatic Genetic Resources, Ministry of Education, Shanghai Ocean University, Shanghai 201306, China.
Fish Shellfish Immunol. 2024 Oct;153:109806. doi: 10.1016/j.fsi.2024.109806. Epub 2024 Aug 3.
Blood transcriptomics has emerged as a vital tool for tracking the immune system and supporting disease diagnosis, prognosis, treatment, and research. The present study was conducted to analyze the gene expression profile and potential biomarker candidates using the whole blood of mandarin fish (Siniperca chuatsi) infected with LPS or poly (I:C) at 0 h, 3 h, 6 h, and 12 h. Our data suggest that 310 shared differentially expressed genes (DEGs) were identified among each comparison group after LPS infection, and 137 shared DEGs were identified after poly (I:C) infection. A total of 62 shared DEGs were differentially expressed in all compared groups after LPS or poly (I:C) infection. Pathways analysis for DEGs in all different compared groups showed that cytokine-cytokine receptor interaction was the most enrichment pathway. The expression levels of genes C-X-C chemokine receptor type 2-like (cxcr2), chemokine (C-C motif) receptor 9a (ccr9a), chemokine (C-C motif) receptor 9b (ccr9b), chemokine (C-X-C motif) receptor 4b (cxcr4b), and interleukin 10 receptor alpha (il10ra) were significantly different in all compared groups and most enriched in cytokine-cytokine receptor interaction pathway. The protein-protein interactions analysis among all shared DEGs showed that cxcr4 was the hub gene with the highest degree. The biomarker candidates discovered in this study may, following validation, prove effective as diagnostic tools in monitoring mandarin fish diseases.
血液转录组学已成为跟踪免疫系统和支持疾病诊断、预后、治疗和研究的重要工具。本研究旨在分析用 LPS 或 poly (I:C) 感染的鳜鱼(Siniperca chuatsi)全血在 0 h、3 h、6 h 和 12 h 时的基因表达谱和潜在的生物标志物候选物。我们的数据表明,在 LPS 感染后,每个比较组之间共鉴定出 310 个差异表达基因(DEGs),在 poly (I:C) 感染后共鉴定出 137 个差异表达基因。在 LPS 或 poly (I:C) 感染后,所有比较组中共有 62 个差异表达基因。对所有不同比较组中 DEGs 的通路分析表明,细胞因子-细胞因子受体相互作用是最富集的通路。在所有比较组中,基因 C-X-C 趋化因子受体型 2 样(cxcr2)、趋化因子(C-C 基元)受体 9a(ccr9a)、趋化因子(C-C 基元)受体 9b(ccr9b)、趋化因子(C-X-C 基元)受体 4b(cxcr4b)和白细胞介素 10 受体 alpha(il10ra)的表达水平在所有比较组中均显著不同,且在细胞因子-细胞因子受体相互作用通路中最富集。在所有共享 DEGs 之间的蛋白质-蛋白质相互作用分析中,cxcr4 是具有最高度数的枢纽基因。本研究发现的生物标志物候选物在验证后可能成为监测鳜鱼疾病的有效诊断工具。