State Key Laboratory of Developmental Biology of Freshwater Fish, Engineering Research Center of Polyploidy fish Reproduction and Breeding of the State Education Ministry, College of Life Science, Hunan Normal University, Changsha 410081, PR China.
Department of Aquatic Animal Medicine, College of Fisheries, Huazhong Agricultural University, Wuhan 430070, PR China.
Int J Biol Macromol. 2024 Oct;278(Pt 3):134898. doi: 10.1016/j.ijbiomac.2024.134898. Epub 2024 Aug 22.
Edwardsiella tarda is an intracellular pathogenic bacteria that can imperil the health of farmed fish. However, the interactive networks of immune regulation and metabolic response in E. tarda-infected fish are still unclear. In this investigation, we aimed to explore immunometabolic interplay in crucian carp after E. tarda infection by utilizing multiomics analyses. Crucian carp (Carassius auratus) receiving E. tarda infection showed increased levels of tissue damage and oxidative injury in liver. Multiomics analyses suggested that carbon and amino acid metabolism may be considered as crucial metabolic pathways in liver of crucian carp following E. tarda infection, while spaglumic acid, isocitric acid and tetrahydrocortisone were the crucial liver biomarkers. After that, a potential antimicrobial peptide (AMP) sequence called apolipoprotein D (ApoD) was identified from omics study. Then, tissue-specific analysis indicated that liver CaApoD showed the highest expression among isolated tissues. After Aeromonas hydrophila stimulated, CaApoD expressions increased sharply in immune-related tissues. Moreover, CaApoD fusion protein could mediate the in vitro binding to A. hydrophila and E. tarda, attenuate bacterial growth as well as diminish bacterial biofilm forming activity. These findings may have a comprehensive implication for understanding immunometabolic response in crucian carp upon infection.
迟缓爱德华氏菌是一种胞内致病性细菌,可危害养殖鱼类的健康。然而,迟缓爱德华氏菌感染鱼类的免疫调节和代谢反应的相互作用网络仍不清楚。在本研究中,我们通过多组学分析旨在探索迟缓爱德华氏菌感染鲤鱼后的免疫代谢相互作用。感染迟缓爱德华氏菌的鲤鱼肝脏组织损伤和氧化损伤水平升高。多组学分析表明,碳和氨基酸代谢可能是迟缓爱德华氏菌感染鲤鱼肝脏中的关键代谢途径,而谷氨酸、异柠檬酸和四氢皮质酮是关键的肝脏生物标志物。之后,从组学研究中鉴定出一种名为载脂蛋白 D (ApoD) 的潜在抗菌肽 (AMP) 序列。然后,组织特异性分析表明,分离组织中肝脏 CaApoD 的表达最高。在嗜水气单胞菌刺激后,免疫相关组织中 CaApoD 的表达急剧增加。此外,CaApoD 融合蛋白可以介导体外与嗜水气单胞菌和迟缓爱德华氏菌的结合,抑制细菌生长并降低细菌生物膜形成活性。这些发现可能对理解感染后鲤鱼的免疫代谢反应具有全面的意义。