多组学综合分析揭示了鱼类虹彩病毒对肝脏代谢的重编程作用以及α-亚麻酸的抗病毒功能。

IF 4 1区 生物学 Q1 ZOOLOGY Zoological Research Pub Date : 2024-05-18 DOI:10.24272/j.issn.2095-8137.2024.028
Lin Liu, Ya Zhang, Meng-Di Yuan, Dong-Miao Xiao, Wei-Hua Xu, Qi Zheng, Qi-Wei Qin, You-Hua Huang, Xiao-Hong Huang
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引用次数: 0

摘要

虹彩病毒因其高死亡率而对全球水产养殖业构成巨大威胁;然而,其致病的分子机制尚未得到很好的阐明。本文采用多组学方法研究了感染新加坡石斑鱼虹彩病毒(SGIV)的石斑鱼,重点研究了关键代谢物的作用。结果表明,SGIV诱发了明显的组织病理学损伤和肝脏内代谢酶的变化。此外,SGIV 还明显降低了脂滴、甘油三酯、胆固醇和脂蛋白的含量。代谢组学分析表明,改变的代谢物富集在 19 个通路中,其中甘油磷酸酯和α-亚麻酸(ALA)等脂质代谢物明显下调,这与肝脏中紊乱的脂质平衡相一致。整合转录组和代谢组数据后发现,富集程度最高的通路与细胞生长和死亡以及核苷酸、碳水化合物、氨基酸和脂质代谢有关,这支持了 SGIV 感染诱导肝脏代谢重编程的结论。进一步的转录组和蛋白质组综合分析表明,SGIV感染激活了吞噬体-免疫抑制-代谢失调-坏死信号级联中的关键分子事件。值得注意的是,多组学综合分析表明,ALA 和亚油酸(LA)代谢物的消耗以及 L-谷氨酸(GA)的积累伴随着免疫、炎症和细胞死亡相关基因的改变。进一步的实验数据显示,ALA(而非 GA)通过激活宿主的抗氧化和抗炎反应抑制了 SGIV 的复制。总之,这些发现为了解鱼类虹彩病毒感染过程中宿主的反应动态提供了全面的资源,并突出了 ALA 在预防和治疗虹彩病毒疾病方面的抗病毒潜力。
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Integrated multi-omics analysis reveals liver metabolic reprogramming by fish iridovirus and antiviral function of alpha-linolenic acid.

Iridovirus poses a substantial threat to global aquaculture due to its high mortality rate; however, the molecular mechanisms underpinning its pathogenesis are not well elucidated. Here, a multi-omics approach was applied to groupers infected with Singapore grouper iridovirus (SGIV), focusing on the roles of key metabolites. Results showed that SGIV induced obvious histopathological damage and changes in metabolic enzymes within the liver. Furthermore, SGIV significantly reduced the contents of lipid droplets, triglycerides, cholesterol, and lipoproteins. Metabolomic analysis indicated that the altered metabolites were enriched in 19 pathways, with a notable down-regulation of lipid metabolites such as glycerophosphates and alpha-linolenic acid (ALA), consistent with disturbed lipid homeostasis in the liver. Integration of transcriptomic and metabolomic data revealed that the top enriched pathways were related to cell growth and death and nucleotide, carbohydrate, amino acid, and lipid metabolism, supporting the conclusion that SGIV infection induced liver metabolic reprogramming. Further integrative transcriptomic and proteomic analysis indicated that SGIV infection activated crucial molecular events in a phagosome-immune depression-metabolism dysregulation-necrosis signaling cascade. Of note, integrative multi-omics analysis demonstrated the consumption of ALA and linoleic acid (LA) metabolites, and the accumulation of L-glutamic acid (GA), accompanied by alterations in immune, inflammation, and cell death-related genes. Further experimental data showed that ALA, but not GA, suppressed SGIV replication by activating antioxidant and anti-inflammatory responses in the host. Collectively, these findings provide a comprehensive resource for understanding host response dynamics during fish iridovirus infection and highlight the antiviral potential of ALA in the prevention and treatment of iridoviral diseases.

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来源期刊
Zoological Research
Zoological Research Medicine-General Medicine
CiteScore
7.60
自引率
10.20%
发文量
1937
审稿时长
8 weeks
期刊介绍: Established in 1980, Zoological Research (ZR) is a bimonthly publication produced by Kunming Institute of Zoology, the Chinese Academy of Sciences, and the China Zoological Society. It publishes peer-reviewed original research article/review/report/note/letter to the editor/editorial in English on Primates and Animal Models, Conservation and Utilization of Animal Resources, and Animal Diversity and Evolution.
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