圣草酚经nrf2-keap1/sod通路激活抗氧化系统发挥抗MRV作用

The eriodictyol exerts anti-MRV effects via activation of nrf2-keap1/sod pathway

  • 摘要:
    目的 探究圣草酚(ER)可以通过激活nrf2-keap1/sod抗氧化通路发挥抗鳜蛙虹彩病毒(MRV)感染的作用。
    方法 本研究在鳜脑细胞系(SCB3)中对超氧化物歧酶(sod)基因分别进行过表达与siRNA敲降,评价sod在抗MRV感染中的作用;通过细胞半数毒性浓度(CC50)与药物半数有效浓度(EC50)测定和定量逆转录聚合酶链式反应(RT-qPCR)、蛋白质印迹法(Western blot)、流式细胞术(FCM)、苏木精-伊红染色法(H.E)、免疫组化(IHC)与免疫荧光(IFA)等方法分析ER在SCB3细胞与大口黑鲈(Micropterus salmoides)体内的抗氧化活性及抗MRV效果。
    结果 SCB3细胞中过表达sod可以显著抑制MRV增殖,敲降sod则促进病毒增殖;ER能够激活SCB3细胞中nrf2基因以及下游sod、谷胱甘肽过氧化物酶4(gpx4a)表达,CC50、EC50分别为43.76 μmol/L、8.522 μmol/L。大口黑鲈灌喂ER后的攻毒实验表明,ER给药可以激活肝组织内nrf2、sod、gpx4a基因表达并提高SOD酶活性与总抗氧化能力(T-AOC),ER可以将MRV感染组织的活性氧(ROS)水平由49.7%降低到12.4%,并能减轻病毒诱导的肝脏组织损伤;ER对MRV的体内抑制率达到99.99%,并将攻毒存活率由27%提高到63%。
    结论 ER通过nrf2-keap1/sod通路激活抗氧化系统,清除ROS,减轻组织损伤,进而发挥抗MRV作用。本研究为ER在抗MRV中的应用提供理论依据。

     

    Abstract: Mandarin fish ranavirus (MRV), a highly pathogenic iridovirus, causes severe tissue damage and high mortality in largemouth bass (Micropterus salmoides), resulting in substantial economic losses. MRV infection induces substantial elevation of host reactive oxygen species (ROS), which mediates multi-tissue inflammatory injury and triggers cellular apoptosis, thereby facilitating viral immune evasion. The antioxidant system is essential for ROS scavenging and preservation of cellular homeostasis. Of the antioxidant enzymes, superoxide dismutase (SOD)-driven antioxidant defense is especially pivotal in mitigating intracellular oxidative stress resulting from ROS accumulation. Eriodictyol (ER), a naturally occurring flavonoid, exhibits potent antioxidant and anti-inflammatory properties. It activates the nuclear factor erythroid 2-related factor 2 (nrf2) signaling cascade, modulates the transcription of downstream antioxidant-responsive genes, augments antioxidant enzyme activities, and ameliorates systemic oxidative stress. This study explored whether ER exerts anti-MRV activity by activating the nrf2-keap1/sod antioxidant pathway. The role of sod against MRV infection was examined via overexpression and siRNA-mediated knockdown in mandarin fish brain SCB3 cells. The antioxidant and antiviral effects of ER were assessed in SCB3 cells and M. salmoides using CC50/EC50 measurement, RT-qPCR, Western blot, flow cytometry, H.E staining, immunohistochemistry, and immunofluorescence assay. sod overexpression markedly inhibited MRV proliferation in SCB3 cells, whereas sod knockdown promoted viral replication. In SCB3 cells, ER upregulated the expression of nrf2 and its downstream targets sod and glutathione peroxidase 4 (gpx4a), with CC50 and EC50 values of 43.76 μmol/L and 8.522 μmol/L, respectively. In vivo, intragastric administration of ER upregulated hepatic nrf2, sod, and gpx4a expression, enhanced SOD and total antioxidant capacity (T-AOC) activities, reduced ROS levels from 49.7% to 12.4%, and attenuated virus-induced liver injury in MRV-infected M. salmoides. ER treatment achieved a 99.99% inhibition rate against MRV and increased host survival from 27% to 63%. Collectively, these results indicate that ER activates the antioxidant system via the nrf2-keap1/sod pathway to scavenge ROS and alleviate tissue damage, which underlies its anti-MRV activity. This study provides a theoretical basis for the application of ER in the prevention and control of MRV infection.

     

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