重组大口黑鲈IFN-γ的生物学活性及其抗LMBV感染的保护机制

BIOLOGICAL ACTIVITY OF RECOMBINANT IFN- Γ FROM LARGEMOUTH BASS (MICROPTERUS SALMOIDES) AND ITS PROTECTIVE MECHANISM AGAINST LMBV INFECTION

  • 摘要: 为了探讨II型干扰素IFN-γ (interferon-γ)在大口黑鲈(Micropterus salmoides)抗大口黑鲈蛙虹彩病毒(Largemouth Bass Ranavirus, LMBV)感染中的作用及机制, 本研究利用pCold-TF/Rosetta (DE3)表达体系原核表达并纯化获得重组蛋白rMsIFN-γ, 随后在大口黑鲈脊髓细胞系(Micropterus salmoides spinal cord cell line, MSSC)及鱼体水平评估其活性与抗LMBV效果。结果显示, rMsIFN-γ分子量约21 kD。体外可显著上调MSSC细胞MxISG15SOCS1IRF9的表达, 并在预防性与治疗性处理条件下均表现出一定抗LMBV作用。体内方面, rMsIFN-γ可诱导脾脏与头肾中MxISG15SOCS1IRF9及促炎因子IL-1βTNF-α和趋化因子IL-8表达。在体内治疗性实验中, 感染早期rMsIFN-γ处理组MxISG15表达水平低于病毒感染对照组, 但IL-1βIL-8显著上调, LMBV即刻早期蛋白ICP46表达下降; 随后组织病毒载量降低并延缓感染鱼的死亡进程。综上, rMsIFN-γ在体外与体内均具有一定抗LMBV作用, 其保护效应可能与典型干扰素诱导的ISGs通路及体内炎症/趋化反应协同参与有关。本研究揭示了IFN-γ在大口黑鲈抗LMBV中的潜在应用价值, 为其免疫防控提供了新思路。

     

    Abstract: Largemouth bass ranavirus (LMBV) is a major pathogen in largemouth bass (Micropterus salmoides) aquaculture, frequently causing high mortality and substantial economic losses. Non-specific immune responses are crucial for host antiviral defence. Although interferons are known to mediate antiviral immunity in teleosts, the function and underlying mechanisms of type II interferon IFN-γ (interferon-γ) in largemouth bass resistance to LMBV infection remain insufficiently elucidated. To address this, recombinant rMsIFN-γ was expressed and purified using a pCold-TF/Rosetta (DE3) prokaryotic system, and its bioactivity and anti-LMBV effects were assessed both in vitro using the Micropterus salmoides spinal cord cell line (MSSC) and in vivo. The results showed that rMsIFN-γ had an apparent molecular mass of approximately 21 kDa. In vitro, rMsIFN-γ markedly upregulated the expression of Mx, ISG15, SOCS1, and IRF9 in MSSC cells, and exhibited measurable anti-LMBV activity under both prophylactic and therapeutic treatment regimens. In vivo, rMsIFN-γ induced the expression of Mx, ISG15, SOCS1, and IRF9, as well as the pro-inflammatory cytokines IL-1β and TNF-α and the chemokine IL-8, in the spleen and head kidney. In therapeutic experiments, early rMsIFN-γ administration after infection resulted in lower Mx and ISG15 expression than that in virus-infected controls, while IL-1β and IL-8 were significantly elevated; concomitantly, expression of the LMBV immediate-early protein ICP-46 was reduced. Thereafter, viral loads in tissues decreased and mortality progression in infected fish was delayed. Collectively, rMsIFN-γ confers demonstrable anti-LMBV effects both in vitro and in vivo, likely associated with the canonical interferon-stimulated genes (ISGs) pathway in conjunction with coordinated inflammatory and chemotactic responses in vivo. These findings highlight the potential utility of IFN-γ for LMBV control and provide a novel perspective for immunological prevention and intervention strategies in largemouth bass.

     

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