College of Veterinary Medicine, China Agricultural University, Beijing, China.
Key Laboratory of Applied Technology on Green-Eco-Healthy Animal Husbandry of Zhejiang Province, College of Animal Science and Technology & College of Veterinary Medicine, Zhejiang A&F University, Hangzhou, China.
Front Cell Infect Microbiol. 2024 Aug 21;14:1431836. doi: 10.3389/fcimb.2024.1431836. eCollection 2024.
Bovine viral diarrhea-mucosal disease (BVD-MD) is a contagious disease in cattle, caused by the bovine viral diarrhea virus (BVDV). This virus continues to spread globally, exerting pressure on both public health and the economy. Despite its impact, there are currently no effective drugs for treating BVDV. This study utilized Madin-Darby bovine kidney (MDBK) cells as a model to investigate the antiviral effects of melatonin against Bovine Viral Diarrhea Virus (BVDV) and its connection with endoplasmic reticulum (ER) stress. Our results show that melatonin can suppress BVDV proliferation in MDBK cells by modulating the endoplasmic reticulum (ER) stress-mediated NF-κB pathway and autophagy. Specifically, melatonin alleviated ER stress, inhibited the activation of IκBα and p65, regulated autophagy, and reduced the expression levels of pro-inflammatory cytokines. Further, when we treated BVDV-infected cells with the ER stress inducer thapsigargin, it led to significant activation of the NF-κB pathway and autophagy. Conversely, treating the cells with the ER stress inhibitor 4-phenylbutyric acid reversed these effects. These findings suggest that melatonin exerts its antiviral effects primarily through the PERK-eIF2α-ATF4 of ER stress-mediated NF-κB pathway and autophagy. Overall, our study underscores the potential of melatonin as an effective protective and therapeutic option against BVDV, offering insights into its anti-infective mechanisms.
牛病毒性腹泻-黏膜病(BVD-MD)是一种牛的传染病,由牛病毒性腹泻病毒(BVDV)引起。这种病毒继续在全球范围内传播,对公共卫生和经济都构成压力。尽管有这种影响,但目前还没有有效的药物来治疗 BVDV。本研究利用 Madin-Darby 牛肾(MDBK)细胞作为模型,研究褪黑素对牛病毒性腹泻病毒(BVDV)的抗病毒作用及其与内质网(ER)应激的关系。我们的研究结果表明,褪黑素可以通过调节内质网(ER)应激介导的 NF-κB 通路和自噬来抑制 MDBK 细胞中的 BVDV 增殖。具体来说,褪黑素减轻 ER 应激,抑制 IκBα和 p65 的激活,调节自噬,降低促炎细胞因子的表达水平。此外,当我们用内质网应激诱导剂他普西龙处理 BVDV 感染的细胞时,NF-κB 通路和自噬明显被激活。相反,用内质网应激抑制剂 4-苯丁酸处理细胞则逆转了这些效应。这些发现表明,褪黑素主要通过内质网应激介导的 NF-κB 通路和自噬中的 PERK-eIF2α-ATF4 发挥其抗病毒作用。总的来说,我们的研究强调了褪黑素作为一种有效保护和治疗 BVDV 的选择的潜力,为其抗感染机制提供了新的见解。