猪流行性腹泻病毒
维罗细胞
病毒学
生物
病毒
病毒复制
冠状病毒
病毒生命周期
微生物学
腹泻
毒性
2019年冠状病毒病(COVID-19)
化学
传染病(医学专业)
医学
疾病
内科学
有机化学
病理
作者
Yiwei Sun,Liyan Wang,Keke Ma,Manman Shen,Jiying Liu,Yujuan Zhang,Liumei Sun
出处
期刊:Animals
[Multidisciplinary Digital Publishing Institute]
日期:2025-04-23
卷期号:15 (9): 1207-1207
被引量:1
摘要
Porcine epidemic diarrhea virus (PEDV), a highly infectious alphacoronavirus, has resulted in substantial economic losses within the global swine industry. Existing vaccines and therapeutic agents have proven inadequate in effectively preventing and controlling PEDV. Natural compounds offer distinct advantages in antiviral research due to their abundant availability, diverse biological activities, and low toxicity. In this study, the antiviral properties of the naturally occurring alkaloid 1-deoxynojirimycin (DNJ) against PEDV were examined. The CC50 of DNJ was determined to be 912.5 μM through experimental analysis on Vero-E6 cells. DNJ demonstrated an inhibitory effect on PEDV activity, with a 50% inhibitory concentration (IC50) of 57.76 μM. The compound primarily inhibited PEDV proliferation during the viral life cycle stages of attachment and replication. Moreover, DNJ mitigated the production of reactive oxygen species (ROS) and inflammation associated with PEDV infection. Computational docking predictions suggest that the viral non-structural proteins include Nsp12, Nsp14, and Nsp16 may serve as potential targets for DNJ. Consequently, DNJ represents a promising candidate for the development of novel therapeutic agents against PEDV.
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