Key Laboratory of Applied Technology on Green-Eco-Healthy Animal Husbandry of Zhejiang Province, Zhejiang Provincial Engineering Research Center for Animal Health Diagnostics & Advanced Technology, Zhejiang International Science and Technology Cooperation Base for Veterinary Medicine and Health Management, China-Australia Joint Laboratory for Animal Health Big Data Analytics, College of Animal Science and Technology & College of Veterinary Medicine of Zhejiang A&F University, Hangzhou, Zhejiang Province 311300, China.
School of Life Science and Technology, Shandong Second Medical University, Shandong, China.
Poult Sci. 2024 Sep;103(9):103944. doi: 10.1016/j.psj.2024.103944. Epub 2024 Jun 6.
Newcastle disease virus, a member of the Paramyxoviridae family, causes significant economic losses in poultry worldwide. To identify novel antiviral agents against NDV, 36 canthin-6-one analogs were evaluated in this study. Our data showed that 8 compounds exhibited excellent inhibitory effects on NDV replication with IC values in the range of 5.26 to 11.76 μM. Besides, these analogs inhibited multiple NDV strains with IC values within 12 μM and exerted antiviral activity against peste des petits ruminants virus (PPRV) and canine distemper virus (CDV). Among these analogs, 16 presented the strongest anti-NDV activity (IC = 5.26 μM) and minimum cytotoxicity (CC > 200 μM) in DF-1 cells. Furthermore, 16 displayed antiviral activity in different cell lines. Our results showed that 16 did not affect the viral adsorption while it can inhibit the entry of NDV by suppressing the Akt pathway. Further study found that 16-treatment inhibited the NDV-activated ERK pathway, thereby promoting the expression of interferon-related genes. Our findings reveal an antiviral mechanism of canthin-6-one analogs through inhibition of the Akt and ERK signaling pathways. These results point to the potential value of canthin-6-one analogs to serve as candidate antiviral agents for NDV.
新城疫病毒(Newcastle disease virus)是副粘病毒科的一员,在全球范围内给家禽养殖业造成了重大的经济损失。为了寻找针对 NDV 的新型抗病毒药物,本研究评估了 36 种喜树碱-6-酮类似物。我们的数据显示,有 8 种化合物对 NDV 复制具有优异的抑制作用,IC 值范围在 5.26 到 11.76 μM 之间。此外,这些类似物能够抑制多种 NDV 毒株,IC 值在 12 μM 以内,并且对小反刍兽疫病毒(Peste des petits ruminants virus,PPRV)和犬瘟热病毒(Canine distemper virus,CDV)具有抗病毒活性。在这些类似物中,化合物 16 在 DF-1 细胞中表现出最强的抗 NDV 活性(IC = 5.26 μM)和最小的细胞毒性(CC > 200 μM)。此外,16 在不同的细胞系中均表现出抗病毒活性。我们的结果表明,16 不影响病毒的吸附,但可以通过抑制 Akt 通路来抑制 NDV 的进入。进一步的研究发现,16 处理抑制了 NDV 激活的 ERK 通路,从而促进了干扰素相关基因的表达。我们的研究结果揭示了喜树碱-6-酮类似物通过抑制 Akt 和 ERK 信号通路发挥抗病毒作用的机制。这些结果表明,喜树碱-6-酮类似物具有作为 NDV 候选抗病毒药物的潜力。