Zhu Song, Miao Bo, Zhang Yu-Zhou, Wang De-Shou, Wang Gao-Xue
College of Fisheries, Southwest University, Chongqing, China.
Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, China.
J Fish Dis. 2022 Mar;45(3):451-459. doi: 10.1111/jfd.13574. Epub 2021 Dec 28.
Outbreaks of viral encephalopathy and retinopathy (VER) in marine and freshwater species severely devastate the aquaculture worldwide. The causative agent of VER is nervous necrosis virus (NNV), which mainly infects the early developmental stages of fish, limiting the effectiveness of vaccines. To counter this case, the anti-NNV potentials of nine drugs with broad-spectrum antiviral activity were explored using ribavirin as a positive drug. Toxicity of the selected drugs to SSN-1 cells and grouper was firstly evaluated to determine the safety concentrations. For screening in vitro, amantadine and oseltamivir phosphate can relieve the cytopathic effects and inhibit NNV replication with the 90% inhibitory concentrations (IC ) of 38.74 and 106.75 mg/L, respectively. Amantadine has a stronger anti-NNV activity than ribavirin at the with- and post-NNV infection stages, indicating that it is a potential therapeutic agent against VER by acting directly on NNV. Similarly, amantadine also has a strong anti-NNV activity in vivo with the IC of 27.91 mg/L at the 7 days post-infection, while that was 73.25 mg/L for ribavirin. Following exposure to amantadine (40 mg/L) and ribavirin (100 mg/L) for 7 days, the survival rates of NNV-infected grouper were increased to 44% and 39%, respectively. The maximum amantadine content (11.88 mg/Kg) in grouper brain was reached following exposure for 24 hr, and amantadine can be quickly excreted from fish, reducing the risk of drug residue. Results so far indicated that amantadine is a promising therapeutic agent against NNV in aquaculture, providing an effective strategy for VER control at the early developmental stages of fish.
海洋和淡水物种中的病毒性脑病和视网膜病(VER)爆发严重破坏了全球水产养殖业。VER的病原体是神经坏死病毒(NNV),它主要感染鱼类的早期发育阶段,限制了疫苗的有效性。为应对这种情况,以利巴韦林作为阳性对照药物,探索了九种具有广谱抗病毒活性药物的抗NNV潜力。首先评估所选药物对SSN-1细胞和石斑鱼的毒性,以确定安全浓度。在体外筛选中,金刚烷胺和磷酸奥司他韦可减轻细胞病变效应并抑制NNV复制,其90%抑制浓度(IC)分别为38.74和106.75mg/L。在NNV感染前和感染后阶段,金刚烷胺的抗NNV活性均强于利巴韦林,表明它通过直接作用于NNV而成为VER的潜在治疗药物。同样,金刚烷胺在体内也具有很强的抗NNV活性,感染后7天的IC为27.91mg/L,而利巴韦林为73.25mg/L。在暴露于金刚烷胺(40mg/L)和利巴韦林(100mg/L)7天后,NNV感染的石斑鱼存活率分别提高到44%和39%。暴露24小时后,石斑鱼脑中金刚烷胺的最大含量达到11.88mg/Kg,且金刚烷胺可迅速从鱼体排出,降低药物残留风险。目前的结果表明,金刚烷胺是水产养殖中抗NNV的一种有前景的治疗药物,为鱼类早期发育阶段的VER控制提供了有效策略。