Sarhan Moustafa, El-Bitar Alaa M H, Mohammadein Amaal, Elshehaby Mohammed, Hotta Hak
Molecular biology Laboratory, Zoology Department, Faculty of Science, Al-Azhar University, Assiut, Egypt.
Department of Microbiology, Kobe University Graduate School of Medicine, Kobe, Japan.
J Venom Anim Toxins Incl Trop Dis. 2021 Nov 19;27:e20210039. doi: 10.1590/1678-9199-JVATITD-2021-0039. eCollection 2021.
Hepatitis C virus (HCV) infection is a major worldwide health problem that can cause liver fibrosis and hepatocellular carcinoma (HCC). The clinical treatment of HCV infection mainly relies on the use of direct-acting antivirals (DAAs) that are usually expensive and have side effects. Therefore, achieving the discovery of more successful agents is always urgent. In this context, antiviral compounds that inhibit viral infections and disease progression with important therapeutic activities have been identified in animal venoms including arthropod toxins. This indicates that arthropod venoms represent a good natural source of promising candidates for new antivirals.
The antiviral activity of the wasp venom (WV), isolated from the Oriental hornet (), was assessed using cell culture technique with human hepatocellular carcinoma-derived cell line (Huh7it-1) and the recombinant strain of HCV genotype 2a (JFH1).
The results revealed that WV inhibited HCV infectivity with 50% inhibitory concentration (IC) of 10 ng/mL, while the 50% cytotoxic concentration (CC) was 11,000 ng/mL. Time of addition experiment showed that the WV blocked HCV attachment/entry to the cells probably through virucidal effect. On the other hand, the venom showed no inhibitory effect on HCV replication.
WV can inhibit the entry stage of HCV infection at non-cytotoxic concentrations. Therefore, it could be considered a potential candidate for characterization of natural anti-HCV agents targeting the entry step.
丙型肝炎病毒(HCV)感染是一个全球性的主要健康问题,可导致肝纤维化和肝细胞癌(HCC)。HCV感染的临床治疗主要依赖于使用直接作用抗病毒药物(DAAs),这些药物通常价格昂贵且有副作用。因此,迫切需要发现更成功的药物。在此背景下,在包括节肢动物毒素在内的动物毒液中已鉴定出具有重要治疗活性、能抑制病毒感染和疾病进展的抗病毒化合物。这表明节肢动物毒液是新抗病毒药物有前景候选物的良好天然来源。
使用人肝癌衍生细胞系(Huh7it-1)和HCV基因2a重组株(JFH1),通过细胞培养技术评估从东方大黄蜂分离的黄蜂毒液(WV)的抗病毒活性。
结果显示,WV抑制HCV感染性,50%抑制浓度(IC)为10 ng/mL,而50%细胞毒性浓度(CC)为11,000 ng/mL。添加时间实验表明,WV可能通过杀病毒作用阻断HCV对细胞的附着/进入。另一方面,该毒液对HCV复制无抑制作用。
WV可在无细胞毒性浓度下抑制HCV感染的进入阶段。因此,它可被视为一种潜在候选物,用于表征靶向进入步骤的天然抗HCV药物。