Li Ping, Du Ruikun, Wang Yanyan, Hou Xuewen, Wang Lin, Zhao Xiujuan, Zhan Peng, Liu Xinyong, Rong Lijun, Cui Qinghua
College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, China.
Qingdao Academy of Chinese Medicinal Sciences, Shandong University of Traditional Chinese Medicine, Qingdao, China.
Front Microbiol. 2020 Feb 28;11:182. doi: 10.3389/fmicb.2020.00182. eCollection 2020.
The influenza A virus (IAV) causes seasonal epidemics and occasional but devastating pandemics, which are of a major public health concern. Although several antiviral drugs are currently available, there is an urgent need to develop novel antiviral therapies with different mechanisms of action due to emergence of drug resistance. In this study, two related compounds, chebulagic acid (CHLA) and chebulinic acid (CHLI), were identified as novel inhibitors against IAV replication. A reporter virus-based infection assay demonstrated that CHLA and CHLI exhibit no inhibitory effect on IAV entry or RNA replication during the virus replication cycle. Results of viral release inhibition assay and neuraminidase (NA) inhibition assay indicated that CHLA and CHLI exert their inhibitory effect on the NA-mediated viral release. Moreover, oseltamivir-resistance mutation NA/H274Y of NA is susceptible to CHLA or CHLI, suggesting a different mechanism of action for CHLA and CHLI. In summary, CHLA and CHLI are promising new NA inhibitors that may be further developed as novel antivirals against IAVs.
甲型流感病毒(IAV)引发季节性流行,偶尔还会引发灾难性的大流行,这是一个重大的公共卫生问题。尽管目前有几种抗病毒药物,但由于耐药性的出现,迫切需要开发具有不同作用机制的新型抗病毒疗法。在本研究中,两种相关化合物,诃子鞣酸(CHLA)和诃子次酸(CHLI),被鉴定为针对IAV复制的新型抑制剂。基于报告病毒的感染试验表明,CHLA和CHLI在病毒复制周期中对IAV进入或RNA复制无抑制作用。病毒释放抑制试验和神经氨酸酶(NA)抑制试验结果表明,CHLA和CHLI对NA介导的病毒释放发挥抑制作用。此外,NA的耐奥司他韦突变体NA/H274Y对CHLA或CHLI敏感,这表明CHLA和CHLI具有不同的作用机制。总之,CHLA和CHLI是有前景的新型NA抑制剂,可能会进一步开发成为针对IAV的新型抗病毒药物。