São Carlos Institute of Physics, University of São Paulo, São Carlos 13563-120, Brazil.
Virology Sector, Department of Preventive Veterinary Medicine, Federal University of Santa Maria, Santa Maria 97105-900, Brazil.
Viruses. 2022 Jun 21;14(7):1351. doi: 10.3390/v14071351.
Chikungunya virus (CHIKV) is the causative agent of chikungunya fever, a disabling disease that can cause long-term severe arthritis. Since the last large CHIKV outbreak in 2015, the reemergence of the virus represents a serious public health concern. The morbidity associated with viral infection emphasizes the need for the development of specific anti-CHIKV drugs. Herein, we describe the development and characterization of a CHIKV reporter replicon cell line and its use in replicon-based screenings. We tested 960 compounds from MMV/DNDi Open Box libraries and identified four candidates with interesting antiviral activities, which were confirmed in viral infection assays employing CHIKV-nanoluc and BHK-21 cells. The most noteworthy compound identified was itraconazole (ITZ), an orally available, safe, and cheap antifungal, that showed high selectivity indexes of >312 and >294 in both replicon-based and viral infection assays, respectively. The antiviral activity of this molecule has been described against positive-sense single stranded RNA viruses (+ssRNA) and was related to cholesterol metabolism that could affect the formation of the replication organelles. Although its precise mechanism of action against CHIKV still needs to be elucidated, our results demonstrate that ITZ is a potent inhibitor of the viral replication that could be repurposed as a broad-spectrum antiviral.
基孔肯雅病毒(CHIKV)是基孔肯雅热的病原体,这种疾病会导致严重的关节炎,使人致残。自 2015 年最后一次大规模 CHIKV 爆发以来,该病毒的再次出现引起了严重的公共卫生关注。与病毒感染相关的发病率强调了开发特异性抗 CHIKV 药物的必要性。在此,我们描述了 CHIKV 报告子复制子细胞系的开发和表征及其在基于复制子的筛选中的应用。我们测试了来自 MMV/DNDi Open Box 文库的 960 种化合物,并在使用 CHIKV-nanoluc 和 BHK-21 细胞的病毒感染实验中鉴定了 4 种具有有趣抗病毒活性的候选化合物。鉴定出的最显著的化合物是伊曲康唑(ITZ),一种口服、安全且廉价的抗真菌药物,在基于复制子和病毒感染的测定中,其选择性指数分别>312 和>294。该分子的抗病毒活性已被描述为针对正链单链 RNA 病毒(+ssRNA),与胆固醇代谢有关,这可能会影响复制细胞器的形成。尽管其针对 CHIKV 的确切作用机制仍有待阐明,但我们的结果表明 ITZ 是一种有效的病毒复制抑制剂,可被重新用作广谱抗病毒药物。