Laboratory of Molecular RNA Virology and Antiviral Strategies, Department of Microbiology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore.
Laboratory of Molecular RNA Virology and Antiviral Strategies, Department of Microbiology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore; Institute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore.
Antiviral Res. 2019 Jul;167:13-24. doi: 10.1016/j.antiviral.2019.04.003. Epub 2019 Apr 5.
Zika virus (ZIKV) is a mosquito-borne virus that has garnered a lot of attention in recent years, due to the explosive epidemic from 2014 to 2016. Since its introduction in the Americas in late 2014, ZIKV has spread at an unprecedented rate and scale throughout the world and infected millions of people. Its infection has also been associated with severe neurological disorders like Guillain-Barré syndrome and microcephaly in fetuses. Despite these, there is currently no approved antiviral against ZIKV. In this study, an immunofluorescence-based high throughput screen was conducted on a library of 483 flavonoid derivatives to identify potential anti-ZIKV compounds. Flavonoids, which are natural polyphenolic compounds found in plants, represent an attractive source of antivirals due to their abundance in food and expected low toxicity. From the primary screen, three hits were selected for validation by cell viability and viral plaque reduction assays. Pinocembrin, a flavanone found in honey, tea and red wine, was chosen for downstream studies as it exhibited the strongest inhibition of ZIKV infection in human placental JEG-3 cells (IC = 17.4 μM). Time-course studies revealed that pinocembrin acts on post-entry process(es) of the ZIKV replication cycle. Furthermore, pinocembrin inhibits viral RNA production and envelope protein synthesis based on quantitative reverse transcription-PCR (qRT-PCR) and Western blot analyses. This study has demonstrated for the first time the in vitro anti-ZIKV activity of pinocembrin.
寨卡病毒(ZIKV)是一种通过蚊子传播的病毒,近年来引起了广泛关注,原因是 2014 年至 2016 年爆发了疫情。自 2014 年底在美洲首次发现以来,ZIKV 以空前的速度和规模在全球范围内传播,并感染了数百万人。其感染还与吉兰-巴雷综合征和胎儿小头畸形等严重神经系统疾病有关。尽管如此,目前尚无针对 ZIKV 的批准抗病毒药物。在这项研究中,我们对 483 种黄酮类衍生物文库进行了基于免疫荧光的高通量筛选,以鉴定潜在的抗 ZIKV 化合物。黄酮类化合物是植物中天然的多酚化合物,由于其在食物中的丰富存在和预期的低毒性,代表了抗病毒药物的一个有吸引力的来源。在初步筛选中,选择了三种化合物进行细胞活力和病毒斑减少测定验证。乔松素是一种在蜂蜜、茶和红酒中发现的黄烷酮,因其对人胎盘 JEG-3 细胞中 ZIKV 感染的最强抑制作用(IC=17.4μM)而被选为下游研究。时间进程研究表明,乔松素作用于 ZIKV 复制周期的进入后过程。此外,基于定量逆转录 PCR(qRT-PCR)和 Western blot 分析,乔松素抑制病毒 RNA 产生和包膜蛋白合成。这项研究首次证明了乔松素在体外抗 ZIKV 的活性。