NHC Key Laboratory of Biosafety, Ministry of Health, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
National Institutes for Food and Drug Control, Beijing, China.
J Virol. 2019 May 29;93(12). doi: 10.1128/JVI.00023-19. Print 2019 Jun 15.
Coronaviruses (CoVs) act as cross-species viruses and have the potential to spread rapidly into new host species and cause epidemic diseases. Despite the severe public health threat of severe acute respiratory syndrome coronavirus and Middle East respiratory syndrome CoV (MERS-CoV), there are currently no drugs available for their treatment; therefore, broad-spectrum inhibitors of emerging and endemic CoVs are urgently needed. To search for effective inhibitory agents, we performed high-throughput screening (HTS) of a 2,000-compound library of approved drugs and pharmacologically active compounds using the established genetically engineered human CoV OC43 (HCoV-OC43) strain expressing luciferase (rOC43-ns2Del-Rluc) and validated the inhibitors using multiple genetically distinct CoVs We screened 56 hits from the HTS data and validated 36 compounds using wild-type HCoV-OC43. Furthermore, we identified seven compounds (lycorine, emetine, monensin sodium, mycophenolate mofetil, mycophenolic acid, phenazopyridine, and pyrvinium pamoate) as broad-spectrum inhibitors according to their strong inhibition of replication by four CoVs at low-micromolar concentrations. Additionally, we found that emetine blocked MERS-CoV entry according to pseudovirus entry assays and that lycorine protected BALB/c mice against HCoV-OC43-induced lethality by decreasing viral load in the central nervous system. This represents the first demonstration of real-time bioluminescence imaging to monitor the effect of lycorine on the spread and distribution of HCoV-OC43 in a mouse model. These results offer critical information supporting the development of an effective therapeutic strategy against CoV infection. Currently, there is no approved therapy to treat coronavirus infection; therefore, broad-spectrum inhibitors of emerging and endemic CoVs are needed. Based on our high-throughput screening assay using a compound library, we identified seven compounds with broad-spectrum efficacy against the replication of four CoVs Additionally, one compound (lycorine) was found to protect BALB/c mice against HCoV-OC43-induced lethality by decreasing viral load in the central nervous system. This inhibitor might offer promising therapeutic possibilities for combatting novel CoV infections in the future.
冠状病毒(CoVs)是跨物种病毒,有潜力快速传播到新的宿主物种并引发流行病。尽管严重急性呼吸系统综合征冠状病毒和中东呼吸系统综合征冠状病毒(MERS-CoV)对公共健康构成严重威胁,但目前尚无针对它们的治疗药物;因此,急需广谱抑制剂来抑制新兴和地方性 CoVs。为了寻找有效的抑制物,我们使用已建立的基因工程人 CoV OC43(HCoV-OC43)表达荧光素酶(rOC43-ns2Del-Rluc)的株进行了高通量筛选(HTS),该株对 2000 种已批准药物和药理学活性化合物的文库进行了筛选,并使用多种遗传不同的 CoV 验证了抑制剂。我们从 HTS 数据中筛选出 56 个阳性结果,并使用野生型 HCoV-OC43 验证了 36 个化合物。此外,我们发现 7 种化合物(石蒜碱、依米丁、莫能菌素钠、霉酚酸酯、霉酚酸、苯佐卡因和吡嗪酰胺)是广谱抑制剂,因为它们能够以低微摩尔浓度抑制四种 CoV 的复制。此外,我们发现依米丁通过假病毒进入测定阻断了 MERS-CoV 的进入,而石蒜碱通过降低中枢神经系统中的病毒载量,保护 BALB/c 小鼠免受 HCoV-OC43 诱导的致死性。这代表了首次使用实时生物发光成像来监测石蒜碱对 HCoV-OC43 在小鼠模型中的传播和分布的影响。这些结果为开发针对 CoV 感染的有效治疗策略提供了关键信息。目前,尚无批准的疗法可用于治疗冠状病毒感染;因此,需要广谱抑制剂来抑制新兴和地方性 CoVs。基于我们使用化合物文库进行的高通量筛选试验,我们鉴定出 7 种对四种 CoV 复制具有广谱疗效的化合物。此外,发现一种化合物(石蒜碱)通过降低中枢神经系统中的病毒载量,保护 BALB/c 小鼠免受 HCoV-OC43 诱导的致死性。这种抑制剂可能为未来对抗新型 CoV 感染提供有前途的治疗可能性。