Center for Cognition and Sociality, Institute for Basic Sciencegrid.410720.0, Daejeon, South Korea.
Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea.
Antimicrob Agents Chemother. 2022 Dec 20;66(12):e0120122. doi: 10.1128/aac.01201-22. Epub 2022 Nov 14.
Several plant-derived natural products with anti-SARS-CoV-2 activity have been evaluated for the potential to serve as chemotherapeutic agents for the treatment of COVID-19. Codonopsis lanceolata (CL) has long been used as a medicinal herb in East Asian countries to treat inflammatory diseases of the respiratory system but its antiviral activity has not been investigated so far. Here, we showed that CL extract and its active compound lancemaside A (LA) displayed potent inhibitory activity against SARS-CoV-2 infection using a pseudotyped SARS-CoV-2 entry assay system. We demonstrated that this inhibitory effect of LA was due to the alteration of membrane cholesterol and blockade of the membrane fusion between SARS-CoV-2 and host cells by filipin staining and cell-based membrane fusion assays. Our findings also showed that LA, as a membrane fusion blocker, could impede the endosomal entry pathway of SARS-CoV-2 and its variants of concern (VOCs), including Alpha (B.1.1.7), Beta (B.1.351), Delta (B.1.617.2), and Omicron (B.1.1.529), in Vero cells with similar of IC values ranging from 2.23 to 3.37 μM as well as the TMPRSS2-mediated viral entry pathway in A549 cells overexpressing ACE2 and TMPRSS2 with IC value of 3.92 μM. We further demonstrated that LA could prevent the formation of multinucleated syncytia arising from SARS-CoV-2 spike protein-mediated membrane fusion. Altogether, the findings reported here suggested that LA could be a broad-spectrum anti-SARS-CoV-2 therapeutic agent by targeting the fusion of viral envelope with the host cell membrane.
几种具有抗 SARS-CoV-2 活性的植物源性天然产物已被评估为治疗 COVID-19 的潜在化学治疗剂。党参(CL)长期以来一直被用作东亚国家的药用植物,用于治疗呼吸系统的炎症性疾病,但迄今为止其抗病毒活性尚未得到研究。在这里,我们使用假型 SARS-CoV-2 进入测定系统表明,党参提取物及其活性化合物刺囊酸 A(LA)对 SARS-CoV-2 感染具有很强的抑制活性。我们证明,LA 的这种抑制作用是由于膜胆固醇的改变以及通过 filipin 染色和基于细胞的膜融合测定阻断 SARS-CoV-2 与宿主细胞之间的膜融合。我们的研究结果还表明,LA 作为一种膜融合阻断剂,可以阻碍 SARS-CoV-2 及其关注变体(VOCs)的内体进入途径,包括 Alpha(B.1.1.7)、Beta(B.1.351)、Delta(B.1.617.2)和 Omicron(B.1.1.529),在 Vero 细胞中的 IC 值相似,范围为 2.23 至 3.37 μM,以及在过表达 ACE2 和 TMPRSS2 的 A549 细胞中 TMPRSS2 介导的病毒进入途径,IC 值为 3.92 μM。我们进一步证明,LA 可以阻止由 SARS-CoV-2 刺突蛋白介导的膜融合引起的多核合胞体的形成。总之,这里报道的研究结果表明,LA 可以通过靶向病毒包膜与宿主细胞膜的融合,成为一种广谱抗 SARS-CoV-2 的治疗剂。