Sadhu Srikanth, Goswami Sandeep, Khatri Ritika, Lohiya Bharat, Singh Virendra, Yadav Rahul, Das Vinayaka, Tripathy Manas Ranjan, Dwivedi Prabhanjan, Srivastava Mitul, Mani Shailendra, Asthana Shailendra, Samal Sweety, Awasthi Amit
Immuno-biology Lab, Infection and Immunology Centre, Translational Health Science and Technology Institute, NCR-Biotech Science Cluster, Faridabad, Haryana 121001, India.
Immunology-Core Lab, Translational Health Science and Technology Institute, NCR-Biotech Science Cluster, Faridabad, Haryana 121001, India.
iScience. 2024 Nov 8;27(12):111347. doi: 10.1016/j.isci.2024.111347. eCollection 2024 Dec 20.
Effective antiviral drugs are essential to combat COVID-19 and future pandemics. Although many compounds show antiviral activity, only a few retain effectiveness against SARS-CoV-2. Here, we show that berbamine (Berb) is effective against SARS-CoV, MER-CoV, SARS-CoV-2 and its variants, including the XBB.1.16 variant. In hACE2.Tg mice, Berb suppresses SARS-CoV-2 replication through two distinct mechanisms: inhibiting spike-mediated viral entry and enhancing antiviral gene expression during infection. The administration of Berb, in combination with remdesivir (RDV), clofazimine (Clof) and fangchinoline (Fcn), nearly eliminated viral load and promoted recovery from acute SARS-CoV-2 infection and its variants. Co-housed mice in direct contact with either pre-treated or untreated infected mice exhibited negligible viral loads, reduced lung pathology, and decreased viral shedding, suggesting that Berb may effectively hinder virus transmission. This broad-spectrum activity positions Berb as a promising preventive or therapeutic option against betacoronaviruses.
有效的抗病毒药物对于对抗新冠病毒及未来的大流行至关重要。尽管许多化合物显示出抗病毒活性,但只有少数对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)仍保持有效性。在此,我们表明小檗胺(Berb)对SARS-CoV、中东呼吸综合征冠状病毒(MER-CoV)、SARS-CoV-2及其变体,包括XBB.1.16变体有效。在人血管紧张素转换酶2转基因(hACE2.Tg)小鼠中,小檗胺通过两种不同机制抑制SARS-CoV-2复制:抑制刺突介导的病毒进入并在感染期间增强抗病毒基因表达。小檗胺与瑞德西韦(RDV)、氯法齐明(Clof)和汉防己甲素(Fcn)联合使用,几乎消除了病毒载量,并促进了急性SARS-CoV-2感染及其变体的恢复。与经过预处理或未处理的感染小鼠直接接触的同笼饲养小鼠表现出可忽略不计的病毒载量、减轻的肺部病理变化以及减少的病毒脱落,这表明小檗胺可能有效地阻碍病毒传播。这种广谱活性使小檗胺成为一种有前景的针对β冠状病毒的预防或治疗选择。