天然化合物特异性组合对SARS-CoV-2及其α、β、γ、δ、Kappa和Mu变体的抑制作用

European Journal of Microbiology & Immunology Pub Date : 2022-01-21 Print Date: 2022-02-03 DOI:10.1556/1886.2021.00022
Anna Goc, Aleksandra Niedzwiecki, Vadim Ivanov, Svetlana Ivanova, Matthias Rath
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引用次数: 12

摘要

尽管有疫苗,但COVID-19的全球传播仍在继续,主要是由于新出现的SARS-CoV-2突变。我们早期的研究表明,植物源性化合物的特定组合可以抑制SARS-CoV-2与其ACE2受体的结合,并控制病毒感染的关键细胞机制。在这项研究中,我们评估了一种确定的植物提取物和微量营养素混合物对原始SARS-CoV-2及其α、β、γ、Delta、Kappa和Mu变体的功效。该组合物含有维生素C、n -乙酰半胱氨酸、白藜芦醇、茶黄素、姜黄素、槲皮素、柚皮素、黄芩苷和西兰花提取物,通过抑制SARS-CoV-2与其细胞ACE2受体的受体结合域(RBD) 90%,显示出最高的功效。在体外将试验伪型变体暴露于该配方1小时,然后或同时施用于人肺细胞,可导致其细胞进入抑制高达60%。此外,该组合物显著抑制病毒感染的其他细胞机制,包括病毒RdRp、furin和组织蛋白酶l的活性。这些发现表明,天然化合物通过多效机制对SARS-CoV-2及其突变形式有效。我们的研究结果表明,同时抑制多种机制的病毒感染宿主细胞可能是预防SARS-CoV-2感染的有效策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inhibitory effects of specific combination of natural compounds against SARS-CoV-2 and its Alpha, Beta, Gamma, Delta, Kappa, and Mu variants.

Inhibitory effects of specific combination of natural compounds against SARS-CoV-2 and its Alpha, Beta, Gamma, Delta, Kappa, and Mu variants.

Inhibitory effects of specific combination of natural compounds against SARS-CoV-2 and its Alpha, Beta, Gamma, Delta, Kappa, and Mu variants.

Inhibitory effects of specific combination of natural compounds against SARS-CoV-2 and its Alpha, Beta, Gamma, Delta, Kappa, and Mu variants.

Despite vaccine availability, the global spread of COVID-19 continues, largely facilitated by emerging SARS-CoV-2 mutations. Our earlier research documented that a specific combination of plant-derived compounds can inhibit SARS-CoV-2 binding to its ACE2 receptor and controlling key cellular mechanisms of viral infectivity. In this study, we evaluated the efficacy of a defined mixture of plant extracts and micronutrients against original SARS-CoV-2 and its Alpha, Beta, Gamma, Delta, Kappa, and Mu variants. The composition containing vitamin C, N-acetylcysteine, resveratrol, theaflavin, curcumin, quercetin, naringenin, baicalin, and broccoli extract demonstrated a highest efficacy by inhibiting the receptor-binding domain (RBD) binding of SARS-CoV-2 to its cellular ACE2 receptor by 90%. In vitro exposure of test pseudo-typed variants to this formula for 1 h before or simultaneously administrated to human pulmonary cells resulted in up to 60% inhibition in their cellular entry. Additionally, this composition significantly inhibited other cellular mechanisms of viral infectivity, including the activity of viral RdRp, furin, and cathepsin L. These findings demonstrate the efficacy of natural compounds against SARS-CoV-2 including its mutated forms through pleiotropic mechanisms. Our results imply that simultaneous inhibition of multiple mechanisms of viral infection of host cells could be an effective strategy to prevent SARS-CoV-2 infection.

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