Composition of naturally occurring compounds decreases activity of Omicron and SARS-CoV-2 RdRp complex.

Anna Goc, Matthias Rath, Aleksandra Niedzwiecki
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Abstract

Naturally-occurring compounds are acknowledged for their broad antiviral efficacy. Little is however known about their mutual cooperation. Here, we evaluated in vitro efficacy of the defined mixture of agents against the RdRp complex of the original SARS-CoV-2 and Omicron variant. This composition of vitamin C, N-acetylcysteine, resveratrol, theaflavin, curcumin, quercetin, naringenin, baicalin, and broccoli extract showed to inhibit activity of RdRp/nsp7/nsp8 both these variants. In vitro exposure of recombinant RdRp complex to individual compounds of this composition pointed to quercetin as the driving inhibitory compound. The outcome of this study supports the motion of antiviral efficacy of natural compounds against SARS-CoV-2 and Omicron and implies that their reciprocal or mutual interaction may augment antiviral action through simultaneous effect on different mechanisms. Consequently, this makes it more difficult for an infectious agent to evade all these mechanisms at the same time. Considering the urgency in finding effective prevention, but also side-effects free treatment of COVID-19 our results call for clinical affirmation of the benefits of this micronutrient combination in both preventive and therapeutic aspects. Whether observed effects can be achieved, by concentrations of the active agents used in these in vitro experiments, in in vivo or clinical setting warrants further study.

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天然化合物的成分降低了 Omicron 和 SARS-CoV-2 RdRp 复合物的活性。
天然化合物具有广泛的抗病毒功效。然而,人们对它们之间的相互合作却知之甚少。在这里,我们评估了确定的混合制剂对原始 SARS-CoV-2 和 Omicron 变体的 RdRp 复合物的体外药效。这种由维生素 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组成的混合物对这两种变体的 RdRp/nsp7/nsp8 的活性都有抑制作用。重组 RdRp 复合物体外暴露于这些成分中的单个化合物后,发现槲皮素是驱动抑制作用的化合物。这项研究的结果支持了天然化合物对 SARS-CoV-2 和 Omicron 的抗病毒功效,并暗示它们之间的相互影响或相互作用可能会通过同时作用于不同的机制来增强抗病毒作用。因此,传染性病原体更难同时避开所有这些机制。考虑到寻找有效预防和无副作用治疗 COVID-19 的方法迫在眉睫,我们的研究结果要求临床证实这种微量营养素组合在预防和治疗方面的益处。这些体外实验中使用的活性剂浓度是否能在体内或临床环境中达到观察到的效果,还有待进一步研究。
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