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新型 A 型原花青素丰富的植物复合物 SP4™ 是一种广谱抗人类呼吸道病毒药物。

The Novel A-Type Proanthocyanidin-Rich Phytocomplex SP4™ Acts as a Broad-Spectrum Antiviral Agent against Human Respiratory Viruses.

机构信息

Microbiology and Virology Unit, Department of Life Sciences and Systems Biology, University of Torino, Via Accademia Albertina 13, 10123 Turin, Italy.

Plant Physiology Unit, Department of Life Sciences and Systems Biology, University of Torino, Via Quarello 15/a, 10135 Torino, Italy.

出版信息

Int J Mol Sci. 2024 Jul 5;25(13):7370. doi: 10.3390/ijms25137370.

Abstract

The appearance of new respiratory virus infections in humans with epidemic or pandemic potential has underscored the urgent need for effective broad-spectrum antivirals (BSAs). Bioactive compounds derived from plants may provide a natural source of new BSA candidates. Here, we investigated the novel phytocomplex formulation SP4™ as a candidate direct-acting BSA against major current human respiratory viruses, including coronaviruses and influenza viruses. SP4™ inhibited the in vitro replication of SARS-CoV-2, hCoV-OC43, hCoV-229E, Influenza A and B viruses, and respiratory syncytial virus in the low-microgram range. Using hCoV-OC43 as a representative respiratory virus, most of the antiviral activity of SP4™ was observed to stem primarily from its dimeric A-type proanthocyanidin (PAC-A) component. Further investigations of the mechanistic mode of action showed SP4™ and its PAC-A-rich fraction to prevent hCoV-OC43 from attaching to target cells and exert virucidal activity. This occurred through their interaction with the spike protein of hCoV-OC43 and SARS-CoV-2, thereby interfering with spike functions and leading to the loss of virion infectivity. Overall, these findings support the further development of SP4™ as a candidate BSA of a natural origin for the prevention of human respiratory virus infections.

摘要

新的呼吸道病毒感染在具有流行或大流行潜力的人类中出现,这突显了迫切需要有效的广谱抗病毒药物(BSA)。源自植物的生物活性化合物可能为新型广谱抗病毒候选药物提供天然来源。在这里,我们研究了新型植物复合物配方 SP4™ 作为一种针对主要当前人类呼吸道病毒(包括冠状病毒和流感病毒)的直接作用广谱抗病毒候选药物。SP4™ 以微克级的低浓度抑制了 SARS-CoV-2、hCoV-OC43、hCoV-229E、甲型和乙型流感病毒以及呼吸道合胞病毒的体外复制。使用 hCoV-OC43 作为代表性呼吸道病毒,SP4™ 的大部分抗病毒活性主要源自其二聚 A 型原花青素(PAC-A)成分。对作用机制模式的进一步研究表明,SP4™及其富含 PAC-A 的部分可防止 hCoV-OC43 附着在靶细胞上并发挥抗病毒活性。这是通过与 hCoV-OC43 和 SARS-CoV-2 的刺突蛋白相互作用来实现的,从而干扰刺突功能并导致病毒粒子失去感染性。总的来说,这些发现支持进一步开发 SP4™ 作为一种天然来源的广谱抗病毒候选药物,用于预防人类呼吸道病毒感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21cd/11242173/a97d4bbcde8e/ijms-25-07370-g001.jpg

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