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来自B512F的硫酸葡聚糖对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)具有强大的抗病毒活性。

Dextran sulfate from B512F exerts potent antiviral activity against SARS-CoV-2 and .

作者信息

Andreu Sabina, von Kobbe Cayetano, Delgado Pilar, Ripa Inés, Buzón María José, Genescà Meritxell, Gironès Núria, Del Moral-Salmoral Javier, Ramírez Gustavo A, Zúñiga Sonia, Enjuanes Luis, López-Guerrero José Antonio, Bello-Morales Raquel

机构信息

Department of Molecular Biology, Universidad Autónoma de Madrid, Madrid, Spain.

Centro de Biología Molecular Severo Ochoa, Spanish National Research Council-Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain.

出版信息

Front Microbiol. 2023 May 3;14:1185504. doi: 10.3389/fmicb.2023.1185504. eCollection 2023.

Abstract

The emergent human coronavirus SARS-CoV-2 and its resistance to current drugs makes the need for new potent treatments for COVID-19 patients strongly necessary. Dextran sulfate (DS) polysaccharides have long demonstrated antiviral activity against different enveloped viruses . However, their poor bioavailability has led to their abandonment as antiviral candidates. Here, we report for the first time the broad-spectrum antiviral activity of a DS-based extrapolymeric substance produced by the lactic acid bacterium B512F. Time of addition assays with SARS-CoV-2 pseudoviruses in models confirm the inhibitory activity of DSs in the early stages of viral infection (viral entry). In addition, this exopolysaccharide substance also reports broad-spectrum antiviral activity against several enveloped viruses such as SARS-CoV-2, HCoV229E, HSV-1, in models and in human lung tissue. The toxicity and antiviral capacity of DS from was tested in mouse models which are susceptible to SARS-CoV-2 infection. The described DS, administered by inhalation, a new route of administration for these types of polymers, shows strong inhibition of SARS-CoV-2 infection , significantly reducing animal mortality and morbidity at non-toxic doses. Therefore, we suggest that it may be considered as a potential candidate for antiviral therapy against SARS-CoV-2.

摘要

新型人类冠状病毒SARS-CoV-2及其对现有药物的耐药性使得为新冠肺炎患者开发新的有效治疗方法变得极为必要。硫酸葡聚糖(DS)多糖长期以来已证明对不同包膜病毒具有抗病毒活性。然而,其较差的生物利用度导致它们被放弃作为抗病毒候选药物。在此,我们首次报道了由乳酸菌B512F产生的一种基于DS的胞外聚合物物质的广谱抗病毒活性。在模型中对SARS-CoV-2假病毒进行的添加时间试验证实了DS在病毒感染早期(病毒进入)的抑制活性。此外,这种胞外多糖物质在模型和人肺组织中也显示出对几种包膜病毒如SARS-CoV-2、HCoV229E、HSV-1的广谱抗病毒活性。在易感染SARS-CoV-2的小鼠模型中测试了来自[具体来源未提及]的DS的毒性和抗病毒能力。所描述的DS通过吸入给药,这是这类聚合物的一种新给药途径,显示出对SARS-CoV-2感染的强烈抑制作用,在无毒剂量下显著降低动物死亡率和发病率。因此,我们建议它可被视为抗SARS-CoV-2抗病毒治疗的潜在候选药物。

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