角叉菜胶抑制关注组号BA.1、BA.2和BA.5 SARS-CoV-2变异体的复制

Christian Setz, M. Große, Maria Fröba, Janina Auth, P. Rauch, A. Herrmann, A. Cordsmeier, A. Ensser, M. Schindler, Martina Morokutti-Kurz, Philipp Graf, Benedikt Engel, Eva Prieschl-Grassauer, A. Grassauer, U. Schubert
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引用次数: 0

摘要

即使已转变为流行病,COVID-19大流行仍然是一种公共卫生威胁,特别是考虑到新出现的关注变体(voc)以及未来需要进行大流行防范。2021年11月,SARS-CoV-2挥发性有机基因出现,其亚型BA.1、BA.2和BA.5占主导地位。尽管蛋白酶抑制剂Paxlovid®和聚合酶抑制剂Molnupiravir和Remdesivir已被批准作为COVID-19感染后早期患者的特异性抗病毒治疗选择,但目前还没有有效的无不良反应的预防作用物质。在最近的一项研究中,我们证明了从红海藻中提取的硫酸化多糖iota-carrageenan能有效抑制SARS-CoV-2武汉型和挥发性有机化合物α、β、γ和δ的复制。现在,我们扩展了这项研究,研究了iota-, lambda-和kappa-卡拉胶对VoC Omicron亚变体BA.1, BA.2和BA.5的抗病毒作用。利用VoC Omicron BA.1刺突假型小鼠白血病病毒(BA.1 MLVOMVLP)和患者源性SARS-CoV-2 Omicron分离物BA.1、BA.2和BA.5 (SARS-CoV-2OM BA.1、SARS-CoV-2OM BA.2和SARS-CoV-2OM BA.5),我们证明了iota- carragenan对所有分析的Omicron亚变体具有相似的抗病毒活性。与之前展示的其他挥发性有机化合物一样,生物惰性的ioa -卡拉胶比kapa -和lambda-卡拉胶更有效。总之,这些结果证实,独立于当前和潜在的未来变体,约塔-卡拉胶提供的物理屏障可能适用于SARS-CoV-2感染的预防和早期治疗。
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Iota-Carrageenan Inhibits Replication of the SARS-CoV-2 Variants of Concern Omicron BA.1, BA.2 and BA.5
Even with its endemic transition, the COVID-19 pandemic remains a public health threat, particularly in the light of emerging variants of concern (VoCs) and the need for pandemic preparedness in the future. In November 2021, the SARS-CoV-2 VoC Omicron emerged and its subvariants BA.1, BA.2 and BA.5 became predominant. Although the protease inhibitor Paxlovid® and the polymerase inhibitors Molnupiravir and Remdesivir were approved as specific antiviral treatment options for COVID-19 patients in the early stages after infection, effective prophylactically acting substances without adverse effects are not available yet. In a recent study, we demonstrated that iota-carrageenan, a sulfated polysaccharide extracted from red seaweed, efficiently inhibits the replication of the SARS-CoV-2 Wuhan Type and the VoCs Alpha, Beta, Gamma and Delta. Now, we extended this study by investigating the antiviral effects of iota-, lambda- and kappa-carrageenans on the VoC Omicron subvariants BA.1, BA.2 and BA.5. Using a VoC Omicron BA.1 spike pseudotyped murine leukemia virus (BA.1 MLVOMVLP) as well as patient-derived SARS-CoV-2 Omicron isolates BA.1, BA.2 and BA.5 (SARS-CoV-2OM BA.1, SARS-CoV-2OM BA.2 and SARS-CoV-2OM BA.5), we demonstrate that iota-carrageenan exhibits similar antiviral activity against all analyzed Omicron subvariants. As with other VoCs shown before, the biologically inert iota-carrageenan was more efficient than kappa- and lambda-carrageenan. Altogether, these results confirm that, independent of the current and potential future variants, the physical barrier provided by iota-carrageenan might be applicable for prophylaxis and early treatment of SARS-CoV-2 infections.
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