Suppr超能文献

针对其高突变率导致 COVID-19 病毒传播的问题:采用非特异性阻止其进入细胞的方法进行干预的方法。

Containing the spread of COVID-19 virus facing to its high mutation rate: approach to intervention using a nonspecific way of blocking its entry into the cells.

机构信息

Department of Medicine, Biochemical Genetics and Metabolism, The Mitochondrial and Metabolic Disease Center, School of Medicine, University of California, San Diego, San Diego, California, USA.

Department of Pediatrics, University of California, San Diego, School of Medicine, La Jolla, California, USA.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2022;41(8):778-814. doi: 10.1080/15257770.2022.2071937. Epub 2022 May 9.

Abstract

Viruses have multiple mutation rates that are higher than any other member of the kingdom of life. This gives them the ability to evolve, even within the course of a single infection, and to evade multiple host defenses, thereby impacting pathogenesis. Additionally, there are also interplays between mutation and recombination and the high multiplicity of infection (MOI) that enhance viral adaptability and increase levels of recombination leading to complex and conflicting effects on genome selection, and the net results is difficult to predict. Recently, the outbreak of COVID-19 virus represents a pandemic threat that has been declared a public health emergency of international concern. Up to present, however, due to the high mutation rate of COVID-19 virus, there are no effective procedures to contain the spread of this virus across the globe. For such a purpose, there is then an urgent need to explore new approaches. As an opinion, the present approach emphasizes on (a) the use of a nonspecific way of blocking the entry of COVID-19 virus as well as its variants into the cells via a therapeutic biocompatible compound (ideally, "in a pill") targeting its spike (S) glycoprotein; and (b) the construction of expression vectors via the glycosyl-phosphatidylinositol, GPI, anchor for studying intermolecular interactions between the spike S of COVID-19 virus as well as its variants and the angiotensin-converting enzyme 2 (ACE2) of its host receptor for checking the efficacy of any therapeutic biocompatible compound of the nonspecific way of blocking. Such antiviral drug would be safer than the ACE1 and ACE2 inhibitors/angiotensin receptor blockers, and recombinant human ACE2 as well as nucleoside analogs or protease inhibitors used for fighting the spread of the virus inside the cells, and it would also be used as a universal one for any eventual future pandemic related to viruses, especially the RNA viruses with high mutation rates.

摘要

病毒具有多个突变率,高于生命王国的任何其他成员。这使它们能够进化,甚至在单次感染过程中,逃避多种宿主防御,从而影响发病机制。此外,突变和重组之间也存在相互作用,以及高感染复数(MOI)增强了病毒的适应性,增加了重组水平,导致对基因组选择的复杂和冲突影响,净结果难以预测。最近,COVID-19 病毒的爆发代表了一种大流行威胁,已被宣布为国际关注的公共卫生紧急事件。然而,迄今为止,由于 COVID-19 病毒的高突变率,没有有效的程序可以在全球范围内遏制这种病毒的传播。出于这个目的,就需要探索新的方法。作为一种观点,本方法强调:(a)使用一种非特异性方法来阻止 COVID-19 病毒及其变体通过针对其刺突(S)糖蛋白的治疗性生物相容性化合物(理想情况下是“一粒药”)进入细胞;(b)通过糖基磷脂酰肌醇(GPI)锚构建表达载体,用于研究 COVID-19 病毒及其变体的刺突 S 与宿主受体的血管紧张素转化酶 2(ACE2)之间的分子间相互作用,以检查任何非特异性阻断方法的治疗性生物相容性化合物的疗效。这种抗病毒药物将比 ACE1 和 ACE2 抑制剂/血管紧张素受体阻滞剂以及重组人 ACE2 以及用于在细胞内抵抗病毒传播的核苷类似物或蛋白酶抑制剂更安全,并且还将作为针对任何与 RNA 病毒相关的未来大流行的通用药物,特别是具有高突变率的 RNA 病毒。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验