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病毒致死性突变的影响不断增加。

The increasing impact of lethal mutagenesis of viruses.

机构信息

Department of Clinical Microbiology, IIS-Fundación Jiménez Díaz, UAM. Av. Reyes Católicos 2, 28040, Madrid, Spain.

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd) del Instituto de Salud Carlos III, 28029, Madrid, Spain.

出版信息

Future Med Chem. 2019 Jul;11(13):1645-1657. doi: 10.4155/fmc-2018-0457.

Abstract

Selection of viral mutants resistant to compounds used in therapy is a major determinant of treatment failure, a problem akin to antibiotic resistance in bacteria. In this scenario, mutagenic base and nucleoside analogs have entered the picture because they increase the mutation rate of viral populations to levels incompatible with their survival. This antiviral strategy is termed lethal mutagenesis. It has found a major impulse with the observation that some antiviral agents, which initially were considered only inhibitors of virus multiplication, may in effect exert part of their antiviral activity through mutagenesis. Here, we review the conceptual basis of lethal mutagenesis, the evidence of virus extinction through mutagenic nucleotide analogs and prospects for application in antiviral designs.

摘要

选择对治疗中使用的化合物具有抗性的病毒突变体是治疗失败的主要决定因素,这是一个类似于细菌对抗生素耐药性的问题。在这种情况下,诱变碱基和核苷类似物已经进入了人们的视野,因为它们会将病毒群体的突变率提高到与它们的生存不相容的水平。这种抗病毒策略被称为致死性诱变。最初被认为只是病毒复制抑制剂的一些抗病毒药物,实际上可能通过诱变发挥部分抗病毒活性,这一观察结果为这种抗病毒策略提供了主要动力。在这里,我们回顾了致死性诱变的概念基础、突变核苷类似物导致病毒灭绝的证据以及在抗病毒设计中的应用前景。

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