Institut für Virologie, Fachbereich Veterinärmedizin, Freie Universität Berlin, Berlin, Germany.
Department of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA.
Mol Biol Evol. 2024 Jul 3;41(7). doi: 10.1093/molbev/msae119.
Antiviral therapy is constantly challenged by the emergence of resistant pathogens. At the same time, experimental approaches to understand and predict resistance are limited by long periods required for evolutionary processes. Here, we present a herpes simplex virus 1 mutant with impaired proofreading capacity and consequently elevated mutation rates. Comparing this hypermutator to parental wild type virus, we study the evolution of antiviral drug resistance in vitro. We model resistance development and elucidate underlying genetic changes against three antiviral substances. Our analyzes reveal no principle difference in the evolutionary behavior of both viruses, adaptive processes are overall similar, however significantly accelerated for the hypermutator. We conclude that hypermutator viruses are useful for modeling adaptation to antiviral therapy. They offer the benefit of expedited adaptation without introducing apparent bias and can therefore serve as an accelerator to predict natural evolution.
抗病毒治疗不断受到耐药病原体的挑战。同时,了解和预测耐药性的实验方法受到进化过程所需时间长的限制。在这里,我们介绍了一种具有受损校对能力的单纯疱疹病毒 1 突变体,因此突变率升高。将这种高突变体与亲本野生型病毒进行比较,我们研究了体外抗病毒药物耐药性的演变。我们针对三种抗病毒物质建立了耐药性发展模型并阐明了潜在的遗传变化。我们的分析表明,两种病毒的进化行为没有本质区别,适应过程总体上是相似的,但对于高突变体来说,适应过程明显加快。我们得出结论,高突变体病毒可用于模拟对抗病毒治疗的适应。它们具有加速适应的优势,而不会引入明显的偏差,因此可以作为预测自然进化的加速器。