Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre of the Hungarian Academy of Sciences, 6726 Szeged, Hungary;
Doctoral School in Biology, Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary.
Proc Natl Acad Sci U S A. 2018 Jun 19;115(25):E5726-E5735. doi: 10.1073/pnas.1801646115. Epub 2018 Jun 5.
Antibiotic development is frequently plagued by the rapid emergence of drug resistance. However, assessing the risk of resistance development in the preclinical stage is difficult. Standard laboratory evolution approaches explore only a small fraction of the sequence space and fail to identify exceedingly rare resistance mutations and combinations thereof. Therefore, new rapid and exhaustive methods are needed to accurately assess the potential of resistance evolution and uncover the underlying mutational mechanisms. Here, we introduce directed evolution with random genomic mutations (DIvERGE), a method that allows an up to million-fold increase in mutation rate along the full lengths of multiple predefined loci in a range of bacterial species. In a single day, DIvERGE generated specific mutation combinations, yielding clinically significant resistance against trimethoprim and ciprofloxacin. Many of these mutations have remained previously undetected or provide resistance in a species-specific manner. These results indicate pathogen-specific resistance mechanisms and the necessity of future narrow-spectrum antibacterial treatments. In contrast to prior claims, we detected the rapid emergence of resistance against gepotidacin, a novel antibiotic currently in clinical trials. Based on these properties, DIvERGE could be applicable to identify less resistance-prone antibiotics at an early stage of drug development. Finally, we discuss potential future applications of DIvERGE in synthetic and evolutionary biology.
抗生素的开发常常受到耐药性迅速出现的困扰。然而,在临床前阶段评估耐药性发展的风险是困难的。标准的实验室进化方法仅探索了一小部分序列空间,无法识别极其罕见的耐药突变及其组合。因此,需要新的快速和详尽的方法来准确评估耐药进化的潜力,并揭示潜在的突变机制。在这里,我们引入了带有随机基因组突变的定向进化(DIvERGE),这是一种方法,可以将多种细菌物种中多个预定义基因座的全长突变率提高到 100 万倍。在一天内,DIvERGE 产生了特定的突变组合,导致对甲氧苄啶和环丙沙星产生了临床显著的耐药性。其中许多突变以前从未被检测到,或者以物种特异性的方式提供耐药性。这些结果表明了病原体特异性的耐药机制和未来窄谱抗菌治疗的必要性。与之前的说法相反,我们检测到了对 gepotidacin 的耐药性迅速出现,gepotidacin 是一种目前正在临床试验中的新型抗生素。基于这些特性,DIvERGE 可以在药物开发的早期阶段用于识别耐药性较低的抗生素。最后,我们讨论了 DIvERGE 在合成和进化生物学中的潜在未来应用。