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Time-Resolved Tracking of Mutations Reveals Diverse Allele Dynamics during Escherichia coli Antimicrobial Adaptive Evolution to Single Drugs and Drug Pairs

机译:时间分辨的突变跟踪揭示了大肠杆菌对单一药物和药物对的抗菌适应性进化过程中的等位基因动力学。

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摘要

Understanding the evolutionary processes that lead to antibiotic resistance can help to achieve better treatment strategies. Yet, little is known about the dynamics of the resistance alleles during adaptation. Here, we use population sequencing to monitor genetic changes in putative resistance loci at several time-points during adaptive evolution experiments involving five different antibiotic conditions. We monitor the mutational spectra in lineages evolved to be resistant to single antibiotics [amikacin (AMK), chloramphenicol (CHL), and ciprofloxacin (CIP)], as well as antibiotic combinations (AMK + CHL and CHL + CIP). We find that lineages evolved to antibiotic combinations exhibit different resistance allele dynamics compared with those of single-drug evolved lineages, especially for a drug pair with reciprocal collateral sensitivity. During adaptation, we observed interfering, superimposing and fixation allele dynamics. To further understand the selective forces driving specific allele dynamics, a subset of mutations were introduced into the ancestral wild type enabling differentiation between clonal interference and negative epistasis.
机译:了解导致抗生素耐药性的进化过程可以帮助实现更好的治疗策略。然而,关于适应过程中抗性等位基因的动力学知之甚少。在这里,我们使用群体测序来监测涉及五个不同抗生素条件的适应性进化实验中几个时间点推定抗性基因座的遗传变化。我们监测进化为对单一抗生素[阿米卡星(AMK),氯霉素(CHL)和环丙沙星(CIP)]具有耐药性的谱系以及抗生素组合(AMK + CHL和CHL + CIP)的突变谱。我们发现进化成抗生素组合的谱系与单药进化谱系相比表现出不同的抗性等位基因动力学,特别是对于具有间接附带敏感性的药物对。在适应过程中,我们观察到干扰,叠加和固定等位基因动力学。为了进一步了解驱动特定等位基因动力学的选择性力,将突变的子集引入祖先野生型,从而能够区分克隆干扰和阴性上位性。

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