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Access to high-impact mutations constrains the evolution of antibiotic resistance in soft agar

机译:获得高影响力突变限制了软琼脂中抗生素抗性的演变

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摘要

Despite widespread resistance to many important antibiotics, the factors that govern the emergence and prevalence of antibiotic-resistant bacteria are still unclear. When exposed to antibiotic gradients in soft agar plates measuring as little as 1.25 × 11 cm we found that Escherichia coli rapidly became resistant to representatives from every class of antibiotics active against Gram-negative bacteria. Evolution kinetics were independent of the frequency of spontaneous mutations that confer antibiotic resistance or antibiotic dose-response curves, and were only loosely correlated to maximal antibiotic concentrations. Instead, rapid evolution required unrealized mutations that could markedly decrease antibiotic susceptibility. When bacteria could not evolve through these “high-impact” mutations, populations frequently bottlenecked, reducing the number of cells from which mutants could arise and prolonging evolution times. This effect was independent of the antibiotic’s mechanism of action, and may affect the evolution of antibiotic resistance in clinical settings.
机译:尽管对许多重要的抗生素有广泛的耐药性,但控制耐药性细菌出现和流行的因素仍不清楚。当暴露于大小仅为1.25×antibiotic11 cm的软琼脂平板中暴露于抗生素梯度时,我们发现大肠杆菌迅速变得对各种对革兰氏阴性细菌有活性的抗生素的代表产生抗性。进化动力学与赋予抗生素抗性或抗生素剂量-反应曲线的自发突变频率无关,并且仅与最大抗生素浓度呈松散相关。取而代之的是,快速进化需要未实现的突变,这可能会大大降低抗生素的敏感性。当细菌无法通过这些“高影响力”突变进化时,种群常常会出现瓶颈,从而减少了可产生突变的细胞数量,并延长了进化时间。这种作用与抗生素的作用机制无关,并且可能会影响临床环境中抗生素耐药性的演变。

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