Lázár Viktória, Nagy István, Spohn Réka, Csörgő Bálint, Györkei Ádám, Nyerges Ákos, Horváth Balázs, Vörös Andrea, Busa-Fekete Róbert, Hrtyan Mónika, Bogos Balázs, Méhi Orsolya, Fekete Gergely, Szappanos Balázs, Kégl Balázs, Papp Balázs, Pál Csaba
1] Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Temesvari krt 62, Szeged 6726, Hungary [2].
1] Sequencing Platform, Institute of Biochemistry, Biological Research Centre, Temesvari krt 62, Szeged 6726, Hungary [2].
Nat Commun. 2014 Jul 8;5:4352. doi: 10.1038/ncomms5352.
Understanding how evolution of antimicrobial resistance increases resistance to other drugs is a challenge of profound importance. By combining experimental evolution and genome sequencing of 63 laboratory-evolved lines, we charted a map of cross-resistance interactions between antibiotics in Escherichia coli, and explored the driving evolutionary principles. Here, we show that (1) convergent molecular evolution is prevalent across antibiotic treatments, (2) resistance conferring mutations simultaneously enhance sensitivity to many other drugs and (3) 27% of the accumulated mutations generate proteins with compromised activities, suggesting that antibiotic adaptation can partly be achieved without gain of novel function. By using knowledge on antibiotic properties, we examined the determinants of cross-resistance and identified chemogenomic profile similarity between antibiotics as the strongest predictor. In contrast, cross-resistance between two antibiotics is independent of whether they show synergistic effects in combination. These results have important implications on the development of novel antimicrobial strategies.
理解抗微生物药物耐药性的进化如何增加对其他药物的耐药性是一个极其重要的挑战。通过结合实验进化和对63个实验室进化菌株的基因组测序,我们绘制了大肠杆菌中抗生素之间交叉耐药性相互作用的图谱,并探索了驱动进化的原理。在这里,我们表明:(1)趋同分子进化在各种抗生素治疗中普遍存在;(2)赋予耐药性的突变同时增强了对许多其他药物的敏感性;(3)27%的累积突变产生了活性受损的蛋白质,这表明抗生素适应性可以部分地在不获得新功能的情况下实现。通过利用抗生素特性的知识,我们研究了交叉耐药性的决定因素,并确定抗生素之间的化学基因组谱相似性是最强的预测指标。相比之下,两种抗生素之间的交叉耐药性与它们联合使用时是否显示协同效应无关。这些结果对新型抗菌策略的开发具有重要意义。