Molecular Biology and Evolution · 2014 · 297 citations · 38 references
Life SciencesGeneticsMicrobiologyAntimicrobial ResistanceMicrobial EvolutionMicrobial GeneticsAntibiotic ResistanceAntibiotic Resistance EvolutionAntibiotic Resistance GeneticsAntibiotic Resistance MechanismsResistance EvolutionResistance GenesAntibiotic Resistance CoevolutionAntibiotic Resistance GenesAntimicrobial Resistance EvolutionEscherichia ColiGenetic Selection PressureIon Transporter GenesPoint Mutation EffectsSelection Pressure On Resistance Alleles
Revealing the genetic changes responsible for antibiotic resistance can be critical for developing novel antibiotic therapies. However, systematic studies correlating genotype to phenotype in the context of antibiotic resistance have been missing. In order to fill in this gap, we evolved 88 isogenic Escherichia coli populations against 22 antibiotics for 3 weeks. For every drug, two populations were evolved under strong selection and two populations were evolved under mild selection. By quantifying evolved populations' resistances against all 22 drugs, we constructed two separate cross-resistance networks for strongly and mildly selected populations. Subsequently, we sequenced representative colonies isolated from evolved populations for revealing the genetic basis for novel phenotypes. Bacterial populations that evolved resistance against antibiotics under strong selection acquired high levels of cross-resistance against several antibiotics, whereas other bacterial populations evolved under milder selection acquired relatively weaker cross-resistance. In addition, we found that strongly selected strains against aminoglycosides became more susceptible to five other drug classes compared with their wild-type ancestor as a result of a point mutation on TrkH, an ion transporter protein. Our findings suggest that selection strength is an important parameter contributing to the complexity of antibiotic resistance problem and use of high doses of antibiotics to clear infections has the potential to promote increase of cross-resistance in clinics.
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