Evolution of antibiotic cross-resistance and collateral sensitivity in Staphylococcus epidermidis using the mutant prevention concentration and the mutant selection window

被引:25
作者
Lozano-Huntelman, Natalie Ann [1 ]
Singh, Nina [1 ]
Valencia, Alondra [1 ]
Mira, Portia [1 ]
Sakayan, Maral [1 ]
Boucher, Ian [1 ]
Tang, Sharon [1 ]
Brennan, Kelley [1 ]
Gianvecchio, Crystal [1 ]
Fitz-Gibbon, Sorel [2 ]
Yeh, Pamela [1 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Mol Cell Dev Biol, Los Angeles, CA USA
[3] Santa Fe Inst, Santa Fe, NM 87501 USA
来源
EVOLUTIONARY APPLICATIONS | 2020年 / 13卷 / 04期
基金
美国国家卫生研究院;
关键词
antibiotic resistance; antimicrobial; bacterial evolution; correlated traits; susceptible; ESCHERICHIA-COLI; ANTIMICROBIAL SUSCEPTIBILITY; DROSOPHILA-MELANOGASTER; 4; FLUOROQUINOLONES; COPACABANA METHOD; AUREUS; CIPROFLOXACIN; MUTATIONS; MECHANISM; PROTEIN;
D O I
10.1111/eva.12903
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In bacteria, evolution of resistance to one antibiotic is frequently associated with increased resistance (cross-resistance) or increased susceptibility (collateral sensitivity) to other antibiotics. Cross-resistance and collateral sensitivity are typically evaluated at the minimum inhibitory concentration (MIC). However, these susceptibility changes are not well characterized with respect to the mutant prevention concentration (MPC), the antibiotic concentration that prevents a single-step mutation from occurring. We measured the MIC and the MPC for Staphylococcus epidermidis and 14 single-drug resistant strains against seven antibiotics. We found that the MIC and the MPC were positively correlated but that this correlation weakened if cross-resistance did not evolve. If any type of resistance did evolve, the range of concentrations between the MIC and the MPC tended to shift right and widen. Similar patterns of cross-resistance and collateral sensitivity were observed at the MIC and MPC levels, though more symmetry was observed at the MIC level. Whole-genome sequencing revealed mutations in both known-target and nontarget genes. Moving forward, examining both the MIC and the MPC may lead to better predictions of evolutionary trajectories in antibiotic-resistant bacteria.
引用
收藏
页码:808 / 823
页数:16
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