磷霉素
生物
背景(考古学)
微生物学
分解代谢抑制
阴沟肠杆菌
抗生素
细胞外
铜绿假单胞菌
抗生素耐药性
人口
肠杆菌科
遗传学
大肠杆菌
肠杆菌
抗药性
基因
质粒
细菌
毒力
基因表达调控
基因表达
恒化器
作者
Jacob E. Choby,David A. Hufnagel,Muqing Ma,Tugba Ozturk,Victor I. Band,Minsu Kim,David S. Weiss
标识
DOI:10.1038/s41467-026-77232-6
摘要
Heteroresistance is a form of antibiotic resistance in which a phenotypically unstable subpopulation of resistant cells coexists with a majority susceptible population. Many mechanisms of heteroresistance are unclear and the impact of the extracellular environment on this phenomenon is unknown. Studying fosfomycin heteroresistance in Enterobacter cloacae complex, we observed that glucose availability greatly increased the frequency of the resistant subpopulation. Glucose downregulated the glycerol and fosfomycin importer GlpT via catabolite repression. Heteroresistance was generated by heterogeneity in single-cell expression of GlpT, in addition to expression of fosA, which acted as a resistance enhancer. Due to the impact of environmental glucose on glpT expression, we observed that the resistant subpopulation was more frequent during infection in murine models of hyperglycemia/diabetes. Thus, we reveal a paradigm where heterogeneity in response to the environment tunes resistant subpopulation frequency, which suggests that the metabolic context of infection in specific disease states may be important to consider in treatment decisions. Choby et al. show an antibiotic-resistant subpopulation is generated by heterogeneity in expression of an antibiotic importer repressed by environmental glucose, suggesting diabetes-related infection environments may influence antibiotic resistance.
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