Heteroresistance in Enterobacter cloacae complex caused by variation in transient gene amplification events.

Johannes Kupke, Julian Brombach, Yuwen Fang, Silver A Wolf, Lakshmipriya Thrukonda, Fereshteh Ghazisaeedi, Benno Kuropka, Dennis Hanke, Torsten Semmler, Niclas Nordholt, Frank Schreiber, Karsten Tedin, Antina Lübke-Becker, Ulrich K Steiner, Marcus Fulde
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Abstract

Heteroresistance (HR) in bacteria describes a subpopulational phenomenon of antibiotic resistant cells of a generally susceptible population. Here, we investigated the molecular mechanisms and phenotypic characteristics underlying HR to ceftazidime (CAZ) in a clinical Enterobacter cloacae complex strain (ECC). We identified a plasmid-borne gene duplication-amplification (GDA) event of a region harbouring an ampC gene encoding a β-lactamase blaDHA-1 as the key determinant of HR. Individual colonies exhibited variations in the copy number of the genes resulting in resistance level variation which correlated with growth onset (lag times) and growth rates in the presence of CAZ. GDA copy number heterogeneity occurred within single resistant colonies, demonstrating heterogeneity of GDA on the single-cell level. The interdependence between GDA, lag time and antibiotic treatment and the strong plasticity underlying HR underlines the high risk for misdetection of antimicrobial HR and subsequent treatment failure.

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由瞬时基因扩增事件变异引起的阴沟肠杆菌复合体的异耐药。
细菌的异耐药(HR)描述了一般易感群体中抗生素耐药细胞的亚群体现象。在这里,我们研究了临床阴沟肠杆菌复合体菌株(ECC) HR对头孢他啶(CAZ)的分子机制和表型特征。我们发现了一个携带ampC基因的区域的质粒基因复制扩增(GDA)事件,该基因编码β-内酰胺酶blaDHA-1,是HR的关键决定因素。单个菌落表现出基因拷贝数的变化,导致抗性水平的变化,这与CAZ存在下的生长开始(滞后时间)和生长速率相关。GDA拷贝数在单个抗性菌落内存在异质性,表明GDA在单细胞水平上存在异质性。GDA、滞后时间和抗生素治疗之间的相互依存关系,以及HR潜在的强可塑性,突显了抗菌HR被误诊和随后治疗失败的高风险。
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