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Biological costs and mechanisms of fosfomycin resistance in Escherichia coli.

机译:大肠杆菌中磷霉素耐药性的生物学成本和机理。

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Fosfomycin is a cell wall inhibitor used mainly for the treatment of uncomplicated lower urinary tract infections. As shown here, resistance to fosfomycin develops rapidly in Escherichia coli under experimental conditions, but in spite of the relatively high mutation rate in vitro, resistance in clinical isolates is rare. To examine this apparent contradiction, we mathematically modeled the probability of resistance development in the bladder during treatment. The modeling showed that during a typical episode of urinary tract infection, the probability of resistance development was high (>10(-2)). However, if resistance was associated with a reduction in growth rate, the probability of resistance development rapidly decreased. To examine if fosfomycin resistance causes a reduced growth rate, we isolated in vitro and in vivo a set of resistant strains. We determined their resistance mechanisms and examined the effect of the different resistance mutations on bacterial growth in the absence and presence of fosfomycin. The types of mutations found in vitro and in vivo were partly different. Resistance in the mutants isolated in vitro was caused by ptsI, cyaA, glpT, uhpA/T, and unknown mutations, whereas no cyaA or ptsI mutants could be found in vivo. All mutations caused a decreased growth rate both in laboratory medium and in urine, irrespective of the absence or presence of fosfomycin. According to the mathematical model, the reduced growth rate of the resistant strains will prevent them from establishing in the bladder, which could explain why fosfomycin resistance remains rare in clinical isolates.
机译:磷霉素是一种细胞壁抑制剂,主要用于治疗简单的下尿路感染。如此处所示,在实验条件下,对磷霉素的抗性在大肠杆菌中迅速发展,尽管体外突变率相对较高,但临床分离株中的抗性却很少。为了检查这种明显的矛盾,我们对治疗过程中膀胱阻力发展的可能性进行了数学建模。该模型显示,在典型的尿路感染发作期间,耐药性发展的可能性很高(> 10(-2))。但是,如果耐药性与生长速度的降低相关,那么耐药性发展的可能性就会迅速降低。为了检查磷霉素抗性是否导致生长速率降低,我们在体内和体外分离出一组抗药性菌株。我们确定了它们的抗药性机制,并研究了在缺乏磷霉素的情况下不同抗药性突变对细菌生长的影响。在体外和体内发现的突变类型部分不同。体外分离的突变体的耐药性是由ptsI,cyaA,glpT,uhpA / T和未知突变引起的,而在体内找不到cyaA或ptsI突变体。无论是否存在磷霉素,所有突变都会导致实验室培养基和尿液的生长速率降低。根据数学模型,耐药菌株的增长率降低将阻止它们在膀胱中建立,这可以解释为什么磷霉素耐药性在临床分离株中仍然罕见。

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