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Inhibitory Concentrations of Ciprofloxacin Induce an Adaptive Response Promoting the Intracellular Survival of Salmonella enterica Serovar Typhimurium

机译:环丙沙星的抑制浓度诱导促进<命名含量含量型=“属型”>沙门氏菌肠道血清癣菌

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ABSTRACT Antimicrobial resistance (AMR) is a pressing global health crisis, which has been fueled by the sustained use of certain classes of antimicrobials, including fluoroquinolones. While the genetic mutations responsible for decreased fluoroquinolone (ciprofloxacin) susceptibility are known, the implications of ciprofloxacin exposure on bacterial growth, survival, and interactions with host cells are not well described. Aiming to understand the influence of inhibitory concentrations of ciprofloxacin in vitro, we subjected three clinical isolates of Salmonella enterica serovar Typhimurium to differing concentrations of ciprofloxacin, dependent on their MICs, and assessed the impact on bacterial growth, morphology, and transcription. We further investigated the differential morphology and transcription that occurred following ciprofloxacin exposure and measured the ability of ciprofloxacin-treated bacteria to invade and replicate in host cells. We found that ciprofloxacin-exposed S. Typhimurium is able to recover from inhibitory concentrations of ciprofloxacin and that the drug induces specific morphological and transcriptional signatures associated with the bacterial SOS response, DNA repair, and intracellular survival. In addition, ciprofloxacin-treated S. Typhimurium has increased capacity for intracellular replication in comparison to that of untreated organisms. These data suggest that S. Typhimurium undergoes an adaptive response under ciprofloxacin perturbation that promotes cellular survival, a consequence that may justify more measured use of ciprofloxacin for Salmonella infections. The combination of multiple experimental approaches provides new insights into the collateral effects that ciprofloxacin and other antimicrobials have on invasive bacterial pathogens.
机译:摘要抗菌抗性(AMR)是一项压制的全球健康危机,其被持续使用某些类别的抗微生物,包括氟喹诺酮类药。虽然已知负责氟喹诺酮(环丙沙星)敏感性降低的遗传突变,但不再详细描述环丙沙星暴露于细菌生长,存活率和与宿主细胞的相互作用的影响。旨在了解抑制环丙沙星在体外的影响,我们将三种临床分离株沙门氏菌肠道毒蕈醋酰硫醇对不同浓度的环丙沙星进行了依赖于其麦盾,并评估了对细菌生长,形态和转录的影响。我们进一步研究了环丙沙星暴露后发生的差异形态和转录,并测量了环丙沙星处理的细菌在宿主细胞中侵入和复制的能力。我们发现环丙沙星暴露的伤寒伤寒毒蕈法能够从环丙沙星的抑制浓度中恢复,并且该药物诱导与细菌SOS反应,DNA修复和细胞内存活相关的具体形态和转录签。此外,与未处理的生物体相比,环丙沙星治疗的伤寒伤寒毒蕈酰硫脲能够增加细胞内复制能力。这些数据表明,S.Typhimurium在促进细胞存活的环丙沙星扰动下进行了适应性的反应,这使得能够为沙门氏菌感染制备更多测量的环氟氟苯甲酸来说。多种实验方法的组合为环丙沙星和其他抗菌药物对侵入性细菌病原体的抵押品效应提供了新的见解。

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