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Changes in microbiome diversity following beta-lactam antibiotic treatment are associated with therapeutic versus subtherapeutic antibiotic exposure in cystic fibrosis

机译:β-内酰胺类抗生素治疗后微生物组多样性的变化与囊性纤维化中治疗性与亚治疗性抗生素暴露的关系

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In persons with cystic fibrosis (CF), decreased airway microbial diversity is associated with lower lung function. Conflicting data exist on the impact of short-term antibiotics for treatment of acute pulmonary exacerbations. However, whether differences in antibiotic exposure impacts airway microbiome changes has not been studied. We hypothesized that subtherapeutic beta-lactam antibiotic exposure, determined by the pharmacokinetics and pharmacodynamics (PK/PD) after intravenous (IV) antibiotic administration, would be associated with different patterns of changes in CF airway microbial diversity. Eligible children were enrolled when well; study assessments were performed around the time of pulmonary exacerbation. Plasma drug concentrations and bacterial minimum inhibitory concentrations (MICs) were used to determine therapeutic versus subtherapeutic beta-lactam antibiotic exposure. Respiratory samples were collected from children, and extracted bacterial DNA was amplified for the V4 region of the 16S rRNA gene. Twenty children experienced 31 APEs during the study; 45% (n?=?14) of antibiotic courses were deemed therapeutic. Those in the therapeutic group had more significant decreases in alpha diversity at end of treatment and post-recovery compared to baseline than those in the subtherapeutic group. Therapeutic and subtherapeutic beta-lactam use is associated with different patterns of changes in CF airway microbial diversity following antibiotic administration.
机译:在患有囊性纤维化(CF)的人中,气道微生物多样性降低与肺功能降低有关。关于短期抗生素治疗急性肺加重的影响存在矛盾的数据。然而,尚未研究抗生素暴露的差异是否影响气道微生物组的变化。我们假设通过静脉(IV)抗生素给药后的药代动力学和药效学(PK / PD)确定的亚治疗性β-内酰胺类抗生素暴露与CF气道微生物多样性变化的不同模式有关。合格的儿童入学时情况良好;在肺部恶化期间进行研究评估。血浆药物浓度和细菌最小抑菌浓度(MICs)用于确定治疗性与亚治疗性β-内酰胺类抗生素的接触情况。从儿童那里收集呼吸道样本,提取的细菌DNA扩增出16S rRNA基因的V4区域。在研究过程中,有20名儿童经历了31次APE。 45%(n?=?14)的抗生素疗程被认为是治疗性的。与亚治疗组相比,与基线相比,治疗组的患者在治疗结束时和恢复后的α多样性下降幅度更大。服用抗生素后,治疗性和亚治疗性β-内酰胺的使用与CF气道微生物多样性变化的不同模式有关。

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