IAME, INSERM, Université de Paris, Paris, France
AP-HP, Bichat Hospital, Département d'Epidémiologie, Biostatistique et Recherche Clinique, Paris, France.
Antimicrob Agents Chemother. 2019 Sep 23;63(10). doi: 10.1128/AAC.00820-19. Print 2019 Oct.
Although the global deleterious impact of antibiotics on the intestinal microbiota is well known, temporal changes in microbial diversity during and after an antibiotic treatment are still poorly characterized. We used plasma and fecal samples collected frequently during treatment and up to one month after from 22 healthy volunteers assigned to a 5-day treatment by moxifloxacin ( = 14) or no intervention ( = 8). Moxifloxacin concentrations were measured in both plasma and feces, and bacterial diversity was determined in feces by 16S rRNA gene profiling and quantified using the Shannon index and number of operational taxonomic units (OTUs). Nonlinear mixed effect models were used to relate drug pharmacokinetics and bacterial diversity over time. Moxifloxacin reduced bacterial diversity in a concentration-dependent manner, with a median maximal loss of 27.5% of the Shannon index (minimum [min], 17.5; maximum [max], 27.7) and 47.4% of the number of OTUs (min, 30.4; max, 48.3). As a consequence of both the long fecal half-life of moxifloxacin and the susceptibility of the gut microbiota to moxifloxacin, bacterial diversity indices did not return to their pretreatment levels until days 16 and 21, respectively. Finally, the model characterized the effect of moxifloxacin on bacterial diversity biomarkers and provides a novel framework for analyzing antibiotic effects on the intestinal microbiome.
虽然抗生素对肠道微生物群的全球有害影响众所周知,但抗生素治疗期间和治疗后微生物多样性的时间变化仍知之甚少。我们使用来自 22 名健康志愿者的血浆和粪便样本,这些志愿者在接受为期 5 天的莫西沙星治疗(n=14)或不接受干预(n=8)期间和治疗结束后一个月内频繁采集。在血浆和粪便中测量了莫西沙星的浓度,并通过 16S rRNA 基因谱分析确定了粪便中的细菌多样性,并使用 Shannon 指数和操作分类单位(OTU)数量进行定量。使用非线性混合效应模型来研究药物药代动力学与细菌多样性随时间的关系。莫西沙星以浓度依赖的方式降低了细菌多样性,Shannon 指数最大损失中位数为 27.5%(最小值 17.5%,最大值 27.7%),OTU 数量最大损失中位数为 47.4%(最小值 30.4%,最大值 48.3%)。由于莫西沙星的粪便半衰期长,以及肠道微生物群对莫西沙星的敏感性,细菌多样性指数直到第 16 天和第 21 天分别才恢复到治疗前水平。最后,该模型描述了莫西沙星对细菌多样性生物标志物的影响,并为分析抗生素对肠道微生物组的影响提供了新的框架。