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量化抗生素对产超广谱β-内酰胺酶耐药性患者内个体动态的影响。

Quantifying antibiotic impact on within-patient dynamics of extended-spectrum beta-lactamase resistance.

机构信息

University of Oxford, Oxford, United Kingdom.

National Institute for Public Health and theEnvironment, Bilthoven, Netherlands.

出版信息

Elife. 2020 May 7;9:e49206. doi: 10.7554/eLife.49206.

Abstract

Antibiotic-induced perturbation of the human gut flora is expected to play an important role in mediating the relationship between antibiotic use and the population prevalence of antibiotic resistance in bacteria, but little is known about how antibiotics affect within-host resistance dynamics. Here we develop a data-driven model of the within-host dynamics of extended-spectrum beta-lactamase (ESBL) producing . We use bla (the most widespread ESBL gene family) and 16S rRNA (a proxy for bacterial load) abundance data from 833 rectal swabs from 133 ESBL-positive patients followed up in a prospective cohort study in three European hospitals. We find that cefuroxime and ceftriaxone are associated with increased bla abundance during treatment (21% and 10% daily increase, respectively), while treatment with meropenem, piperacillin-tazobactam, and oral ciprofloxacin is associated with decreased bla (8% daily decrease for all). The model predicts that typical antibiotic exposures can have substantial long-term effects on bla carriage duration.

摘要

抗生素诱导的人类肠道菌群紊乱预计将在介导抗生素使用与细菌对抗生素耐药性的人群流行率之间的关系方面发挥重要作用,但对于抗生素如何影响宿主内耐药性动态变化知之甚少。在这里,我们开发了一个针对产超广谱β-内酰胺酶(ESBL)的宿主内动力学的数据分析模型。我们使用了来自三个欧洲医院的前瞻性队列研究中 133 名 ESBL 阳性患者的 833 个直肠拭子中的 bla(最广泛的 ESBL 基因家族)和 16S rRNA(细菌负荷的替代物)丰度数据。我们发现,头孢呋辛和头孢曲松在治疗期间与 bla 丰度增加相关(分别为每天增加 21%和 10%),而美罗培南、哌拉西林他唑巴坦和口服环丙沙星治疗与 bla 减少相关(所有药物均为每天减少 8%)。该模型预测,典型的抗生素暴露可以对 bla 携带持续时间产生重大的长期影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3d6/7205461/5f36953b4efb/elife-49206-fig1.jpg

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