1South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
2South Australian Health and Medical Research Institute Microbiome Research Laboratory, College of Medicine and Public Health, Flinders University, Bedford Park, South Australia, Australia.
Am J Respir Crit Care Med. 2019 Aug 1;200(3):309-317. doi: 10.1164/rccm.201809-1739OC.
The macrolide antibiotic azithromycin reduces exacerbations in adults with persistent symptomatic asthma. However, owing to the pleotropic properties of macrolides, unintended bacteriological consequences such as augmented pathogen colonization or dissemination of antibiotic-resistant organisms can occur, calling into question the long-term safety of azithromycin maintenance therapy. To assess the effects of azithromycin on the airway microbiota, pathogen abundance, and carriage of antibiotic resistance genes. 16S rRNA sequencing and quantitative PCR were performed to assess the effect of azithromycin on sputum microbiology from participants of the AMAZES (Asthma and Macrolides: The Azithromycin Efficacy and Safety) trial: a 48-week, double-blind, placebo-controlled trial of thrice-weekly 500 mg oral azithromycin in adults with persistent uncontrolled asthma. Pooled-template shotgun metagenomic sequencing, quantitative PCR, and isolate whole-genome sequencing were performed to assess antibiotic resistance. Paired sputum samples were available from 61 patients ( = 34 placebo, = 27 azithromycin). Azithromycin did not affect bacterial load ( = 0.37) but did significantly decrease Faith's phylogenetic diversity ( = 0.026) and load ( < 0.0001). Azithromycin did not significantly affect levels of , , , or . Of the 89 antibiotic resistance genes detected, five macrolide resistance genes and two tetracycline resistance genes were increased significantly. In patients with persistent uncontrolled asthma, azithromycin reduced airway load compared with placebo but did not change total bacterial load. Macrolide resistance increased, reflecting previous studies. These results highlight the need for studies assessing the efficacy of nonantibiotic macrolides as a long-term therapy for patients with persistent uncontrolled asthma.
大环内酯类抗生素阿奇霉素可减少持续性有症状哮喘成人的恶化。然而,由于大环内酯类药物的多效性,可能会出现意想不到的细菌学后果,如病原体定植增加或抗生素耐药体的传播,从而质疑阿奇霉素维持治疗的长期安全性。评估阿奇霉素对气道微生物群、病原体丰度和抗生素耐药基因携带的影响。使用 16S rRNA 测序和定量 PCR 评估 AMAZES(哮喘和大环内酯类药物:阿奇霉素的疗效和安全性)试验参与者的痰微生物组学,这是一项为期 48 周、双盲、安慰剂对照的试验,在持续性未控制的哮喘成人中每周三次口服 500mg 阿奇霉素。进行了 pooled-template shotgun 宏基因组测序、定量 PCR 和分离株全基因组测序来评估抗生素耐药性。从 61 名患者中获得了配对的痰样本( = 34 名安慰剂, = 27 名阿奇霉素)。阿奇霉素未影响细菌负荷( = 0.37),但显著降低了 Faith 的系统发育多样性( = 0.026)和负荷( < 0.0001)。阿奇霉素未显著影响 、 、 或 的水平。在检测到的 89 个抗生素耐药基因中,5 个大环内酯类耐药基因和 2 个四环素耐药基因显著增加。在持续性未控制的哮喘患者中,与安慰剂相比,阿奇霉素降低了气道 负荷,但并未改变总细菌负荷。大环内酯类耐药性增加,反映了之前的研究。这些结果强调了需要研究评估非抗生素大环内酯类药物作为持续性未控制哮喘患者长期治疗的疗效。