Division of Pulmonary and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Antimicrob Agents Chemother. 2017 Sep 22;61(10). doi: 10.1128/AAC.01146-17. Print 2017 Oct.
Macrolide antibiotics are mainstays in the treatment of lung disease due to the complex. Although previous studies have reported development of acquired macrolide resistance in this species, limited data are available on the outcomes of lung disease due to macrolide-resistant subsp. This study evaluated the clinical features, treatment outcomes, and molecular characteristics of macrolide-resistant isolates of subsp. We performed a retrospective review of medical records and genetic analysis of clinical isolates from 13 patients who had acquired macrolide-resistant subsp. lung disease between November 2006 and March 2016. Eleven (85%) patients had the nodular bronchiectatic form of the disease, and two (15%) patients had the fibrocavitary form. When acquired macrolide resistance was detected, 10 (77%) patients were on antibiotic therapy for subsp. , and three (23%) patients were on therapy for lung disease due to other nontuberculous mycobacteria. The median treatment duration after detecting resistance was 24.0 months (interquartile range, 16.0 to 43.0 months). Treatment outcomes were poor, and final sputum culture conversion was achieved in only one (8%) patient, after resectional surgery. All 13 clinical isolates demonstrated point mutations at position 2058 ( = 10) or 2059 ( = 3) of the 23S rRNA gene, which resulted in acquired macrolide resistance. This study indicates that treatment outcomes are very poor after the development of acquired macrolide resistance in patients with subsp. lung disease. Thus, more effective measures are needed to prevent development and effectively treat macrolide-resistant subsp. lung disease.
大环内酯类抗生素是治疗肺部疾病的主要药物,因为该病原体结构复杂。尽管以前的研究已经报道了该物种获得大环内酯类耐药性的发展,但关于大环内酯类耐药亚种引起的肺部疾病的结果数据有限。本研究评估了获得性大环内酯类耐药亚种引起的肺部疾病患者的临床特征、治疗结果和分子特征。我们对 2006 年 11 月至 2016 年 3 月期间获得大环内酯类耐药亚种的 13 例肺部疾病患者的病历和临床分离株的遗传分析进行了回顾性研究。11 例(85%)患者患有结节性支气管扩张型疾病,2 例(15%)患者患有纤维空洞型疾病。当检测到大环内酯类耐药性时,10 例(77%)患者正在接受针对亚种的抗生素治疗,3 例(23%)患者正在接受针对其他非结核分枝杆菌引起的肺部疾病的治疗。在检测到耐药性后,中位治疗时间为 24.0 个月(四分位距,16.0 至 43.0 个月)。治疗结果不佳,只有 1 例(8%)患者在切除手术后最终实现了痰培养转换。13 例临床分离株均在 23S rRNA 基因的 2058 位(= 10)或 2059 位(= 3)发生点突变,导致获得性大环内酯类耐药性。本研究表明,在患有亚种肺部疾病的患者中出现获得性大环内酯类耐药性后,治疗结果非常差。因此,需要采取更有效的措施来预防和有效治疗大环内酯类耐药亚种引起的肺部疾病。