Division of Infectious Diseases, Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Center for Nontuberculous Mycobacteria and Bronchiectasis, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
mSphere. 2023 Apr 20;8(2):e0066522. doi: 10.1128/msphere.00665-22. Epub 2023 Mar 13.
Mycobacteroides abscessus is an opportunistic pathogen in people with structural lung conditions such as bronchiectasis, chronic obstructive pulmonary disease, and cystic fibrosis. Pulmonary M. abscessus infection causes progressive symptomatic and functional decline as well as diminished lung function and is often incurable with existing antibiotics. We investigated the efficacy of a new tetracycline, omadacycline, in combination with existing antibiotics recommended to treat this indication, in a mouse model of M. abscessus lung disease. Amikacin, azithromycin, bedaquiline, biapenem, cefoxitin, clofazimine, imipenem, linezolid, and rifabutin were selected as companions to omadacycline. M. abscessus burden in the lungs of mice over a 4-week treatment duration was considered the endpoint. Omadacycline in combination with linezolid, imipenem, cefoxitin, biapenem, or rifabutin exhibited early bactericidal activity compared to any single drug. Using three M. abscessus isolates, we also determined the frequency of spontaneous resistance against omadacycline to be between 1.9 × 10 and 6.2 × 10 and the frequency of persistence against omadacycline to be between 5.3 × 10 and 1.3 × 10. Based on these findings, the combination of omadacycline and select drugs that are included in the recent treatment guidelines may exhibit improved potency to treat M. abscessus lung disease. M. abscessus disease incidence is increasing in the United States. This disease is difficult to cure with existing antibiotics. In this study, we describe the efficacy of a new tetracycline antibiotic, omadacycline, in combination with an existing antibiotic to treat this disease. A mouse model of M. abscessus lung disease was used to assess the efficacies of these experimental treatment regimens. Omadacycline in combination with select existing antibiotics exhibited bactericidal activity during the early phase of treatment.
脓肿分枝杆菌是一种机会性病原体,存在于结构性肺病患者中,如支气管扩张症、慢性阻塞性肺疾病和囊性纤维化。肺部脓肿分枝杆菌感染导致进行性症状和功能下降以及肺功能下降,并且通常无法用现有抗生素治愈。我们研究了一种新型四环素药物奥马环素与现有抗生素联合治疗该疾病的疗效,在脓肿分枝杆菌肺部疾病的小鼠模型中进行了研究。选择氨基糖苷类抗生素阿米卡星、大环内酯类抗生素阿奇霉素、噁二唑类抗生素贝达喹啉、碳青霉烯类抗生素比阿培南、头孢菌素类抗生素头孢西丁、氯法齐明、碳青霉烯类抗生素亚胺培南、利奈唑胺和利福布汀作为奥马环素的伴侣药物。在 4 周的治疗期间,通过检测小鼠肺部脓肿分枝杆菌的负荷来评估终点。与任何单药治疗相比,奥马环素与利奈唑胺、亚胺培南、头孢西丁、比阿培南或利福布汀联合治疗具有早期杀菌活性。使用三种脓肿分枝杆菌分离株,我们还确定了奥马环素的自发耐药频率在 1.9×10和 6.2×10之间,对奥马环素的持续耐药频率在 5.3×10和 1.3×10之间。基于这些发现,奥马环素与包含在最近治疗指南中的选择药物的联合治疗可能具有提高治疗脓肿分枝杆菌肺部疾病的效力。在美国,脓肿分枝杆菌病的发病率正在增加。这种疾病用现有抗生素很难治愈。在这项研究中,我们描述了一种新型四环素抗生素奥马环素与现有抗生素联合治疗这种疾病的疗效。使用脓肿分枝杆菌肺部疾病的小鼠模型来评估这些实验治疗方案的疗效。奥马环素与选择的现有抗生素联合治疗在治疗早期具有杀菌活性。