Feng Jie, Shi Wanliang, Zhang Shuo, Sullivan David, Auwaerter Paul G, Zhang Ying
Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore MD, USA.
Fisher Center for Environmental Infectious Diseases, School of Medicine, Johns Hopkins University, Baltimore MD, USA.
Front Microbiol. 2016 May 23;7:743. doi: 10.3389/fmicb.2016.00743. eCollection 2016.
Although currently recommended antibiotics for Lyme disease such as doxycycline or amoxicillin cure the majority of the patients, about 10-20% of patients treated for Lyme disease may experience lingering symptoms including fatigue, pain, or joint and muscle aches. Under experimental stress conditions such as starvation or antibiotic exposure, Borrelia burgdorferi can develop round body forms, which are a type of persister bacteria that appear resistant in vitro to customary first-line antibiotics for Lyme disease. To identify more effective drugs with activity against the round body form of B. burgdorferi, we established a round body persister model induced by exposure to amoxicillin (50 μg/ml) and then screened the Food and Drug Administration drug library consisting of 1581 drug compounds and also 22 drug combinations using the SYBR Green I/propidium iodide viability assay. We identified 23 drug candidates that have higher activity against the round bodies of B. burgdorferi than either amoxicillin or doxycycline. Eleven individual drugs scored better than metronidazole and tinidazole which have been previously described to be active against round bodies. In this amoxicillin-induced round body model, some drug candidates such as daptomycin and clofazimine also displayed enhanced activity which was similar to a previous screen against stationary phase B. burgdorferi persisters not exposure to amoxicillin. Additional candidate drugs active against round bodies identified include artemisinin, ciprofloxacin, nifuroxime, fosfomycin, chlortetracycline, sulfacetamide, sulfamethoxypyridazine and sulfathiozole. Two triple drug combinations had the highest activity against amoxicillin-induced round bodies and stationary phase B. burgdorferi persisters: artemisinin/cefoperazone/doxycycline and sulfachlorpyridazine/daptomycin/doxycycline. These findings confirm and extend previous findings that certain drug combinations have superior activity against B. burgdorferi persisters in vitro, even when pre-treated with amoxicillin. These findings may have implications for improved treatment of Lyme disease.
尽管目前推荐用于治疗莱姆病的抗生素,如多西环素或阿莫西林,能治愈大多数患者,但约10%-20%接受莱姆病治疗的患者可能会出现持续症状,包括疲劳、疼痛或关节及肌肉酸痛。在饥饿或抗生素暴露等实验应激条件下,伯氏疏螺旋体可形成圆体形态,这是一种在体外对莱姆病常用一线抗生素具有耐药性的持留菌。为了鉴定对伯氏疏螺旋体圆体形态具有活性的更有效药物,我们建立了一个由阿莫西林(50μg/ml)诱导的圆体持留菌模型,然后使用SYBR Green I/碘化丙啶活力测定法筛选了由1581种药物化合物以及22种药物组合组成的美国食品药品监督管理局药物库。我们鉴定出了23种对伯氏疏螺旋体圆体形态活性高于阿莫西林或多西环素的候选药物。11种单一药物的得分优于先前已描述对圆体具有活性的甲硝唑和替硝唑。在这个阿莫西林诱导的圆体模型中,一些候选药物,如达托霉素和氯法齐明,也表现出增强的活性,这与之前针对未暴露于阿莫西林的静止期伯氏疏螺旋体持留菌的筛选结果相似。鉴定出的其他对圆体具有活性的候选药物包括青蒿素、环丙沙星、硝呋肟、磷霉素、金霉素、磺胺醋酰、磺胺甲氧嗪和磺胺噻唑。两种三联药物组合对阿莫西林诱导的圆体和静止期伯氏疏螺旋体持留菌具有最高活性:青蒿素/头孢哌酮/多西环素和磺胺氯哒嗪/达托霉素/多西环素。这些发现证实并扩展了先前的发现,即某些药物组合在体外对伯氏疏螺旋体持留菌具有卓越活性,即使在预先用阿莫西林处理后也是如此。这些发现可能对改善莱姆病的治疗具有重要意义。