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联合用药消除体外伯氏疏螺旋体持续感染:达托霉素联合头孢哌酮和多西环素可实现完全清除。

Drug combinations against Borrelia burgdorferi persisters in vitro: eradication achieved by using daptomycin, cefoperazone and doxycycline.

机构信息

Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, United States of America.

Fisher Center for Environmental Infectious Diseases, School of Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America.

出版信息

PLoS One. 2015 Mar 25;10(3):e0117207. doi: 10.1371/journal.pone.0117207. eCollection 2015.

Abstract

Although most Lyme disease patients can be cured with antibiotics doxycycline or amoxicillin using 2-4 week treatment durations, some patients suffer from persistent arthritis or post-treatment Lyme disease syndrome. Why these phenomena occur is unclear, but possibilities include host responses, antigenic debris, or B. burgdorferi organisms remaining despite antibiotic therapy. In vitro, B. burgdorferi developed increasing antibiotic tolerance as morphology changed from typical spirochetal form in log phase growth to variant round body and microcolony forms in stationary phase. B. burgdorferi appeared to have higher persister frequencies than E. coli as a control as measured by SYBR Green I/propidium iodide (PI) viability stain and microscope counting. To more effectively eradicate the different persister forms tolerant to doxycycline or amoxicillin, drug combinations were studied using previously identified drugs from an FDA-approved drug library with high activity against such persisters. Using a SYBR Green/PI viability assay, daptomycin-containing drug combinations were the most effective. Of studied drugs, daptomycin was the common element in the most active regimens when combined with doxycycline plus either beta-lactams (cefoperazone or carbenicillin) or an energy inhibitor (clofazimine). Daptomycin plus doxycycline and cefoperazone eradicated the most resistant microcolony form of B. burgdorferi persisters and did not yield viable spirochetes upon subculturing, suggesting durable killing that was not achieved by any other two or three drug combinations. These findings may have implications for improved treatment of Lyme disease, if persistent organisms or detritus are responsible for symptoms that do not resolve with conventional therapy. Further studies are needed to validate whether such combination antimicrobial approaches are useful in animal models and human infection.

摘要

虽然大多数莱姆病患者可以通过使用 2-4 周疗程的抗生素多西环素或阿莫西林治愈,但有些患者患有持续性关节炎或治疗后莱姆病综合征。为什么会出现这些现象尚不清楚,但可能性包括宿主反应、抗原碎片或尽管经过抗生素治疗但仍存在的 B. burgdorferi 生物体。在体外,B. burgdorferi 在形态从对数生长期的典型螺旋体形式变为静止期的变体圆形体和微菌落形式时,表现出越来越强的抗生素耐药性。与作为对照的大肠杆菌相比,B. burgdorferi 似乎具有更高的持久性频率,如通过 SYBR Green I/碘化丙啶 (PI) 活力染色和显微镜计数测量的那样。为了更有效地消除对多西环素或阿莫西林具有耐药性的不同持久性形式,研究了使用先前从具有针对此类持久性菌高活性的 FDA 批准药物库中鉴定出的药物进行药物组合。使用 SYBR Green/PI 活力测定法,含达托霉素的药物组合最有效。在所研究的药物中,当与多西环素联合使用时,达托霉素是与β-内酰胺(头孢哌酮或羧苄西林)或能量抑制剂(氯法齐明)联合使用的最有效方案中的共同元素。达托霉素联合多西环素和头孢哌酮根除了最耐药的 B. burgdorferi 持久性微菌落形式,并且在传代培养后没有产生有活力的螺旋体,这表明持久的杀伤作用是任何其他两种或三种药物组合都无法实现的。如果持续存在的生物体或残余物是导致常规治疗无法解决的症状的原因,这些发现可能对改善莱姆病的治疗有影响。需要进一步的研究来验证这种联合抗菌方法在动物模型和人类感染中的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d244/4373819/875d9e414a16/pone.0117207.g001.jpg

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