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纯化亚甲蓝在溃疡分枝杆菌感染实验模型中的效果。

Effectiveness of purified methylene blue in an experimental model of Mycobacterium ulcerans infection.

机构信息

Aix-Marseille Université, INSERM, CNRS, IRD, URMITE, Marseille, France.

Aix-Marseille Université, INSERM, CNRS, IRD, URMITE, Marseille, France.

出版信息

Int J Antimicrob Agents. 2017 Mar;49(3):290-295. doi: 10.1016/j.ijantimicag.2016.11.012. Epub 2017 Jan 9.

DOI:10.1016/j.ijantimicag.2016.11.012
PMID:28131607
Abstract

Mycobacterium ulcerans is responsible for Buruli ulcer, characterised by extensive, disabling ulcers. Standard treatment combining rifampicin and streptomycin exposes patients to toxicity and daily painful injections. In this study, the in vitro susceptibilities of 3 M. ulcerans strains, 1 Mycobacterium marinum strain and 18 strains representative of eleven other Mycobacterium species and subspecies to methylene blue were determined. Whilst growth of M. ulcerans was inhibited by 0.0125 g/L methylene blue, growth of all other tested strains was not inhibited by 1 g/L methylene blue. The effectiveness of methylene blue in a murine model of M. ulcerans infection was then tested. Topical treatment by brushing a methylene blue solution on the skin lesion, systemic treatment by intraperitoneal injection of methylene blue, and a combined treatment (topical and systemic) were tested. The three treatment groups exhibited a significantly lower clinical score compared with the non-treated control group (P <0.05). Moreover, subcutaneous nodules were significantly smaller in the systemic treatment group (excluding males) (3 ± 0.7 mm) compared with the other groups (P <0.05). The M. ulcerans insertion sequence IS2404 and the KR-B gene were detected in all challenged mice, but not in negative controls. The density of M. ulcerans (mycobacteria/cell) was significantly lower in the combined treatment group compared with the other groups. These data provide evidence for the effectiveness of purified methylene blue against the initial stage of Buruli ulcer.

摘要

溃疡分枝杆菌是造成溃疡分枝杆菌溃疡的原因,其特征是广泛且使人丧失能力的溃疡。结合使用利福平(rifampicin)和链霉素(streptomycin)的标准治疗方案使患者面临毒性和每日痛苦注射的风险。在这项研究中,测定了 3 株溃疡分枝杆菌、1 株海分枝杆菌(Mycobacterium marinum)和 18 株代表 11 种其他分枝杆菌物种和亚种的菌株对亚甲蓝的体外敏感性。虽然 0.0125 g/L 的亚甲蓝抑制了溃疡分枝杆菌的生长,但 1 g/L 的亚甲蓝未抑制所有其他测试菌株的生长。然后在溃疡分枝杆菌感染的小鼠模型中测试了亚甲蓝的有效性。通过在皮肤损伤处刷涂亚甲蓝溶液进行局部治疗、通过腹腔内注射亚甲蓝进行全身治疗以及联合治疗(局部和全身)进行了测试。与未治疗的对照组相比,三组治疗组的临床评分显著降低(P <0.05)。此外,与其他组相比,全身治疗组(不包括雄性)的皮下结节明显更小(3 ± 0.7 mm)(P <0.05)。所有受挑战的小鼠中均检测到了溃疡分枝杆菌插入序列 IS2404 和 KR-B 基因,但阴性对照中未检测到。与其他组相比,联合治疗组中溃疡分枝杆菌(细菌/细胞)的密度显著降低。这些数据为纯化的亚甲蓝针对溃疡分枝杆菌溃疡的初始阶段的有效性提供了证据。

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