莫匹罗星和α-蒎烯对耐甲氧西林金黄色葡萄球菌耐多药临床菌株的新型协同疗法

Puerto Rico health sciences journal Pub Date : 2024-06-01
Paulo Cáceres-Guido, Nicolás Martín-Vázquez, Adriana Ojeda-Sana, Catalina Van Baren, Ziomara Balbarrey, Silvia Moreno
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引用次数: 0

摘要

目的:莫匹罗星使用量的增加会导致莫匹罗星耐药性的产生,并与耐甲氧西林金黄色葡萄球菌(MRSA)携带者的持续存在、住院时间的延长以及卫生系统的重大经济负担有关。本研究旨在利用从儿科患者中分离的样本,研究迷迭香(原名 Rosmarinus officinalis)化合物单独使用或与莫匹罗星联用对耐多药 MRSA 的抗菌活性:方法:通过测定迷迭香精油成分单萜α-蒎烯(α-Pi)对耐多种药物的临床 MRSA 菌株的最小抑菌浓度、最小杀菌浓度(MBCs)、分数抑菌浓度指数(FICIs)和分数杀菌浓度指数,评估了迷迭香精油成分单萜α-蒎烯(α-Pi)单独或与莫匹罗星联用的体外抗菌活性。采用优化的小鼠 MRSA 感染伤口模型,测定了 α-Pi 单独使用或与莫匹罗星联用时根除 MRSA 感染的体内疗效。对小鼠皮肤样本(通过活检获得)和兔子皮肤样本进行了毒性和刺激性评估:结果:在体外和体内,α-Pi 对 MRSA 菌株都有活性,而且与莫匹罗星一起对 MRSA 菌株有协同作用。莫匹罗星-单萜组合的 FICI 值为 0.2 至 0.4,使局部莫匹罗星的 MBC 降低了 33 倍。含有α-Pi和莫匹罗星的外用制剂增强了莫匹罗星在体内MRSA感染小鼠皮肤模型中的疗效,而不会对小鼠和兔子的皮肤造成明显伤害:结论:莫匹罗星和 α-Pi 的外用制剂可能有助于开发治疗 MRSA 感染的创新药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Synergistic Combination Therapy of Mupirocin and α-Pinene Against Multidrug-Resistant Clinical Strains of Methicillin-Resistant Staphylococcus aureus.

Objective: Increased mupirocin use leads to mupirocin resistance and is associated with persistence of methicillin-resistant Staphylococcus aureus (MRSA) carriers, prolonged hospitalization, and significant economic burdens for health systems. The study aimed to investigate the antimicrobial activity of compounds of Salvia rosmarinus L. ("rosemary", formerly Rosmarinus officinalis), alone or in combination with mupirocin, against multidrug resistant MRSA using isolates obtained from pediatric patients.

Methods: The in vitro antibacterial activity of the monoterpene α-pinene (α-Pi), a rosemary essential oil constituent, alone and in combination with mupirocin, was evaluated by determining the minimum inhibitory concentrations and minimum bactericidal concentrations (MBCs) and the fractional inhibitory concentration indices (FICIs) and fractional bactericidal concentration indices against multidrug-resistant clinical MRSA strains. The in vivo efficacy of α-Pi, alone and in combination with mupirocin, to eradicate MRSA infection was determined using an optimized mouse model of MRSA-infected wounds. Mouse skin samples (obtained via biopsy) were assessed for toxicity, and rabbit skin samples for irritation.

Results: Both in vitro and in vivo, α-Pi was active against MRSA strains and acted synergistically with mupirocin against MRSA strains. Mupirocin-monoterpene combinations exhibited FICI values of 0.2 to 0.4, reducing the MBC of topical mupirocin 33-fold. A topical formulation containing α-Pi and mupirocin enhanced the efficacy of mupirocin in an in vivo MRSA-infected mouse skin model without significantly harming the skin of mice and rabbits.

Conclusions: A topical formulation combining mupirocin and α-Pi may aid in the development of innovative agents for treating MRSA infections.

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