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角鲨胺软膏对金黄色葡萄球菌皮肤定植的抑制作用在小鼠模型中的研究

Squalamine ointment for Staphylococcus aureus skin decolonization in a mouse model.

机构信息

Unité de Recherche sur les Maladies Infectieuses et Tropicales Émergentes (URMITE) UMR 6236 CNRS, Faculté de Médecine et de Pharmacie, Université de la Méditerranée, 27 boulevard Jean Moulin, 13385 Marseille 05, France.

出版信息

J Antimicrob Chemother. 2011 Jun;66(6):1306-10. doi: 10.1093/jac/dkr114. Epub 2011 Mar 29.

Abstract

OBJECTIVES

Staphylococcus aureus colonization of the skin and the nostrils remains a major cause of surgical-site infections despite preoperative and preventive procedures. To date, many compounds have been used for S. aureus decolonization, including mupirocin ointments and antiseptics, with variable results. The emergence of mupirocin-resistant S. aureus strains has led to the search for new antimicrobial agents specifically for S. aureus decolonization. In this work we evaluated squalamine and related parent-derived ointments (1%) as potential new compounds for S. aureus decolonization in a new mouse model.

METHODS

We report the development and application of squalamine and related parent-derived ointments in a new mouse skin model. After skin shaving, mice were colonized with an S. aureus suspension that was calibrated to 10⁴-10⁶ cfu/mL. The remaining bacterial load was monitored for 2 days after a single application of squalamine by spreading.

RESULTS

We found that S. aureus colonization of the skin was stable for at least 2 days before it was naturally eliminated. Using this model we found that squalamine ointment (1%) could reduce S. aureus viable cells by up to 4 log with a single, 1 h application of ointment, whereas mupirocin application reduced viable cell numbers by only 1.3 log during that same time (P < 0.05).

CONCLUSIONS

Our results suggest that such compounds may be useful for S. aureus nasal and skin decolonization and may constitute a potent alternative for skin and nasal antisepsis before surgery.

摘要

目的

尽管术前和预防措施已经实施,但金黄色葡萄球菌在皮肤和鼻腔中的定植仍然是手术部位感染的主要原因。迄今为止,已经使用了许多化合物来消除金黄色葡萄球菌的定植,包括莫匹罗星软膏和防腐剂,但结果各不相同。耐莫匹罗星金黄色葡萄球菌菌株的出现导致人们寻找专门用于金黄色葡萄球菌定植消除的新抗菌剂。在这项工作中,我们评估了鲨肝醇和相关母体衍生的软膏(1%)作为一种新的金黄色葡萄球菌定植消除的潜在新化合物,在一个新的小鼠模型中进行了评估。

方法

我们报告了鲨肝醇和相关母体衍生的软膏在一种新的小鼠皮肤模型中的开发和应用。在皮肤剃毛后,用 10⁴-10⁶ cfu/mL 校准的金黄色葡萄球菌悬浮液对小鼠进行定植。在单次涂抹鲨肝醇后,通过扩散监测 2 天内的剩余细菌负荷。

结果

我们发现金黄色葡萄球菌在皮肤中的定植至少稳定 2 天,然后才自然消除。使用该模型,我们发现鲨肝醇软膏(1%)可以在单次 1 小时的涂抹后将金黄色葡萄球菌的活菌减少多达 4 对数级,而莫匹罗星在同一时间内仅减少了 1.3 对数级的活菌数量(P<0.05)。

结论

我们的结果表明,这些化合物可能对金黄色葡萄球菌的鼻腔和皮肤定植有用,并且可能是手术前皮肤和鼻腔消毒的有效替代物。

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