开发由金黄色葡萄球菌(包括耐甲氧西林菌株)引起的猪皮肤和软组织感染模型,用于测试局部抗菌剂。

Q1 Health Professions
Filip Raška, Břetislav Lipový, Šárka Kobzová, Lukáš Vacek, Rea Jarošová, Dominika Kleknerová, Katarína Matiašková, Peter Makovický, Monika Vícenová, Edita Jeklová, Roman Pantůček, Martin Faldyna, Lubomír Janda
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引用次数: 0

摘要

背景:鉴于对各种抗生素产生抗药性的葡萄球菌菌株日益增多,开发用于评估新型抗菌药物的体内模型至关重要:本文介绍了一种完全免疫功能健全的猪大面积皮肤和软组织损伤模型的开发过程,该模型适用于测试局部抗菌药物,与临床实际情况相符。该模型分三个阶段连续开发,每个阶段的方案都根据前一个阶段的结果进行了修改:在最终模型中,每头猪都在全身麻醉的情况下切除了 10 处皮肤和下层软组织,并在缺损处的基底切开筋膜,然后立即接种金黄色葡萄球菌悬浮液。一头猪没有接种,作为阴性对照。随后,在第 4、8、11 和 15 天更换绷带。在这些时间点,对每个伤口进行滤纸压印技术(FPIT),以进行半定量微生物学评估。从每头猪的伤口底部和随机选取的三个缺损的邻近完整组织中提取组织样本,进行微生物学、组织病理学和分子生物学检查。经 FPIT 和组织样本证实,在整个实验过程中,接种的金黄色葡萄球菌菌株感染充分。实验还描述了炎症标志物的动态变化和感染的临床症状:成功开发的猪模型适用于新型短效局部抗菌剂的体内试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a porcine model of skin and soft-tissue infection caused by Staphylococcus aureus, including methicillin-resistant strains suitable for testing topical antimicrobial agents.

Background: In view of the ever-increasing representation of Staphylococcus spp. strains resistant to various antibiotics, the development of in vivo models for evaluation of novel antimicrobials is of utmost importance.

Methods: In this article, we describe the development of a fully immunocompetent porcine model of extensive skin and soft tissue damage suitable for testing topical antimicrobial agents that matches the real clinical situation. The model was developed in three consecutive stages with protocols for each stage amended based on the results of the previous one.

Results: In the final model, 10 excisions of the skin and underlying soft tissue were created in each pig under general anesthesia, with additional incisions to the fascia performed at the base of the defects and immediately inoculated with Staphylococcus aureus suspension. One pig was not inoculated and used as the negative control. Subsequently, the bandages were changed on Days 4, 8, 11, and 15. At these time points, a filter paper imprint technique (FPIT) was made from each wound for semi-quantitative microbiological evaluation. Tissue samples from the base of the wound together with the adjacent intact tissue of three randomly selected defects of each pig were taken for microbiological, histopathological, and molecular-biological examination. The infection with the inoculated S. aureus strains was sufficient during the whole experiment as confirmed by both FPIT and from tissue samples. The dynamics of the inflammatory markers and clinical signs of infection are also described.

Conclusions: A successfully developed porcine model is suitable for in vivo testing of novel short-acting topical antimicrobial agents.

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CiteScore
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