Moshynets Olena V, Baranovskyi Taras P, Iungin Olga S, Krikunov Alexey A, Potochilova Viktoria V, Rudnieva Kateryna L, Potters Geert, Pokholenko Ianina
Biofilm Study Group, Department of Cell Regulatory Mechanisms, Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Zabolotnoho Str. 150, 03680 Kyiv, Ukraine.
CeMM, Research Center for Molecular Medicine of the Austrian Academy of Sciences, Lazarettgasse 14, A-1090 Vienna, Austria.
Antibiotics (Basel). 2023 Feb 1;12(2):293. doi: 10.3390/antibiotics12020293.
A therapeutic combination of azithromycin (AZM) and colistin methanesulfonate (CMS) was shown to be effective against both non-PDR and PDR biofilms in vitro. These anti-biofilm effects, however, may not correlate with effects observed in standard plate assays, nor will they representative of in vivo therapeutic action. After all, biofilm-associated infection processes are also impacted by the presence of wound bed components, such as host cells or wound fluids, which can all affect the antibiotic effectiveness. Therefore, an in vitro wound model of biofilm infection which partially mimics the complex microenvironment of infected wounds was developed to investigate the therapeutic potential of an AZM-CMS combination against XDR isolates. The model consists of a 3D collagen sponge-like scaffold seeded with HEK293 cells submerged in a fluid milieu mimicking the wound bed exudate. Media that were tested were all based on different strengths of Dulbecco's modified Eagles/high glucose medium supplemented with fetal bovine serum, and/or Bacto Proteose peptone. Use of this model confirmed AZM to be a highly effective antibiofilm component, when applied alone or in combination with CMS, whereas CMS alone had little antibacterial effectiveness or even stimulated biofilm development. The wound model proposed here proves therefore, to be an effective aid in the study of drug combinations under realistic conditions.
阿奇霉素(AZM)和粘菌素甲磺酸盐(CMS)的治疗组合在体外对非泛耐药和泛耐药生物膜均显示出有效性。然而,这些抗生物膜作用可能与标准平板试验中观察到的效果不相关,也不能代表体内治疗作用。毕竟,生物膜相关感染过程还受到伤口床成分(如宿主细胞或伤口液体)的影响,这些都可能影响抗生素的有效性。因此,开发了一种部分模拟感染伤口复杂微环境的生物膜感染体外伤口模型,以研究AZM-CMS组合对广泛耐药菌株的治疗潜力。该模型由一个三维胶原海绵状支架组成,接种有HEK293细胞,浸没在模拟伤口床渗出液的液体环境中。所测试的培养基均基于不同浓度的杜氏改良伊格尔氏/高糖培养基,并添加胎牛血清和/或细菌蛋白胨。使用该模型证实,单独使用AZM或与CMS联合使用时,AZM是一种高效的抗生物膜成分,而单独使用CMS几乎没有抗菌效果,甚至会刺激生物膜的形成。因此,这里提出的伤口模型被证明是在实际条件下研究药物组合的有效辅助工具。