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新型齐墩果酸和山楂酸衍生物有望治疗医院感染中的细菌生物膜:一项体外和体内研究

Novel Oleanolic and Maslinic Acid Derivatives as a Promising Treatment against Bacterial Biofilm in Nosocomial Infections: An in Vitro and in Vivo Study.

作者信息

Blanco-Cabra Núria, Vega-Granados Karina, Moya-Andérico Laura, Vukomanovic Marija, Parra Andrés, Álvarez de Cienfuegos Luis, Torrents Eduard

机构信息

Bacterial Infections and Antimicrobial Therapies Group , Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST) , Baldiri Reixac 15-21 , 08028 Barcelona , Spain.

Department of Organic Chemistry, Faculty of Science , University of Granada , Campus Universitario Fuentenueva s/n, 18071 Granada , Spain.

出版信息

ACS Infect Dis. 2019 Sep 13;5(9):1581-1589. doi: 10.1021/acsinfecdis.9b00125. Epub 2019 Jul 16.

Abstract

Oleanolic acid (OA) and maslinic acid (MA) are pentacyclic triterpenic compounds that abound in industrial olive oil waste. These compounds have renowned antimicrobial properties and lack cytotoxicity in eukaryotic cells as well as resistance mechanisms in bacteria. Despite these advantages, their antimicrobial activity has only been tested in vitro, and derivatives improving this activity have not been reported. In this work, a set of 14 OA and MA C-28 amide derivatives have been synthesized. Two of these derivatives, MA-HDA and OA-HDA, increase the in vitro antimicrobial activity of the parent compounds while reducing their toxicity in most of the Gram-positive bacteria tested, including a methicillin-resistant -MRSA. MA-HDA also shows an enhanced in vivo efficacy in a invertebrate animal model of infection. A preliminary attempt to elucidate their mechanism of action revealed that these compounds are able to penetrate and damage the bacterial cell membrane. More significantly, their capacity to reduce antibiofilm formation in catheters has also been demonstrated in two sets of conditions: a static and a more challenged continuous-flow biofilm.

摘要

齐墩果酸(OA)和山楂酸(MA)是五环三萜类化合物,大量存在于工业橄榄油废料中。这些化合物具有显著的抗菌特性,在真核细胞中缺乏细胞毒性,在细菌中也不存在耐药机制。尽管有这些优点,它们的抗菌活性仅在体外进行了测试,且尚未有提高这种活性的衍生物的报道。在这项工作中,合成了一组14种OA和MA的C-28酰胺衍生物。其中两种衍生物,MA-HDA和OA-HDA,提高了母体化合物的体外抗菌活性,同时降低了它们在大多数测试的革兰氏阳性菌中的毒性,包括耐甲氧西林金黄色葡萄球菌(MRSA)。MA-HDA在无脊椎动物感染模型中也显示出增强的体内疗效。初步尝试阐明它们的作用机制表明,这些化合物能够穿透并损伤细菌细胞膜。更重要的是,在两组条件下也证明了它们减少导管中生物膜形成的能力:静态和更具挑战性的连续流生物膜。

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