Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, Via Pansini 5, 80131 Naples, Italy.
Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Universitario Monte S. Angelo, Via Cintia 4, 80126 Napoli, Italy.
Toxins (Basel). 2020 Jul 8;12(7):444. doi: 10.3390/toxins12070444.
Many pathogens involved in human infection have rapidly increased their antibiotic resistance, reducing the effectiveness of therapies in recent decades. Most of them can form biofilms and effective drugs are not available to treat these formations. Natural products could represent an efficient solution in discovering and developing new drugs to overcome antimicrobial resistance and treat biofilm-related infections. In this study, 20 secondary metabolites produced by pathogenic fungi of forest plants and belonging to diverse classes of naturally occurring compounds were evaluated for the first time against clinical isolates of antibiotic-resistant Gram-negative and Gram-positive bacteria. -Epoformin, sphaeropsidone, and sphaeropsidin A showed antimicrobial activity on all test strains. In particular, sphaeropsidin A was effective at low concentrations with Minimum Inhibitory Concentration (MIC) values ranging from 6.25 μg/mL to 12.5 μg/mL against all reference and clinical test strains. Furthermore, sphaeropsidin A at sub-inhibitory concentrations decreased methicillin-resistant (MRSA) and biofilm formation, as quantified by crystal violet staining. Interestingly, mixtures of sphaeropsidin A and -epoformin have shown antimicrobial synergistic effects with a concomitant reduction of cytotoxicity against human immortalized keratinocytes. Our data show that sphaeropsidin A and -epoformin possess promising antimicrobial properties.
许多与人类感染相关的病原体迅速增加了其抗生素耐药性,降低了近几十年来治疗的效果。它们大多数可以形成生物膜,而针对这些生物膜的有效药物尚不存在。天然产物可能是发现和开发新药以克服抗微生物药物耐药性并治疗生物膜相关感染的有效方法。在这项研究中,首次评估了 20 种由森林植物病原体产生的次级代谢产物,这些产物属于多种天然存在的化合物类别,针对耐抗生素的革兰氏阴性和革兰氏阳性临床分离株。-Epoformin、sphaeropsidone 和 sphaeropsidin A 对所有测试菌株均表现出抗菌活性。特别是 sphaeropsidin A 在低浓度下有效,对所有参考和临床测试菌株的最小抑菌浓度 (MIC) 值范围为 6.25 μg/mL 至 12.5 μg/mL。此外,亚抑制浓度的 sphaeropsidin A 可降低耐甲氧西林金黄色葡萄球菌 (MRSA) 和生物膜形成,这通过结晶紫染色进行定量。有趣的是,sphaeropsidin A 和 -epoformin 的混合物显示出抗菌协同作用,同时降低了对人永生化角质形成细胞的细胞毒性。我们的数据表明,sphaeropsidin A 和 -epoformin 具有有前景的抗菌特性。