College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.
State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun 130062, China.
Int J Mol Sci. 2024 Jul 14;25(14):7704. doi: 10.3390/ijms25147704.
The synergetic strategy has created tremendous advantages in drug-resistance bacterial infection treatment, whereas challenges related to novel compound discovery and identifying drug-binding targets still remain. The mechanisms of antimicrobial resistance involving -lactamase catalysis and the degradation of -lactam antibiotics are being revealed, with relevant therapies promising to improve the efficacy of existing major classes of antibiotics in the foreseeable future. In this study, it is demonstrated that nordalbergin, a coumarin isolated from the wood bark of , efficiently potentiated the activities of -lactam antibiotics against methicillin-resistant (MRSA) by suppressing -lactamase performance and improving the bacterial biofilm susceptibility to antibiotics. Nordalbergin was found to destabilize the cell membrane and promote its permeabilization. Moreover, nordalbergin efficiently improved the therapeutic efficacy of amoxicillin against MRSA pneumonia in mice, as supported by the lower bacterial load, attenuated pathological damage, and decreased inflammation level. These results demonstrate that nordalbergin might be a promising synergist of amoxicillin against MRSA infections. This study provided a new approach for developing potentiators for -lactam antibiotics against MRSA infections.
协同策略在耐药菌感染治疗中创造了巨大的优势,然而,与新型化合物发现和确定药物结合靶点相关的挑战仍然存在。涉及β-内酰胺酶催化和β-内酰胺抗生素降解的抗菌药物耐药机制正在被揭示,相关治疗方法有望在可预见的未来提高现有主要类别的抗生素的疗效。在这项研究中,从白皮松木材树皮中分离得到的香豆素化合物 Nordalbergin 被证明能够通过抑制β-内酰胺酶的活性和提高细菌生物膜对抗生素的敏感性,有效地增强β-内酰胺类抗生素对耐甲氧西林金黄色葡萄球菌 (MRSA) 的活性。Nordalbergin 被发现能够破坏细胞膜并促进其通透性。此外,Nordalbergin 能够有效地提高阿莫西林治疗 MRSA 肺炎的疗效,这一点得到了小鼠模型中较低的细菌负荷、减轻的病理损伤和降低的炎症水平的支持。这些结果表明,Nordalbergin 可能是一种有前途的阿莫西林与 MRSA 感染协同作用的增效剂。本研究为开发针对 MRSA 感染的β-内酰胺类抗生素增效剂提供了一种新方法。