Lin Hang, Zhou Cui, Yu Kai-Hang, Lin Yi-Shuai, Wang Ling-Bo, Zhang Ying, Liu Shi-Xing, Xu Wen-Ya, Sun Yao, Zhou Tie-Li, Cao Jian-Ming, Ye Jian-Zhong
Department of Clinical Laboratory, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province, People's Republic of China.
School of the First Clinical Medical Sciences, Wenhzou Medical University, Wenzhou, Zhejiang Province, People's Republic of China.
Infect Drug Resist. 2023 Aug 30;16:5697-5705. doi: 10.2147/IDR.S417751. eCollection 2023.
is a hazardous bacterium that causes hospital-acquired nosocomial infections, and the advent of multidrug-resistant (MDR-AB) strains is concerning. Novel antibacterial therapeutic strategies must be developed. The biological effects of glabridin on MDR-AB were investigated in this study.
The minimum inhibitory concentrations (MICs) of glabridin against eight clinical MDR-AB strains were determined using the broth microdilution technique. Crystal violet staining was used to assess biofilm development, which has significant contribution to bacterial resistance. Swarming motility was measured according to surface growth zone of MDR-AB on LB agar medium. qRT-PCR was used to evaluate the expression of quorum sensing genes and . Glabridin and routinely used therapeutic antimicrobial agents were tested for synergistic action using the checkerboard method.
According to our findings, glabridin suppressed MDR-AB growth at high doses (512-1024 μg/mL). The 1/4 MIC of glabridin significantly decreased MDR-AB biofilm formation by 19.98% ( < 0.05), inhibited MDR-AB motility by 44.27% ( < 0.05), whereas the 1/2 MIC of glabridin dramatically reduced MDR-AB biofilm development by 27.43% ( < 0.01), suppressed MDR-AB motility by 50.64% ( < 0.05). Mechanistically, glabridin substantially downregulated the expression of quorum sensing-related genes and by up to 39.12% (P < 0.001) and 25.19% (P < 0.01), respectively. However, no synergistic effect between glabridin and antibacterial drugs was found.
Glabridin might be a quorum sensing inhibitor that inhibits MDR-AB biofilm development and swarming motility.
鲍曼不动杆菌是一种可导致医院获得性感染的有害细菌,多重耐药鲍曼不动杆菌(MDR-AB)菌株的出现令人担忧。必须开发新的抗菌治疗策略。本研究调查了光甘草定对MDR-AB的生物学效应。
采用肉汤微量稀释技术测定光甘草定对8株临床MDR-AB菌株的最低抑菌浓度(MIC)。采用结晶紫染色评估生物膜形成,生物膜形成对细菌耐药性有重要影响。根据MDR-AB在LB琼脂培养基上的表面生长区域测量群游运动能力。采用qRT-PCR评估群体感应基因和的表达。使用棋盘法测试光甘草定与常规使用的治疗性抗菌药物的协同作用。
根据我们的研究结果,高剂量(512-1024μg/mL)的光甘草定可抑制MDR-AB生长。光甘草定的1/4 MIC可使MDR-AB生物膜形成显著降低19.98%(P<0.05),抑制MDR-AB运动能力44.27%(P<0.05),而光甘草定的1/2 MIC可使MDR-AB生物膜形成显著降低27.43%(P<0.01),抑制MDR-AB运动能力50.64%(P<0.05)。从机制上讲,光甘草定可使群体感应相关基因和的表达分别显著下调高达39.12%(P<0.001)和25.19%(P<0.01)。然而,未发现光甘草定与抗菌药物之间有协同作用。
光甘草定可能是一种群体感应抑制剂,可抑制MDR-AB生物膜形成和群游运动能力。