Lan Shihua, Chen Xiaofeng, Yin Chuanping, Xie Shengjun, Wang Shuaishuai, Deng Rongrong, Shen Zhibin
School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Guangzhou Hipower Pharmaceutical R&D Co., Ltd., Guangzhou, China.
Front Microbiol. 2023 Jan 19;14:999449. doi: 10.3389/fmicb.2023.999449. eCollection 2023.
infections are an important concern in worldwide, especially when associated with biofilms, and resistance of this agent to many drugs makes the situation even worse. We investigated the inhibitory effect of Disaspidin BB obtained from plant extracts and purifications on clinical strains and their biofilms, and preliminarily investigated its mechanism of of its anti-biofilm activity.
The broth dilution method was used to determine the minimum inhibitory concentrations (MIC) of Disaspidin BB on 11 clinical strains (MIC value of 0.63 ~ 2.5 μg/ml). SEP-05 was found to be erythromycin-resistant (MIC value>8 μg/ml) and Disaspidin BB sensitive with an MIC value of 0.63 μg/ml. The time-kill curve assay indicated that the antibacterial activity of Disaspidin BB against SEP-05 with concentration dependence. The metabolic activity and total biomass of the drug-treated SEP-05 biofilm in each stage were significantly inhibited by the crystalline violet and XTT assay, and the scavenging effect of Disaspidin BB on SEP-05 biofilm was also confirmed by SEM observation. The results of real-time quantitative PCR showed that subinhibitory concentrations Disaspidin BB can inhibit biofilm formation by affecting the expression level of key genes (, , , , ) in SEP-05 biofilm formation. In addition, the content of polysaccharides, proteins and extracellular DNA in biofilm matrix after the intervention of Disaspidin BB was significantly reduced, and it was tentatively determined that the ability of SEP-05 biofilm formation and its stability were thus disturbed.
The results show that Disaspidin BB has promising antibacterial effect on erythromycin-resistant and significant scavenging effect on its biofilm, which provides a theoretical basis for the further development of BB as a new drug for the treatment of skin infections caused by .
感染是全球范围内的一个重要问题,尤其是与生物膜相关的感染,而这种病原体对多种药物的耐药性使情况更加恶化。我们研究了从植物提取物和纯化中获得的双齿鞘氨醇BB对临床菌株及其生物膜的抑制作用,并初步研究了其抗生物膜活性的机制。
采用肉汤稀释法测定双齿鞘氨醇BB对11株临床菌株的最低抑菌浓度(MIC)(MIC值为0.63~2.5μg/ml)。发现SEP - 05对红霉素耐药(MIC值>8μg/ml),而对双齿鞘氨醇BB敏感,MIC值为0.63μg/ml。时间 - 杀菌曲线分析表明双齿鞘氨醇BB对SEP - 05的抗菌活性具有浓度依赖性。通过结晶紫和XTT分析,药物处理后的SEP - 05生物膜在各阶段的代谢活性和总生物量均受到显著抑制,扫描电子显微镜观察也证实了双齿鞘氨醇BB对SEP - 05生物膜的清除作用。实时定量PCR结果表明,亚抑菌浓度的双齿鞘氨醇BB可通过影响SEP - 05生物膜形成中关键基因(,,,,)的表达水平来抑制生物膜形成。此外,双齿鞘氨醇BB干预后生物膜基质中多糖、蛋白质和细胞外DNA的含量显著降低,初步确定SEP - 05生物膜的形成能力及其稳定性因此受到干扰。
结果表明,双齿鞘氨醇BB对耐红霉素菌株具有良好的抗菌作用,对其生物膜具有显著的清除作用,为进一步开发双齿鞘氨醇BB作为治疗由引起的皮肤感染的新药提供了理论依据。