Qiu Zhilang, Ran Jun, Yang Yifan, Wang Yue, Zeng Yang, Jiang Yinhui, Hu Zuquan, Zeng Zhu, Peng Jian
Key Laboratory of Infectious Immune and Antibody Engineering of Guizhou Province, Cellular Immunotherapy Engineering Research Center of Guizhou Province, School of Biology and Engineering/School of Basic Medical Sciences, Guizhou Medical University, Guiyang, Guizhou, 550025, People's Republic of China.
The Engineering Research Center of Health Medicine Biotechnology of Institution of Higher Education of Guizhou Province, Guizhou Medical University, Guiyang, Guizhou, 550025, People's Republic of China.
Drug Des Devel Ther. 2024 Dec 7;18:5795-5810. doi: 10.2147/DDDT.S481225. eCollection 2024.
The emergence of carbapenem-resistant (CRAB) poses great difficulties in clinical treatment, and has been listed by the World Health Organization as a class of pathogens in urgent need of new antibiotic development. In our previous report, the novel antimicrobial peptide Cec4 showed great potential in decreasing the clinical CRAB biofilm, but its mechanism of action is still illusive. Therefore, in order to evaluate the clinical therapeutic potential of Cec4, it is necessary to explore the mechanism of how Cec4 decreases mature biofilms.
Key genes involved in the removal of CRAB biofilms by Cec4 were analyzed using transcriptomics. Based on the results of the bioinformatics analysis, the CRISPR-Cas9 method was used to construct the deletion strain of the key gene. The pYMAb2 plasmid was used for the complementation strain construction. Finally, the roles of key genes in biofilm removal by Cec4 were determined by crystal violet staining, podocyte staining, laser confocal imaging, and MBC and MBEC.
Combined with transcriptome analysis, we hypothesized that is a key gene involved in the removal of CRAB biofilms by Cec4. Deletion of the gene did not affect growth, but decreased capsule thickness, increasing biofilm production, and made biofilm-state more sensitive to Cec4.
Cec4 decreases biofilms formed by CRAB targeting . Deletion of the gene results in an increase in biofilms and greater sensitivity to Cec4, which enhances the removal of biofilms by Cec4.
耐碳青霉烯类鲍曼不动杆菌(CRAB)的出现给临床治疗带来了巨大困难,已被世界卫生组织列为急需开发新型抗生素的一类病原体。在我们之前的报告中,新型抗菌肽Cec4在减少临床CRAB生物膜方面显示出巨大潜力,但其作用机制仍不清楚。因此,为了评估Cec4的临床治疗潜力,有必要探索Cec4如何减少成熟生物膜的机制。
利用转录组学分析参与Cec4去除CRAB生物膜的关键基因。基于生物信息学分析结果,采用CRISPR-Cas9方法构建关键基因的缺失菌株。使用pYMAb2质粒构建互补菌株。最后,通过结晶紫染色、足细胞染色、激光共聚焦成像以及MBC和MBEC测定关键基因在Cec4去除生物膜中的作用。
结合转录组分析,我们推测[具体基因名称]是参与Cec4去除CRAB生物膜的关键基因。缺失该基因不影响[细菌名称]生长,但会降低[细菌名称]荚膜厚度,增加生物膜产生,并使生物膜状态的[细菌名称]对Cec4更敏感。
Cec4通过靶向[具体基因名称]减少CRAB形成的生物膜。缺失该基因会导致生物膜增加且对Cec4更敏感,从而增强Cec4对[细菌名称]生物膜的去除作用。