生物膜
铜绿假单胞菌
调节器
微生物学
病菌
机会性病原体
响应调节器
多重耐药
人类病原体
流出
抗菌剂
生物
细胞外
化学
序列(生物学)
细菌
体外
抗生素耐药性
计算生物学
假单胞菌
抗药性
绿脓素
群体感应
抗生素
最小抑制浓度
胞外聚合物
肽序列
体内
作者
Himanshi Kain,Akanksha Haldiya,Mayur Sonkusare,Janhavi Tripathi,Pramodkumar P. Gupta,Anupam Jyoti,Vijay Kumar Srivastava,Vinay Sharma,Sanket Kaushik
摘要
The pathogen Pseudomonas aeruginosa (P. aeruginosa) is recognized as an international pathogen of significance due to its multidrug resistance and strong ability to create biofilm as the basis of chronic and device-associated infections. The two-component regulatory system PprAB is important in the biofilm network, where the response regulator PprB regulates binding, aggregation, and biofilm production in the extracellular environment. The current research took PprB as a probable anti-biofilm target and assessed two biogenic ligands, atropine and α-ketoglutarate, as potential inhibitory substrates. PprB was purified and structural studies were conducted to investigate ligand-binding interactions and structural stability. Conserved regulatory motifs were identified through sequence analysis and multiple sequence alignments. Biofilm inhibition, combinatory assays, antimicrobial study, fluorescence spectroscopy, and FESEM were conducted to experimentally validate the interactions and functional analysis of PprB. Collectively, our findings highlight PprB as a promising therapeutic target and demonstrate the potential of atropine and α-ketoglutarate as effective modulators of P. aeruginosa biofilm formation.
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