In Silico Screening and Experimental Validation of Novel MexAB-OprM Efflux Pump Inhibitors of Pseudomonas aeruginosa .
Suzanne M A AbdelmalekMalak HajarLuma SalahHeba Abdel-HalimPublished in: Microbial drug resistance (Larchmont, N.Y.) (2023)
The emergence of multidrug-resistant Pseudomonas aeruginosa possesses a significant public health concern. Constitutively expressed MexAB-OprM efflux pumps in P. aeruginosa significantly contribute to its resistance to a variety of antibiotics. The development of efflux pump inhibitors (EPIs) has emerged as an attractive strategy in reversing antibiotic resistance. In this study, structure-based virtual screening techniques were used for the identification of new MexAB-OprM efflux inhibitors. The predicted poses were thoroughly filtered by induced fit docking procedures followed by in vitro microbiological assays for the validation of in silico results. Two compounds, NSC-147850 and NSC-112703, were able to restore tetracycline susceptibility in MexAB-OprM overexpressing Pseudomonas aeruginosa ATCC ® 27853™ strain. This correlation observed between in silico screening and positive efflux inhibitory activity in vitro suggests that NSC-147850 and NSC-112703 have potential as EPIs and may be effective in combination therapy against drug-resistant strains of P. aeruginosa .
Keyphrases
- pseudomonas aeruginosa
- drug resistant
- acinetobacter baumannii
- multidrug resistant
- combination therapy
- cystic fibrosis
- public health
- molecular docking
- biofilm formation
- gram negative
- escherichia coli
- molecular dynamics
- klebsiella pneumoniae
- molecular dynamics simulations
- high glucose
- oxidative stress
- small molecule
- protein protein
- magnetic resonance imaging
- diabetic rats