Advanced transcriptomic analysis reveals the role of efflux pumps and media composition in antibiotic responses of Pseudomonas aeruginosa.
Akanksha RajputHannah TsunemotoAnand V SastryRichard SzubinKevin RychelSiddharth M ChauhanJoe PoglianoBernhard O PalssonPublished in: Nucleic acids research (2022)
Pseudomonas aeruginosa is an opportunistic pathogen and major cause of hospital-acquired infections. The virulence of P. aeruginosa is largely determined by its transcriptional regulatory network (TRN). We used 411 transcription profiles of P. aeruginosa from diverse growth conditions to construct a quantitative TRN by identifying independently modulated sets of genes (called iModulons) and their condition-specific activity levels. The current study focused on the use of iModulons to analyze the biofilm production and antibiotic resistance of P. aeruginosa. Our analysis revealed: (i) 116 iModulons, 81 of which show strong association with known regulators; (ii) novel roles of regulators in modulating antibiotics efflux pumps; (iii) substrate-efflux pump associations; (iv) differential iModulon activity in response to beta-lactam antibiotics in bacteriological and physiological media; (v) differential activation of 'Cell Division' iModulon resulting from exposure to different beta-lactam antibiotics and (vi) a role of the PprB iModulon in the stress-induced transition from planktonic to biofilm lifestyle. In light of these results, the construction of an iModulon-based TRN provides a transcriptional regulatory basis for key aspects of P. aeruginosa infection, such as antibiotic stress responses and biofilm formation. Taken together, our results offer a novel mechanistic understanding of P. aeruginosa virulence.
Keyphrases
- pseudomonas aeruginosa
- biofilm formation
- transcription factor
- stress induced
- cystic fibrosis
- candida albicans
- staphylococcus aureus
- acinetobacter baumannii
- escherichia coli
- single cell
- gene expression
- healthcare
- metabolic syndrome
- cardiovascular disease
- genome wide identification
- physical activity
- weight loss
- genome wide
- high resolution
- dna methylation
- type diabetes
- signaling pathway
- drug induced
- heat shock protein
- cell therapy