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Antibiotic resistance pattern in Pseudomonas aeruginosa strains isolated from clinical specimens 

Antibiotic resistance pattern in Pseudomonas aeruginosa strains isolated from clinical specimens 

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Introduction and Objectives: Pseudomonas aeruginosa is an opportunistic human pathogen which causes serious problems especially in people who have immunodeficiency. This pathogen is intrinsically resistant to many antibacterial agents. The aim of this study was to detect and survey the antibiotic resistance pattern of Pseudomonas (P.) aeruginosa st...

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... Such infections are especially difficult to treat because of emerging antibiotic resistant strains, a trend that could be attributed to selective pressures from antibiotic treatment, as well as the organism's intrinsic ability to adapt to drug-stressed environments (17,18). P. aeruginosa can persist during feast, famine, and stress conditions such as nutrient limitation, antibiotics, heat, osmotic, and high pH in many different environments (2). ...
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Background: Sigma factors are proteins that regulate transcription in bacteria. Sigma factors can be activated in response to different environmental conditions. The rpoS (RNA polymerase, sigma S) gene encodes sigma-38 (σ38, or RpoS), a 37.8 kDa protein in Pseudomonas aeruginosa (P. aeruginosa) strains. RpoS is a central regulator of the general stress response and operates in both retroactive and proactive manners; not only does it allow the cell to survive environmental challenges; it also prepares the cell for subsequent stresses (cross-protection). Methods: The significance of RpoS for stress resistance and protein expression in stationary-phase P. aeruginosa cells was assessed. The goal of the current study was to characterize RpoS of P. aeruginosa PAO1 using bioinformatics tools. Results: The results showed that RpoS is an unstable protein that belongs to the sigma-70 factor family. Secondary structure analysis predicted that random coil is the predominant structure followed by extended alpha helix. The three-dimensional (3D) structure was modeled using SWISS-MODEL Workspace. Conclusion: Determination of sequence, function, structure, and predicted epitopes of RpoS is important for modeling of inhibitors that will help in the design of new drugs to combat multi-drug-resistant (MDR) strains. Such information may aid in the development of new diagnostic tools, drugs, and vaccines for treatment in endemic regions.