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In vitro Investigation of the MexAB Efflux Pump From Pseudomonas aeruginosa
Published on: February 17, 2014
Identification of Efflux Pump Mutations in Pseudomonas aeruginosa from Clinical Samples
Sonia Quddus1, Zainab Liaqat1, Sadiq Azam1
1Centre of Biotechnology and Microbiology, University of Peshawar, Peshawar 25120, Pakistan.
Abstract:
Efflux pumps are a specialized tool of antibiotic resistance used by Pseudomonas aeruginosa to expel antibiotics. The current study was therefore conducted to examine the expression of MexAB-OprM and MexCD-OprJ efflux pump genes. In this study, 200 samples were collected from Khyber Teaching Hospital (KTH) and Hayatabad Medical Complex (HMC) in Peshawar, Pakistan. All the isolates were biochemically identified by an Analytical Profile Index kit and at the molecular level by Polymerase Chain Reaction (PCR) utilizing specific primers for the OprL gene. A total of 26 antibiotics were tested in the current study using the guidelines of the Clinical and Laboratory Standard Institute (CLSI) and high-level resistance was shown to amoxicillin-clavulanic acid (89%) and low-level to chloramphenicol (1%) by the isolates. The antibiotic-resistant efflux pump genes MexA, MexB, OprM, MexR, MexC, MexD, OprJ, and NfxB were detected in 178 amoxicillin-clavulanic acid-resistant isolates. Mutations were detected in MexA, MexB, and OprM genes but no mutation was found in the MexR gene as analyzed by I-Mutant software. Statistical analysis determined the association of antibiotics susceptibility patterns by ANOVA: Single Factor p = 0.05. The in silico mutation impact on the protein structure stability was determined via the Dynamut server, which revealed the mutations might increase the structural stability of the mutants. The docking analysis reported that MexA wild protein showed a binding energy value of -6.1 kcal/mol with meropenem and the mexA mutant (E178K) value is -6.5 kcal/mol. The mexB wild and mutant binding energy value was -5.7 kcal/mol and -8.0 kcal/mol, respectively. Efflux pumps provide resistance against a wide range of antibiotics. Determining the molecular mechanisms of resistance in P. aeruginosa regularly will contribute to the efforts against the spread of antibiotic resistance globally.
Insights
Pseudomonas aeruginosa`s MexAB-OprM and MexCD-OprJ efflux pumps confer antibiotic resistance. Mutations in MexA, MexB, and OprM genes were identified, potentially increasing protein stability and contributing to resistance against antibiotics like meropenem.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Efflux pumps are key mechanisms of antibiotic resistance in Pseudomonas aeruginosa.
- Understanding these pumps is crucial for combating antimicrobial resistance.
Purpose of the Study:
- To investigate the expression of MexAB-OprM and MexCD-OprJ efflux pump genes in Pseudomonas aeruginosa.
- To identify mutations within these efflux pump genes and assess their impact on protein stability and antibiotic binding.
Main Methods:
- Collected 200 Pseudomonas aeruginosa samples from hospitals in Peshawar, Pakistan.
- Identified isolates biochemically and molecularly using PCR.
- Tested antibiotic susceptibility against 26 antibiotics.
- Detected efflux pump genes (MexA, MexB, OprM, MexR, MexC, MexD, OprJ, NfxB) and analyzed mutations using I-Mutant and Dynamut software.
- Performed in silico docking analysis with meropenem.
Main Results:
- High-level resistance to amoxicillin-clavulanic acid (89%) and low-level resistance to chloramphenicol (1%) were observed.
- Efflux pump genes were detected in 178 amoxicillin-clavulanic acid-resistant isolates.
- Mutations were found in MexA, MexB, and OprM genes, but not in MexR.
- In silico analysis suggested mutations may increase protein structural stability.
- Docking analysis showed increased binding affinity of mexA and mexB mutants to meropenem.
Conclusions:
- MexAB-OprM and MexCD-OprJ efflux pumps play a significant role in Pseudomonas aeruginosa antibiotic resistance.
- Identified mutations in key efflux pump genes can enhance antibiotic resistance.
- Continuous monitoring of molecular resistance mechanisms is vital for global antimicrobial resistance control efforts.
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