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Integrons and multidrug resistance across phylogenetic groups of clinical isolates of Escherichia coli
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Objective: This study was aimed to investigate the multidrug resistance patterns in clinical isolates of Escherichia coli and their correlation with integrons and phylogenetic groupings.
Methods: A total of 37 clinical E. coli isolates were evaluated for drug resistance patterns by disk diffusion method. Phylogenetic groupings and the presence of integrons among E. coli were determined by multiplex PCR assays.
Results: Multidrug resistance was identified in 84% of the clinical isolates of E. coli with higher resistance found against cephalosporins (94.6%) and fluoroquinolones (83.8%), while lower resistance was observed against polymyxins (24.3%) and carbapenems (29.7%). Metallo-β-lactamases were found in all carbapenem resistant isolates. The phylogenetic group B2 was the most dominant (40.5%), followed by groups A (35.1%), D (13.5%) and B1 (10.8%). Integrons were detected in 25 (67.6%) isolates and intI1, intI2, and intI3 genes were found in 62.2%, 18.9% and 10.8% of isolates respectively.
Conclusion: Our results show that phylogenetic classification of E. coli is not relevant with antimicrobial resistance. However, there was strong association between the integron classes and resistance against β-lactam and fluoroquinolones antimicrobials. Additionally, this study highlighted that the presence of integrons plays a crucial role in the development of multidrug resistance in clinical isolates of E. coli. Most significantly, this is the first report of detection of three classes of integron among clinical isolates of E. coli in Pakistan.
doi: https://doi.org/10.12669/pjms.40.6.8886
How to cite this: Razzaq R, Sheraz A, Arshad MM, Awan AB, Haque A. Integrons and multidrug resistance across phylogenetic groups of clinical isolates of Escherichia coli. Pak J Med Sci. 2024;40(6):1190-1195. doi: https://doi.org/10.12669/pjms.40.6.8886
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Pakistan Journal of Medical Sciences
Title: Integrons and multidrug resistance across phylogenetic groups of clinical isolates of Escherichia coli
Description:
Objective: This study was aimed to investigate the multidrug resistance patterns in clinical isolates of Escherichia coli and their correlation with integrons and phylogenetic groupings.
Methods: A total of 37 clinical E.
coli isolates were evaluated for drug resistance patterns by disk diffusion method.
Phylogenetic groupings and the presence of integrons among E.
coli were determined by multiplex PCR assays.
Results: Multidrug resistance was identified in 84% of the clinical isolates of E.
coli with higher resistance found against cephalosporins (94.
6%) and fluoroquinolones (83.
8%), while lower resistance was observed against polymyxins (24.
3%) and carbapenems (29.
7%).
Metallo-β-lactamases were found in all carbapenem resistant isolates.
The phylogenetic group B2 was the most dominant (40.
5%), followed by groups A (35.
1%), D (13.
5%) and B1 (10.
8%).
Integrons were detected in 25 (67.
6%) isolates and intI1, intI2, and intI3 genes were found in 62.
2%, 18.
9% and 10.
8% of isolates respectively.
Conclusion: Our results show that phylogenetic classification of E.
coli is not relevant with antimicrobial resistance.
However, there was strong association between the integron classes and resistance against β-lactam and fluoroquinolones antimicrobials.
Additionally, this study highlighted that the presence of integrons plays a crucial role in the development of multidrug resistance in clinical isolates of E.
coli.
Most significantly, this is the first report of detection of three classes of integron among clinical isolates of E.
coli in Pakistan.
doi: https://doi.
org/10.
12669/pjms.
40.
6.
8886
How to cite this: Razzaq R, Sheraz A, Arshad MM, Awan AB, Haque A.
Integrons and multidrug resistance across phylogenetic groups of clinical isolates of Escherichia coli.
Pak J Med Sci.
2024;40(6):1190-1195.
doi: https://doi.
org/10.
12669/pjms.
40.
6.
8886
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.
org/licenses/by/3.
0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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