Transformation mediated transfer of Extended Spectrum Beta lactamases (ESBLs) and Sul 1 genes obtained from trimethoprim-sulfamethoxazole resistant (TSR) Escherichia coli and Pseudomonas aeruginosa clinical isolates | ||||
| Microbes and Infectious Diseases | ||||
| Article 21, Volume 5, Issue 4, November 2024, Page 1450-1460 PDF (564.09 K) | ||||
| Document Type: Original Article | ||||
| DOI: 10.21608/mid.2024.295964.1986 | ||||
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| Authors | ||||
Olivia Sochi Egbule1; Bernard Onyekweli Ejechi1; Ubreye Benjamin Uwhe-Ureghe1; Ogi Okwumabua2; Benson C IWERIEBOR   3; LC Obi* 3
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| 1Department of microbiology, Faculty of Science, Delta State University, Abraka, Nigeria | ||||
| 2Department of Pathobiological Sciences, School of Verterinary Medicine, University of Wisconsin, Madison, WI | ||||
| 3School of Science and Technology, Sefako Makgatho Health Sciences University, Ga Rankuwa, South Africa | ||||
| Abstract | ||||
| Background: Plasmid mediated Multi-Drug Resistant (MDR) Sul1 and ESBL resistance encoding genes are the major threats due to their ability to be transferred horizontally in any environment. In this study, the prevalence of Sul1 gene and ESBL coding genes (blaCTX-M, blaTEM or blaSHV) in E. coli and P. aeruginosa and determined their ability to transfer resistance through transformation. Methods: Ninety-two trimethoprim-sulfamethoxazole resistant TSR isolates belonging to E. coli and P. aeruginosa species were obtained from clinical samples such as urine, wound, and blood from patients in 3 government hospitals in Delta State, Nigeria. Resistance to antimicrobial agents was determined by disc diffusion methods. PCR amplification was performed on extracted plasmid DNAs for the detection of ESBL and Sul1 genes using specific primers. Extracted plasmid DNAs of ESBL producing and Sul1 positive isolates were used in transforming a competent E. coli K-12 adopting CaCl2 method. Results: All 92 TSR isolates were MDR with a vast majority of resistant patterns associated with the cephalosporins, amoxicillin-clavulanic acid, and the fluoroquinolones. Sul1 gene and ESBL genotypes were produced in 29.3% of E. coli and 58.7% of P. aeruginosa isolates, respectively. E. coli was more prevalent ESBL producer (75.9%) than P. aeruginosa (24.1%) and the blaCTX-M was the most prevalent gene (30.4%). Conclusion: Twenty-three isolates transferred several antibiotic resistances which includes ceftazidime, cefotaxime, cefuroxime, cefixime, gentamicin, ciprofloxacin, ofloxacin trimethoprim-sulfamethoxazole and amoxicillin-clavulanic acid, Sul1 gene and ESBL genotypes by transformation, thereby indicating a high potential for dissemination of resistance markers in hospitals. These findings are of health concern because of the rise in antimicrobial resistance associated with ESBL isolates. | ||||
| Keywords | ||||
| : Sul1 gene; Extended Spectrum β-lactamase; E. coli; P. aeruginosa; plasmid transformation | ||||
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