2021•Records of Pharmaceutical and Biomedical Sciences/Records of Pharmaceutical & Biomedical SciencesOpen access

Phenotypic and genotypic characterization of Extended Spectrum β-lactamases producing Proteus mirabilis isolates.

Lamiaa A. Salama, Hazem Hamed Saleh, Shaymaa Hassan Abdel-Rhman, Rasha Fathy Barwa, Ramadan Hassan

Open full text 15 citations

Abstract

Background: The Extended spectrum β-lactamases (ESBLs) production is one of the most essential mechanism of drug resistance in Proteus mirabilis (P. mirabilis). Objective: Phenotypic and genotypic detection of extended spectrum β -lactamases production in P. mirabilis and its antimicrobial resistance among clinical isolates. Methods: A total of Sixty P. mirabilis clinical isolates were tested for Extended spectrum β lactamase production by modified double disc synergy test (MDDST). Polymerase chain reaction (PCR) was done to detect Extended spectrum β-lactamases genes in the clinical isolates. Antimicrobial susceptibility testing was done by means of Kirby Bauer disc diffusion method. Results: Out of the 60 P. mirabilis clinical isolates, 17 isolates (28.33%) were ESBL producers by phenotypic test. Genotypically; ESBLs genes were detected and the most prevalent ESBL resistance gene was TEM (91.7%) followed by SHV (75%), CTX-2-59 (56.7%) and CtxM-15 (51.7%). Moderate level of resistance to ofloxacin, ciprofloxacin, amoxicillin/ clavulanic acid, cefotaxime and ceftazidime (60.0%, 58.3%, 45.0%, 41.7% and 40.0% respectively) was recorded. In addition, 73.33% of isolates were classified as multidrug resistant (MDR). Conclusion: Monitoring of Extended spectrum β-lactamase producing P. mirabilis is very important because of its high prevalence among urinary tract infections. Also; increasing awareness for clinicians and enhancing laboratories

Open-access reader

About this research paper

What this paper is about

Background: The Extended spectrum β-lactamases (ESBLs) production is one of the most essential mechanism of drug resistance in Proteus mirabilis (P. mirabilis). Objective: Phenotypic and genotypic detection of extended spectrum β -lactamases production in P. mirabilis and its antimicrobial resistance among clinical isolates. Methods: A total of Sixty P. mirabilis clinical isolates were tested for Extended spectrum β lactamase production by modified double disc synergy test (MDDST). Polymerase chain reaction (PCR) was done to detect Extended spectrum β-lactamases genes in the clinical isolates. Antimicrobial susceptibility testing was done by means of Kirby Bauer disc diffusion method. Results: Out of the 60 P. mirabilis clinical isolates, 17 isolates (28.33%) were ESBL producers by phenotypic test. Genotypically; ESBLs genes were detected and the most prevalent ESBL resistance gene was TEM (91.7%) followed by SHV (75%), CTX-2-59 (56.7%) and CtxM-15 (51.7%). Moderate level of resistance to ofloxacin, ciprofloxacin, amoxicillin/ clavulanic acid, cefotaxime and ceftazidime (60.0%, 58.3%, 45.0%, 41.7% and 40.0% respectively) was recorded. In addition, 73.33% of isolates were classified as multidrug resistant (MDR). Conclusion: Monitoring of Extended spectrum β-lactamase producing P. mirabilis is very important because of its high prevalence among urinary tract infections. Also; increasing awareness for clinicians and enhancing laboratories

Why it matters

OpenAlex reports 15 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Background: The Extended spectrum β-lactamases (ESBLs) production is one of the most essential mechanism of drug resistance in Proteus mirabilis (P. mirabilis). Objective: Phenotypic and genotypic detection of extended spectrum β -lactamases production in P. mirabilis and its antimicrobial resistance among clinical isolates. Methods: A total of Sixty P. mirabilis clinical isolates were tested for Extended spectrum β lactamase production by modified double disc synergy test (MDDST). Polymerase chain reaction (PCR) was done to detect Extended spectrum β-lactamases genes in the clinical isolates. Antimicrobial susceptibility testing was done by means of Kirby Bauer disc diffusion method. Results: Out of the 60 P. mirabilis clinical isolates, 17 isolates (28.33%) were ESBL producers by phenotypic test. Genotypically; ESBLs genes were detected and the most prevalent ESBL resistance gene was TEM (91.7%) followed by SHV (75%), CTX-2-59 (56.7%) and CtxM-15 (51.7%). Moderate level of resistance to ofloxacin, ciprofloxacin, amoxicillin/ clavulanic acid, cefotaxime and ceftazidime (60.0%, 58.3%, 45.0%, 41.7% and 40.0% respectively) was recorded. In addition, 73.33% of isolates were classified as multidrug resistant (MDR). Conclusion: Monitoring of Extended spectrum β-lactamase producing P. mirabilis is very important because of its high prevalence among urinary tract infections. Also; increasing awareness for clinicians and enhancing laboratories

Key concepts: Proteus mirabilis, Ceftazidime, Microbiology, Cefotaxime, Clavulanic acid, Biology, Genotype, Multiple drug resistance

Related papers

Back to paper searchBrowse research topicsOriginal source
Phenotypic and genotypic characterization of Extended Spectrum β-lactamases producing Proteus mirabilis isolates. — Research Paper | ScholarLens