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Shahanara, B., Abdus Salam, MD., Faisal Alam, KH., Nurjaham, B., Harsan, JA. Detection of extended spectrum beta- lactamase in Pseudomonas spp isolated from two tertiary hospitals in Bangladesh. 2013, BMC Research Notes, 6, 1-6.

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Article

Extended-Spectrum Beta-Lactamase and AmpC Beta-lactamase Mediated Resistance in Escherichia coli from Clinical Sources

1Department of Microbiology Faculty of Science University of Port Harcourt, Rivers State Nigeria, P.M.B. 5323 East-West Road Choba


American Journal of Microbiological Research. 2017, Vol. 5 No. 5, 107-112
DOI: 10.12691/ajmr-5-5-3
Copyright © 2017 Science and Education Publishing

Cite this paper:
Agbagwa OE, Aminofifori J. Extended-Spectrum Beta-Lactamase and AmpC Beta-lactamase Mediated Resistance in Escherichia coli from Clinical Sources. American Journal of Microbiological Research. 2017; 5(5):107-112. doi: 10.12691/ajmr-5-5-3.

Correspondence to: Agbagwa  OE, Department of Microbiology Faculty of Science University of Port Harcourt, Rivers State Nigeria, P.M.B. 5323 East-West Road Choba. Email: obakpororo.agbagwa@uniport.edu.ng

Abstract

The development of antibiotic resistance in bacteria following the introduction of antimicrobial agents has emerged as an important medical problem worldwide. Antibiotic resistance has made the treatment of infectious diseases a global challenge. The study was carried out to detect Extended Spectrum Beta-Lactamase (ESBL) and Amp C Beta-lactamase mediated resistance of Escherichia coli. Twelve isolates were collected from the University of Port Harcourt, department of Microbiology; nine out of the 12 were identified to be E. coli after series of biochemical test. Antimicrobial susceptibility testing was carried out on all the isolates using the disc diffusion method. High level of antimicrobial resistance was observed in the test organism against Augmentin and Ampicillin. ESBL preliminary screening, ESBL phenotypic confirmatory test and double disk synergy test was performed on all the isolates to detect ESBL producers. Results obtained from the study showed that 5(55.5%) out of the nine E. coli isolates were confirmed to be ESBL producers. AmpC production was detected in only one of the E. coli isolate which was from wound swab. The study revealed a high rate of ESBL- producing E. coli from clinical specimen. Further studies should be carried out using molecular method to detect ESBL genes and a wider range of E. coli from different sources should be used.

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