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Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain

BACKGROUND: Enterobacteriaceae with AmpC β-lactamase are multidrug-resistant organisms and represent a significant challenge to patient care. This study aims to determine the prevalence of plasmid-derived AmpC β-lactamase among extended spectrum β-lactamases (ESBL)-producing Enterobacteriaceae strai...

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Autores principales: Joji, Ronni Mol, Al-Mahameed, Ali Ebrahim, Jishi, Thamer Al, Fatani, Dania Ismail, Saeed, Nermin K., Jaradat, Ahmed, Ezzat, Hicham, Bindayna, Khalid Mubarak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388573/
https://www.ncbi.nlm.nih.gov/pubmed/34484445
http://dx.doi.org/10.4103/atm.ATM_523_20
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author Joji, Ronni Mol
Al-Mahameed, Ali Ebrahim
Jishi, Thamer Al
Fatani, Dania Ismail
Saeed, Nermin K.
Jaradat, Ahmed
Ezzat, Hicham
Bindayna, Khalid Mubarak
author_facet Joji, Ronni Mol
Al-Mahameed, Ali Ebrahim
Jishi, Thamer Al
Fatani, Dania Ismail
Saeed, Nermin K.
Jaradat, Ahmed
Ezzat, Hicham
Bindayna, Khalid Mubarak
author_sort Joji, Ronni Mol
collection PubMed
description BACKGROUND: Enterobacteriaceae with AmpC β-lactamase are multidrug-resistant organisms and represent a significant challenge to patient care. This study aims to determine the prevalence of plasmid-derived AmpC β-lactamase among extended spectrum β-lactamases (ESBL)-producing Enterobacteriaceae strains in Bahrain. METHODS: It was a cross-sectional study. A total of 185 ESBL-producing Enterobacteriaceae isolates were recovered from clinically significant specimens from January 2018 to December 2019. The samples underwent initial screen for cefoxitin resistance by disc diffusion test and subsequent phenotypic confirmation of AmpC production with phenyl boronic acid assays as well as genotypic analysis by multiplex polymerase chain reactions for AmpC subtypes. Drug-resistant features of these clinical isolates were also examined. RESULTS: Twenty-nine ESBL-producing Enterobacteriaceae isolates were cefoxitin resistant. Phenotypic and genotypic analyses confirmed that 8 and 12 cefoxitin-resistant isolates are AmpC positive, respectively. These AmpC producers are multidrug resistant, and Escherichia coli is the dominant strain among them. CONCLUSIONS: Plasmid-mediated spread of AmpC is present in clinically relevant Enterobacteriaceae species in Bahrain. Rational antimicrobial therapy against these multidrug-resistant organisms and continued surveillance of antimicrobial resistance mechanisms among the clinical isolates are recommended for optimal patient care.
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spelling pubmed-83885732021-09-03 Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain Joji, Ronni Mol Al-Mahameed, Ali Ebrahim Jishi, Thamer Al Fatani, Dania Ismail Saeed, Nermin K. Jaradat, Ahmed Ezzat, Hicham Bindayna, Khalid Mubarak Ann Thorac Med Original Article BACKGROUND: Enterobacteriaceae with AmpC β-lactamase are multidrug-resistant organisms and represent a significant challenge to patient care. This study aims to determine the prevalence of plasmid-derived AmpC β-lactamase among extended spectrum β-lactamases (ESBL)-producing Enterobacteriaceae strains in Bahrain. METHODS: It was a cross-sectional study. A total of 185 ESBL-producing Enterobacteriaceae isolates were recovered from clinically significant specimens from January 2018 to December 2019. The samples underwent initial screen for cefoxitin resistance by disc diffusion test and subsequent phenotypic confirmation of AmpC production with phenyl boronic acid assays as well as genotypic analysis by multiplex polymerase chain reactions for AmpC subtypes. Drug-resistant features of these clinical isolates were also examined. RESULTS: Twenty-nine ESBL-producing Enterobacteriaceae isolates were cefoxitin resistant. Phenotypic and genotypic analyses confirmed that 8 and 12 cefoxitin-resistant isolates are AmpC positive, respectively. These AmpC producers are multidrug resistant, and Escherichia coli is the dominant strain among them. CONCLUSIONS: Plasmid-mediated spread of AmpC is present in clinically relevant Enterobacteriaceae species in Bahrain. Rational antimicrobial therapy against these multidrug-resistant organisms and continued surveillance of antimicrobial resistance mechanisms among the clinical isolates are recommended for optimal patient care. Wolters Kluwer - Medknow 2021 2021-02-19 /pmc/articles/PMC8388573/ /pubmed/34484445 http://dx.doi.org/10.4103/atm.ATM_523_20 Text en Copyright: © 2021 Annals of Thoracic Medicine https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Joji, Ronni Mol
Al-Mahameed, Ali Ebrahim
Jishi, Thamer Al
Fatani, Dania Ismail
Saeed, Nermin K.
Jaradat, Ahmed
Ezzat, Hicham
Bindayna, Khalid Mubarak
Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain
title Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain
title_full Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain
title_fullStr Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain
title_full_unstemmed Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain
title_short Molecular detection of plasmid-derived AmpC β-lactamase among clinical strains of Enterobacteriaceae in Bahrain
title_sort molecular detection of plasmid-derived ampc β-lactamase among clinical strains of enterobacteriaceae in bahrain
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388573/
https://www.ncbi.nlm.nih.gov/pubmed/34484445
http://dx.doi.org/10.4103/atm.ATM_523_20
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