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Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases

BACKGROUND: Resistance to contemporary broad-spectrum β-lactams, mediated by extended-spectrum β-lactamases (ESBL), is an increasing problem worldwide. Many of the emerging antimicrobial resistance problems of this decade have been characterized by difficulty in the recognition of resistance in the...

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Autores principales: Cagatay, Atahan A, Kocagoz, Tanil, Eraksoy, Haluk
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC222987/
https://www.ncbi.nlm.nih.gov/pubmed/14511397
http://dx.doi.org/10.1186/1471-2334-3-22
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author Cagatay, Atahan A
Kocagoz, Tanil
Eraksoy, Haluk
author_facet Cagatay, Atahan A
Kocagoz, Tanil
Eraksoy, Haluk
author_sort Cagatay, Atahan A
collection PubMed
description BACKGROUND: Resistance to contemporary broad-spectrum β-lactams, mediated by extended-spectrum β-lactamases (ESBL), is an increasing problem worldwide. Many of the emerging antimicrobial resistance problems of this decade have been characterized by difficulty in the recognition of resistance in the laboratory, particularly by rapid susceptibility test methods. The plasmid-encoded ESBL represent such a resistance phenomenon that is difficult to recognize. We compared Dio-Sensimedia-ES (DSM-ES; Diomed, Istanbul, Turkey) and Mueller-Hinton (MH) agar in the double-disk synergy test (DDST) as a novel rapid system for detecting ESBL directly from bacterial culture. METHODS: Sixty ESBL-producing Klebsiella pneumoniae isolates cultured from blood (30), endotracheal aspirates (20), urine (5) and pus (5), as well as 40 Escherichia coli isolates cultured from endotracheal aspirates (15), urine (10), blood (8) and pus (7) were studied. Isolates positive for ESBL by the combined disk tests were tested with the DDST using MH and DSM-ES agar to detect ESBL-mediated resistance in K. pneumoniae and E. coli. DSM-ES agar was also used to determine the susceptibility of Enterobacteriaceae and staphylococci. RESULTS: Among 60 ESBL-producing K. pneumoniae isolates, 59 (98.3%) were identified as ESBL-positive by the DDST using MH, and 58 (96.6%), using DSM-ES agar. Of 40 ESBL-producing E. coli isolates, 38 (95%) were ESBL-positive by the DDST on MH agar, and 37 (92.5%), on DSM-ES agar. The average incubation period required for ESBL detection by the DDST on DSM-ES agar was 4 hours. CONCLUSIONS: Since the DDST results were available within 4 hours when DSM-ES agar was used, the use of this media may significantly lower the length of hospital stay, the total cost for patient care and even the mortality rate by fascilitating early treatment against ESBL-producing organisms.
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spelling pubmed-2229872003-10-24 Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases Cagatay, Atahan A Kocagoz, Tanil Eraksoy, Haluk BMC Infect Dis Research Article BACKGROUND: Resistance to contemporary broad-spectrum β-lactams, mediated by extended-spectrum β-lactamases (ESBL), is an increasing problem worldwide. Many of the emerging antimicrobial resistance problems of this decade have been characterized by difficulty in the recognition of resistance in the laboratory, particularly by rapid susceptibility test methods. The plasmid-encoded ESBL represent such a resistance phenomenon that is difficult to recognize. We compared Dio-Sensimedia-ES (DSM-ES; Diomed, Istanbul, Turkey) and Mueller-Hinton (MH) agar in the double-disk synergy test (DDST) as a novel rapid system for detecting ESBL directly from bacterial culture. METHODS: Sixty ESBL-producing Klebsiella pneumoniae isolates cultured from blood (30), endotracheal aspirates (20), urine (5) and pus (5), as well as 40 Escherichia coli isolates cultured from endotracheal aspirates (15), urine (10), blood (8) and pus (7) were studied. Isolates positive for ESBL by the combined disk tests were tested with the DDST using MH and DSM-ES agar to detect ESBL-mediated resistance in K. pneumoniae and E. coli. DSM-ES agar was also used to determine the susceptibility of Enterobacteriaceae and staphylococci. RESULTS: Among 60 ESBL-producing K. pneumoniae isolates, 59 (98.3%) were identified as ESBL-positive by the DDST using MH, and 58 (96.6%), using DSM-ES agar. Of 40 ESBL-producing E. coli isolates, 38 (95%) were ESBL-positive by the DDST on MH agar, and 37 (92.5%), on DSM-ES agar. The average incubation period required for ESBL detection by the DDST on DSM-ES agar was 4 hours. CONCLUSIONS: Since the DDST results were available within 4 hours when DSM-ES agar was used, the use of this media may significantly lower the length of hospital stay, the total cost for patient care and even the mortality rate by fascilitating early treatment against ESBL-producing organisms. BioMed Central 2003-09-25 /pmc/articles/PMC222987/ /pubmed/14511397 http://dx.doi.org/10.1186/1471-2334-3-22 Text en Copyright © 2003 Cagatay et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Cagatay, Atahan A
Kocagoz, Tanil
Eraksoy, Haluk
Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
title Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
title_full Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
title_fullStr Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
title_full_unstemmed Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
title_short Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
title_sort dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC222987/
https://www.ncbi.nlm.nih.gov/pubmed/14511397
http://dx.doi.org/10.1186/1471-2334-3-22
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