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Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran

BACKGROUND: In the context of growing health concerns over antibiotic resistance, the evaluation of the minimum inhibitory concentration (MIC) of vancomycin for Streptococcus pneumoniae (S. pneumoniae) strains resistant to ceftazidime becomes important for guiding health policy makers. The aim of th...

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Autores principales: Ataee, Ramezan Ali, Habibian, Samira, Mehrabi-Tavana, Ali, Ahmadi, Zyanab, Jonaidi, Nematollah, Salesi, Mahmood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261561/
https://www.ncbi.nlm.nih.gov/pubmed/25384528
http://dx.doi.org/10.1186/s12941-014-0053-1
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author Ataee, Ramezan Ali
Habibian, Samira
Mehrabi-Tavana, Ali
Ahmadi, Zyanab
Jonaidi, Nematollah
Salesi, Mahmood
author_facet Ataee, Ramezan Ali
Habibian, Samira
Mehrabi-Tavana, Ali
Ahmadi, Zyanab
Jonaidi, Nematollah
Salesi, Mahmood
author_sort Ataee, Ramezan Ali
collection PubMed
description BACKGROUND: In the context of growing health concerns over antibiotic resistance, the evaluation of the minimum inhibitory concentration (MIC) of vancomycin for Streptococcus pneumoniae (S. pneumoniae) strains resistant to ceftazidime becomes important for guiding health policy makers. The aim of this study was to determine vancomycin MIC of ceftazidime resistant S. pneumoniae strains. METHODS: Fifty identified serotypes of ceftazidime resistant S. pneumoniae strains were included in the study. The vancomycin MIC of the above mentioned bacteria was determined based on the 0.5 McFarland standards, by using a microdilution broth and the Etest method. RESULTS: The results showed that out of 50 ceftazidime resistant strains of S. pneumoniae, 46 strains (92%) have shown a vancomycin MIC ≤0.19 − 0.1.5 μg/ml and only four strains (8%) have shown a vancomycin MIC equal to 1.5 μg/ml and the related maximum zone of inhibition was of 10 millimeter diameters. CONCLUSIONS: The results of this investigation point out the emergence of S. pneumoniae strains with a vancomycin MIC ≥1.5 μg/ml, which were resistant to ceftazidime. This finding uncovers a major health concern: a vancomycin MIC higher than 1.5 μg/ml and maximum zone of inhibition of only 10 millimeter. These findings represent an important warning for health authorities globally, concerning the treatment of patients, as the occurrence of S. pneumoniae strains with decreased vancomycin susceptibility has been demonstrated.
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spelling pubmed-42615612014-12-10 Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran Ataee, Ramezan Ali Habibian, Samira Mehrabi-Tavana, Ali Ahmadi, Zyanab Jonaidi, Nematollah Salesi, Mahmood Ann Clin Microbiol Antimicrob Research BACKGROUND: In the context of growing health concerns over antibiotic resistance, the evaluation of the minimum inhibitory concentration (MIC) of vancomycin for Streptococcus pneumoniae (S. pneumoniae) strains resistant to ceftazidime becomes important for guiding health policy makers. The aim of this study was to determine vancomycin MIC of ceftazidime resistant S. pneumoniae strains. METHODS: Fifty identified serotypes of ceftazidime resistant S. pneumoniae strains were included in the study. The vancomycin MIC of the above mentioned bacteria was determined based on the 0.5 McFarland standards, by using a microdilution broth and the Etest method. RESULTS: The results showed that out of 50 ceftazidime resistant strains of S. pneumoniae, 46 strains (92%) have shown a vancomycin MIC ≤0.19 − 0.1.5 μg/ml and only four strains (8%) have shown a vancomycin MIC equal to 1.5 μg/ml and the related maximum zone of inhibition was of 10 millimeter diameters. CONCLUSIONS: The results of this investigation point out the emergence of S. pneumoniae strains with a vancomycin MIC ≥1.5 μg/ml, which were resistant to ceftazidime. This finding uncovers a major health concern: a vancomycin MIC higher than 1.5 μg/ml and maximum zone of inhibition of only 10 millimeter. These findings represent an important warning for health authorities globally, concerning the treatment of patients, as the occurrence of S. pneumoniae strains with decreased vancomycin susceptibility has been demonstrated. BioMed Central 2014-11-11 /pmc/articles/PMC4261561/ /pubmed/25384528 http://dx.doi.org/10.1186/s12941-014-0053-1 Text en © Ataee et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ataee, Ramezan Ali
Habibian, Samira
Mehrabi-Tavana, Ali
Ahmadi, Zyanab
Jonaidi, Nematollah
Salesi, Mahmood
Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran
title Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran
title_full Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran
title_fullStr Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran
title_full_unstemmed Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran
title_short Determination of vancomycin minimum inhibitory concentration for ceftazidime resistant Streptococcus pneumoniae in Iran
title_sort determination of vancomycin minimum inhibitory concentration for ceftazidime resistant streptococcus pneumoniae in iran
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261561/
https://www.ncbi.nlm.nih.gov/pubmed/25384528
http://dx.doi.org/10.1186/s12941-014-0053-1
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