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Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales

BACKGROUND AND OBJECTIVES: This study was designed to determine the in vitro efficacy of mecillinam against extended spectrum beta lactamse producing Enterobacterales. MATERIALS AND METHODS: After proper permission from Ethical Review Committee of the Institute, all samples yielding growth of ESBL p...

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Autores principales: Kaleem, Fatima, Aftab, Irum, Farwa, Umme, Saleem, Hassan, Ishtiaq, Saima, Syed, Saima, Abbasi, Shahid Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723427/
https://www.ncbi.nlm.nih.gov/pubmed/36531808
http://dx.doi.org/10.18502/ijm.v14i5.10959
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author Kaleem, Fatima
Aftab, Irum
Farwa, Umme
Saleem, Hassan
Ishtiaq, Saima
Syed, Saima
Abbasi, Shahid Ahmad
author_facet Kaleem, Fatima
Aftab, Irum
Farwa, Umme
Saleem, Hassan
Ishtiaq, Saima
Syed, Saima
Abbasi, Shahid Ahmad
author_sort Kaleem, Fatima
collection PubMed
description BACKGROUND AND OBJECTIVES: This study was designed to determine the in vitro efficacy of mecillinam against extended spectrum beta lactamse producing Enterobacterales. MATERIALS AND METHODS: After proper permission from Ethical Review Committee of the Institute, all samples yielding growth of ESBL producing Enterobacterales were part of the study and were processed according to routine microbiological procedures. Routine antibiotic sensitivity testing was done on Muller Hinton Agar by Modified Kirby Bauer Method. All Gram negative isolates were subjected to concomitant detection of ESBL production by double disc synergy method. All ESBL producers were then subjected to the mecillinam Minimum Inhibitory Concentration (MIC) determination by E test. The results were interpreted as per CLSI Guidelines. RESULTS: A total of 120 ESBL producing Enterobacterales isolates were included in the study. The mean age of patients with ESBL infection was 45 ± 18.7 years. There were 44% male and 55% female patients. Majority of the ESBL producing Enterobacterales were isolated from urine samples (56%), followed by pus. Among the isolated organisms, Escherichia coli (45%) was the most frequently isolated organism followed by Klebsiella spp. (22%). Overall 83% of the isolates turned out to be sensitive to mecillinam. MIC50 of mecillinam against ESBL producing Gram negative rods (GNR) turned out to be 1 ug/ml and MIC90 turned out to be 2 ug/ml. CONCLUSION: Mecillinam shows good in vitro efficacy against ESBL producing Enterobacterales in our study. Further studies with more sample size and from diverse areas across the country should be done to evaluate its efficacy.
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spelling pubmed-97234272022-12-15 Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales Kaleem, Fatima Aftab, Irum Farwa, Umme Saleem, Hassan Ishtiaq, Saima Syed, Saima Abbasi, Shahid Ahmad Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: This study was designed to determine the in vitro efficacy of mecillinam against extended spectrum beta lactamse producing Enterobacterales. MATERIALS AND METHODS: After proper permission from Ethical Review Committee of the Institute, all samples yielding growth of ESBL producing Enterobacterales were part of the study and were processed according to routine microbiological procedures. Routine antibiotic sensitivity testing was done on Muller Hinton Agar by Modified Kirby Bauer Method. All Gram negative isolates were subjected to concomitant detection of ESBL production by double disc synergy method. All ESBL producers were then subjected to the mecillinam Minimum Inhibitory Concentration (MIC) determination by E test. The results were interpreted as per CLSI Guidelines. RESULTS: A total of 120 ESBL producing Enterobacterales isolates were included in the study. The mean age of patients with ESBL infection was 45 ± 18.7 years. There were 44% male and 55% female patients. Majority of the ESBL producing Enterobacterales were isolated from urine samples (56%), followed by pus. Among the isolated organisms, Escherichia coli (45%) was the most frequently isolated organism followed by Klebsiella spp. (22%). Overall 83% of the isolates turned out to be sensitive to mecillinam. MIC50 of mecillinam against ESBL producing Gram negative rods (GNR) turned out to be 1 ug/ml and MIC90 turned out to be 2 ug/ml. CONCLUSION: Mecillinam shows good in vitro efficacy against ESBL producing Enterobacterales in our study. Further studies with more sample size and from diverse areas across the country should be done to evaluate its efficacy. Tehran University of Medical Sciences 2022-10 /pmc/articles/PMC9723427/ /pubmed/36531808 http://dx.doi.org/10.18502/ijm.v14i5.10959 Text en Copyright © 2022 The Authors. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Kaleem, Fatima
Aftab, Irum
Farwa, Umme
Saleem, Hassan
Ishtiaq, Saima
Syed, Saima
Abbasi, Shahid Ahmad
Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales
title Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales
title_full Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales
title_fullStr Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales
title_full_unstemmed Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales
title_short Reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales
title_sort reviving the role of mecillinam against extended spectrum beta-lactamase producing enterobacterales
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723427/
https://www.ncbi.nlm.nih.gov/pubmed/36531808
http://dx.doi.org/10.18502/ijm.v14i5.10959
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