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Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh

OBJECTIVES: A growing incidence of pathogens producing carbapenemases has been observed in many countries including Bangladesh. The present study was carried out to determine the presence of carbapenemase producers among uropathogens. MATERIALS AND METHODS: A total of 138 Gram-negative uropathogens...

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Autores principales: Begum, Nurjahan, Shamsuzzaman, S.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442910/
https://www.ncbi.nlm.nih.gov/pubmed/28757733
http://dx.doi.org/10.1016/j.tcmj.2016.04.005
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author Begum, Nurjahan
Shamsuzzaman, S.M.
author_facet Begum, Nurjahan
Shamsuzzaman, S.M.
author_sort Begum, Nurjahan
collection PubMed
description OBJECTIVES: A growing incidence of pathogens producing carbapenemases has been observed in many countries including Bangladesh. The present study was carried out to determine the presence of carbapenemase producers among uropathogens. MATERIALS AND METHODS: A total of 138 Gram-negative uropathogens were isolated and identified by conventional methods and were screened for carbapenemase production using imipenem discs. Phenotypic identification of carbapenemase production was done by the double disc synergy test, combined disc assay, and modified Hodge test. The minimum inhibitory concentration of imipenem was determined by the agar dilution method. Genes encoding blaNDM-1, blaIMP, blaVIM, blaKPC and blaOXA-48/blaOXA-181 were identified by polymerase chain reaction. RESULTS: Twenty (14.49%) imipenem resistant strains were detected among 138 Gram-negative uro-pathogens. The most common isolates were Escherichia coli and Klebsiella spp. Among 20 imipenem resistant strains, 16 (80%) carbapenemase producers were detected by polymerase chain reaction, 13 (65%) by double disc synergy, 15 (75%) by combined disc assay, and seven (35%) by modified Hodge test. The blaNDM-1 gene was most prevalent (55%), followed by blaOXA-48/OXA-181, blaKPC (20%), blaVIM (15%), and blaIMP (10%). More than one carbapenemase gene was present in nine (45%) of the isolates. The minimum inhibitory concentration of imipenem of the carbapenemase producers ranged from ≥128 μg/mL to 4 μg/mL. Overall, carbapenemase encoding genes were detected in 11.6% (16/138) of the studied Gram-negative uropathogens. All (100%) of the carbapenemase-producing organisms were resistant to all tested antibiotics apart from colistin. CONCLUSION: The study shows a significant rate of urinary isolates were carbapenemase producers, including a high prevalence of blaNDM-1, in Bangladesh.
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spelling pubmed-54429102017-07-26 Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh Begum, Nurjahan Shamsuzzaman, S.M. Tzu Chi Med J Original Article OBJECTIVES: A growing incidence of pathogens producing carbapenemases has been observed in many countries including Bangladesh. The present study was carried out to determine the presence of carbapenemase producers among uropathogens. MATERIALS AND METHODS: A total of 138 Gram-negative uropathogens were isolated and identified by conventional methods and were screened for carbapenemase production using imipenem discs. Phenotypic identification of carbapenemase production was done by the double disc synergy test, combined disc assay, and modified Hodge test. The minimum inhibitory concentration of imipenem was determined by the agar dilution method. Genes encoding blaNDM-1, blaIMP, blaVIM, blaKPC and blaOXA-48/blaOXA-181 were identified by polymerase chain reaction. RESULTS: Twenty (14.49%) imipenem resistant strains were detected among 138 Gram-negative uro-pathogens. The most common isolates were Escherichia coli and Klebsiella spp. Among 20 imipenem resistant strains, 16 (80%) carbapenemase producers were detected by polymerase chain reaction, 13 (65%) by double disc synergy, 15 (75%) by combined disc assay, and seven (35%) by modified Hodge test. The blaNDM-1 gene was most prevalent (55%), followed by blaOXA-48/OXA-181, blaKPC (20%), blaVIM (15%), and blaIMP (10%). More than one carbapenemase gene was present in nine (45%) of the isolates. The minimum inhibitory concentration of imipenem of the carbapenemase producers ranged from ≥128 μg/mL to 4 μg/mL. Overall, carbapenemase encoding genes were detected in 11.6% (16/138) of the studied Gram-negative uropathogens. All (100%) of the carbapenemase-producing organisms were resistant to all tested antibiotics apart from colistin. CONCLUSION: The study shows a significant rate of urinary isolates were carbapenemase producers, including a high prevalence of blaNDM-1, in Bangladesh. Medknow Publications & Media Pvt Ltd 2016 2016-05-27 /pmc/articles/PMC5442910/ /pubmed/28757733 http://dx.doi.org/10.1016/j.tcmj.2016.04.005 Text en Copyright: © 2016, Buddhist Compassion Relief Tzu Chi Foundation http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Begum, Nurjahan
Shamsuzzaman, S.M.
Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh
title Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh
title_full Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh
title_fullStr Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh
title_full_unstemmed Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh
title_short Emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in Dhaka, Bangladesh
title_sort emergence of carbapenemase-producing urinary isolates at a tertiary care hospital in dhaka, bangladesh
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442910/
https://www.ncbi.nlm.nih.gov/pubmed/28757733
http://dx.doi.org/10.1016/j.tcmj.2016.04.005
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