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Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene
INTRODUCTION: The aim of this study was to show the emergence of the qnrD gene among fluoroquinolone-resistant Morganella morganii isolate. The occurrence of mutations in DNA gyrase (gyrA and gyrB) and topoisomerase IV (parC,parE) genes was also investigated in this strain. METHODOLOGY: 95 clinical...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236555/ https://www.ncbi.nlm.nih.gov/pubmed/25106550 http://dx.doi.org/10.1186/s12941-014-0034-4 |
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author | Nasri Yaiche, Mariem Denden Rafraf, Ikbel Guo, Qinglan Mastouri, Maha Aouni, Mahjoub Wang, Minggui |
author_facet | Nasri Yaiche, Mariem Denden Rafraf, Ikbel Guo, Qinglan Mastouri, Maha Aouni, Mahjoub Wang, Minggui |
author_sort | Nasri Yaiche, Mariem |
collection | PubMed |
description | INTRODUCTION: The aim of this study was to show the emergence of the qnrD gene among fluoroquinolone-resistant Morganella morganii isolate. The occurrence of mutations in DNA gyrase (gyrA and gyrB) and topoisomerase IV (parC,parE) genes was also investigated in this strain. METHODOLOGY: 95 clinical Enterobacteria were screened for harbouring the qnrD gene. The clinical isolate of M. morganii was recovered from urine from a patient hospitalized in the urology unit at Fattouma Bourguiba Hospital, Tunisia. Antibiotic susceptibility was tested with the agar disk diffusion method. Quinolone susceptibility was studied with microbroth dilution technique. The investigations of plasmid mediated quinolone resistance (PMQR) and topoisomerases mutations were performed by polymerase chain reaction and nucleotide sequencing. RESULTS: This isolate showed high level of resistance to quinolones. The MIC with microbroth dilution technique was 512 μg/ml for norfloxacin, 256 μg/ml for ofloxacin and ciprofloxacin and 64μg/ml for levofloxacin. This strain was found to harbour the quinolone resistance determinant qnrD. In addition, this strain harboured two new gyrB mutations (S463A, S464Y) and one parC mutation (S80I). CONCLUSIONS: This is the first report in Tunisia of qnrD determinant and tow new gyrB muations in M. morganii. The nosocomial infection due to this proteeae invites further study of its epidemiologic evolution. |
format | Online Article Text |
id | pubmed-4236555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42365552014-11-19 Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene Nasri Yaiche, Mariem Denden Rafraf, Ikbel Guo, Qinglan Mastouri, Maha Aouni, Mahjoub Wang, Minggui Ann Clin Microbiol Antimicrob Research INTRODUCTION: The aim of this study was to show the emergence of the qnrD gene among fluoroquinolone-resistant Morganella morganii isolate. The occurrence of mutations in DNA gyrase (gyrA and gyrB) and topoisomerase IV (parC,parE) genes was also investigated in this strain. METHODOLOGY: 95 clinical Enterobacteria were screened for harbouring the qnrD gene. The clinical isolate of M. morganii was recovered from urine from a patient hospitalized in the urology unit at Fattouma Bourguiba Hospital, Tunisia. Antibiotic susceptibility was tested with the agar disk diffusion method. Quinolone susceptibility was studied with microbroth dilution technique. The investigations of plasmid mediated quinolone resistance (PMQR) and topoisomerases mutations were performed by polymerase chain reaction and nucleotide sequencing. RESULTS: This isolate showed high level of resistance to quinolones. The MIC with microbroth dilution technique was 512 μg/ml for norfloxacin, 256 μg/ml for ofloxacin and ciprofloxacin and 64μg/ml for levofloxacin. This strain was found to harbour the quinolone resistance determinant qnrD. In addition, this strain harboured two new gyrB mutations (S463A, S464Y) and one parC mutation (S80I). CONCLUSIONS: This is the first report in Tunisia of qnrD determinant and tow new gyrB muations in M. morganii. The nosocomial infection due to this proteeae invites further study of its epidemiologic evolution. BioMed Central 2014-08-09 /pmc/articles/PMC4236555/ /pubmed/25106550 http://dx.doi.org/10.1186/s12941-014-0034-4 Text en Copyright © 2014 Nasri Yaiche et al.; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/4.0 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 Nasri Yaiche, Mariem Denden Rafraf, Ikbel Guo, Qinglan Mastouri, Maha Aouni, Mahjoub Wang, Minggui Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene |
title | Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene |
title_full | Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene |
title_fullStr | Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene |
title_full_unstemmed | Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene |
title_short | Type II and type IV topoisomerase mutations in clinical isolates of Morganella morganii harbouring the qnrD gene |
title_sort | type ii and type iv topoisomerase mutations in clinical isolates of morganella morganii harbouring the qnrd gene |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236555/ https://www.ncbi.nlm.nih.gov/pubmed/25106550 http://dx.doi.org/10.1186/s12941-014-0034-4 |
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