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Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil
The objective of this study was to identify mutations in the Quinolone Resistance Determining sources Regions (QRDR) of the gyrA, gyrB, parC, and parE genes and to determine if any of the qnr variants or the aac(6′)-Ib-cr variant were present in strains of Salmonella spp. isolated in Brazil. A total...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Brazilian Society of Microbiology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833171/ https://www.ncbi.nlm.nih.gov/pubmed/24294265 http://dx.doi.org/10.1590/S1517-83822013000200046 |
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author | Ferrari, Rafaela Galiana, Antonio Cremades, Rosa Rodríguez, Juan Carlos Magnani, Marciane Tognim, M.C.B. Oliveira, Tereza C.R.M. Royo, Gloria |
author_facet | Ferrari, Rafaela Galiana, Antonio Cremades, Rosa Rodríguez, Juan Carlos Magnani, Marciane Tognim, M.C.B. Oliveira, Tereza C.R.M. Royo, Gloria |
author_sort | Ferrari, Rafaela |
collection | PubMed |
description | The objective of this study was to identify mutations in the Quinolone Resistance Determining sources Regions (QRDR) of the gyrA, gyrB, parC, and parE genes and to determine if any of the qnr variants or the aac(6′)-Ib-cr variant were present in strains of Salmonella spp. isolated in Brazil. A total of 126 Salmonella spp. strains from epidemic (n = 114) and poultry (n = 12) origin were evaluated. One hundred and twelve strains (88.8%) were resistant to nalidixic acid (NAL) and 29 (23.01%) showed a reduced susceptibility to ciprofloxacin (Cip). The mutations identified were substitutions limited to the QRDR of the gyrA gene in the codons for Serine 83, Aspartate 87 and Alanine 131. The sensitivity to NAL seems to be a good phenotypic indication of distinguishing mutated and non-mutated strains in the QRDR, however the double mutation in gyrA did not cause resistance to ciprofloxacin. The qnrA1 and qnrB19 genes were detected, respectively, in one epidemic strain of S. Enteritidis and one strain of S. Corvallis of poultry origin. Despite previous detection of qnr genes in Brazil, this is the first report of qnr gene detection in Salmonella, and also the first detection of qnrB19 gene in this country. The results alert for the continuous monitoring of quinolone resistance determinants in order to minimize the emergence and selection of Salmonella spp. strains showing reduced susceptibility or resistance to quinolones. |
format | Online Article Text |
id | pubmed-3833171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Brazilian Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-38331712013-11-30 Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil Ferrari, Rafaela Galiana, Antonio Cremades, Rosa Rodríguez, Juan Carlos Magnani, Marciane Tognim, M.C.B. Oliveira, Tereza C.R.M. Royo, Gloria Braz J Microbiol Research Paper The objective of this study was to identify mutations in the Quinolone Resistance Determining sources Regions (QRDR) of the gyrA, gyrB, parC, and parE genes and to determine if any of the qnr variants or the aac(6′)-Ib-cr variant were present in strains of Salmonella spp. isolated in Brazil. A total of 126 Salmonella spp. strains from epidemic (n = 114) and poultry (n = 12) origin were evaluated. One hundred and twelve strains (88.8%) were resistant to nalidixic acid (NAL) and 29 (23.01%) showed a reduced susceptibility to ciprofloxacin (Cip). The mutations identified were substitutions limited to the QRDR of the gyrA gene in the codons for Serine 83, Aspartate 87 and Alanine 131. The sensitivity to NAL seems to be a good phenotypic indication of distinguishing mutated and non-mutated strains in the QRDR, however the double mutation in gyrA did not cause resistance to ciprofloxacin. The qnrA1 and qnrB19 genes were detected, respectively, in one epidemic strain of S. Enteritidis and one strain of S. Corvallis of poultry origin. Despite previous detection of qnr genes in Brazil, this is the first report of qnr gene detection in Salmonella, and also the first detection of qnrB19 gene in this country. The results alert for the continuous monitoring of quinolone resistance determinants in order to minimize the emergence and selection of Salmonella spp. strains showing reduced susceptibility or resistance to quinolones. Brazilian Society of Microbiology 2013-10-30 /pmc/articles/PMC3833171/ /pubmed/24294265 http://dx.doi.org/10.1590/S1517-83822013000200046 Text en Copyright © 2013, Sociedade Brasileira de Microbiologia All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License CC BY-NC. |
spellingShingle | Research Paper Ferrari, Rafaela Galiana, Antonio Cremades, Rosa Rodríguez, Juan Carlos Magnani, Marciane Tognim, M.C.B. Oliveira, Tereza C.R.M. Royo, Gloria Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil |
title | Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil |
title_full | Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil |
title_fullStr | Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil |
title_full_unstemmed | Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil |
title_short | Plasmid-mediated quinolone resistance (PMQR) and mutations in the topoisomerase genes of Salmonella enterica strains from Brazil |
title_sort | plasmid-mediated quinolone resistance (pmqr) and mutations in the topoisomerase genes of salmonella enterica strains from brazil |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833171/ https://www.ncbi.nlm.nih.gov/pubmed/24294265 http://dx.doi.org/10.1590/S1517-83822013000200046 |
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