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Characterization of plasmids harbouring qnrS1, qnrB2 and qnrB19 genes in Salmonella
被引:231
作者:

Garcia-Fernandez, Aurora
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h-index: 0
机构:
Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy

Fortini, Daniela
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Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy

Veldman, Kees
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h-index: 0
机构:
Wageningen UR, Cent Vet Inst, NL-8203 AA Lelystad, Netherlands Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy

Mevius, Dik
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机构:
Wageningen UR, Cent Vet Inst, NL-8203 AA Lelystad, Netherlands
Univ Utrecht, Fac Vet Med, Utrecht, Netherlands Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy

Carattoli, Alessandra
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h-index: 0
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Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy
机构:
[1] Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy
[2] Wageningen UR, Cent Vet Inst, NL-8203 AA Lelystad, Netherlands
[3] Univ Utrecht, Fac Vet Med, Utrecht, Netherlands
关键词:
MEDIATED QUINOLONE RESISTANCE;
SPECTRUM-BETA-LACTAMASE;
COMPLETE NUCLEOTIDE-SEQUENCE;
ESCHERICHIA-COLI;
KLEBSIELLA-PNEUMONIAE;
DETERMINANT QNRS1;
ENTEROBACTER-CLOACAE;
MODIFYING ENZYME;
UNITED-STATES;
ENTERICA;
D O I:
10.1093/jac/dkn470
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
The aim of this study was to identify and characterize plasmids carrying qnrS1, qnrB2 and qnrB19 genes identified in Salmonella strains from The Netherlands. The identification of plasmids may help to follow the dissemination of these resistance genes in different countries and environments. Plasmids from 33 qnr-positive Salmonella strains were transferred to Escherichia coli and analysed by restriction, Southern blot hybridization, PCR and sequencing of resistance determinants. They were also assigned to incompatibility groups by PCR-based replicon typing, including three additional PCR assays for the IncU, IncR and ColE groups. The collection included isolates from humans and one from chicken meat. Five IncN plasmids carrying qnrS1, qnrB2 and qnrB19 genes were identified in Salmonella enterica Bredeney, Typhimurium PT507, Kentucky and Saintpaul. qnrS1 genes were also located on three further plasmid types, belonging to the ColE (in Salmonella Corvallis and Anatum), IncR (in Salmonella Montevideo) and IncHI2 (in Salmonella Stanley) groups. Multiple events of mobilization, transposition and replicon fusion generate the complexity observed in qnr-positive isolates that are emerging worldwide. Despite the fact that the occurrence of qnr genes in bacteria from animals is scarcely reported, these genes are associated with genetic elements and located on plasmids that are recurrent in animal isolates.
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页码:274 / 281
页数:8
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