High frequency of the combined presence of QRDR mutations and PMQR determinants in multidrug-resistant Klebsiella pneumoniae and Escherichia coli isolates from nosocomial and community-acquired infections

Plasmid-mediated quinolone resistance (PMQR) determinants combined with mutations in quinolone resistance-determining regions (QRDRs) and clonal dissemination were investigated in 40 fluoroquinolone-resistant Klebsiellapneumoniae and Escherichiacoli isolates from nosocomial and community-acquired in...

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Veröffentlicht in:Journal of medical microbiology 2017-08, Vol.66 (8), p.1144-1150
Hauptverfasser: Araújo, Bruna Fuga, Campos, Paola Amaral de, Royer, Sabrina, Ferreira, Melina Lorraine, Gonçalves, Iara Rossi, Batistão, Deivid William da Fonseca, Resende, Daiane Silva, Brito, Cristiane Silveira de, Gontijo-Filho, Paulo Pinto, Ribas, Rosineide Marques
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Sprache:eng
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Zusammenfassung:Plasmid-mediated quinolone resistance (PMQR) determinants combined with mutations in quinolone resistance-determining regions (QRDRs) and clonal dissemination were investigated in 40 fluoroquinolone-resistant Klebsiellapneumoniae and Escherichiacoli isolates from nosocomial and community-acquired infections. We observed nucleotide substitutions in gyrA (Ser83Ile, Val37Leu, Lys154Arg, Ser171Ala, Ser19Asn, Ile198Val, Ser83Tyr, Ser83Leu, Asp87Asn and Asp87Gly) and parC genes (Ser80Ile, Glu84Lys, Ala129Ser, Val141Ala and Glu84Gly). Two novel substitutions were detected in the gyrA gene (Val37Leu and Ile198Val). The presence of PMQR genes predominated in community isolates (55.5 %). In addition to the frequent presence of the class 1 integron in isolates from community-acquired infections, the genetic similarity results obtained by PFGE showed high genomic diversity. This study suggests that management of multidrug-resistant Enterobacteriaceae isolates from the community are a possible source of genetic mobile elements that carry genes that confer resistance to fluoroquinolones. More attention should be paid to the surveillance of community-acquired infections.
ISSN:0022-2615
1473-5644
DOI:10.1099/jmm.0.000551