2015
DOI: 10.1016/j.ijantimicag.2014.09.019
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Co-existence of plasmid-mediated quinolone resistance determinants and mutations in gyrA and parC among fluoroquinolone-resistant clinical Enterobacteriaceae isolated in a tertiary hospital in Warsaw, Poland

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Cited by 64 publications
(78 citation statements)
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“…In Enterobacteriaceae, qnrS, qnrB and aac(6 )-Ib-cr genes have been implicated in plasmid-mediated quinolone resistance (PMQR) [57,58]. A combination of low-level resistance to fluoroquinolones caused by PMQR mechanism, with QRDR mutation can lead to clinically relevant resistance [59]. We did not find any PMQR in the fluoroquinolone resistant isolates exhibiting QRDR, indicating that these mutations were only identified in resistant isolates.…”
Section: Concordance Of Amr Phenotype and Genotypementioning
confidence: 74%
“…In Enterobacteriaceae, qnrS, qnrB and aac(6 )-Ib-cr genes have been implicated in plasmid-mediated quinolone resistance (PMQR) [57,58]. A combination of low-level resistance to fluoroquinolones caused by PMQR mechanism, with QRDR mutation can lead to clinically relevant resistance [59]. We did not find any PMQR in the fluoroquinolone resistant isolates exhibiting QRDR, indicating that these mutations were only identified in resistant isolates.…”
Section: Concordance Of Amr Phenotype and Genotypementioning
confidence: 74%
“…Analysis of quinolone resistance-determining regions of gyrA and parC genes revealed the presence of multiple and diverse mutations in gyrA (S83Y, S83F, D87A)and parC (S80I, N304S) in isolates that were clonally distinct. Mutations in gyrA and parC genes have been reported as major mechanisms of fluoroquinolone/quinolone resistance associated with DNA gyrase and topoisomerase IV alterations in Enterobacteriaceae (Alvi et al, 2018;Piekarska et al, 2015; Sekyere and Amoako, 2017), as the plasmid-mediated quinolone resistance genes (PMQR) and extrusion by intrinsic efflux pumps commonly mediate low-level fluoroquinolone/quinolone resistance (Sekyere and Amoako, 2017). However, mutations in both gyrA and parC are often common and associated with high-level quinolone resistance in Enterobacteriaceae compared with alterations in gyrB (Piekarska et al, 2015) as evident in this study.…”
Section: Discussionmentioning
confidence: 99%
“…Mutations in gyrA and parC genes have been reported as major mechanisms of fluoroquinolone/quinolone resistance associated with DNA gyrase and topoisomerase IV alterations in Enterobacteriaceae (Alvi et al, 2018;Piekarska et al, 2015; Sekyere and Amoako, 2017), as the plasmid-mediated quinolone resistance genes (PMQR) and extrusion by intrinsic efflux pumps commonly mediate low-level fluoroquinolone/quinolone resistance (Sekyere and Amoako, 2017). However, mutations in both gyrA and parC are often common and associated with high-level quinolone resistance in Enterobacteriaceae compared with alterations in gyrB (Piekarska et al, 2015) as evident in this study. ST101 (P26-75, P26-81) and ST152 (P26-66) isolates were of the same mutation codons 83 and 87 of the gyrA and at 80 in parC genes with no mutation in gyrB gene among isolates with a ciprofloxacin MIC of 4 mg/L.…”
Section: Discussionmentioning
confidence: 99%
“…Efflux pump QepA was the most common isolated genes. According to Piekarska K et al 2015, PMQR determinants were present in 49 urinary isolates (22.8%), among which aac(6')-Ib-cr and proteins Qnr predominated (85.7% and 26.5%, respectively) [15]. But Marchisio M et al did not find any plasmid-mediated quinolone resistance determinants among Enterobacteriaceae isolated from urinary tract infections patients [23].…”
Section: Discussionmentioning
confidence: 96%