2016
DOI: 10.1007/s40291-016-0191-6
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Molecular Characterization of Intermediate Susceptible Typhoidal Salmonella to Ciprofloxacin, and its Impact

Abstract: It was clear that the molecular mechanism of ciprofloxacin resistance correlates better with the EUCAST criteria than the CLSI criteria, which is also in agreement with the pefloxacin results, suggesting it as a surrogate marker for identifying fluoroquinolone susceptibility.

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Cited by 15 publications
(12 citation statements)
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“…This study showed only 8 isolates could be amplified both the gyrB and parE genes. Previous studies from Brazil and Senegal were showed similar results with our results [28][29][30][31].…”
Section: Discussionsupporting
confidence: 92%
See 1 more Smart Citation
“…This study showed only 8 isolates could be amplified both the gyrB and parE genes. Previous studies from Brazil and Senegal were showed similar results with our results [28][29][30][31].…”
Section: Discussionsupporting
confidence: 92%
“…The main mechanism of resistance to quinolones is linked to chromosomal mutations especially in the gyrA or parC genes and more rarely at the gyrB and parE genes [28,29]. This study showed only 8 isolates could be amplified both the gyrB and parE genes.…”
Section: Discussionmentioning
confidence: 68%
“…However, in the past decade there have been reports of treatment failures using fluoroquinolones in patients with typhoid fever and the isolate being susceptible to fluoroquinolones and resistant to nalidixic acid in vitro [33]. Studies have reported that plasmid-mediated resistance showed reduced susceptibility to ciprofloxacin (MIC of 0.125–1.0 μg/ml), which could not be picked up by the nalidixic acid test [34]. However, the mechanism is not well understood.…”
Section: Discussionmentioning
confidence: 99%
“…Quinolone resistance is due to mutations in the quinolone-resistance determining regions of chromosomal genes such as gyrA , gyrB , parC and parE and plasmid-mediated qnr, qepA and aacs(6′)-Ib-cr genes [ 42 ]. Studies have reported that plasmid-mediated resistance showed reduced susceptibility to ciprofloxacin (MIC of 0.125–1.0 μg/ml), which could not be picked up by the nalidixic acid test [ 43 ]. Therefore, the CLSI and EUCAST recommend a new screening surrogate marker of pefloxacin (5 μg) disc diffusion for detecting both chromosomal- and plasmid-mediated resistance.…”
Section: Fluoroquinolonesmentioning
confidence: 99%