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Characterization of Quinolone-Resistant Clinical Isolates of Escherichia coli in Korea

Authors
오유정박서형하미선이연희
Issue Date
Jun-2002
Publisher
한국미생물학회
Keywords
clinical isolate; Escherichia coli; norfloxacin; QRDR; RAPD; resistanceQuinolone is a specific inhibitor of DNA gyrase andtopoisomerase IV (Bauernfeind; 1971; Chen et al.; 1996; O'Dea et al.; 1996). DNA gyrase is encoded by gyrA andgyrB and unwinds t
Citation
The Journal of Microbiology, v.40, no.2, pp 98 - 103
Pages
6
Journal Title
The Journal of Microbiology
Volume
40
Number
2
Start Page
98
End Page
103
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/65993
ISSN
1225-8873
1976-3794
Abstract
Twenty-eight clinical isolates of Escherichia coli, composed of thirteen norfloxacin resistant isolates (MIC of >16 mg/ml), one intermediately resistant isolate (MIC of 8 mg/ml), and fourteen susceptible isolates (MIC of <4 mg/ml), were randomly selected to study the norfloxacin resistance mechanism and phylogeny in clinical isolates in Korea. Eleven norfloxacin resistant isolates and one susceptible isolate were multi-drug resistant (MDR). Every norfloxacin resistant isolate with MIC higher than 32 mg/ml had the same three mutations Ser83 Leu and Asp87 Asn or Tyr in GyrA and Ser80 Ile in ParC. Whereas a resistant isolate with MIC of 16 mg/ml had three mutations but Asp87 in GyrA was replaced with Gly instead of Asn. The intermediately resistant isolate had the same two mutations in GyrA but a different mutation in ParC, Glu84 Lys. Among the susceptible isolates, two isolates with MIC of 4 mg/ml had one mutation Ser83 Leu in GyrA, and no mutation was found in the susceptible isolates. Resistant isolates showed higher efflux activity than the susceptible ones, with random amplification of polymorphic DNA (RAPD), six susceptible isolates form a separate group from the rest of the isolates.
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