Characterization of Quinolone-Resistant Clinical Isolates of Escherichia coli in Korea
- Authors
- 오유정; 박서형; 하미선; 이연희
- 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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