Abstract |
The presence of fluoroquinolone resistance-associated mutations within the quinolone resistance-determining region of DNA gyrase and topoisomerase IV was investigated genetically in clinical isolates of Proteus mirabilis recovered from patients with urinay tract infections. Two isolates of fluoroquinolone-resistant P. mirabilis possessed the mutations in GyrA (Ser-83 --> Arg or Ile), GyrB (Ser-464 --> Tyr or Phe) and ParC (Ser-80 --> Ile). A novel mutation with Glu-87 --> Lys in GyrA, where suggested to be responsible for fluoroquinolone resistance, was identified. These results demonstrate that the presence of an additional mutation at Glu-87 in GyrA may contribute to high-level fluoroquinolone resistance, too.
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Authors | Ryoichi Saito, Kenya Sato, Wakako Kumita, Natsuko Inami, Hiroyuki Nishiyama, Noboru Okamura, Kyoji Moriya, Kazuhiko Koike |
Journal | The Japanese journal of antibiotics
(Jpn J Antibiot)
Vol. 59
Issue 1
Pg. 41-3
(Feb 2006)
ISSN: 0368-2781 [Print] Japan |
PMID | 16673582
(Publication Type: Journal Article)
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Chemical References |
- Fluoroquinolones
- DNA Topoisomerase IV
- DNA Gyrase
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Topics |
- DNA Gyrase
(genetics)
- DNA Topoisomerase IV
(genetics)
- Drug Resistance, Bacterial
- Fluoroquinolones
(pharmacology)
- Humans
- Mutation
- Proteus mirabilis
(drug effects, enzymology, genetics, isolation & purification)
- Urinary Tract Infections
(microbiology)
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