HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

[Mutations of DNA gyrase and topoisomerase IV in clinical isolates of fluoroquinolone-resistant Proteus mirabilis].

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.
AuthorsRyoichi Saito, Kenya Sato, Wakako Kumita, Natsuko Inami, Hiroyuki Nishiyama, Noboru Okamura, Kyoji Moriya, Kazuhiko Koike
JournalThe Japanese journal of antibiotics (Jpn J Antibiot) Vol. 59 Issue 1 Pg. 41-3 (Feb 2006) ISSN: 0368-2781 [Print] Japan
PMID16673582 (Publication Type: Journal Article)
Chemical References
  • Fluoroquinolones
  • DNA Topoisomerase IV
  • DNA Gyrase
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)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: