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Among 73 clinical isolates of Pseudomonas aeruginosa 48 strains were Ciprofloxacine (CIP) susceptible and 25 CIP resistant (Minimal inhibitory concentration - MIC>32 μg/ml - 14 strains) or of intermediate susceptibility to CIP (MIC≥ 1,5-32 μg/ml - 11 isolates). Mutations in the quinolone-resistance-determining region (QRDR) of gyrA gene were searched in groups of CIP resistant and of intermediate susceptibility to CIP isolates. Two methods: restriction fragment length polymorphism (RFLP) analysis and DNA sequencing analysis allowed to detect three different mutations. The nucleotide substitutions observed led to the following amino acid replacements: Thr-83 —> Ile, Asp-87—>Asn, Asp-87—>Gly. One mutated strain among the group of mutants analyzed showed double mutation (Thr-83—>Ile, Asp-87—>Gly) and additional silent mutation (Val-103—> Val); whilst the rest of the isolates showed different single missense mutations. The most frequently detected mutation in the gyrA gene (16 out of 25 mutants) was the Thr-83—>Ile substitution.
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p.201-206,fig.,ref.
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- Medical University of Silesia, Sosnowiec, Poland
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Bibliografia
- Akasaka T., M. Tanaka, A. Yamaguchi and K. Sato. 2001. Type II topoisomerase mutations in fluoroquinolone-resistant clinical strains Pseudomonas aeruginosa isolated in 1998 and 1999: role of target enzyme in mechanism of fluoroquinolone resistance. Antimicrob. Agents Chemother. 45: 2263-2268.
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- Kureishi A., J.M. Diver, B. Beckthold, T. Schollaardt, L.E. Bryan. 1994. Cloning and nucleotide sequence of Pseudomonas aeruginosa DNA gyrase gyrA gene from strain PAOl and quinolone-resistant clinical isolates. Antimicrob. Agents Chemother. 38: 1944-1952.
- Mouneimné H., J. Robert, V. Jarlier and E. Cambau. 1999. Type II topoisomerase mutations in ciprofloxacin-resistant strains of Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 43: 62-66.
- Nakajima A., Y. Sugimotoo, H. Yoneyama and T. Nakae. 2002. High-level fluoroquinolone resistance in Pseudomonas aeruginosa due to interplay of the MexAB-OprM efflux pump and the DNA gyrase mutation. Microbiol. Immun. 46: 391-395.
- Nakano M., T. Deguchi, T. Kawamura, M. Yasuda, M. Kimura, Y. Okano and Y. Kawada. 1997. Mutations in the gyrA and parC genes in fluoroquinolone-resistant clinical isolates of Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 41: 2289-2291.
- National Committee for Clinical Laboratory Standards. 2000. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. 5th edn. Approved standard. NCCLS document M7-A5. Wayne, Pennsylvania.
- Takenouchi T., E. Sakagawa, M. Sugawara. 1999. Detection of gyrA mutations among 335 Pseudomonas aeruginosa strains isolated in Japan and their susceptibilities to fluoroquinolones. Antimicrob. Agents Chemother. 43: 406-409.
- Weigel L.M., Ch.D. Steward and F.C. Tenover. 1998. gyrA mutations associated with fluoroquinolone resistance in eight species of Enterobacteriaceae. Antimicrob. Agents Chemother. 42: 2661-2667.
- Yonezawa M., M. Takahata, N. Matsubara, Y. Watanabe and H. Narita. 1995. DNA gyrase gyrA mutations in quinolone-resistant clinical isolates of Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 39: 1970-1972.
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Bibliografia
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