High occurrence of simultaneous mutations in target enzymes and MtrRCDE efflux system in quinolone-resistant Neisseria gonorrhoeae

被引:28
作者
Dewi, BE
Akira, S
Hayashi, H
Ba-Thein, W [1 ]
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Infect Biol, Tsukuba, Ibaraki 3058575, Japan
[2] Mito Chuo Clin, Dept Urol, Mito, Ibaraki, Japan
[3] Chugoku Gakuen Univ, Fac Contemporary Sci, Dept Human Nutr, Okayama, Japan
[4] Univ Indonesia, Fac Med, Dept Microbiol, Jakarta, Indonesia
关键词
D O I
10.1097/00007435-200406000-00007
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Emergence of multidrug-resistant Neisseria gonorrhoeae resulting from new genetic mutations is a serious threat to controlling gonorrhea. Goal: To determine 1) antimicrobial susceptibilities and the corresponding genetic mutations and 2) the role of MtrRCDE efflux system in gonococcal resistance to fluoroquinolones. Study Design: Antimicrobial susceptibility testing and sequence analysis of gyrA, parC, and mtrR loci of 131 N. gonorrhoeae isolates from Japan. Results: The proportion of N. gonorrhoeae strains resistant and intermediate-resistant to antimicrobials was 25.2% and 48.9% for ciprofloxacin, 25.2% and 30.5% for ofloxacin, 12.2% and 53.4% for penicillin; and 17.6 % and 51.1 % for tetracycline, respectively. Strains were categorized into 22 mutation profiles, with GyrA-S91F/ParCD86N/MtrR-G45D being the most predominant profile. The frequency of mutation in gyrA, parC, mtrR, and the mtrR promoter was 71 %, 47.3%, 77.1 %, and 23.7%, respectively. Seventy-one percent of strains carried mutations in both gyrA and mtrR. Conclusion: This study reports simultaneous mutations in fluoroquinolone target enzymes and the MtrRCDE efflux system as a fluoroquinolone- resistant mechanism in N. gonorrhoeae.
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页码:353 / 359
页数:7
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