Kanematsu E, Deguchi T, Yasuda M, Kawamura T, Nishino Y, Kawada Y
Department of Urology, Gifu University School of Medicine, Gifu City, Japan.
Antimicrob Agents Chemother. 1998 Feb;42(2):433-5. doi: 10.1128/AAC.42.2.433.
The gyrA and parC genes of 31 clinical isolates of Enterococcus faecalis, including fluoroquinolone-resistant isolates, were partially sequenced and analyzed for target alterations. Topoisomerase IV may be a primary target in E. faecalis, but high-level fluoroquinolone resistance was associated with simultaneous alterations in both GyrA and ParC.
对31株粪肠球菌临床分离株(包括耐氟喹诺酮类分离株)的gyrA和parC基因进行了部分测序,并分析了靶点改变情况。拓扑异构酶IV可能是粪肠球菌中的主要靶点,但高水平氟喹诺酮耐药性与GyrA和ParC同时发生改变有关。