Hirose K, Kawasaki Y, Kotani K, Abiko K, Sato H
Clinical Research Center of Animal Health, Meiji Seika Kaisha Ltd, Yokohama, Kanagawa 222-8567.
J Vet Med B Infect Dis Vet Public Health. 2004 May;51(4):169-75. doi: 10.1111/j.1439-0450.2004.00748.x.
Quinolone-resistant (QR) mutants of Mycoplasma bovirhinis strain PG43 (type strain) were generated by stepwise selection in increasing concentrations of enrofloxacin (ENR). An alteration was found in the quinolone resistance-determining region (QRDR) of the parC gene coding for the ParC subunit of topoisomerase IV from these mutants, but not in the gyrA, gyrB, and parE gene coding for the GyrA and GyrB subunits of DNA gyrase and the ParE subunit of topoisomerase IV. Similarly, such an alteration in QRDR of parC was found in the field isolates of M. bovirhinis, which possessed various levels of QR. The substitution of leucine (Leu) by serine (Ser) at position 80 of QRDR of ParC was observed in both QR-mutants and QR-isolates. This is the first report of QR based on a point mutation of the parC gene in M. bovirhinis.
通过在浓度递增的恩诺沙星(ENR)中逐步筛选,产生了牛鼻支原体PG43株(模式菌株)的喹诺酮抗性(QR)突变体。在这些突变体中,编码拓扑异构酶IV的ParC亚基的parC基因的喹诺酮抗性决定区域(QRDR)发生了改变,但编码DNA促旋酶的GyrA和GyrB亚基以及拓扑异构酶IV的ParE亚基的gyrA、gyrB和parE基因未发生改变。同样,在具有不同水平QR的牛鼻支原体野外分离株中也发现了parC的QRDR发生这种改变。在QR突变体和QR分离株中均观察到ParC的QRDR第80位的亮氨酸(Leu)被丝氨酸(Ser)取代。这是关于基于牛鼻支原体parC基因点突变的QR的首次报道。