›› 2010, Vol. 37 ›› Issue (9): 43-47.

• 生理生化 • 上一篇    下一篇

耐氟喹诺酮类药物鸡毒支原体DNA回旋酶及拓扑异构酶Ⅳ的突变特征

魏飞龙,周云雷,沈祥广,蒋红霞   

  1. (华南农业大学兽医学院 广东省兽药研制与安全评价重点实验室,广州 510642)
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2010-09-20 发布日期:2010-09-20
  • 通讯作者: 蒋红霞

Characterization of Mutations in DNA Gyrase and Topoisomerase Ⅳ Involved in Quinolone Resistance of Clinical Mycoplasma gallisepticum Isolates

WEI Fei-long, ZHOU Yun-lei,SHEN Xiang-guang,JIANG Hong-xia   

  1. (Guangdong Key Laboratory for Veterinary Drug Development and Safety Evaluation,College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China)
  • Received:1900-01-01 Revised:1900-01-01 Online:2010-09-20 Published:2010-09-20
  • Contact: JIANG Hong-xia

摘要: 采用二倍稀释法测定临床分离的4株鸡毒支原体对常用抗菌药物的敏感性,PCR方法和基因测序法对鸡毒支原体DNA回旋酶编码基因gyrA、gyrB及拓扑异构酶Ⅳ编码基因gyrC和gyrE耐药决定区进行分析。敏感性测定结果表明,4株分离鸡毒支原体对泰乐菌素、泰妙林、沃尼妙林和替米考星有很高的敏感性,对四环素和红霉素中度敏感,对林可霉素、氟苯尼考和氟喹诺酮类药物呈现不同程度的耐药性。4株耐氟喹诺酮类药物鸡毒支原体均在GyrA和ParC的喹诺酮类耐药决定区(QRDR)发生氨基酸的改变,GyrA的氨基酸取代模式有两种,分别为Ser81→Gly和Ser83→Ile,ParC仅在80位发生氨基酸取代(Ser80→Leu),GyrB和ParE均未发生氨基酸改变。

关键词: 鸡毒支原体; 最低抑菌浓度; DNA回旋酶; 拓扑异构酶Ⅳ

Abstract: Susceptibilities of 4 isolated M. gallisepticum to common used antimicrobials were determined by broth dilution method. PCR and sequencing were applied for analysis of quinolone resistance-determining regions of the four target genes encoding DNA gyrase and topoisomerase Ⅳ from 4 isolates. The results showed that 4 isolates presented higher susceptible to tylosin, tiamulin, valnemulin and tilmicosin,moderate susceptible to tetracycline and erythromycin, and resistant to lincomycin, florfenicol and 3 fluroquinolone drugs to a certain extent. Several mutations were found in the two fluoroquinolone targets GyrA and ParC. Double mutations within QRDR of GyrA were found among 4 isolated M. gallisepticum, with the same substitution patterns of Ser81→Gly and Ser83→Ile. There was only one alteration existed within QRDR of ParC (Ser80→Leu) among 4 isolates. No mutations were found within QRDR of GyrB and ParE in 4 isolates.

Key words: Mycoplasma gallisepticum; minimum inhibitory concentration; DNA gyrase; topoisomerase Ⅳ

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