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淋病奈瑟菌中导致低水平萘啶酸耐药的gyrB突变的特征分析。

Characterization of a gyrB mutation responsible for low-level nalidixic acid resistance in Neisseria gonorrhoeae.

作者信息

Stein D C, Danaher R J, Cook T M

机构信息

Department of Microbiology, University of Maryland, College Park 20742.

出版信息

Antimicrob Agents Chemother. 1991 Apr;35(4):622-6. doi: 10.1128/AAC.35.4.622.

Abstract

Nalidixic acid-resistant derivatives of Neisseria gonorrhoeae WR302 were identified and categorized into two classes on the basis of their susceptibilities to this antimicrobial agent. The MIC of nalidixic acid for the derivative strain MUG116 was fourfold greater than that for its isogenic parental strain WR302 (2 versus 0.5 micrograms/ml, respectively). MUG324 was significantly more resistant to nalidixic acid (greater than 64 micrograms/ml). The MICs of other antimicrobial agents known to interact with either the gyrA or gyrB gene products were determined. Although the nalidixic acid MIC for MUG116 increased, no significant increases in the MICs of other agents that interact with the gyrA gene product were seen. The MICs of all agents that interact with the gyrA gene product were significantly increased for MUG324. The gene that imparts low-level nalidixic acid resistance was cloned from strain MUG116. The DNA sequence of this gene was determined, and by comparing the deduced amino acid sequence with sequences of proteins in data bases, this protein was found to be approximately 70% homologous with the gyrB gene product of Escherichia coli.

摘要

淋病奈瑟菌WR302的耐萘啶酸衍生物被鉴定出来,并根据它们对这种抗菌剂的敏感性分为两类。萘啶酸对衍生菌株MUG116的最低抑菌浓度(MIC)比对其同基因亲本菌株WR302的MIC高四倍(分别为2微克/毫升和0.5微克/毫升)。MUG324对萘啶酸的耐药性明显更高(大于64微克/毫升)。测定了已知与gyrA或gyrB基因产物相互作用的其他抗菌剂的MIC。虽然MUG116的萘啶酸MIC增加了,但与gyrA基因产物相互作用的其他药物的MIC没有明显增加。对于MUG324,与gyrA基因产物相互作用的所有药物的MIC都显著增加。从菌株MUG116中克隆出赋予低水平萘啶酸耐药性的基因。确定了该基因的DNA序列,并通过将推导的氨基酸序列与数据库中的蛋白质序列进行比较,发现该蛋白质与大肠杆菌的gyrB基因产物约有70%的同源性。

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