耐氟喹诺酮类淋病奈瑟菌gyrA和parC基因的转化

S. Walter de Walthoffen
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引用次数: 1

摘要

淋病奈瑟菌是最常见的性传播疾病之一的病原学病原体之一。淋球菌产生了许多与细菌进化有关的耐药机制。自然转化是奈瑟菌属细菌水平基因转移的基本方法,它可以导致编码DNA旋转酶的gyrA基因发生突变。本研究的目的是验证gyrA蛋白91位和95位突变对淋病奈瑟菌对喹诺酮类抗生素敏感性的意义。方法:采用遗传转化的方法,将GyrA基因导入淋球菌敏感分离株。检测抗性基因供体、受体和转化菌株的敏感性,并对gyrA基因进行测序。结果:经研究表明,在CIP敏感淋病乳杆菌中,GyrA蛋白91和95位氨基酸序列的双突变可使MIC值从0.003 mg / L增加到0.125 mg / L。结论:91位和95位氨基酸序列的突变影响了菌株对环丙沙星的敏感性,但这不是改变喹诺酮类药物MIC值的唯一机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transformation of fluoroquinolone-resistance Neisseria gonorrhoeae gyrA and parC genes
Introduction: N. gonorrhoeae is one of the etiological causative agents of one of the most common sexually transmitted diseases. Gonococci has created many resistance mechanisms, which is associated with bacterial evolution. Natural transformation is the basic method of horizontal gene transfer in bacteria of the genus Neisseria, which can lead to a mutation in the gyrA gene encoding DNA gyrase. The aim of the study was to verify the view on the significance of mutations at positions 91 and 95 of the gyrA protein on the sensitivity of N. gonorrhoeae to antibiotics of the quinolone type. Methods: GyrA gene was introduced into an sensitive isolate of N. gonorrhoeae using genetic transformation. Resistance gene donor, recipient and transform strains were tested for susceptibility and the gyrA gene was sequenced. Results: It has been shown that double mutation in amino acid acid sequence of the GyrA protein at positions 91 and 95 increase the value of MIC from 0,003 mg / L to 0,125 mg / L at CIP sensitive N. gonorrhoeae strain. Conclusions: Mutations in the amino acid sequence at positions 91 and 95 affet the strain’s sensitivity to ciprofloxacin, but it is not the only mechanism which could alter the MIC value of quinolones.
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