体外诱导人型支原体对氟喹诺酮类药物耐药的实验研究  被引量:1

Study on drug resistance of mycoplasma hominis induced by fluoroquinolones in vitro

在线阅读下载全文

作  者:叶萍[1] 邓超干[1] 王辉 王晓川[1] 

机构地区:[1]广东省深圳市罗湖区人民医院,518001 [2]广东省深圳市龙岗区中心医院,518116

出  处:《重庆医学》2009年第6期659-660,共2页Chongqing medicine

基  金:深圳市科技计划基金资助项目(200603087)

摘  要:目的探讨体外短期和长期诱导后人型支原体(Mh)对氟喹诺酮类药物的耐药和交叉耐药情况。方法将Mh标准株PG21在分别含有次抑菌浓度环丙沙星、氧氟沙星、司帕沙星和加替沙星的液体培养基中传代培养3代和12代后,筛选诱导株并分别检测其对4种药物的MIC值。结果经体外诱导后,分别筛选出4株短期诱导株(传3代)和4株长期诱导株(传12代)。4株短期诱导株对诱导药物和非诱导药物均产生耐药和交叉耐药,但耐药程度较低;4株长期诱导株的耐药和交叉耐药程度大大提高;且这种体外获得性耐药具有较好的稳定性。结论体外长时间、次抑菌浓度的氟喹诺酮类药物刺激将诱导Mh产生稳定的耐药和交叉耐药;短期诱导产生低度耐药,长期诱导产生高度耐药。Objective To explore the drug resistance or cross-resistance of mycoplasma hominis after 3-passage and 12-passage induction by fluoroquinolones in vitro. Methods The mycoplasma hominis standard strain PG21 were cultured stepwise for 3 and 12 passages respectively with ciprofloxacin,ofloxacin, sparfloxacin and gatifloxacin at subinhibitory concentrations and the minimum inhibition concentrations(MICs) to these drugs were detected before and after induction. Results Four 3-passage and four 12-passage resistant strains were selected respectively after induced by fluoroquinolones in vitro. Four 3-passage selected strains exhibited low-lever resistance or cross-resistance and another four 12-passage selected strains exhibited high lever resistance or cross resistance to these fluoroquinolones. The resistance or cross-resistance of mycoplasma hominis induced by fluoroquinolones in vitro were stable. Conclusion The resistance and cross-resistance of mycopiasma hominis to fluoroquinolones can be induced after long time and subinhibitory concentration stimulation with the fluoroquinolones in vitro. Low-lever and high lever resistance or cross-resistance were selected after 3-passage and 12 passage induction respectively.

关 键 词:人型支原体 氟喹诺酮 耐药性 

分 类 号:R375[医药卫生—病原生物学] R969.3[医药卫生—基础医学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象