摘要
目的:了解我院临床分离泛耐铜绿假单胞菌(PDRPA)16S rRNA甲基化酶基因、氨基糖苷类药物修饰酶基因存在状况,探讨PDRPA氨基糖苷类耐药机制。方法:GNS-448药敏卡及K-B法测定抗菌药物的敏感性,聚合酶链反应(PCR)检测氨基糖苷类修饰酶基因、16S rRNA甲基化酶基因。结果:22株PDRPA对20种常用抗菌药物耐药,16S rRNA甲基化酶rmtB阳性1株(4.5%);氨基糖苷类修饰酶aac(6′)-Ⅰb阳性4株(18.2%),ant(3″)-Ⅰ阳性12株(54.5%),ant(2″)-Ⅰ阳性8株(36.4%),其他基因均阴性。共18株检出氨基糖苷类修饰酶基因。结论:PDRPA氨基糖苷类耐药为多重耐药机制,我院PDRPA氨基糖苷类耐药机制主要与氨基糖苷类修饰酶基因相关。
Objective:To investigate the status of the 16SrRNA methylases gene and aminoglycoside-modifying en-zyme gene in pan-drug resistant Pseudomonas aeruginosa(PDRPA) isolated from clinic,and further understand the resistant mechanisms of aminoglycoside drug.Methods:GNS-448 and K-B test was performed to detect the susceptibility of 19 kinds of antimicrobial agents against 22 strains of PDRPA.16SrRNA methylase genes and aminoglycoside-modifying enzyme genes were detected by polymerase chain reaction(PCR) and verified by DNA sequencer.Results:22 strains of PDRPA were resistant to 20 kinds of antimicrobial agents,the positive rate of rmtB,aac(6′)-Ⅰb,ant(3″)-Ⅰand ant(2″)-Ⅰgenes were 4.5%(1/22),18.2%(4/22),54.5%(12/22) and 36.4%(8/22),respectively.The rest detected genes were negative.The total positive rate of AMEs gene was 81.8%(18/22).Conclusion:PDRPA is of multi-resistant mechanism.The resistant mechanism of aminoglycoside is mainly related to aminoglycoside-modifying en-zyme gene aac(6′)-Ⅰb,ant(3″)-Ⅰ,ant(2″)-Ⅰin our hospital.
出处
《中国卫生检验杂志》
CAS
2010年第4期709-711,共3页
Chinese Journal of Health Laboratory Technology
基金
宁波市自然科学基金(2008A610090)