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耐碳青霉烯类肠杆菌科细菌对喹诺酮类耐药机制的研究
引用本文:苏珊珊,张吉生,王英,王勇,王宇超,李慧玲,张晓丽. 耐碳青霉烯类肠杆菌科细菌对喹诺酮类耐药机制的研究[J]. 中国感染控制杂志, 2019, 18(2): 99-104. DOI: 10.12138/j.issn.1671-9638.20193929
作者姓名:苏珊珊  张吉生  王英  王勇  王宇超  李慧玲  张晓丽
作者单位:耐碳青霉烯类肠杆菌科细菌对喹诺酮类耐药机制的研究
基金项目:黑龙江省自然科学基金(D201224);黑龙江省卫生计生委科研项目(2017-405);佳木斯大学学科交叉项目(12J201505)
摘    要:目的研究质粒介导喹诺酮耐药(PMQR)基因在耐碳青霉烯类肠杆菌(CRE)中的流行情况及耐药机制。方法收集2015年3月—2018年3月某院临床分离的CRE菌株,VITEK2 Compact分析仪对其进行鉴定及药物敏感试验,采用聚合酶链反应(PCR)及测序确定PMQR基因qnrA、qnrB、qnrS、qepA、acc(6’)Ib-cr携带情况,通过质粒接合试验验证PMQR基因的水平转移。结果耐碳青霉烯类大肠埃希菌对喹诺酮类药物的耐药率达100%,耐碳青霉烯类肺炎克雷伯菌对喹诺酮类药物的耐药率为15.56%~33.33%。acc(6’)Ib-cr基因检出率最高(87.72%),其次为qnrB(77.19%)和qnrS(17.54%),有2株菌携带qnrA基因(3.51%),未分离出qepA基因,菌株同时含有2种或3种PMQR基因(84.21%)。8株接合成功的菌株均存在PMQR基因转入,但喹诺酮药物对其最低抑菌浓度无明显改变。结论虽然该院CRE质粒介导喹诺酮耐药基因检出率高,但对喹诺酮类药物仍存在一定敏感性。

关 键 词:喹诺酮耐药基因  肠杆菌科细菌  耐碳青霉烯类肠杆菌  耐药性  
收稿时间:2018-05-23

Mechanisms of quinolone resistance of carbapenem-resistant Enterobacte-riaceae
SU Shan-shan,ZHANG Ji-sheng,WANG Ying,WANG Yong,WANG Yu-chao,LI Hui-ling,ZHANG Xiao-li. Mechanisms of quinolone resistance of carbapenem-resistant Enterobacte-riaceae[J]. Chinese Journal of Infection Control, 2019, 18(2): 99-104. DOI: 10.12138/j.issn.1671-9638.20193929
Authors:SU Shan-shan  ZHANG Ji-sheng  WANG Ying  WANG Yong  WANG Yu-chao  LI Hui-ling  ZHANG Xiao-li
Affiliation:Department of Laboratory Medicine, First Affiliated Hospital of Jiamusi University, Jiamusi 154007, China
Abstract:Objective To study the prevalence of plasmid-mediated quinolone resistance (PMQR) genes in carbapenem-resistant Enterobacteriaceae (CRE) and its resistance mechanism. Methods Clinically isolated CRE strains in a hospital from March 2015 to March 2018 were collected, then identified and performed antimicrobial susceptibility test by VITEK 2 Compact analyzer, carriage of PMQR genes qnrA, qnrB, qnrS, qepA and acc (6')Ib-cr were determined by polymerase chain reaction (PCR) and sequencing, the horizontal transfer of PMQR genes were verified by plasmid conjugation test. Results Resistance rates of carbapenem-resistant Escherichia coli and carbapenem-resistant Klebsiella pneumoniae to quinolones were 100% and 15.56%-33.33% respectively. Detection rate of acc (6')Ib-cr gene was the highest (87.72%), followed by qnrB (77.19%) and qnrS (17.54%), 2 strains (3.51%) carried qnrA gene, qepA gene was not isolated, 84.21% of strains harbored 2 or 3 PMQR genes. PMQR gene was transfected into all the 8 conjugated strains, but minimum inhibitory concentration value of quinolones didn't change significantly. Conclusion The detection rate of PMQR genes in CRE in this hospital is high, but there is a certain sensitivity to quinolones.
Keywords:quinolone resistance gene  Enterobacteriaceae  carbapenem-resistant Enterobacteriaceae  drug resistance  
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