首页> 外文期刊>Journal of Medical Microbiology: An Official Journal of the Pathological Society of Great Britain and Ireland >Prevalence of plasmid-mediated quinolone resistance determinants in Citrobacter freundii isolates from Anhui province, PR China
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Prevalence of plasmid-mediated quinolone resistance determinants in Citrobacter freundii isolates from Anhui province, PR China

机译:在中国安徽省的弗氏柠檬酸杆菌中,质粒介导的喹诺酮耐药性决定因素的流行

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This study was conducted to detect and analyse the presence of plasmid-mediated quinolone resistance (PMQR) determinants [qnr, aac(6′)-Ib-cr and qepA] among Citrobacter freundii isolates from patients in Anhui province, PR China. During 2009–2010, 31 C. freundii strains were collected from various hospital units and patient specimens. Using PCR, qnr genes were detected in eight isolates, but aac(6′)-Ib-cr and qepA genes were not found. The genes qnrA1, qnrB1, qnrB2, qnrB4, qnrB10 and qnrB24 were present in 6.5, 3.2, 6.5, 3.2, 3.2 and 3.2 % of C. freundii isolates, respectively. A new subgene of qnrB variant (qnrB24) was found and identified for what we believe to be the first time. PFGE after XbaI digestion of genomic DNA indicated that qnr-positive strains were not clonally related. Conjugation experiments were conducted to determine whether the qnr-carrying plasmids were self-transferable, and plasmids of transconjugants were extracted and analysed. The qnr genes were transferred from three clinical isolates to their transconjugants. Two qnrA1 genes transferred quinolone resistance with a plasmid of ~11 kb, whilst the size of the plasmid carrying the qnrB4 gene was ~64 kb. The susceptibility of positive isolates and transconjugants was tested using an agar dilution method according to Clinical and Laboratory Standards Institute guidelines, and the MICs of ciprofloxacin and levofloxacin were determined using Etest strips. Most isolates with qnr genes were resistant to fluoroquinolones and other antimicrobial agents. The MICs of transconjugants showed reduced susceptibility to fluoroquinolones.
机译:这项研究旨在检测和分析来自中国安徽省患者的弗氏柠檬酸杆菌分离株中质粒介导的喹诺酮耐药性(PMQR)决定簇[qnr,aac(6')-Ib-cr和qepA]的存在。在2009–2010年期间,从各个医院单位和患者标本中采集了31株弗氏梭菌。使用PCR,在八个分离物中检测到qnr基因,但未发现aac(6')-Ib-cr和qepA基因。基因qnrA1,qnrB1,qnrB2,qnrB4,qnrB10和qnrB24分别存在于6.9%,3.2%,6.5%,3.2%,3.2%和3.2%的弗氏梭菌中。我们发现并鉴定了qnrB变体的新亚基因(qnrB24),这是我们第一次相信。 XbaI消化基因组DNA后的PFGE表明qnr阳性菌株无克隆相关性。进行缀合实验以确定携带qnr的质粒是否可自我转移,并提取和分析转缀合物的质粒。将qnr基因从三种临床分离株转移至其转导结合体。两个qnrA1基因通过〜11 kb的质粒转移了喹诺酮耐药性,而携带qnrB4基因的质粒的大小为〜64 kb。根据临床和实验室标准协会的指南,使用琼脂稀释法测试阳性分离物和转导结合剂的敏感性,并使用Etest试纸条测定环丙沙星和左氧氟沙星的MIC。大多数具有qnr基因的分离株对氟喹诺酮类药物和其他抗菌剂具有抗性。转导结合剂的MICs显示出对氟喹诺酮类药物的敏感性降低。

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