首页> 外文期刊>Japanese journal of infectious diseases >Plasmid-Mediated Quinolone Resistance Genes, aac(6′)-Ib-cr, qnrS, qnrB, and qnrA, in Urinary Isolates of Escherichia coli and Klebsiella pneumoniae at a Teaching Hospital, Thailand
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Plasmid-Mediated Quinolone Resistance Genes, aac(6′)-Ib-cr, qnrS, qnrB, and qnrA, in Urinary Isolates of Escherichia coli and Klebsiella pneumoniae at a Teaching Hospital, Thailand

机译:质粒介导的喹诺酮抗性基因aac(6')-Ib-cr,qnrS,qnrB和qnrA在泰国教学医院的大肠杆菌和肺炎克雷伯菌的尿分离物中

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References(28) Cited-By(8) A total of 121 Escherichia coli (47 extended-spectrum β-lactamase [ESBL] and 74 non-ESBL producers) and 75 Klebsiella pneumoniae isolates (49 ESBL and 26 non-ESBL producers) were collected from urine samples between October 2010 and April 2011 at a university hospital and assessed for the presence of plasmid-mediated quinolone resistance (PMQR) genes. Twenty-seven E. coli (22.3%) and 49 K. pneumoniae (65.3%) isolates harbored PMQR genes, which mostly consisted of aac(6′)-Ib-cr and qnrS, followed by qnrB and qnrA. Among the 76 PMQR-positive isolates, 15 (19.7%) and 2 (2.6%) carried 2 and 3 different PMQR genes, respectively. However, qnrC, qnrD, and qepA were not found in any isolate. The PMQR genes were more prevalent in ESBL producers than in non-ESBL producers (42.6% versus 9.5% in E. coli and 81.6% versus 34.6% in K. pneumoniae). Approximately 35%–60% of the PMQR-positive isolates were susceptible or intermediately susceptible to fluoroquinolones. The enterobacterial repetitive intergenic consensus-PCR method revealed that most PMQR-positive isolates belonged to different strains, indicating the spread of these resistance determinants. PMQR gene transfer by conjugation was successful in 10%–25% of the test donors. This study showed a high prevalence of PMQR genes among both organisms. Clinical use of fluoroquinolones for the treatment of infections caused by fluoroquinolone-susceptible strains harboring PMQR genes may lead to decreased therapeutic efficacy.
机译:参考文献(28)被引(8)总共有121株大肠杆菌(47例广谱β-内酰胺酶[ESBL]和74例非ESBL的生产者)和75株肺炎克雷伯菌分离株(49例ESBL和26例非ESBL的生产者)在2010年10月至2011年4月间从某大学医院的尿液样本中收集样本,并评估是否存在质粒介导的喹诺酮耐药性(PMQR)基因。 27个大肠杆菌(22.3%)和49例肺炎克雷伯菌(65.3%)分离株带有PMQR基因,其中大多数由aac(6')-Ib-cr和qnrS组成,其次是qnrB和qnrA。在76个PMQR阳性分离株中,分别有15个(19.7%)和2个(2.6%)携带2个和3个不同的PMQR基因。但是,在任何分离物中均未发现qnrC,qnrD和qepA。 PMQR基因在ESBL生产者中比在非ESBL生产者中更为普遍(大肠杆菌中42.6%相对于9.5%,肺炎克雷伯氏菌中81.6%相对于34.6%)。大约35%–60%的PMQR阳性分离株对氟喹诺酮类药物敏感或中等敏感。肠细菌重复基因间共有-PCR方法显示大多数PMQR阳性分离株属于不同菌株,表明这些抗性决定簇的传播。通过缀合转移PMQR基因在10%–25%的测试供体中成功完成。这项研究表明两种生物中PMQR基因的患病率很高。临床上使用氟喹诺酮类药物治疗由携带PMQR基因的氟喹诺酮敏感性菌株引起的感染可能会导致治疗效果下降。

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