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Extended-spectrum beta-lactamases in Enterobacteriaceae isolated in Brazil carry distinct types of plasmid-mediated quinolone resistance genes

机译:巴西分离的肠杆菌科细菌中的广谱β-内酰胺酶携带不同类型的质粒介导的喹诺酮抗性基因

摘要

One hundred and six nalidixic acid-resistant Enterobacteriaceae isolates from two Brazilian hospitals isolated from June to October 2010 were evaluated to characterize the co-existence of plasmid-mediated quinolone resistant (PMQR) and extended-spectrum beta-lactamase (ESBL) determinants. the qnr genetic environment was determined by PCR and sequencing. Conjugation and hybridization experiments determined whether qnr-carrying plasmids were self-transferable. the aac(6')-lb-cr and qepA genes were also screened. Thirteen qnr-like genes (12.3%) were identified, with qnrB1 the most common, followed by qnrS1, qnrB2 and qnrB19. No qnrA, qnrC, qnrD or qepA determinant was detected. All qnr-positive strains possessed chromosomal substitutions in gyrase- and topoisomerase-encoding genes and four harboured a aac(6')-lb-cr gene. the co-production of bla(CTX-M) was observed in ten qnr-positive strains. These results indicate the dissemination of PMQR genes shown in clinical isolates from Brazil, and their co-existence with ESBL genes emphasizes the complexity of plasmid-mediated resistance determinants among Enterobacteriaceae.
机译:评估了从2010年6月至2010年10月从两家巴西医院分离出的一百零六种耐萘啶酸的肠杆菌科细菌,以鉴定质粒介导的喹诺酮抗药性(PMQR)和广谱β-内酰胺酶(ESBL)决定簇的共存。通过PCR和测序确定qnr遗传环境。缀合和杂交实验确定携带qnr的质粒是否可自我转移。还筛选了aac(6')-lb-cr和qepA基因。鉴定出13个qnr样基因(12.3%),其中qnrB1最常见,其次是qnrS1,qnrB2和qnrB19。未检测到qnrA,qnrC,qnrD或qepA决定簇。所有qnr阳性菌株在回旋酶和拓扑异构酶编码基因中均具有染色体取代,其中四个具有aac(6')-lb-cr基因。在十个qnr阳性菌株中观察到bla(CTX-M)的联合生产。这些结果表明,PMQR基因在巴西临床分离株中的传播,与ESBL基因的共存强调了肠杆菌科细菌介导的耐药决定簇的复杂性。

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