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首页> 外文期刊>British Microbiology Research Journal >Molecular Characterization of ESBL and AmpCβ-Lactamases among Blood Isolates ofKlebsiella pneumoniae and Escherichia coli
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Molecular Characterization of ESBL and AmpCβ-Lactamases among Blood Isolates ofKlebsiella pneumoniae and Escherichia coli

机译:肺炎克雷伯菌和大肠埃希菌血液分离株中ESBL和AmpCβ-内酰胺酶的分子表征

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The purpose of this study was to determine the mechanisms of third generation cephalosporins resistance among blood isolates of Klebsiella pneumoniae and Escherichia coli. A total of 549 isolates, Klebsiella pneumoniae (n=369) and Escherichia coli (n=180) were included. Antibiotic susceptibility pattern, phenotypic and genotypic detection of ESBL and AmpC production were carried out. The genetic environment surrounding blaCTX-M gene was assessed for insertion sequences. The plasmid-mediated quinolone resistance (PMQR) and integron carriage rate of ESBL producers were studied. The clonality was assessed by pulsed-field gel electrophoresis. Also, the plasmids bearing the ESBL, AmpC genes were studied by incompatibility typing and conjugation assay. By phenotypic tests, K. pneumoniae (79.8%) and E. coli (74.1%) were ESBL producers. Similarly, K. pneumoniae (70.5%) and E. coli (76.8%) were AmpC producers. By PCR, K. pneumoniae (68%) and E. coli (62%) carried ESBL genes. blaCTX-M- 15 was the prevalent type (98.1%). The linkage of ISEcp1 with blaCTX-M-15 gene was found in 92.5% of the blaCTX-M-15 genes. blaCMY-2 was present in 57% isolates. PFGE showed no clonal relatedness however; replicon typing revealed that ESBL genes were carried on 5 different replicon types, IncA/C being the commonest type present in this region. Also, PMQR was found in 19.3% of the ESBL producers. As high as 21.5% of class 2 integron was noted for first time from this region. A high prevalence of ESBL and AmpC genes was noticed. The clonal diversity, transferability of blaCTX-M plasmids suggest a higher incidence and wider distribution of ESBL and AmpC producing bacteria existing in the South India.
机译:这项研究的目的是确定肺炎克雷伯菌和大肠杆菌的血液分离株中第三代头孢菌素耐药性的机制。总共包括549个分离株,肺炎克雷伯菌(n = 369)和大肠杆菌(n = 180)。进行了抗生素敏感性分析,ESBL和AmpC产生的表型和基因型检测。评估blaCTX-M基因周围的遗传环境的插入序列。研究了质粒介导的喹诺酮抗药性(PMQR)和ESBL产生者的整联体携带率。通过脉冲场凝胶电泳评估克隆性。另外,通过不相容性分型和缀合试验研究了带有ESBL,AmpC基因的质粒。通过表型测试,肺炎克雷伯菌(79.8%)和大肠杆菌(74.1%)是ESBL的生产者。同样,肺炎克雷伯氏菌(70.5%)和大肠杆菌(76.8%)是AmpC的生产者。通过PCR,肺炎克雷伯氏菌(68%)和大肠杆菌(62%)携带ESBL基因。 blaCTX-M-15是流行的类型(98.1%)。在92.5%的blaCTX-M-15基因中发现ISEcp1与blaCTX-M-15基因的连锁。 blaCMY-2存在于57%的分离物中。 PFGE显示无克隆相关性。复制子分型显示ESBL基因携带5种不同的复制子类型,IncA / C是该区域中最常见的类型。此外,在ESBL生产者中有19.3%的人发现了PMQR。首次从该区域注意到高达21.5%的2类整联子。注意到ESBL和AmpC基因的高流行。 blaCTX-M质粒的克隆多样性,可转移性表明,存在于印度南部的ESBL和AmpC产生细菌的发生率更高,分布更广。

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