Frequency and Molecular Characterization of β-lactamases Producing Escherichia coli Isolated from North of Palestine

G. Adwan, A. Jaber
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引用次数: 11

Abstract

Aims: The aim of this study was to determine the prevalence and molecular characterization of AmpC β-lactamases and extended-spectrum β-lactamases (ESβLs) among E. coli isolates. Place and Duration of Study: Department of Biology and Biotechnology, An-Najah National University, Palestine, during February-April 2015. Methodology: A total 52 isolates of E. coli were recovered from different hospitals and private labs in Jennin district-Palestine. These isolates were used to detect ESβLs and AmpC β-lactamases using phenotypic tests and molecular techniques. Results: The prevalence of ESβLs and AmpC β-lactamases using conventional methods was 32.7% and 26.9%, respectively. Whereas, the prevalence using PCR technique was 67.3% and 5.8% for ESβLs and AmpC β-lactamases, respectively. TEM gene was the dominant (82.9%) Original Research Article Adwan and Jaber; BMRJ, 11(5): 1-13, 2016; Article no.BMRJ.22631 2 among E. coli that carried ESβL genes. Other genes were (0.0%), (2.9%) and (15.4%) for CTX-M, SHV and OXA genes, respectively. Whereas, AmpC β-lactamases only DHA gene was detected and the prevalence was (5.8%). Molecular analysis by construction phylogenetic tree showed that all sequenced TEM, SHV, OXA and DHA genes were belonged to TEM-1, SHV-1, OXA-1 and DHA-1, respectively. ERIC results showed that these strains were diverse and unrelated clones. Conclusions: Our results showed high frequency of ESβLs and AmpC β-lactamases among E. coli isolates in Palestine. According to these results we recommend the continuous monitoring and surveillance of the prevalence, proper control and prevention practices and effective antibiotic use will limit the further spread of Amp-C β-lactamases and ESβLs producing isolates within hospitals in Palestine.
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巴勒斯坦北部产β-内酰胺酶大肠杆菌的频率及分子特性研究
目的:研究大肠杆菌AmpC β-内酰胺酶和广谱β-内酰胺酶(ESβLs)在大肠杆菌中的流行程度和分子特征。学习地点和时间:2015年2月- 4月,巴勒斯坦安纳杰国立大学生物与生物技术系。方法:从巴勒斯坦杰宁地区不同医院和私人实验室共分离出52株大肠杆菌。利用表型检测和分子技术检测这些分离株ESβLs和AmpC β-内酰胺酶。结果:常规方法检测ESβLs和AmpC β-内酰胺酶的阳性率分别为32.7%和26.9%。而PCR检测的es β l和AmpC β-内酰胺酶的阳性率分别为67.3%和5.8%。TEM基因为显性基因(82.9%);中国生物医学工程学报,2016,31 (5):1104 - 1104;文章no.BMRJ。在大肠杆菌中携带ESβL基因。CTX-M、SHV和OXA基因分别为(0.0%)、(2.9%)和(15.4%)。而AmpC β-内酰胺酶仅检测到DHA基因,患病率为5.8%。构建系统发育树的分子分析结果表明,TEM、SHV、OXA和DHA基因分别属于TEM-1、SHV-1、OXA-1和DHA-1。ERIC结果表明,这些菌株是不同的、不相关的克隆。结论:巴勒斯坦地区大肠杆菌分离株中ESβLs和AmpC β-内酰胺酶含量较高。根据这些结果,我们建议对流行情况进行持续监测和监测,采取适当的控制和预防措施以及有效使用抗生素将限制Amp-C β-内酰胺酶和产生es β l的分离株在巴勒斯坦医院内的进一步传播。
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