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首页> 外文期刊>Karbala International Journal of Modern Science >Comparison of Five Methods for Detection of Extended Spectrum β-Lactamases in Gram Negative Enteric Bacteria
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Comparison of Five Methods for Detection of Extended Spectrum β-Lactamases in Gram Negative Enteric Bacteria

机译:革兰阴性肠溶细菌中扩展光谱β-内酰胺酶的五种方法的比较

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摘要

The presence of extended-spectrum β-lactamases in 55 isolates of Gram negative enteric bacteria isolated from lower respiratory tract infections, was investigated by using the Clinical Laboratory Standards Institute CLSI method which showed that 41.8% of the isolates produced this type of β-lactamases, and that Klebsiella pneumoniae isolates were the most producing species with a production rate of 61.1%, followed by Escherichia coli isolates 43.75%. Five confirmatory methods were used to detect these enzymes: ceftazidime agar method, double-disk synergy method, combination disk method, modified 3D extract method and enzymatic disks method. The study indicated that ceftazidime agar method was the best method in detecting extended-spectrum β-lactamases as it gave a detection rate of 95.7%, followed by the double-disk synergy method with a rate of 87%, then enzymatic disks method with a rate of 73.9%.
机译:通过使用临床实验室标准研究所的CLSI方法研究了55分离出从低呼吸道感染中分离的革兰阴性肠溶细菌的分离物中的扩展光谱β-乳酰胺酶的存在,表明41.8%的分离物产生这种类型的β-内酰胺酶 ,肺炎群岛肺炎群岛分离物是生产率最大的物种,产量为61.1%,其次是大肠杆菌分离株43.75%。 五种确认方法用于检测这些酶:头孢他啶琼脂法,双磁盘协同方法,组合盘法,改进的3D提取方法和酶磁盘法。 该研究表明,CeTtazidime琼脂法检测延长光谱β-内酰胺酶的最佳方法,因为它使检测率为95.7%,然后是速率为87%的双磁盘协同方法,然后酶磁盘方法 率为73.9%。

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