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首页> 外文期刊>Journal of Clinical Microbiology >Sensitive EDTA-Based Microbiological Assays for Detection of Metallo-β-Lactamases in Nonfermentative Gram-Negative Bacteria
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Sensitive EDTA-Based Microbiological Assays for Detection of Metallo-β-Lactamases in Nonfermentative Gram-Negative Bacteria

机译:基于灵敏的EDTA的微生物学检测非发酵革兰氏阴性细菌中的金属β-内酰胺酶

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The worldwide spread of metallo-β-lactamase (MBL)-producing gram-negative bacilli represents a great concern nowadays. Sensitive assays for their specific detection are increasingly demanded to aid infection control and to prevent their dissemination. We have developed a novel microbiological assay employing crude bacterial extracts, designated EDTA-imipenem microbiological assay (EIM), to identify MBLs in nonfermentative gram-negative clinical strains. We also evaluated the ability of EIM to detect MBLs in comparison to those of other currently employed screening methods, such as the EDTA disk synergy test (EDS) with imipenem as a substrate and the Etest method. The sensitivities of EIM and Etest were similar (1 versus 0.92, respectively) and much higher than that of EDS (0.67). Moreover, both EIM and Etest displayed the maximum specificity. Modifications were introduced to EDS, including the simultaneous testing of three different β-lactams (imipenem, meropenem, and ceftazidime) and two different EDTA concentrations. This resulted in a sensitivity improvement (0.92), albeit at a cost to its specificity. A simple strategy to accurately detect MBL producers is proposed; this strategy combines (i) an initial screening of the isolates by the extended EDS assay to select the potential candidates and (ii) confirmation of the true presence of MBL activity by EIM.
机译:如今,金属β-内酰胺酶(MBL)产生的革兰氏阴性杆菌在全球范围内的传播引起了人们的极大关注。越来越需要针对其特异性检测的灵敏测定法,以帮助控制感染并防止其传播。我们已经开发了一种使用粗细菌提取物的新型微生物测定法,称为EDTA-亚胺培南微生物测定法(EIM),以鉴定非发酵革兰氏阴性临床菌株中的MBL。我们还评估了EIM与其他目前采用的筛选方法(例如以亚胺培南为底物的EDTA盘协同试验(EDS))和Etest方法相比检测MBL的能力。 EIM和Etest的灵敏度相似(分别为1和0.92),远高于EDS(0.67)。此外,EIM和Etest均显示出最大的特异性。对EDS进行了修改,包括同时测试三种不同的β-内酰胺(亚胺培南,美罗培南和头孢他啶)和两种不同的EDTA浓度。这导致灵敏度提高(0.92),尽管会牺牲其特异性。提出了一种准确检测MBL生产者的简单策略。该策略结合了(i)通过扩展EDS分析对菌株进行初步筛选以选择潜在的候选对象,以及(ii)通过EIM确认MBL活性的真实存在。

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