Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, New York, USA.
Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
J Clin Microbiol. 2019 Apr 26;57(5). doi: 10.1128/JCM.01757-18. Print 2019 May.
The increase in the prevalence and impact of infections caused by carbapenemase-producing is a global health concern. Therefore, rapid and accurate methods to detect these organisms in any clinical microbiology laboratory, including those in resource-limited settings, are essential to prevent and contain their spread. It is also important to differentiate between serine- and metal-dependent carbapenemases elaborated by carbapenemase-producing isolates for epidemiologic, infection control and prevention, and therapeutic purposes. Here, we describe the development and evaluation of the EDTA-modified carbapenem inactivation method (eCIM), an assay for discriminating between serine- and metal-dependent (i.e., metallo-β-lactamases [MBLs]) carbapenemases when used in conjunction with the modified carbapenem inactivation method (mCIM). The eCIM had an overall sensitivity and specificity of 100% and was adopted by the Clinical and Laboratory Standards Institute as a method to use in combination with the mCIM to identify MBL-producing .
产碳青霉烯酶的 感染的流行率和影响增加是全球关注的健康问题。因此,在任何临床微生物学实验室,包括资源有限的环境中,快速准确地检测这些生物体对于预防和控制其传播至关重要。区分产碳青霉烯酶分离株产生的丝氨酸依赖和金属依赖碳青霉烯酶对于流行病学、感染控制和预防以及治疗目的也很重要。在这里,我们描述了 EDTA 修饰的碳青霉烯失活方法(eCIM)的开发和评估,该方法是一种在与改良碳青霉烯失活方法(mCIM)联合使用时用于区分丝氨酸依赖和金属依赖(即金属-β-内酰胺酶 [MBLs])碳青霉烯酶的检测方法。eCIM 的总体敏感性和特异性均为 100%,并被临床和实验室标准协会采用,作为与 mCIM 联合使用以鉴定产 MBL 的 的方法。