Department of Infectious Diseases and Clinical Microbiology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People's Republic of China.
Pol J Microbiol. 2021 Sep;70(3):387-394. doi: 10.33073/pjm-2021-036. Epub 2021 Sep 17.
This study was conducted to develop a cheap, rapid, and accurate modified combined-disk test (mCDT) approach to detect and differentiate KPC and MBL carbapenemases among clinical carbapenem-resistant Enterobacterales (CRE) isolates and simultaneously distinguish them from carbapenem-susceptible Enterobacterales (CSE) isolates. A total of 163 CRE and 90 third-generation cephalosporin-resistant Enterobacterales isolates were tested using imipenem and meropenem disks and different concentrations of carbapenemase inhibitors. The optimal sensitivity and specificity for detecting KPC carbapenemase were 97.2% and 100%, respectively. The sensitivity and specificity for detecting MBL carbapenemase were 100% and 100% with imipenem or meropenem and carbapenemase inhibitors within six hours. The inhibitory zone diameter of 18 mm for imipenem or meropenem disks without inhibitor could distinguish CRE from CSE isolates. Therefore, this mCDT approach may be a useful tool in clinical laboratories to detect CRE isolates and differentiate KPC and MBL producers, which is beneficial for patient management and hospital infection prevention and control.
本研究旨在开发一种廉价、快速且准确的改良联合盘试验(mCDT)方法,用于检测和区分临床耐碳青霉烯肠杆菌科(CRE)分离株中的 KPC 和 MBL 碳青霉烯酶,并将其与耐碳青霉烯肠杆菌科(CSE)分离株区分开来。共检测了 163 株 CRE 和 90 株第三代头孢菌素耐药肠杆菌科分离株,使用亚胺培南和美罗培南纸片和不同浓度的碳青霉烯酶抑制剂。检测 KPC 碳青霉烯酶的最佳灵敏度和特异性分别为 97.2%和 100%。对于检测 MBL 碳青霉烯酶,在 6 小时内使用亚胺培南或美罗培南和碳青霉烯酶抑制剂的灵敏度和特异性均为 100%。无抑制剂的亚胺培南或美罗培南纸片的抑菌圈直径为 18 毫米,可将 CRE 与 CSE 分离株区分开来。因此,这种 mCDT 方法可能是临床实验室检测 CRE 分离株并区分 KPC 和 MBL 产生菌的有用工具,有助于患者管理和医院感染防控。