Srisrattakarn Arpasiri, Lulitanond Aroonlug, Charoensri Nicha, Wonglakorn Lumyai, Kenprom Suthida, Sukkasem Chutipapa, Kuwatjanakul Waewta, Piyapatthanakul Sirikan, Luanphairin Onphailin, Phukaw Wichuda, Khanchai Kunthida, Pasuram Jantira, Wilailuckana Chotechana, Daduang Jureerut, Chanawong Aroonwadee
Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand.
Clinical Microbiology Unit, Srinagarind Hospital, Khon Kaen University, Khon Kaen 40002, Thailand.
Antibiotics (Basel). 2022 May 18;11(5):684. doi: 10.3390/antibiotics11050684.
Carbapenemase-producing Gram-negative bacteria have been increasingly reported. Simple and sensitive methods for carbapenemase detection are still needed. In this study, a gold nanoparticle (AuNP) solution was modified by the addition of zinc sulfate (ZnSO) for improving the conventional GoldNano Carb (cGoldC) test, and the modified GoldC (mGoldC) test was then evaluated for phenotypic detection of carbapenemase production in Gram-negative bacilli clinical isolates. ZnSO was added to give final concentrations of 0.25, 0.5, 0.75, and 1 mM. The performance of the mGoldC test was evaluated in Enterobacterales, spp., and isolates from six hospitals in different regions using polymerase chain reaction (PCR) as a gold standard. The AuNP solution with 0.25 mM ZnSO was used for the mGoldC test. Evaluation of the mGoldC test in 495 Enterobacterales, 212 spp., and 125 isolates (including 444 carbapenemase producers and 388 non-carbapenemase producers) revealed sensitivity, specificity, a positive likelihood ratio, and a negative likelihood ratio of 98.6%, 98.2%, 54.7, and 0.01, respectively. This test is fast, easy to perform, cost-effective (~0.25 USD per test), and highly sensitive and specific for routine carbapenemase detection, thus leading to effective antimicrobial therapy and infection control measures.
产碳青霉烯酶革兰氏阴性菌的报道日益增多。仍需要简单且灵敏的碳青霉烯酶检测方法。在本研究中,通过添加硫酸锌(ZnSO)对金纳米颗粒(AuNP)溶液进行修饰,以改进传统的金纳米碳(cGoldC)试验,然后对修饰后的金纳米碳(mGoldC)试验进行评估,用于革兰氏阴性杆菌临床分离株中产碳青霉烯酶的表型检测。添加ZnSO使其终浓度分别为0.25、0.5、0.75和1 mM。以聚合酶链反应(PCR)作为金标准,在来自不同地区六家医院的肠杆菌科、假单胞菌属和不动杆菌属分离株中评估mGoldC试验的性能。使用含0.25 mM ZnSO的AuNP溶液进行mGoldC试验。对495株肠杆菌科细菌、212株假单胞菌属细菌和125株不动杆菌属细菌(包括444株产碳青霉烯酶菌株和388株非产碳青霉烯酶菌株)进行mGoldC试验评估,结果显示其敏感性、特异性、阳性似然比和阴性似然比分别为98.6%、98.2%、54.7和0.01。该试验快速、易于操作、成本效益高(每次试验约0.25美元),并且对常规碳青霉烯酶检测具有高度敏感性和特异性,从而能够实现有效的抗菌治疗和感染控制措施。