Pragasam Agila Kumari, Sahni Rani Diana, Anandan Shalini, Sharma Archa, Gopi Radha, Hadibasha Noorjahan, Gunasekaran Priya, Veeraraghavan Balaji
Research Associate, Department of Clinical Microbiology, Christian Medical College , Vellore, India .
Professor, Department of Clinical Microbiology, Christian Medical College , Vellore, India .
J Clin Diagn Res. 2016 Jul;10(7):DC09-13. doi: 10.7860/JCDR/2016/16417.8152. Epub 2016 Jul 1.
Rapid identification of carbapenemase producing organisms is of great importance for timely detection, treatment and implementation of control measures to prevent the spread. The Modified Hodge Test (MHT) and Carba NP test is recommended by CLSI for the detection of carbapenemases in Enterobacteriaceae. However, MHT may give false positive results or fail to detect metallo β-lactamases (MBLs). In the US, MHT is the most widely used test for detection of carbapenemases and has been found to have a sensitivity and specificity of >90% for bla KPC producers. However, in India, the prevalence of bla NDM is higher than bla KPC producers.
To evaluate the usefulness of CarbaNP in an Indian setting.
A total of 260 isolates of carbapenem resistant E.coli (n=57), Klebsiella spp. (n=85), Pseudomonas aeruginosa (n=60), and Acinetobacter baumannii (58) isolated from clinical specimens between 2012-2014 at the Christian Medical College, Vellore were included in the study. All the carbapenem resistant isolates were subjected to CarbaNP, MHT and multiplex PCR for detection of carbapenemase genes.
CarbaNP was found to be positive in 88% (n=50/57), 81% (n=69/51), 38% (n=23/60) and 81% (n=47/58) for E.coli, Klebsiella spp., P. aeruginosa, and A. baumannii respectively. While in MHT it showed, 89% (n=51/57) and 81 % (n=69/85) for E.coli and Klebsiella spp. respectively. In P.aeruginosa, synergy testing of imipenem plus cloxacillin showed that, 65% of CarbaNP negatives were ampC producers. Overall, the sensitivity and specificity of CarbaNP was found to be 94% and 100 for bla NDM; 77% and 100 % for bla OXA-48 like producers and 81% and 100% for CarbAcinetoNP respectively.
This observation was more than what was reported in CLSI guidelines. Therefore, it is advisable to evaluate an assay for better laboratory diagnosis at respective regions.
快速鉴定产碳青霉烯酶的微生物对于及时检测、治疗以及实施控制措施以防止其传播至关重要。美国临床和实验室标准协会(CLSI)推荐使用改良 Hodge 试验(MHT)和 Carba NP 试验来检测肠杆菌科细菌中的碳青霉烯酶。然而,MHT 可能会给出假阳性结果或无法检测到金属β-内酰胺酶(MBL)。在美国,MHT 是检测碳青霉烯酶最广泛使用的试验,并且已发现其对 blaKPC 产生菌的敏感性和特异性均>90%。然而,在印度,blaNDM 的流行率高于 blaKPC 产生菌。
评估 CarbaNP 在印度环境中的实用性。
本研究纳入了 2012 年至 2014 年期间在韦洛尔基督教医学院从临床标本中分离出的总共 260 株耐碳青霉烯的大肠杆菌(n = 57)、克雷伯菌属(n = 85)、铜绿假单胞菌(n = 60)和鲍曼不动杆菌(58)。所有耐碳青霉烯的分离株均接受 CarbaNP、MHT 和多重 PCR 检测以检测碳青霉烯酶基因。
对于大肠杆菌、克雷伯菌属、铜绿假单胞菌和鲍曼不动杆菌,CarbaNP 检测呈阳性的比例分别为 88%(n = 50/57)、81%(n = 69/51)、38%(n = 23/60)和 81%(n = 47/58)。而在 MHT 检测中,大肠杆菌和克雷伯菌属的阳性比例分别为 89%(n = 51/57)和 81%(n = 69/85)。在铜绿假单胞菌中,亚胺培南加氯唑西林的协同试验表明,65%的 CarbaNP 阴性菌株为 AmpC 产生菌。总体而言,CarbaNP 对 blaNDM 的敏感性和特异性分别为 94%和 100%;对 blaOXA - 48 样产生菌的敏感性和特异性分别为 77%和 100%;对 CarbAcinetoNP 的敏感性和特异性分别为 81%和 100%。
这一观察结果高于 CLSI 指南中所报告的。因此,建议在各个地区评估一种检测方法以实现更好的实验室诊断。