Dhanalakshmi Sankaramoorthy, Meenachi Chidambaram, Parija Subhash Chandra
Ph.D Scholar, Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research , Puducherry, Tamil Nadu, India .
Junior Resident, Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research , Puducherry, Tamil Nadu, India .
J Clin Diagn Res. 2016 Aug;10(8):DC05-8. doi: 10.7860/JCDR/2016/21566.8326. Epub 2016 Aug 1.
Diagnosis of amoebiasis is based on combination of tests like microscopy, imaging, serology and molecular methods. In absence of molecular techniques, serology can be used as an alternative aid. Various serological techniques were reported with different sensitivity and specificity. The diagnostic efficiency of these assays mainly depends on the characteristics of antigen that is being used and various conditions of performance.
To evaluate the efficiency of recombinant calcium binding domain containing protein by Indirect Haemagglutination Assay (IHA) against a commercial ELISA among amoebic liver abscess cases and control group.
The study was carried out during the period of 2011-2015 and blood samples were collected from suspected amoebiasis cases who were attending the clinics of Medicine and Paediatrics department, JIPMER. A total of 200 sera samples which included 100 Amoebic Liver Abscess (ALA), 50 cases of other parasitic infections and liver diseases and 50 presumed healthy controls were examined by IHA and commercial ELISA. In brief, chick cells were stabilized by Double Aldehyde Sensitization (DAS) method. Optimum Sensitizing Dose (OSD) of the antigen was determined. The test was performed in a U-bottomed microtiter plate with recombinant amoebic antigen (12.5μg/ml), incubated at Room Temperature (RT) for 2 hours. RIDASCREEN Entamoeba IgG ELISA kit which is commercially available was used to evaluate the samples as per manufacturer's instruction.
The overall sensitivity and specificity of the IHA was 62% and 96%, respectively when compared to ELISA having sensitivity and specificity of 69% and 90%, respectively. The positive predictive value of the IHA was 91% while negative predictive value was 79%. Similarly, the positive predictive value of the ELISA was 87% while negative predictive value was 74%.
As serology heavily suffers due to lack of a standardised test system employing the native antigen, there arises need to identify alternative source of recombinant antigen which could effectively improvise the existing lacunae in the current system. Serology acts as an adjunct in clinical decision making if properly interpreted. This is an important consideration in endemic region where health services resources are limited.
阿米巴病的诊断基于显微镜检查、影像学、血清学和分子方法等多种检测方法的综合应用。在缺乏分子技术的情况下,血清学可作为一种辅助手段。已报道了各种血清学技术,其敏感性和特异性各不相同。这些检测方法的诊断效率主要取决于所使用抗原的特性和各种检测条件。
通过间接血凝试验(IHA)评估含重组钙结合结构域蛋白对商业酶联免疫吸附测定(ELISA)在阿米巴肝脓肿病例和对照组中的检测效率。
研究于2011年至2015年期间进行,从就诊于贾瓦哈拉尔·尼赫鲁医学研究理事会医学和儿科门诊的疑似阿米巴病病例中采集血样。总共200份血清样本,包括100例阿米巴肝脓肿(ALA)、50例其他寄生虫感染和肝脏疾病病例以及50例推定健康对照,通过IHA和商业ELISA进行检测。简而言之,采用双醛致敏(DAS)方法使鸡细胞稳定。确定抗原的最佳致敏剂量(OSD)。试验在U型微量滴定板中进行,加入重组阿米巴抗原(12.5μg/ml),在室温(RT)下孵育2小时。使用市售的RIDASCREEN Entamoeba IgG ELISA试剂盒按照制造商的说明对样本进行评估。
与ELISA相比,IHA的总体敏感性和特异性分别为62%和96%,而ELISA的敏感性和特异性分别为69%和90%。IHA的阳性预测值为91%,阴性预测值为79%。同样,ELISA的阳性预测值为87%,阴性预测值为74%。
由于缺乏使用天然抗原的标准化检测系统,血清学受到严重影响,因此需要确定重组抗原的替代来源,以有效改善当前系统中存在的缺陷。如果解释得当,血清学可作为临床决策的辅助手段。在卫生服务资源有限的流行地区,这是一个重要的考虑因素。