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用于粪便样本中溶组织内阿米巴抗原检测的侧向流动试纸条检测方法的开发与初步评估。

Development and initial evaluation of a lateral flow dipstick test for antigen detection of Entamoeba histolytica in stool sample.

作者信息

Saidin Syazwan, Yunus Muhammad Hafiznur, Othman Nurulhasanah, Lim Yvonne Ai-Lian, Mohamed Zeehaida, Zakaria Nik Zairi, Noordin Rahmah

机构信息

a Institute for Research in Molecular Medicine , Universiti Sains Malaysia , Penang , Malaysia.

b Faculty of Medicine, Department of Parasitology , University of Malaya , Kuala Lumpur , Malaysia.

出版信息

Pathog Glob Health. 2017 May;111(3):128-136. doi: 10.1080/20477724.2017.1300421. Epub 2017 Mar 24.

Abstract

Entamoeba histolytica infection remains a public health concern in developing countries. Early diagnosis of amoebiasis can avoid disease complications, thus this study was aimed at developing a test that can rapidly detect the parasite antigens in stool samples. Rabbits were individually immunized with recombinant pyruvate phosphate dikinase (rPPDK) and E. histolytica excretory-secretory antigens to produce polyclonal antibodies. A rapid dipstick test was produced using anti-rPPDK PAb lined on the dipstick as capture reagent and anti-EhESA PAb conjugated to colloidal gold as the detector reagent. Using E. histolytica-spiked in stool sample of a healthy individual, the detection limit of the dipstick test was found to be 1000 cells ml. Meanwhile when rPPDK was spiked in the stool sample, the minimum concentration detected by the dipstick test was 0.1 μg ml. The performances of the dipstick, commercial Techlab E. histolytica II enzyme-linked immunosorbent assays (ELISA) and real-time PCR were compared using 70 stool samples from patients infected with Entamoeba species (n = 45) and other intestinal pathogens (n = 25). When compared to real-time PCR, the diagnostic sensitivity of the dipstick for detection of E. histolytica was 65.4% (n = 17/26); while the diagnostic specificity when tested with stool samples containing other intestinal pathogens was 92% (23/25). In contrast, Techlab E. histolytica II ELISA detected 19.2% (5/26) of the E. histolytica-positive samples as compared to real-time PCR. The lateral flow dipstick test produced in this study enabled rapid detection of E. histolytica, thus it showed good potential to be further developed into a diagnostic tool for intestinal amoebiasis.

摘要

溶组织内阿米巴感染在发展中国家仍然是一个公共卫生问题。早期诊断阿米巴病可以避免疾病并发症,因此本研究旨在开发一种能够快速检测粪便样本中寄生虫抗原的检测方法。用重组丙酮酸磷酸双激酶(rPPDK)和溶组织内阿米巴排泄分泌抗原分别免疫兔子,以产生多克隆抗体。使用固定在试纸条上的抗rPPDK多克隆抗体作为捕获试剂,与胶体金偶联的抗EhESA多克隆抗体作为检测试剂,制作了一种快速试纸条检测方法。使用添加了溶组织内阿米巴的健康个体粪便样本,发现试纸条检测方法的检测限为每毫升1000个细胞。同时,当在粪便样本中添加rPPDK时,试纸条检测方法检测到的最低浓度为每毫升0.1微克。使用来自感染溶组织内阿米巴物种的患者(n = 45)和其他肠道病原体的患者(n = 25)的70份粪便样本,比较了试纸条、商业Techlab溶组织内阿米巴II酶联免疫吸附测定(ELISA)和实时PCR的性能。与实时PCR相比,试纸条检测溶组织内阿米巴的诊断敏感性为65.4%(n = 17/26);而用含有其他肠道病原体的粪便样本进行检测时,诊断特异性为92%(23/25)。相比之下,与实时PCR相比,Techlab溶组织内阿米巴II ELISA检测到19.2%(5/26)的溶组织内阿米巴阳性样本。本研究中制作的侧向流动试纸条检测方法能够快速检测溶组织内阿米巴,因此显示出进一步开发成为肠道阿米巴病诊断工具的良好潜力。

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