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J Clin Microbiol. 2015 Feb;53(2):493-7. doi: 10.1128/JCM.02836-14. Epub 2014 Nov 26.
2
Production of recombinant Entamoeba histolytica pyruvate phosphate dikinase and its application in a lateral flow dipstick test for amoebic liver abscess.重组溶组织内阿米巴丙酮酸磷酸二激酶的生产及其在阿米巴肝脓肿侧向流试纸条检测中的应用。
BMC Infect Dis. 2014 Apr 4;14:182. doi: 10.1186/1471-2334-14-182.
3
The effects of size and synthesis methods of gold nanoparticle-conjugated MαHIgG4 for use in an immunochromatographic strip test to detect brugian filariasis.金纳米粒子缀合的 MαHIgG4 大小和合成方法对用于检测盘尾丝虫病的免疫层析条试验的影响。
Nanotechnology. 2012 Dec 14;23(49):495719. doi: 10.1088/0957-4484/23/49/495719. Epub 2012 Nov 19.
4
Differentiating Entamoeba histolytica, Entamoeba dispar and Entamoeba moshkovskii using nested polymerase chain reaction (PCR) in rural communities in Malaysia.利用巢式聚合酶链反应(PCR)在马来西亚农村社区区分溶组织内阿米巴、迪斯帕内阿米巴和莫氏内阿米巴。
Parasit Vectors. 2012 Sep 4;5:187. doi: 10.1186/1756-3305-5-187.
5
Comparison of the Triage Micro Parasite Panel and Microscopy for the Detection of Entamoeba histolytica/Entamoeba dispar, Giardia lamblia, and Cryptosporidium parvum in Stool Samples Collected in Kenya.肯尼亚粪便样本中检测溶组织内阿米巴/迪斯帕内阿米巴、蓝氏贾第鞭毛虫和微小隐孢子虫的微寄生虫检测试剂盒与显微镜检查的比较。
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6
Evaluation of a rapid point-of-care fecal antigen detection test for Entamoeba histolytica.评估一种用于检测溶组织内阿米巴的即时粪便抗原检测试验。
Am J Trop Med Hyg. 2012 Jun;86(6):980-1. doi: 10.4269/ajtmh.2012.11-0661.
7
Evaluation of an immunochromatographic dip strip test for simultaneous detection of Cryptosporidium spp, Giardia duodenalis, and Entamoeba histolytica antigens in human faecal samples.评估一种免疫胶体金渗滤法检测试条,用于同时检测人粪便样本中的隐孢子虫属、蓝氏贾第鞭毛虫和溶组织内阿米巴抗原。
Eur J Clin Microbiol Infect Dis. 2012 Aug;31(8):2077-82. doi: 10.1007/s10096-012-1544-7. Epub 2012 Jan 20.
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Public health and clinical importance of amoebiasis in Malaysia: a review.马来西亚阿米巴病的公共卫生及临床重要性:综述
Trop Biomed. 2011 Aug;28(2):194-222.
9
Analysis of Entamoeba histolytica excretory-secretory antigen and identification of a new potential diagnostic marker.溶组织内阿米巴排泄分泌抗原分析及一种新的潜在诊断标志物的鉴定。
Clin Vaccine Immunol. 2011 Nov;18(11):1913-7. doi: 10.1128/CVI.05356-11. Epub 2011 Sep 14.
10
Application of real-time polymerase chain reaction in detection of Entamoeba histolytica in pus aspirates of liver abscess patients.实时聚合酶链反应在肝脓肿患者脓液抽吸物中溶组织内阿米巴检测中的应用。
Foodborne Pathog Dis. 2010 Jun;7(6):637-41. doi: 10.1089/fpd.2009.0427.

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.

DOI:10.1080/20477724.2017.1300421
PMID:28335696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5445638/
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。