Development and performance evaluation of a novel immunofluorescence chromatographic assay for histidine-rich protein 2 of Plasmodium falciparum

被引:3
作者
Kang, Keren [1 ,2 ]
Dzakah, Emmanuel E. [3 ]
Huang, Yongping [2 ]
Xie, Mingquan [1 ]
Luo, Xiaochun [1 ]
Li, Wenmei [2 ]
Wang, Jihua [2 ]
机构
[1] S China Univ Technol, Sch Biosci & Bioengn, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangzhou Wondfo Biotech Co Ltd, Natl Engn Lab Rapid Diagnost Tests, Guangzhou 510663, Guangdong, Peoples R China
[3] Univ Cape Coast, Coll Agr & Nat Sci, Sch Biol Sci, Dept Mol Biol & Biotechnol, Cape Coast, Ghana
关键词
Plasmodium falciparum; Immunofluorescence chromatographic assay; Histidine-rich protein 2; Rapid diagnostic test; TRANSMISSION SETTINGS; MALARIA; DIAGNOSIS; ANTIGEN; TESTS;
D O I
10.1186/s12936-015-0740-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: The low sensitivity and specificity of Plasmodium falciparum diagnostic tests pose a serious health threat to people living in endemic areas. The objective of the study was to develop a rapid assay for the detection of histidine-rich protein 2 (HRP2) of P. falciparum in whole blood by immunofluorescence chromatographic technology. Methods: A total of 1163 positive and negative blood samples were screened. The double-antibody sandwich assay was used to establish the kit and its performance was evaluated for sensitivity, specificity, accuracy, precision, stability, and clinical effectiveness. Results: The cut-off level of detection of the kit was 25 parasites/mu l. Common interfering substances in human blood specimens, such as bilirubin, triglyceride and cholesterol had no significant effect on HRP2 antigen detection. The precision of the kit was run with different concentration of standard calibrators and the values were less than 10 %. The performance of this diagnostic kit in the detection of the calibrators has shown that a shelf life of about 12 months gives a more reliable result. Among clinical samples tested, the HRP2 test kit and the reference products had good coincidence rate in a parallel experiment and this test kit had a more sensitive detecting level to the target protein than the reference kits used in this study. The specificity and sensitivity for this test were 99.6 % (800/803) and 99.7 % (1160/1163), respectively. Conclusions: A novel HRP2 immunofluorescence detection method was developed in this study. Overall performance evaluation indicated that the kit has a rapid, high sensitivity and on-spot method for detecting P. falciparum.
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页数:8
相关论文
共 20 条
[1]   Malaria diagnostic testing and treatment practices in three different Plasmodium falciparum transmission settings in Tanzania: before and after a government policy change [J].
Bastiaens, Guido J. H. ;
Schaftenaar, Erik ;
Ndaro, Arnold ;
Keuter, Monique ;
Bousema, Teun ;
Shekalaghe, Seif A. .
MALARIA JOURNAL, 2011, 10
[2]  
Bell D, 2006, NAT REV MICROBIOL, pS34, DOI [10.1038/nrmico1524, 10.1038/nrmicro1524]
[3]  
CFDA, 2010, GUID PERF EV IN VITR
[4]  
Das P, 1984, J Diarrhoeal Dis Res, V2, P238
[5]   Sample Preincubation Strategy for Sensitive and Quantitative Detection of Clenbuterol in Swine Urine Using a Fluorescent Microsphere-Based Immunochromatographic Assay [J].
Deng, Sheng L. ;
Shan, Shan ;
Xu, Chao L. ;
Liu, Dao F. ;
Xiong, Yong H. ;
Wei, Hua ;
Lai, Wei H. .
JOURNAL OF FOOD PROTECTION, 2014, 77 (11) :1998-2003
[6]   Stage-dependent production and release of histidine-rich protein 2 by Plasmodium falciparum [J].
Desakorn, V ;
Dondorp, AM ;
Silamut, K ;
Pongtavornpinyo, W ;
Sahassananda, D ;
Chotivanich, K ;
Pitisuttithum, P ;
Smithyman, AM ;
Day, NPJ ;
White, NJ .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2005, 99 (07) :517-524
[7]   Preparedness for Malaria Resurgence in China: Case Study on Imported Cases in 2000-2012 [J].
Feng, Jun ;
Xia, Zhi-Gui ;
Vong, Sirenda ;
Yang, Wei-Zhong ;
Zhou, Shui-Sen ;
Xiao, Ning .
MALARIA CONTROL AND ELIMINATION PROGRAM IN THE PEOPLE'S REPUBLIC OF CHINA, 2014, 86 :231-265
[8]   Genome sequence of the human malaria parasite Plasmodium falciparum [J].
Gardner, MJ ;
Hall, N ;
Fung, E ;
White, O ;
Berriman, M ;
Hyman, RW ;
Carlton, JM ;
Pain, A ;
Nelson, KE ;
Bowman, S ;
Paulsen, IT ;
James, K ;
Eisen, JA ;
Rutherford, K ;
Salzberg, SL ;
Craig, A ;
Kyes, S ;
Chan, MS ;
Nene, V ;
Shallom, SJ ;
Suh, B ;
Peterson, J ;
Angiuoli, S ;
Pertea, M ;
Allen, J ;
Selengut, J ;
Haft, D ;
Mather, MW ;
Vaidya, AB ;
Martin, DMA ;
Fairlamb, AH ;
Fraunholz, MJ ;
Roos, DS ;
Ralph, SA ;
McFadden, GI ;
Cummings, LM ;
Subramanian, GM ;
Mungall, C ;
Venter, JC ;
Carucci, DJ ;
Hoffman, SL ;
Newbold, C ;
Davis, RW ;
Fraser, CM ;
Barrell, B .
NATURE, 2002, 419 (6906) :498-511
[9]   Defining Falciparum-Malaria-Attributable Severe Febrile Illness in Moderate-to-High Transmission Settings on the Basis of Plasma PfHRP2 Concentration [J].
Hendriksen, Ilse C. E. ;
White, Lisa J. ;
Veenemans, Jacobien ;
Mtove, George ;
Woodrow, Charles ;
Amos, Ben ;
Saiwaew, Somporn ;
Gesase, Samwel ;
Nadjm, Behzad ;
Silamut, Kamolrat ;
Joseph, Sarah ;
Chotivanich, Kesinee ;
Day, Nicholas P. J. ;
von Seidlein, Lorenz ;
Verhoef, Hans ;
Reyburn, Hugh ;
White, Nicholas J. ;
Dondorp, Arjen M. .
JOURNAL OF INFECTIOUS DISEASES, 2013, 207 (02) :351-361
[10]  
[康可人 Kang Keren], 2014, [中华检验医学杂志, Chinese Journal of Laboratory Medicine], V37, P842