Piezoelectric immunochip for the detection of dengue fever in viremia phase

被引:60
作者
Wu, TZ
Su, CC
Chen, LK
Yang, HH
Tai, DF
Peng, KC [1 ]
机构
[1] Natl Dong Hwa Univ, Dept Life Sci, Hualien, Taiwan
[2] Natl Dong Hwa Univ, Inst Biotechnol, Hualien, Taiwan
[3] Buddhist Tzu Chi Univ, Sch Med, Dept Emergency Med, Hualien, Taiwan
[4] Natl Dong Hwa Univ, Dept Chem, Hualien, Taiwan
关键词
dengue virus; clinical detection; quartz crystal microbalance; immunochip; antibody immobilization; monoclonal antibody;
D O I
10.1016/j.bios.2004.12.019
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The global prevalence of dengue fever has grown so dramatically in recent years that it is endemic in more than 100 countries and has become a major international public health concern. Moreover, since the flu-like symptoms that accompany dengue fever are atypical and varied, the detection procedures currently used to identify it are cumbersome and time-consuming, making early stage epidemiological control and effective medical treatment of this epidemic almost impossible. In this study, a QCM-based detection system was developed in which two monoclonal antibodies against dengue E and NS-1 protein, respectively, were control orientated immobilized on QCM via protein A to produce an immunochip. Various sample pretreatment procedures were evaluated to ascertain the most suitable combination, and both the simulating samples and the clinical specimen were examined by the immunochip. The results revealed that the cibacron blue 3GA gel-heat denature (CB-HD) method was the most effective sample pretreatment technique. Due to the complex composition of the serum, the immunochip could only effectively quantify dengue viral antigens in a 1/1000 untreated simulated sample. With the help of the CB-HD method, the dilution folds were found to capable of being reduced from 1000 to 100, and the detection limit lowered to 1.727 mu g/ml (E protein) and 0.740 mu g/ml (NS-1 protein) in the original sample. While the cocktail immunochip could not quantify both antigens separately, the higher signal level rendered it a more effective qualification tool for suspect screening. Moreover, the results of the analysis of clinical specimens also proved the ability and future potential of cocktail immunochip in discriminating dengue-positive cases from negative serum specimens in the viremia phase. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:689 / 695
页数:7
相关论文
共 20 条
[1]   Piezoelectric quartz crystal biosensors [J].
Bunde, RL ;
Jarvi, EJ ;
Rosentreter, JJ .
TALANTA, 1998, 46 (06) :1223-1236
[2]   QUARTZ-CRYSTAL MICROBALANCE DETECTION OF VIBRIO-CHOLERAE O139 SEROTYPE [J].
CARTER, RM ;
MEKALANOS, JJ ;
JACOBS, MB ;
LUBRANO, GJ ;
GUILBAULT, GG .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 187 (01) :121-125
[3]   Diagnosis of dengue infection by detecting specific immunoglobulin M antibodies in saliva samples [J].
de Oliveira, SA ;
Rodrigues, CVN ;
Camacho, LAB ;
Miagostovich, MP ;
Araújo, ESM ;
Nogueira, RMR .
JOURNAL OF VIROLOGICAL METHODS, 1999, 77 (01) :81-86
[4]  
DEUBEL V, 2001, ENCY ARTHR TRANSMITT
[5]   Dengue: an escalating problem [J].
Gibbons, RV ;
Vaughn, DW .
BMJ-BRITISH MEDICAL JOURNAL, 2002, 324 (7353) :1563-1566
[6]   Impact of dengue/dengue hemorrhagic fever on the developing world [J].
Gubler, DJ ;
Meltzer, M .
ADVANCES IN VIRUS RESEARCH, VOL 53, 1999, 53 :35-70
[7]   Dengue and dengue hemorrhagic fever [J].
Gubler, DJ .
CLINICAL MICROBIOLOGY REVIEWS, 1998, 11 (03) :480-+
[8]   Dengue:: an update [J].
Guzmán, MG ;
Kouri, G .
LANCET INFECTIOUS DISEASES, 2002, 2 (01) :33-42
[9]   The future of dengue vaccines [J].
Halstead, SB ;
Deen, J .
LANCET, 2002, 360 (9341) :1243-1245
[10]   Dengue virus infection: Epidemiology, pathogenesis, clinical presentation, diagnosis, and prevention [J].
Kautner, I ;
Robinson, MJ ;
Kuhnle, U .
JOURNAL OF PEDIATRICS, 1997, 131 (04) :516-524