Visual DNA microarrays for simultaneous detection of Ureaplasma urealyticum and Chlamydia trachomatis coupled with multiplex asymmetrical PCR

被引:35
作者
Cao, Xuan [1 ]
Wang, Ye-Fu [1 ]
Zhang, Chu-Fu [1 ]
Gao, Wen-Juan [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, Wuhan 430072, Peoples R China
关键词
Ureaplasma urealyticum; Chlamydia trachomatis; DNA microarrays; gold nanoparticles; gold-conjugated streptavidins; gold label silver stain; multiplex asymmetrical PCR;
D O I
10.1016/j.bios.2006.05.011
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Visual DNA microarrays, based on gold label silver stain (GLSS) and coupled with multiplex asymmetrical PCR, were developed for simultaneous, sensitive and specific detection of Ureaplasma urealyticum and Chlanzydia trachomatis. 5'-end-amino-modified oligonucleotides, which were immobilized on glass surface, acted as capturing probes that were designed to bind complementary biotinylated targets DNA. The gold-conjugated streptavidins were introduced to the microarray for specific binding to biotin. The black image of microarray spots, resulting from the precipitation of silver onto nanogold particles bound to streptavidins, were used to detect biotinylated targets DNA visually or with a visible light scanner. Multiplex asymmetrical PCR of U. urealyticum, C. trachomatis and Bacillus subtilis (used as positive control) was performed to prepare abundant biotinylated single-stranded targets DNA, which affected detection efficiency and sensitivity of hybridization on microarray. Plenty of clinical samples of U. urealyticuin and C. trachomatis from infected patients were tested using home-made DNA microarrays. For its high sensitivity, good specificity, simplicity, cheapness and speed, the present visual gene-detecting technique has potential applications in clinical fields. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:393 / 398
页数:6
相关论文
共 16 条
[1]   Colorimetric silver detection of DNA microarrays [J].
Alexandre, I ;
Hamels, S ;
Dufour, S ;
Collet, J ;
Zammatteo, N ;
De Longueville, F ;
Gala, JL ;
Remacle, J .
ANALYTICAL BIOCHEMISTRY, 2001, 295 (01) :1-8
[2]  
BOWTELLD L, 1999, NAT GENET, V21, P25
[3]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[4]   DELETION SCREENING OF THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS VIA MULTIPLEX DNA AMPLIFICATION [J].
CHAMBERLAIN, JS ;
GIBBS, RA ;
RANIER, JE ;
NGUYEN, PN ;
CASKEY, CT .
NUCLEIC ACIDS RESEARCH, 1988, 16 (23) :11141-11156
[5]   Covalent attachment of synthetic DNA to self-assembled monolayer films [J].
Chrisey, LA ;
Lee, GU ;
OFerrall, CE .
NUCLEIC ACIDS RESEARCH, 1996, 24 (15) :3031-3039
[6]   PREPARATION AND CHARACTERIZATION OF AU COLLOID MONOLAYERS [J].
GRABAR, KC ;
FREEMAN, RG ;
HOMMER, MB ;
NATAN, MJ .
ANALYTICAL CHEMISTRY, 1995, 67 (04) :735-743
[7]   Methods for genotyping single nucleotide polymorphisms [J].
Kwok, PY .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2001, 2 :235-258
[8]   Genomics, gene expression and DNA arrays [J].
Lockhart, DJ ;
Winzeler, EA .
NATURE, 2000, 405 (6788) :827-836
[9]  
Sambrook J, 1989, MOL CLONING LAB MANU
[10]   Microarrays: biotechnology's discovery platform for functional genomics [J].
Schena, M ;
Heller, RA ;
Theriault, TP ;
Konrad, K ;
Lachenmeier, E ;
Davis, RW .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (07) :301-306