Electronic microarray analysis of 16S rDNA amplicons for bacterial detection

被引:24
作者
Barlaan, EA
Sugimori, M
Furukawa, S
Takeuchi, K
机构
[1] Nagasaki Ind Promot Fdn, Nagasaki 8560026, Japan
[2] Mitsubishi Heavy Ind Co Ltd, Tech Headquarters, Nagasaki Res & Dev Ctr, Nagasaki 8510392, Japan
关键词
electronic microarray; NanoChip; DNA chip; probes; pathogenic bacteria; 16S rDNA;
D O I
10.1016/j.jbiotec.2004.07.015
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Electronic microarray technology is a potential alternative in bacterial detection and identification. However, conditions for bacterial detection by electronic microarray need optimization. Using the NanoChip electronic microarray, we investigated eight marine bacterial species. Based on the 16S rDNA sequences of these species, we constructed primers, reporter probes, and species-specific capture probes. We carried out two separate analyses for longer (533 bp) and shorter (350 and 200 bp) amplified products (amplicons). To detect simultaneously the hybridization signals for the 350- and 200-bp amplicons, we designed a common reporter probe from an overlapping sequence within both fragments. We developed methods to optimize detection of hybridization signals for processing the DNA chips. A matrix analysis was performed for different bacterial species and complementary capture probes on electronic microarrays. Results showed that, when using the longer amplicon, not all bacterial targets hybridized with the complementary capture probes, which was characterized by the presence of false-positive signals. However, with the shorter amplicons, all bacterial species were correctly and completely detected using the constructed complementary capture probes. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 21
页数:11
相关论文
共 29 条
[1]   Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray [J].
Borsting, C ;
Sanchez, JJ ;
Morling, N .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2004, 118 (02) :75-82
[2]   Nocardiosis in tank-reared Atlantic salmon, Salmo salar L. [J].
Bransden, MP ;
Carson, J ;
Munday, BL ;
Handlinger, JH ;
Carter, CG ;
Nowak, BF .
JOURNAL OF FISH DISEASES, 2000, 23 (01) :83-85
[3]   Detection of Flexibacter maritimus in fish tissue using nested PCR amplification [J].
Cepeda, C ;
García-Márquez, S ;
Santos, Y .
JOURNAL OF FISH DISEASES, 2003, 26 (02) :65-70
[4]   Sequence versus structure for the direct detection of 16S rRNA on planar oligonucleotide microarrays [J].
Chandler, DP ;
Newton, GJ ;
Small, JA ;
Daly, DS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (05) :2950-2958
[5]   Development of a universal probe for electronic microarray and its application in characterization of the Staphylococcus aureus po/C gene [J].
Cooper, KLF ;
Goering, RV .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2003, 5 (01) :28-33
[6]  
Edman CF, 2000, J INVEST MED, V48, P93
[7]   Electric field directed nucleic acid hybridization on microchips [J].
Edman, CF ;
Raymond, DE ;
Wu, DJ ;
Tu, EG ;
Sosnowski, RG ;
Butler, WF ;
Nerenberg, M ;
Heller, MJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (24) :4907-4914
[8]  
Eldar A, 1999, APPL ENVIRON MICROB, V65, P1005
[9]   Lactococcus garvieae endocarditis:: Report of a case and review of the literature [J].
Fefer, JJ ;
Ratzan, KR ;
Sharp, SE ;
Saiz, E .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1998, 32 (02) :127-130
[10]   Single nucleotide polymorphic discrimination by an electronic dot blot assay on semiconductor microchips [J].
Gilles, PN ;
Wu, DJ ;
Foster, CB ;
Dillon, PJ ;
Chanock, SJ .
NATURE BIOTECHNOLOGY, 1999, 17 (04) :365-370