Recent developments in pathogen detection arrays: Implications for fungal plant pathogens and use in practice

被引:111
作者
Lievens, B
Thomma, BPHJ
机构
[1] Katholieke Univ Leuven, CMPG, B-3001 Heverlee, Belgium
[2] Scientia Terrae Res Inst, B-2860 St Katelijne Waver, Belgium
[3] Wageningen Univ, Phytopathol Lab, NL-6709 PD Wageningen, Netherlands
关键词
diagnosis; disease management; high-throughput; phytopathogen;
D O I
10.1094/PHYTO-95-1374
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The failure to adequately identify plant pathogens from culture-based morphological techniques has led to the development of culture-independent molecular approaches. Increasingly, diagnostic laboratories are pursuing fast routine methods that provide reliable identification, sensitive detection, and accurate quantification of plant pathogens. In addition, since plants or parts thereof can be infected by multiple pathogens, multiplex assays that can detect and quantify different pathogens simultaneously are highly desirable. Technologies that can meet these requirements, especially those involving polymerase chain reaction, are being developed and implemented in horticultural and agricultural practice. Currently, DNA array technology is the most suitable technique for multiplex detection of plant pathogens. Recently, a quantitative aspect was added to this technology, making DNA arrays highly attractive for various research and practical applications. Here, we review the most important recent advances in molecular plant pathogen diagnostics, with special attention to fungal molecular diagnostics. In addition to their applicability in practice, the different criteria that have to be fulfilled for developing robust detection procedures that can routinely be used by diagnostic laboratories are discussed.
引用
收藏
页码:1374 / 1380
页数:7
相关论文
共 64 条
[11]   Vertical niche differentiation of ectomycorrhizal hyphae in soil as shown by T-RFLP analysis [J].
Dickie, IA ;
Xu, B ;
Koide, RT .
NEW PHYTOLOGIST, 2002, 156 (03) :527-535
[12]  
EGGERS M, 2000, INNOV PHARM TECHNOL, V6, P36
[13]   Multiplex PCR: Optimization and application in diagnostic virology [J].
Elnifro, EM ;
Ashshi, AM ;
Cooper, RJ ;
Klapper, PE .
CLINICAL MICROBIOLOGY REVIEWS, 2000, 13 (04) :559-+
[14]   An oligonucleotide array for the identification and differentiation of bacteria pathogenic on potato [J].
Fessehaie, A ;
De Boer, SH ;
Lévesque, CA .
PHYTOPATHOLOGY, 2003, 93 (03) :262-269
[15]   Rapid detection and diagnosis of Septoria tritici epidemics in wheat using a polymerase chain reaction PicoGreen assay [J].
Fraaije, BA ;
Lovell, DJ ;
Rohel, EA ;
Hollomon, DW .
JOURNAL OF APPLIED MICROBIOLOGY, 1999, 86 (04) :701-708
[16]   Real-time PCR: what relevance to plant studies? [J].
Gachon, C ;
Mingam, A ;
Charrier, B .
JOURNAL OF EXPERIMENTAL BOTANY, 2004, 55 (402) :1445-1454
[17]   Barcoding animal life:: cytochrome c oxidase subunit 1 divergences among closely related species [J].
Hebert, PDN ;
Ratnasingham, S ;
deWaard, JR .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2003, 270 :S96-S99
[18]   Real time quantitative PCR [J].
Heid, CA ;
Stevens, J ;
Livak, KJ ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :986-994
[19]   Persistence of DNA of Gaeumannomyces graminis var. tritici in soil as measured by a DNA-based assay [J].
Herdina ;
Neate, S ;
Jabaji-Hare, S ;
Ophel-Keller, K .
FEMS MICROBIOLOGY ECOLOGY, 2004, 47 (02) :143-152
[20]   QUANTIFICATION OF VERTICILLIUM BIOMASS IN WILT DISEASE DEVELOPMENT [J].
HU, X ;
NAZAR, RN ;
ROBB, J .
PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 1993, 42 (01) :23-36