Exploiting generic platform technologies for the detection and identification of plant pathogens

被引:70
作者
Boonham, Neil [1 ]
Glover, Rachel [1 ]
Tomlinson, Jenny [1 ]
Mumford, Rick [1 ]
机构
[1] Cent Sci Lab, York, N Yorkshire, England
关键词
plant health; diagnostics; detection; real-time PCR; DNA barcoding; microarrays; isothermal amplification; LAMP; direct tuber testing; molecular diagnostics; TaqMan; de novo sequencing; pyrosequencing;
D O I
10.1007/s10658-008-9284-3
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The detection and identification of plant pathogens currently relies upon a very diverse range of techniques and skills, from traditional culturing and taxonomic skills to modern molecular-based methods. The wide range of methods employed reflects the great diversity of plant pathogens and the hosts they infect. The well-documented decline in taxonomic expertise, along with the need to develop ever more rapid and sensitive diagnostic methods has provided an impetus to develop technologies that are both generic and able to complement traditional skills and techniques. Real-time polymerase chain reaction (PCR) is emerging as one such generic platform technology and one that is well suited to high-throughput detection of a limited number of known target pathogens. Real-time PCR is now exploited as a front line diagnostic screening tool in human health, animal health, homeland security, biosecurity as well as plant health. Progress with developing generic techniques for plant pathogen identification, particularly of unknown samples, has been less rapid. Diagnostic microarrays and direct nucleic acid sequencing (de novo sequencing) both have potential as generic methods for the identification of unknown plant pathogens but are unlikely to be suitable as high-throughput detection techniques. This paper will review the application of generic technologies in the routine laboratory as well as highlighting some new techniques and the trend towards multi-disciplinary studies.
引用
收藏
页码:355 / 363
页数:9
相关论文
共 42 条
[21]   Development of a multiplex AmpliDet RNA for the simultaneous detection of Potato leafroll virus and Potato virus Y in potato tubers [J].
Klerks, MM ;
Leone, GOM ;
Verbeek, M ;
van den Heuvel, JFJM ;
Schoen, CD .
JOURNAL OF VIROLOGICAL METHODS, 2001, 93 (1-2) :115-125
[22]   Rapid sequencer puts virus in the frame for deaths [J].
Ledford, Heidi .
NATURE, 2007, 447 (7140) :12-13
[23]   Direct detection of potato leafroll virus in potato tubers by immunocapture and the isothermal nucleic acid amplification method NASBA [J].
Leone, G ;
vanSchijndel, HB ;
vanGemen, B ;
Schoen, CD .
JOURNAL OF VIROLOGICAL METHODS, 1997, 66 (01) :19-27
[24]   THE DETECTION OF TOMATO SPOTTED WILT VIRUS USING THE POLYMERASE CHAIN-REACTION [J].
MUMFORD, RA ;
BARKER, I ;
WOOD, KR .
JOURNAL OF VIROLOGICAL METHODS, 1994, 46 (03) :303-311
[25]   Advances in molecular phytodiagnostics - new solutions for old problems [J].
Mumford, Rick ;
Boonham, Neil ;
Tomlinson, Jenny ;
Barker, Ian .
EUROPEAN JOURNAL OF PLANT PATHOLOGY, 2006, 116 (01) :1-19
[26]   Using COI barcodes to identify forensically and medically important blowflies [J].
Nelson, L. A. ;
Wallman, J. F. ;
Dowton, M. .
MEDICAL AND VETERINARY ENTOMOLOGY, 2007, 21 (01) :44-52
[27]   Loop-mediated isothermal amplification of DNA [J].
Notomi, Tsugunori ;
Okayama, Hiroto ;
Masubuchi, Harumi ;
Yonekawa, Toshihiro ;
Watanabe, Keiko ;
Amino, Nobuyuki ;
Hase, Tetsu .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12)
[28]  
ODONNELL KJ, 1996, BCPC S P, V65, P187
[29]   Development of microarray-based diagnostics of voles and shrews for use in biodiversity monitoring studies, and evaluation of mitochondrial cytochrome oxidase I vs. cytochrome b as genetic markers [J].
Pfunder, M ;
Holzgang, O ;
Frey, JE .
MOLECULAR ECOLOGY, 2004, 13 (05) :1277-1286
[30]   SEQUENCE-ANALYSIS OF MINUTE AMOUNTS OF VIROID RNA USING THE POLYMERASE CHAIN-REACTION (PCR) [J].
PUCHTA, H ;
SANGER, HL .
ARCHIVES OF VIROLOGY, 1989, 106 (3-4) :335-340