The use of real-time PCR and species-specific primers for the identification and monitoring of Paecilomyces lilacinus

被引:111
作者
Atkins, SD
Clark, IM
Pande, S
Hirsch, PR
Kerry, BR
机构
[1] Rothamsted Res, Harpenden AL5 2JQ, Herts, England
[2] Univ Reading, Reading RG6 6AH, Berks, England
基金
英国生物技术与生命科学研究理事会;
关键词
Paecilomyces lilacinus; PCR diagnostics; species-specific primers; potato cyst nematodes; real-time PCR;
D O I
10.1016/j.femsec.2004.09.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Paecilomyces lilacinus is the most widely tested fungus for the control of root-knot and cyst nematodes. The fungus has also been implicated in a number of human and animal infections, difficulties in diagnosis often result in misdiagnosis or delays identification leading to a delay in treatment. Here, we report the development of species-specific primers for the identification of P. lilacinus based on sequence information from the ITS gene, and their use in identifying P. lilacinus isolates, including clinical isolates of the fungus. The primer set generated a single PCR fragment of 130 bp in length that was specific to P. lilacinus and was also used to detect the presence of P. lilacinus from soil, roots and nematode eggs. Real-time PCR primers and a TaqMang(R) probe were also developed and provided quantitative data on the population size of the fungus in two field sites. PCR, bait and culture methods were combined to investigate the presence and abundance of the fungus from two field sites in the United Kingdom where potato cyst nematode populations were naturally declining, and results demonstrated the importance of using a combination of methods to investigate population size and activity of fungi. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 264
页数:8
相关论文
共 33 条
[1]   Detection and quantification of Plectosphaerella cucumerina, a potential biological control agent of potato cyst nematodes, by using conventional PCR, real-time PCR, selective media, and baiting [J].
Atkins, SD ;
Clark, IM ;
Sosnowska, D ;
Hirsch, PR ;
Kerry, BR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (08) :4788-4793
[2]   Approaches for monitoring the release of Pochonia chlamydosporia var. catenulata, a biocontrol agent of root-knot nematodes [J].
Atkins, SD ;
Hidalgo-Diaz, L ;
Clark, IM ;
Morton, CO ;
de Oca, NM ;
Gray, PA ;
Kerry, BR .
MYCOLOGICAL RESEARCH, 2003, 107 :206-212
[3]  
ATKINS SD, 2003, IOBC B, V27, P1
[4]   Approaches to molecular characterization of fungal biocontrol agents:: some case studies [J].
Avis, TJ ;
Hamelin, RC ;
Bélanger, RR .
CANADIAN JOURNAL OF PLANT PATHOLOGY, 2001, 23 (01) :8-12
[5]   The application of real-time PCR to the identification, detection and quantification of Pyrenophora species in barley seed [J].
Bates, J. A. ;
Taylor, E. J. A. ;
Kenyon, D. M. ;
Thomas, J. E. .
MOLECULAR PLANT PATHOLOGY, 2001, 2 (01) :49-57
[6]   Real-time quantitative PCR:: DNA determination in isolated spores of the mycorrhizal fungus Glomus mosseae and monitoring of Phytophora infestans and Phytophthora citricola in their respective host plants [J].
Böhm, J ;
Hahn, A ;
Schubert, R ;
Bahnweg, G ;
Adler, N ;
Nechwatal, J ;
Oehlmann, R ;
Osswald, W .
JOURNAL OF PHYTOPATHOLOGY-PHYTOPATHOLOGISCHE ZEITSCHRIFT, 1999, 147 (7-8) :409-416
[7]   Molecular diagnostics in clinical parasitology and mycology: limits of the current polymerase chain reaction (PCR) assays and interest of the real-time PCR assays [J].
Bretagne, S .
CLINICAL MICROBIOLOGY AND INFECTION, 2003, 9 (06) :505-511
[8]  
CRUMP DH, 1998, ASPECTS APPL BIOL, V52, P383
[9]   Conventional PCR and real-time quantitative PCR detection of Helminthosporium solani in soil and on potato tubers [J].
Cullen, DW ;
Lees, AK ;
Toth, IK ;
Duncan, JM .
EUROPEAN JOURNAL OF PLANT PATHOLOGY, 2001, 107 (04) :387-398
[10]  
Diaz-Silveira MF, 1998, NEMATROPICA, V28, P151