Detection and Quantification of Leveillula taurica Growth in Pepper Leaves

被引:22
作者
Zheng, Zheng [1 ]
Nonomura, Teruo [2 ]
Boka, Karoly [3 ]
Matsuda, Yoshinori [2 ]
Visser, Richard G. F. [1 ]
Toyoda, Hideyoshi [2 ]
Kiss, Levente [4 ]
Bai, Yuling [1 ]
机构
[1] Univ Wageningen & Res Ctr, Wageningen UR Plant Breeding, NL-6708 PB Wageningen, Netherlands
[2] Kinki Univ, Lab Phytoprotect Sci & Technol, Fac Agr, Nara 6318505, Japan
[3] Eotvos Lorand Univ, Dept Plant Anat, H-1117 Budapest, Hungary
[4] Hungarian Acad Sci, Inst Plant Protect, Agr Res Ctr, H-1525 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
INTERNAL TRANSCRIBED SPACER; POWDERY-MILDEW; GENUS LEVEILLULA; RESISTANCE; SEQUENCES; PCR; DNA; ERYSIPHALES; MYCELIUM; MARKER;
D O I
10.1094/PHYTO-08-12-0198-R
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Leveillula taurica is an obligate fungal pathogen that causes powdery mildew disease on a broad range of plants, including important crops such as pepper, tomato, eggplant, onion, cotton, and so on. The early stage of this disease is difficult to diagnose and the disease can easily spread unobserved; for example, in pepper and tomato production fields and greenhouses. The objective of this study was to develop a detection and quantification method of L. taurica biomass in pepper leaves with special regard to the early stages of infection. We monitored the development of the disease to time the infection process on the leaf surface as well as inside the pepper leaves. The initial and final steps of the infection taking place on the leaf surface were consecutively observed using a dissecting microscope and a scanning electron microscope. The development of the intercellular mycelium in the mesophyll was followed by light and transmission electron microscopy. A pair of L. taurica-specific primers was designed based on the internal transcribed spacer sequence of L. taurica and used in real-time polymerase chain reaction (PCR) assay to quantify the fungal DNA during infection. The specificity of this assay was confirmed by testing the primer pair with DNA from host plants and also from another powdery mildew species, Oidium neolycopersici, infecting tomato. A standard curve was obtained for absolute quantification of L. taurica biomass. In addition, we tested a relative quantification method by using a plant gene as reference and the obtained results were compared with the visual disease index scoring. The real-time PCR assay for L. taurica provides a valuable tool for detection and quantification of this pathogen in breeding activities as well in plant microbe interaction studies.
引用
收藏
页码:623 / 632
页数:10
相关论文
共 37 条
[1]   QTLs for tomato powdery mildew resistance (Oidium lycopersici) in Lycopersicon parviflorum G1.1601 co-localize with two qualitative powdery mildew resistance genes [J].
Bai, YL ;
Huang, CC ;
van der Hulst, R ;
Meijer-Dekens, F ;
Bonnema, G ;
Lindhout, P .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2003, 16 (02) :169-176
[2]   Visual rating and the use of image analysis for assessing different symptoms of citrus canker on grapefruit leaves [J].
Bock, C. H. ;
Parker, P. E. ;
Cook, A. Z. ;
Gottwald, T. R. .
PLANT DISEASE, 2008, 92 (04) :530-541
[3]   In vivo monitoring of obligate biotrophic pathogen growth by kinetic PCR [J].
Boyle, B ;
Hamelin, RC ;
Séguin, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (03) :1546-1552
[4]  
Braun U., 2012, TAXONOMIC MANUAL ERY
[5]   CONIDIA AND CONIDIAL GERMINATION IN LEVEILLULA TAURICA (LEV) ARN [J].
CLERK, GC ;
AYESUOFF.EN .
ANNALS OF BOTANY, 1967, 31 (124) :749-&
[6]   RESISTANCE TO LEVEILLULA-TAURICA IN PEPPER (CAPSICUM-ANNUUM) IS OLIGOGENICALLY CONTROLLED AND STABLE IN MEDITERRANEAN REGIONS [J].
DAUBEZE, AM ;
HENNART, JW ;
PALLOIX, A .
PLANT BREEDING, 1995, 114 (04) :327-332
[7]   Resistance to Leveillula taurica in the genus Capsicum [J].
de Souza, VL ;
Café, AC .
PLANT PATHOLOGY, 2003, 52 (05) :613-619
[8]   Ultrastructural chances of chloroplasts caused by tobamovirus infections in different pepper varieties [J].
Gáborjányi, R ;
Almási, A ;
Sárvári, E ;
Bóka, K ;
Lózsa, R ;
Sági, Z .
CEREAL RESEARCH COMMUNICATIONS, 2006, 34 (01) :449-452
[9]   Real-time PCR monitoring of fungal development in Arabidopsis thaliana infected by Alternaria brassicicola and Botrytis cinerea [J].
Gachon, C ;
Saindrenan, P .
PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2004, 42 (05) :367-371
[10]   ERGOSTEROL DETERMINATION IN ACTIVATED-SLUDGE AND ITS APPLICATION AS A BIOCHEMICAL MARKER FOR MONITORING FUNGAL BIOMASS [J].
GARDNER, RM ;
TINDALL, GW ;
CLINE, SM ;
BROWN, KL .
JOURNAL OF MICROBIOLOGICAL METHODS, 1993, 17 (01) :49-60