DNA polymorphism and molecular diagnosis in Inonotus spp.

被引:16
作者
Germain, H [1 ]
Laflamme, G [1 ]
Bernier, L [1 ]
Boulet, B [1 ]
Hamelin, RC [1 ]
机构
[1] Nat Resources Canada, Canadian Forestry Serv, Laurentian Forestry Ctr, St Foy, PQ G1V 4C7, Canada
来源
CANADIAN JOURNAL OF PLANT PATHOLOGY-REVUE CANADIENNE DE PHYTOPATHOLOGIE | 2002年 / 24卷 / 02期
关键词
Inonotus; root rot; molecular diagnosis; ribosomal DNA;
D O I
10.1080/07060660309506995
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Specific polymerase chain reaction (PCR) primers were developed for the internal transcribed spacer (ITS) region of the rDNA gene of Inonotus tomentosus, the causal agent of tomentosus root rot of conifers. The primers were designed to specifically amplify DNA from I. tomentosus and allow its differentiation from Inonotus leporinus and from Phellinus pini s.l., which are morphologically very similar to L tomentosus in culture. The PCR amplification was carried out successfully from DNA extracted from fruiting bodies and cultures and can potentially be used to detect the pathogen from environmental samples for survey and management purposes. The PCR assay was validated with 42 samples from seven coniferous hosts originating from eight provinces or states across the North American continent. No cross reaction was observed with DNA of several other species of the same genus, with Phellinus pini or with white spruce (Picea glauca), a conifer host of I. tomentosus. Phylogenetic analysis of the ITS region for six species of Inonotus suggests that these resulted from the adaptation of a generalist ancestor to different ecological niches. It also appears that divergent evolution of an ancestor occupying different ecological niches has driven the speciation process, which subsequently conferred specificity to either coniferous or deciduous trees.
引用
收藏
页码:194 / 199
页数:6
相关论文
共 20 条
[1]   Identification of ectomycorrhizal fungi of the genus Tuber by species-specific ITS primers [J].
Amicucci, A ;
Zambonelli, A ;
Giomaro, G ;
Potenza, L ;
Stocchi, V .
MOLECULAR ECOLOGY, 1998, 7 (03) :273-277
[2]  
BOULET B, 1995, AUBELLE, V111, P1
[3]   Polymerase chain reaction-based assay for specific detection of Rhizoctonia solani AG-3 isolates [J].
Bounou, S ;
Jabaji-Hare, SH ;
Hogue, R ;
Charest, PM .
MYCOLOGICAL RESEARCH, 1999, 103 :1-8
[4]  
Dai YC, 1997, MYCOTAXON, V65, P273
[5]   ITS PRIMERS WITH ENHANCED SPECIFICITY FOR BASIDIOMYCETES - APPLICATION TO THE IDENTIFICATION OF MYCORRHIZAE AND RUSTS [J].
GARDES, M ;
BRUNS, TD .
MOLECULAR ECOLOGY, 1993, 2 (02) :113-118
[6]  
Gilbertson R. L, 1986, N AM POLYPORES, V1
[7]   PCR detection of Gremmeniella abietina, the causal agent of Scleroderris canker of pine [J].
Hamelin, RC ;
Bourassa, M ;
Rail, J ;
Dusabenyagasani, M ;
Jacobi, V ;
Laflamme, G .
MYCOLOGICAL RESEARCH, 2000, 104 :527-532
[8]   Identification of root rot fungi in nursery seedlings by nested multiplex PCR [J].
Hamelin, RC ;
Berube, P ;
Gignac, M ;
Bourassa, M .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (11) :4026-4031
[9]  
Hunt RS, 1999, EUR J FOREST PATHOL, V29, P259
[10]   Differential medium for Phellinus pini and Inonotus tomentosus [J].
Hunt, RS .
CANADIAN JOURNAL OF PLANT PATHOLOGY, 1997, 19 (03) :307-309