Genetic analysis of Eutypa strains from California supports the presence of two pathogenic species

被引:22
作者
DeScenzo, RA [1 ]
Engel, SR
Gomez, G
Jackson, EL
Munkvold, GP
Weller, J
Irelan, NA
机构
[1] E&J Gallo Winery, Biotechnol Res Grp, Modesto, CA 95353 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO 80262 USA
[3] Iowa State Univ, Dept Plant Pathol, Ames, IA 50011 USA
[4] Natl Ctr Genome Resources, Santa Fe, NM 87505 USA
关键词
D O I
10.1094/PHYTO.1999.89.10.884
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Eutypa dieback is a perennial canker disease that adversely affects grape (Vitis vinifera) production throughout the world. The causal agent has been known as either Eutypa armeniacae or E. lata, and it has been unclear whether the two taxa are separate species. We analyzed 115 isolates of Eutypa and conspecific strains, including 106 from California, using amplified fragment length polymorphism (AFLP) and sequence analysis of the ribosomal DNA (rDNA) internal transcribed spacer (ITS) sequence. Strains from cultivated plant species exhibited an average genetic distance of 0.34, as calculated by the DICE coefficient (NTSYS-pc software). An unweighted pair-group method with arithmetic averages dendrogram revealed a genetically distinct (distance of 0.73) group of Eutypa strains from valley oak (Quercus lobata) and madrone (Arbutus menziesii) and a strain from grape. Analysis of rDNA ITS sequences strongly supported the genetically distinct cluster detected in the AFLP data. Combined data indicated the presence of two species of Eutypa (E, armeniacae and E. lata) in our sample population. However, both Eutypa species were capable of infecting native and cultivated hosts, suggesting the potential for native tree species to serve as inoculum sources for grape infection in California. Further investigations of E. armeniacae and E, lata would contribute to the development of a successful disease management strategy.
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页码:884 / 893
页数:10
相关论文
共 60 条
[21]   Differentiation and grouping of isolates of the Ganoderma lucidum complex by random amplified polymorphic DNA-PCR compared with grouping on the basis of internal transcribed spacer sequences [J].
Hseu, RS ;
Wang, HH ;
Wang, HF ;
Moncalvo, JM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (04) :1354-1363
[22]   Application of the logistic-normal-binomial distribution to the analysis of Eutypa dieback disease incidence [J].
Hughes, G ;
Munkvold, GP ;
Samita, S .
INTERNATIONAL JOURNAL OF PEST MANAGEMENT, 1998, 44 (01) :35-42
[23]   Evaluation of the DNA fingerprinting method AFLP as a new tool in bacterial taxonomy [J].
Janssen, P ;
Coopman, R ;
Huys, G ;
Swings, J ;
Bleeker, M ;
Vos, P ;
Zabeau, M ;
Kersters, K .
MICROBIOLOGY-UK, 1996, 142 :1881-1893
[24]  
JOHNSON DA, 1985, PHYTOPATHOLOGY, V75, P1370
[25]  
JU YM, 1991, MYCOTAXON, V41, P311
[27]   RELATIONSHIP BETWEEN PATHOGENICITY AND PHYLOGENY BASED ON RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM IN LEPTOSPHAERIA-MACULANS [J].
KOCH, E ;
SONG, K ;
OSBORN, TC ;
WILLIAMS, PH .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1991, 4 (04) :341-349
[28]   Genetic variation among field isolates of Pyrenopeziza brassicae [J].
Majer, D ;
Lewis, BG ;
Mithen, R .
PLANT PATHOLOGY, 1998, 47 (01) :22-28
[29]   The use of AFLP fingerprinting for the detection of genetic variation in fungi [J].
Majer, D ;
Mithen, R ;
Lewis, BG ;
Vos, P ;
Oliver, RP .
MYCOLOGICAL RESEARCH, 1996, 100 :1107-1111
[30]   A HYPHOMYCETOUS SYNANAMORPH OF EUTYPA-ARMENIACAE IN ARTIFICIAL CULTURE [J].
MCKEMY, JM ;
GLAWE, DA ;
MUNKVOLD, GP .
MYCOLOGIA, 1993, 85 (06) :941-944