Phylogenetic Analysis of Verticillium dahliae Vegetative Compatibility Groups

• Published in: Phytopathology 2008-09, Vol.98 (9), p.1019-1028
• Main Authors: Collado-Romero, M, Mercado-Blanco, J, Olivares-Garcia, C, Jimenez-Diaz, R.M
• Format: Article
• Language: English
• Subjects: amplified fragment length polymorphism; Amplified Fragment Length Polymorphism Analysis; assays; Biological and medical sciences; Consensus Sequence; DNA Fingerprinting; DNA Primers; DNA, Fungal - genetics; DNA, Ribosomal - genetics; Ecosystem; Evolution, Molecular; Fundamental and applied biological sciences. Psychology; Fungal plant pathogens; Fungal Proteins - genetics; genetic polymorphism; genetic relationships; genetic variation; geographical variation; Geography; mutation; Phylogeny; Phytopathology. Animal pests. Plant and forest protection; plant pathogenic fungi; Polymorphism, Restriction Fragment Length - genetics; selfing; sequence analysis; Verticillium - classification; Verticillium - genetics; Verticillium dahliae; Verticillium wilt
• ISSN: 0031-949X; 1943-7684
• DOI: 10.1094/PHYTO-98-9-1019

The evolutionary relationships among Verticillium dahliae vegetative compatibility (VCG) subgroups VCG1A, VCG1B, VCG2A, VCG2B, VCG4A, VCG4B, and VCG6 were investigated by parsimony analysis of amplified fragment length polymorphism (AFLP) fingerprints and sequences of six DNA regions (actin, β-tubulin, calmodulin, and histone 3 genes, the ITS 1 and 2 regions of the rDNA, and a V. dahliae-specific sequence), using 101 isolates of diverse host and geographic origin. Polymorphisms in gene sequences among isolates of different VCGs were very low and individual gene genealogies provided very little resolution at the VCG level. The combined analysis of all DNA regions differentiated all VCG subgroups except for isolates in VCG1A and VCG1B. VCG clonal lineages in V. dahliae and evolutionary relationships among them were resolved independently by analyses of AFLP fingerprints, multiple gene genealogies, and the combined data set of AFLP fingerprinting and multiple gene genealogies. Two main lineages (I and II) were identified with lineage II comprising two closely related subgroups of VCGs. Lineage I included VCG1A, VCG1B, and VCG2B334; and lineage II included, VCG2A and VCG4B (subclade 1); and VCG2B824, VCG4A, and VCG6 (subclade 2). VCG subgroups were monophyletic except for VCG2B that appeared polyphyletic. Limiting the parsimony analysis either to AFLP fingerprints or DNA sequences would have obscured intra-VCG differentiation. Therefore, the dual approach represented by the independent and combined analyses of AFLP fingerprints and DNA sequences was a highly valuable method for the identification of phylogenetic relationships at the intraspecific level in V. dahliae.