4.5 Article

Phylogenetic analysis of Verticillium dahliae vegetative compatibility groups

Journal

PHYTOPATHOLOGY
Volume 98, Issue 9, Pages 1019-1028

Publisher

AMER PHYTOPATHOLOGICAL SOC
DOI: 10.1094/PHYTO-98-9-1019

Keywords

defoliating pathotype; genetic diversity; Verticillium wilt

Categories

Funding

  1. Comision Interministerial de Ciencia y Tecnologia (CICYT) of Spain [AGL2000-1444]
  2. 'Verticilosis del olivo' from Fundacion Ramon Areces [AGL2003-00503]
  3. Spanish Ministry of Education and Science (MEC)
  4. Ramon y Cajal-Programme of MEC

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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, beta-tubulin, calmodulin, and histone 3 genes, the ITS I 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 11) were identified with lineage 11 comprising two closely related subgroups of VCGs. Lineage I included VCG I A, VCG I B, and VCG2B(334) and lineage 11 included, VCG2A and VCG4B (subclade 1); and VCG2B(824). 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.

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