Clonal Expansion and Migration of a Highly Virulent, Defoliating Lineage of Verticillium dahliae

• Published in: Phytopathology Vol. 106; no. 9; pp. 1038 - 1046
• Main Authors: Milgroom, Michael G, Del Mar Jiménez-Gasco, María, Olivares-García, Concepción, Jiménez-Díaz, Rafael M
• Format: Journal Article
• Language: English
• Published: United States 01-09-2016
• Subjects: Abelmoschus - microbiology; Crops, Agricultural; Genetic Variation; Genetics, Population; Genomics; Genotype; Gossypium - microbiology; Greece; Haplotypes; Host Specificity; Israel; Olea; Olea - microbiology; Plant Diseases - microbiology; Polymorphism, Single Nucleotide - genetics; Spain; Turkey; United States; Verticillium - genetics; Verticillium - isolation & purification; Verticillium - pathogenicity; Verticillium dahliae
• ISSN: 0031-949X; 1943-7684
• DOI: 10.1094/PHYTO-11-15-0300-R

We used a population genomics approach to test the hypothesis of clonal expansion of a highly fit genotype in populations of Verticillium dahliae. This fungal pathogen has a broad host range and can be dispersed in contaminated seed or other plant material. It has a highly clonal population structure, with several lineages having nearly worldwide distributions in agricultural crops. Isolates in lineage 1A are highly virulent and cause defoliation in cotton, okra, and olive (denoted 1A/D), whereas those in other lineages cause wilting but not defoliation (ND). We tested whether the highly virulent lineage 1A/D could have spread from the southwestern United States to the Mediterranean basin, as predicted from historical records. We found 187 single-nucleotide polymorphisms (SNPs), determined by genotyping by sequencing, among 91 isolates of lineage 1A/D and 5 isolates in the closely related lineage 1B/ND. Neighbor-joining and maximum-likelihood analyses on the 187 SNPs showed a clear divergence between 1A/D and 1B/ND haplotypes. Data for only 77 SNPs were obtained for all 96 isolates (no missing data); lineages 1A/D and 1B/ND differed by 27 of these 77 SNPs, confirming a clear divergence between the two lineages. No evidence of recombination was detected within or between these two lineages. Phylogenetic and genealogical analyses resulted in five distinct subclades of 1A/D isolates that correlated closely with geographic origins in the Mediterranean basin, consistent with the hypothesis that the D pathotype was introduced at least five times in independent founder events into this region from a relatively diverse source population. The inferred ancestral haplotype was found in two isolates sampled before 1983 from the southwestern United States, which is consistent with historical records that 1A/D originated in North America. The five subclades coalesce with the ancestral haplotype at the same time, consistent with a hypothesis of rapid population expansion in the source population during the emergence of 1A/D as a severe pathogen of cotton in the United States.