Clonal Expansion from Standing Genetic Variation Underpins the Evolution of Curtobacterium flaccumfaciens pv. flaccumfaciens in AustraliaExport / Share PlumX View Altmetrics View AltmetricsSparks, A. H., Adorada, D. L., Colombi, E., Kelly, L. A., Young, A., Knight, N. L. and Vaghefi, N. (2025) Clonal Expansion from Standing Genetic Variation Underpins the Evolution of Curtobacterium flaccumfaciens pv. flaccumfaciens in Australia. Phytopathology® (ja). null. Full text not currently attached. Access may be available via the Publisher's website or OpenAccess link. Article Link: https://doi.org/10.1094/PHYTO-01-25-0032-R Publisher URL: https://apsjournals.apsnet.org/doi/abs/10.1094/PHYTO-01-25-0032-R AbstractPathogens can evolve rapidly, leading to the emergence of novel strains that can overcome commercially deployed host plant resistance. Understanding the genetic and phenotypic diversity and population dynamics of plant pathogens is crucial to inform breeding programs targeting resistance. Tan spot, otherwise known as bacterial wilt, caused by Curtobacterium flaccumfaciens pv. flaccumfaciens, is an increasingly significant pathogen affecting beans and mungbean worldwide. Since the 1990s, several mungbean cultivars with partial resistance to tan spot have been released in Australia; however, cultivars initially rated as moderately resistant were later rated as moderately susceptible to tan spot. This study investigated the genetic and phenotypic diversity and temporal evolutionary dynamics of C. flaccumfaciens pv. flaccumfaciens in Australian mungbean fields. Whole-genome sequencing of 119 isolates collected from mungbean and other legumes (1986 to 2019) enabled analyses of pathogen evolution in Australia and in a global context. Results revealed that clonal expansion from standing genetic variation, rather than introduction of novel genotypes, has driven the evolution of this pathogen in Australia since the 1980s. Glasshouse trials confirmed the role of a plasmid in pathogenicity of C. flaccumfaciens pv. flaccumfaciens but found no significant differences in aggressiveness between clonal lineages. Our research provides insights into genetic and phenotypic diversity of this important plant pathogen and temporal changes in its population structure in Australia and highlights the need for further studies on the competitive fitness of isolates and characterisation of private alleles linked to dominant clonal lineages.
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