Dispensable chromosomes in Fusarium oxysporum f. sp. lycopersici

Mol Plant Pathol. 2016 Dec;17(9):1455-1466. doi: 10.1111/mpp.12440. Epub 2016 Aug 21.

Abstract

The genomes of many filamentous fungi consist of a 'core' part containing conserved genes essential for normal development as well as conditionally dispensable (CD) or lineage-specific (LS) chromosomes. In the plant-pathogenic fungus Fusarium oxysporum f. sp. lycopersici, one LS chromosome harbours effector genes that contribute to pathogenicity. We employed flow cytometry to select for events of spontaneous (partial) loss of either the two smallest LS chromosomes or two different core chromosomes. We determined the rate of spontaneous loss of the 'effector' LS chromosome in vitro at around 1 in 35 000 spores. In addition, a viable strain was obtained lacking chromosome 12, which is considered to be a part of the core genome. We also isolated strains carrying approximately 1-Mb deletions in the LS chromosomes and in the dispensable core chromosome. The large core chromosome 1 was never observed to sustain deletions over 200 kb. Whole-genome sequencing revealed that some of the sites at which the deletions occurred were the same in several independent strains obtained for the two chromosomes tested, indicating the existence of deletion hotspots. For the core chromosome, this deletion hotspot was the site of insertion of the marker used to select for loss events. Loss of the core chromosome did not affect pathogenicity, whereas loss of the effector chromosome led to a complete loss of pathogenicity.

Keywords: chromosome deletions; conditionally dispensable chromosomes; flow cytometry; pathogenic fungi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon / pharmacology
  • Chromosomes, Fungal / metabolism*
  • Fungal Proteins / metabolism
  • Fusarium / genetics
  • Fusarium / growth & development
  • Fusarium / metabolism*
  • Fusarium / pathogenicity
  • Gene Duplication / drug effects
  • Genes, Fungal
  • Genetic Markers
  • Karyotyping
  • Phylogeny
  • Sequence Analysis, DNA
  • Sequence Deletion / genetics
  • Xylem / metabolism

Substances

  • Fungal Proteins
  • Genetic Markers
  • Carbon