Global perspective on the genetic architecture of susceptibility to spot form net blotch in barley

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Abstract

The necrotrophic fungal pathogen Pyrenophora teres f. maculata causes spot form net blotch (SFNB), a global disease of barley. This fungus uses effector proteins to promote infection, which act in an inverse gene-for-gene manner by targeting dominant host susceptibility genes. Currently, there is a general understanding of the genetics of resistance/susceptibility in the host; however, there are still gaps in our understanding of global pathogen virulence and how it has evolved to target the host and cause disease. Because the P. teres f. maculata -barley interaction conforms to an inverse gene-for-gene model, we crossed three different susceptible barley lines (Hockett, TR 326, and PI 392501) with the resistant line PI 67381 and developed and mapped recombinant inbred populations to characterize the susceptibility in these lines based on their response to ten pathogen isolates collected from globally diverse barley growing regions on five continents. Four independent quantitative trait loci (QTL) showed associations with susceptibility and mapped to barley chromosomes (Chr) 2HS, 4HS, 4HL, and 7HL. In all three populations, the same genomic position on Chr7H was associated with the highest susceptibility levels and was targeted by seven of the ten fungal isolates. The QTL identified on Chr2HS mapped to the same position in two populations and was also targeted by seven of the ten isolates. However, the Chr4HS and Chr4HL susceptibilities were targeted by only three and two of the global isolates, respectively. This work shows that pathogen populations under different host selection pressures can evolve to target different barley susceptibilities.

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