Poster
MARK JAVE BAUTISTA
PhD student
The Sainsbury Laboratory
Norwich, England, United Kingdom
Neftaly Cruz-Mireles
Postdoctoral scientist
The Sainsbury Laboratory
Norwich, England, United Kingdom
Xia Yan
Postdoctoral Scientist
The Sainsbury Laboratory
Norwich, England, United Kingdom
Vincent Were
Postdoctoral scientist
The Sainsbury Laboratory
Norwich, England, United Kingdom
Luyao Huang
Postdoctoral scientist
The Sainsbury Laboratory
Norwich, England, United Kingdom
Paul Derbyshire
The Sainsbury Laboratory
Norwich, England, United Kingdom
Neha Sahu
Postdoctoral scientist
The Sainsbury Laboratory
Norwich, England, United Kingdom
Yu Sugihara
Postdoctoral scientist
The Sainsbury Laboratory
NORWICH, England, United Kingdom
Frank L.H. Menke
The Sainsbury Laboratory
Norwich, England, United Kingdom
Nicholas J. Talbot
Group Leader
The Sainsbury Laboratory
Norwich, England, United Kingdom
The rice blast fungus Magnaporthe oryzae secretes a battery of effector proteins to manipulate host defence and colonise its host. The pathogenicity MAP kinase Pmk1 governs M. oryzae appressorium formation and tissue colonisation, but most of its downstream targets remain unknown. In this study, we used a comparative phosphoproteomics approach to investigate plant infection by the blast fungus. We identified a group of seven phosphorylated effector proteins dependent upon Pmk1 MAPK activity for their expression. These Pmk1-Regulated Effectors (PREs) are specifically expressed between 24-48h after plant infection when the fungus rapidly colonises rice tissue. PRE genes are highly conserved in 163 available genomes of M. oryzae including numerous host-limited forms of the fungus. Subcellular localisation of GFP-tagged PREs showed that they accumulate at the Biotrophic Interfacial Complex during invasive growth, indicating that they are cytoplasmic effectors delivered to host cells. Targeted gene deletion of PREs has so far provided evidence for a role for Pre2 in fungal virulence. Immunoprecipitation-mass spectrometry of YFP-tagged PREs transiently expressed in Nicotiana benthamiana revealed that PREs are phosphorylated in planta. Taken together, our work provides evidence that a sub-set of effectors can be phosphorylated during host plant infection and are regulated as part of a developmental programme controlled by the M. oryzae Pmk1 MAP kinase.