A Downy mildew Effector Attenuates Salicylic Acid-Triggered Immunity in Arabidopsis by interacting with the host Mediator complex

MARIE-CECILE CAILLAUD; SHUTA ASAI; GANASHYAM RALLAPALLI; SOPHIE J.M. PIQUEREZ; GEORGINA FABRO; JONATHAN D. G. JONES

PLOS BIOLOGY

PUBLIC LIBRARY SCIENCE

Lugar: San Francisco; Año: 2013 p. 1 - 18

1544-9173

Plants are continually exposed to pathogen attack but usually remain healthy because they can activate defences upon perception of microbes. However, pathogens have evolved to overcome plant immunity by delivering effectors into the plant cell to attenuate defence, resulting in disease. Recent studies suggest that some effectors may manipulate host transcription, but the specific mechanisms by which such effectors promote susceptibility remain unclear. We study the oomycete downy mildew pathogen of Arabidopsis, Hyaloperonsopora arabidopsidis (Hpa), and show here that the nuclear-localized effector HaRxL44 interacts with Mediator subunit 19a (MED19a), resulting in the degradation of MED19a in proteasome-dependent manner. The Mediator complex of ~25 proteins is broadly conserved in eukaryotes and mediates the interaction between transcriptional regulators and RNA polymerase II. We found Med19a to be a positive regulator of immunity against Hpa. Expression profiling experiments reveal transcriptional changes resembling jasmonic acid/ethylene (JA/ET) signalling in the presence of HaRxL44, and also three days after infection with Hpa. Elevated JA/ET signalling is associated with a decrease in salicylic acid (SA)-triggered immunity (STI) in Arabidopsis plants expressing HaRxL44 and in med19a loss-offunction mutants, whereas STI is elevated in plants overexpressing MED19a. Using a PR1::GUS reporter, we discovered that Hpa suppresses PR1 expression specifically in cells containing haustoria, into which RxLR effectors are delivered, but not in nonhaustoriatedadjacent cells, which show high PR1::GUS expression levels. Thus, HaRxL44 interferes with Mediator function by degrading Med19, shifting the balance of defence transcription from SA-responsive defence to JA/ET-signalling, and enhancing susceptibility to biotrophs by attenuating SA-dependent gene expression.