4.5 Article

Phytophthora infestans RxLR Effector PITG06478 Hijacks 14-3-3 to Suppress PMA Activity Leading to Necrotrophic Cell Death

Journal

MOLECULAR PLANT-MICROBE INTERACTIONS
Volume 36, Issue 3, Pages 150-158

Publisher

AMER PHYTOPATHOLOGICAL SOC
DOI: 10.1094/MPMI-06-22-0135-R

Keywords

14-3-3 protein; cell death; Phytophthora infestans; plasma membrane proton ATPase; RxLR effector

Ask authors/readers for more resources

Pathogens induce cell death in host plants for successful proliferation, and the regulation of plasma membrane H+-ATPases (PMAs) plays a crucial role in this process. This study reveals a mechanism by which pathogens manipulate PMA activity through interaction with host proteins, leading to cell death.
Pathogens often induce cell death for their successful proliferation in the host plant. Plasma membrane H+-ATPases (PMAs) are targeted by either pathogens or plant immune receptors in immune response regulation. Although PMAs play pivotal roles in host cell death, the molecular mechanism of effector-mediated regulation of PMA activity has not been described. Here, we report that the Phytophthora infestans RxLR effector PITG06478 can induce cell death in Nicotiana benthamiana but the induced cell death is inhibited by fusicoccin (FC), an irreversible PMA activator. PITG06478, which is localized at the plasma membrane, is not directly associated with the PMA but is associated with Nb14-3-3s, a PMA activator. Immunoblot analyses revealed that the interaction between PITG06478 and Nb14-3-3s was disrupted by FC. PMA activity in PITG06478-expressing plants was eventually inhibited, and cell death likely occurred because the 14-3-3 protein was hijacked. Our results further confirm the significance of PMA activity in host cell death and provide new insight into how pathogens utilize essential host components to sustain their life cycle.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available