Abstract

Plants have evolved pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) and effector-triggered immunity (ETI) to protect themselves from infection by diverse pathogens. Avirulence (Avr) effectors that trigger plant ETI as a result of recognition by plant resistance (R) gene products have been identified in many plant pathogenic oomycetes and fungi. However, the virulence functions of oomycete and fungal Avr effectors remain largely unknown. Here, we combined bioinformatics and genetics to identify Avr3b, a new Avr gene from Phytophthora sojae, an oomycete pathogen that causes soybean root rot. Avr3b encodes a secreted protein with the RXLR host-targeting motif and C-terminal W and Nudix hydrolase motifs. Some isolates of P. sojae evade perception by the soybean R gene Rps3b through sequence mutation in Avr3b and lowered transcript accumulation. Transient expression of Avr3b in Nicotiana benthamiana increased susceptibility to P. capsici and P. parasitica, with significantly reduced accumulation of reactive oxygen species (ROS) around invasion sites. Biochemical assays confirmed that Avr3b is an ADP-ribose/NADH pyrophosphorylase, as predicted from the Nudix motif. Deletion of the Nudix motif of Avr3b abolished enzyme activity. Mutation of key residues in Nudix motif significantly impaired Avr3b virulence function but not the avirulence activity. Some Nudix hydrolases act as negative regulators of plant immunity, and thus Avr3b might be delivered into host cells as a Nudix hydrolase to impair host immunity. Avr3b homologues are present in several sequenced Phytophthora genomes, suggesting that Phytophthora pathogens might share similar strategies to suppress plant immunity.

Highlights

  • Plant innate immunity, which has been continuously refined by challenges from a diversity of pathogens during evolution, employs at least two defense systems in response to pathogen attacks [1]

  • In this paper we identified an RXLRcarrying protein from P. sojae as Avr effector Avr3b based on genetic mapping, sequence polymorphisms, and transient expression

  • We hypothesized that Avr3b was likely encoded by an infection-expressed RXLR effector that is polymorphic among P. sojae strains

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Summary

Introduction

Plant innate immunity, which has been continuously refined by challenges from a diversity of pathogens during evolution, employs at least two defense systems in response to pathogen attacks [1]. One is basal defense through host receptor recognition of conserved pathogen-associated molecular patterns (PAMPs), termed PAMP-triggered immunity (PTI). The basal defense response can successfully prevent infections from becoming established. Successful pathogens deliver secreted proteins (effectors) to suppress basal defense. Plants have developed a second immunity system that relies on plant resistance (R) protein perception of specific pathogen effectors and is called effector-triggered immunity (ETI). Pathogen effectors recognized by plant R proteins have historically been termed avirulence (Avr) effectors [1,2]. ETI usually results in faster and stronger plant resistance responses, including programmed cell death (PCD), reactive oxygen species (ROS) accumulation, and induction of plant hormone-mediated signal pathways [1]. The interaction between host R proteins and pathogen Avr effectors can determine the outcome of an infection

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