Abstract

Oomycetes are filamentous organisms that cause notorious diseases, several of which have a high economic impact. Well known is Phytophthora infestans, the causal agent of potato late blight. Previously, in silico analyses of the genome and transcriptome of P. infestans resulted in the annotation of a large number of genes encoding proteins with an N-terminal signal peptide. This set is collectively referred to as the secretome and comprises proteins involved in, for example, cell wall growth and modification, proteolytic processes, and the promotion of successful invasion of plant cells. So far, proteomic profiling in oomycetes was primarily focused on subcellular, intracellular or cell wall fractions; the extracellular proteome has not been studied systematically. Here we present the first comprehensive characterization of the in vivo secretome and extracellular proteome of P. infestans. We have used mass spectrometry to analyze P. infestans proteins present in seven different growth media with mycelial cultures and this resulted in the consistent identification of over two hundred proteins. Gene ontology classification pinpointed proteins involved in cell wall modifications, pathogenesis, defense responses, and proteolytic processes. Moreover, we found members of the RXLR and CRN effector families as well as several proteins lacking an obvious signal peptide. The latter were confirmed to be bona fide extracellular proteins and this suggests that, similar to other organisms, oomycetes exploit non-conventional secretion mechanisms to transfer certain proteins to the extracellular environment.

Highlights

  • From the ‡Laboratory of Phytopathology, Wageningen University, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands; §Proteomics Unit, Center of Genomics Regulation (CRG), Carrer Dr Aiguader 88, 08003 Barcelona, Spain; ¶Proteomics Unit, Universitat Pompeu Fabra (UPF), Carrer Dr Aiguader 88, 08003 Barcelona, Spain; ʈCentre for BioSystems Genomics, Droevendaalsesteeg, 16708 PB Wageningen, The Netherlands

  • Phospholipase D Activity Release is Dependent on Media Composition—We previously showed that phospholipase D (PLD) activity was present in extracellular medium of P. infestans strains, as demonstrated by the production of phosphatidic acid (PA) and the PLD specific marker phosphatidylalcohol (PPro), when cultured on V8-agar or RS-agar plates flooded with V8 juice medium [44]

  • It was deduced that PLD activity in the extracellular medium could act as an enzymatic marker to monitor P. infestans response to changing nutritional conditions

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Summary

Introduction

From the ‡Laboratory of Phytopathology, Wageningen University, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands; §Proteomics Unit, Center of Genomics Regulation (CRG), Carrer Dr Aiguader 88, 08003 Barcelona, Spain; ¶Proteomics Unit, Universitat Pompeu Fabra (UPF), Carrer Dr Aiguader 88, 08003 Barcelona, Spain; ʈCentre for BioSystems Genomics, Droevendaalsesteeg, 16708 PB Wageningen, The Netherlands. Apoplastic and cytosolic effector classes are mostly small modular proteins that contain an N-terminal signal peptide to facilitate secretion. Their C-terminal part comprises additional effector modules including host targeting signals, as is the case for RXLRs and CRNs, and a functional domain exerting its function [8]. Both RXLR and CRNЈs were originally identified as inducers of plant cell death and defense-related gene expression during in planta expression [3, 9] not all CRNs promote infection [10]. It can be anticipated that similar mechanisms exist in oomycetes

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