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      Effector Polymorphisms of the Sunflower Downy Mildew Pathogen Plasmopara halstedii and Their Use to Identify Pathotypes from Field Isolates

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          Abstract

          The obligate biotroph oomycete Plasmopara halstedii causes downy mildew on sunflower crop, Helianthus annuus. The breakdown of several Pl resistance genes used in sunflower hybrids over the last 25 years came along with the appearance of new Pl. halstedii isolates showing modified virulence profiles. In oomycetes, two classes of effector proteins, key players of pathogen virulence, are translocated into the host: RXLR and CRN effectors. We identified 54 putative CRN or RXLR effector genes from transcriptomic data and analyzed their genetic diversity in seven Pl. halstedii pathotypes representative of the species variability. Pl. halstedii effector genes were on average more polymorphic at both the nucleic and protein levels than random non-effector genes, suggesting a potential adaptive dynamics of pathogen virulence over the last 25 years. Twenty-two KASP (Competitive Allele Specific PCR) markers designed on polymorphic effector genes were genotyped on 35 isolates belonging to 14 Pl. halstedii pathotypes. Polymorphism analysis based on eight KASP markers aims at proposing a determination key suitable to classify the eight multi-isolate pathotypes into six groups. This is the first report of a molecular marker set able to discriminate Pl. halstedii pathotypes based on the polymorphism of pathogenicity effectors. Compared to phenotypic tests handling living spores used until now to discriminate Pl. halstedii pathotypes, this set of molecular markers constitutes a first step in faster pathotype diagnosis of Pl. halstedii isolates. Hence, emerging sunflower downy mildew isolates could be more rapidly characterized and thus, assessment of plant resistance breakdown under field conditions should be improved.

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          Most cited references25

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          A translocation signal for delivery of oomycete effector proteins into host plant cells.

          Bacterial, oomycete and fungal plant pathogens establish disease by translocation of effector proteins into host cells, where they may directly manipulate host innate immunity. In bacteria, translocation is through the type III secretion system, but analogous processes for effector delivery are uncharacterized in fungi and oomycetes. Here we report functional analyses of two motifs, RXLR and EER, present in translocated oomycete effectors. We use the Phytophthora infestans RXLR-EER-containing protein Avr3a as a reporter for translocation because it triggers RXLR-EER-independent hypersensitive cell death following recognition within plant cells that contain the R3a resistance protein. We show that Avr3a, with or without RXLR-EER motifs, is secreted from P. infestans biotrophic structures called haustoria, demonstrating that these motifs are not required for targeting to haustoria or for secretion. However, following replacement of Avr3a RXLR-EER motifs with alanine residues, singly or in combination, or with residues KMIK-DDK--representing a change that conserves physicochemical properties of the protein--P. infestans fails to deliver Avr3a or an Avr3a-GUS fusion protein into plant cells, demonstrating that these motifs are required for translocation. We show that RXLR-EER-encoding genes are transcriptionally upregulated during infection. Bioinformatic analysis identifies 425 potential genes encoding secreted RXLR-EER class proteins in the P. infestans genome. Identification of this class of proteins provides unparalleled opportunities to determine how oomycetes manipulate hosts to establish infection.
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            Genome evolution following host jumps in the Irish potato famine pathogen lineage.

            Many plant pathogens, including those in the lineage of the Irish potato famine organism Phytophthora infestans, evolve by host jumps followed by specialization. However, how host jumps affect genome evolution remains largely unknown. To determine the patterns of sequence variation in the P. infestans lineage, we resequenced six genomes of four sister species. This revealed uneven evolutionary rates across genomes with genes in repeat-rich regions showing higher rates of structural polymorphisms and positive selection. These loci are enriched in genes induced in planta, implicating host adaptation in genome evolution. Unexpectedly, genes involved in epigenetic processes formed another class of rapidly evolving residents of the gene-sparse regions. These results demonstrate that dynamic repeat-rich genome compartments underpin accelerated gene evolution following host jumps in this pathogen lineage.
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              Phytophthora infestans effector AVR3a is essential for virulence and manipulates plant immunity by stabilizing host E3 ligase CMPG1.

              Fungal and oomycete plant pathogens translocate effector proteins into host cells to establish infection. However, virulence targets and modes of action of their effectors are unknown. Effector AVR3a from potato blight pathogen Phytophthora infestans is translocated into host cells and occurs in two forms: AVR3a(KI), which is detected by potato resistance protein R3a, strongly suppresses infestin 1 (INF1)-triggered cell death (ICD), whereas AVR3a(EM), which evades recognition by R3a, weakly suppresses host ICD. Here we show that AVR3a interacts with and stabilizes host U-box E3 ligase CMPG1, which is required for ICD. In contrast, AVR3a(KI/Y147del), a mutant with a deleted C-terminal tyrosine residue that fails to suppress ICD, cannot interact with or stabilize CMPG1. CMPG1 is stabilized by the inhibitors MG132 and epoxomicin, indicating that it is degraded by the 26S proteasome. CMPG1 is degraded during ICD. However, it is stabilized by mutations in the U-box that prevent its E3 ligase activity. In stabilizing CMPG1, AVR3a thus modifies its normal activity. Remarkably, given the potential for hundreds of effector genes in the P. infestans genome, silencing Avr3a compromises P. infestans pathogenicity, suggesting that AVR3a is essential for virulence. Interestingly, Avr3a silencing can be complemented by in planta expression of Avr3a(KI) or Avr3a(EM) but not the Avr3a(KI/Y147del) mutant. Our data provide genetic evidence that AVR3a is an essential virulence factor that targets and stabilizes the plant E3 ligase CMPG1, potentially to prevent host cell death during the biotrophic phase of infection.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                4 February 2016
                2016
                : 11
                : 2
                : e0148513
                Affiliations
                [1 ]Institut National de la Recherche Agronomique, INRA, Laboratoire des Interactions Plantes-Microorganismes (LIPM), Unité Mixte de Recherches UMR441, F-31326 Castanet-Tolosan, France
                [2 ]Centre National de la Recherche Scientifique, CNRS, Laboratoire des Interactions Plantes-Microorganismes (LIPM), Unité Mixte de Recherches UMR2594, F-31326 Castanet-Tolosan, France
                Agriculture and Agri-Food Canada, CANADA
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: PV LG. Performed the experiments: QG AB. Analyzed the data: QG ES SC FR PV LG. Contributed reagents/materials/analysis tools: NP. Wrote the paper: QG FR PV LG. Constructed the S1 Table: PV.

                [¤]

                Current address: INRA, Unité Mixte de Recherches UMR1332 BFP, Biologie du Fruit et Pathologie, CS20032, F-33882 Villenave d'Ornon cedex, France

                Article
                PONE-D-15-40780
                10.1371/journal.pone.0148513
                4742249
                26845339
                d1843a43-2f61-4798-ad21-1a115199218e
                © 2016 Gascuel et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 15 September 2015
                : 19 January 2016
                Page count
                Figures: 5, Tables: 1, Pages: 19
                Funding
                This work was supported by the French INRA Project “Bioressources 2009”, the CETIOM, and the French Laboratory of Excellence project "TULIP" (Toward a unified theory of biotic interactions: role of environmental perturbations) (ANR-10-LABX-41; ANR-11-IDEX-0002-02).
                Categories
                Research Article
                Biology and Life Sciences
                Organisms
                Plants
                Flowering Plants
                Sunflower
                Biology and Life Sciences
                Organisms
                Fungi
                Oomycetes
                Biology and Life Sciences
                Microbiology
                Oomycetes
                Research and Analysis Methods
                Database and Informatics Methods
                Biological Databases
                Genomic Databases
                Biology and Life Sciences
                Computational Biology
                Genome Analysis
                Genomic Databases
                Biology and Life Sciences
                Genetics
                Genomics
                Genome Analysis
                Genomic Databases
                Biology and Life Sciences
                Plant Science
                Plant Pathology
                Plant Pathogens
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Sequencing Techniques
                Sequence Analysis
                Sequence Motif Analysis
                Research and Analysis Methods
                Molecular Biology Techniques
                Sequencing Techniques
                Sequence Analysis
                Sequence Motif Analysis
                Biology and Life Sciences
                Genetics
                Genomics
                Plant Genomics
                Biology and Life Sciences
                Biotechnology
                Plant Biotechnology
                Plant Genomics
                Biology and Life Sciences
                Plant Science
                Plant Biotechnology
                Plant Genomics
                Biology and Life Sciences
                Genetics
                Plant Genetics
                Plant Genomics
                Biology and Life Sciences
                Plant Science
                Plant Genetics
                Plant Genomics
                Biology and Life Sciences
                Plant Science
                Plant Pathology
                Plant Pathogens
                Plant Bacterial Pathogens
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Sequencing Techniques
                Sequence Analysis
                Sequence Alignment
                Research and Analysis Methods
                Molecular Biology Techniques
                Sequencing Techniques
                Sequence Analysis
                Sequence Alignment
                Custom metadata
                All relevant data are within the paper and its Supporting Information files ( S1 Table and S1 File). All the ESTs and cDNA data (more than 800 000 clean sequences) obtained from spores or from infected sunflower hypocotyls have been deposited at SRA (Sequence Read Archive), accession numbers SRR1141084 to SRR1141091.

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