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454‐pyrosequencing of Coffea arabica leaves infected by the rust fungus Hemileia vastatrix reveals in planta‐expressed pathogen‐secreted proteins and plant functions in a late compatible plant–rust interaction

Identifieur interne : 001E71 ( Main/Exploration ); précédent : 001E70; suivant : 001E72

454‐pyrosequencing of Coffea arabica leaves infected by the rust fungus Hemileia vastatrix reveals in planta‐expressed pathogen‐secreted proteins and plant functions in a late compatible plant–rust interaction

Auteurs : Diana Fernandez [France] ; Emilie Tisserant [France] ; Pedro Talhinhas [Portugal] ; Helena Azinheira [Portugal] ; Ana Vieira [Portugal] ; Anne-Sophie Petitot [France] ; Andreia Loureiro [Portugal] ; Julie Poulain [France] ; Corinne Da Silva [France] ; Maria Do Céu Silva [Portugal] ; Sébastien Duplessis [France]

Source :

RBID : ISTEX:7A719BED9B3DF8F156CB19E10C8E712C6BF0FE5A

English descriptors

Abstract

Coffee (Coffea arabica L.), one of the key export and cash crops in tropical and subtropical countries, suffers severe losses from the rust fungus Hemileia vastatrix. The transcriptome of H. vastatrix was analysed during a compatible interaction with coffee to obtain an exhaustive repertoire of the genes expressed during infection and to identify potential effector genes. Large‐scale sequencing (454‐GS‐FLEX Titanium) of mixed coffee and rust cDNAs obtained from 21‐day rust‐infected leaves generated 352 146 sequences which assembled into 22 774 contigs. In the absence of any reference genomic sequences for Coffea or Hemileia, specific trinucleotide frequencies within expressed sequence tags (ESTs) and blast homology against a set of dicots and basidiomycete genomes were used to distinguish pathogen from plant sequences. About 30% (6763) of the contigs were assigned to H. vastatrix and 61% (13 951) to C. arabica. The majority (60%) of the rust sequences did not show homology to any genomic database, indicating that they were potential novel fungal genes. In silico analyses of the 6763 H. vastatrix contigs predicted 382 secreted proteins and identified homologues of the flax rust haustorially expressed secreted proteins (HESPs) and bean rust transferred protein 1 (RTP1). These rust candidate effectors showed conserved amino‐acid domains and conserved patterns of cysteine positions suggestive of conserved functions during infection of host plants. Quantitative reverse transcription‐polymerase chain reaction profiling of selected rust genes revealed dynamic expression patterns during the time course of infection of coffee leaves. This study provides the first valuable genomic resource for the agriculturally important plant pathogen H. vastatrix and the first comprehensive C. arabica EST dataset.

Url:
DOI: 10.1111/j.1364-3703.2011.00723.x


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Abundant contigs</term>
<term>Amino</term>
<term>Amino acid transport</term>
<term>Amino acids</term>
<term>Arabica</term>
<term>Arabica leaf tissues</term>
<term>Asparagine synthase</term>
<term>Avirulence</term>
<term>Avirulence genes</term>
<term>Basidiomycete</term>
<term>Bean rust fungus</term>
<term>Best blast</term>
<term>Bicolor</term>
<term>Bioinformatic</term>
<term>Bioinformatic procedure</term>
<term>Biotechnology information</term>
<term>Blackwell publishing</term>
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<term>Blastx</term>
<term>Blastx searches</term>
<term>Bspp</term>
<term>Cahv</term>
<term>Cahv contigs</term>
<term>Carbohydrate</term>
<term>Carbohydrate transport</term>
<term>Catanzariti</term>
<term>Cdna</term>
<term>Coffea</term>
<term>Coffea arabica</term>
<term>Coffee plants</term>
<term>Coffee rust</term>
<term>Coffee rust fungus</term>
<term>Columns detail</term>
<term>Compatible interaction</term>
<term>Contig</term>
<term>Contig sequences</term>
<term>Contigs</term>
<term>Database</term>
<term>Dehydrogenase</term>
<term>Distinct patterns</term>
<term>Duplessis</term>
<term>Effector</term>
<term>Encoding</term>
<term>Est</term>
<term>Est3</term>
<term>Est3 program</term>
<term>Eukaryotic orthologous group</term>
<term>Experimental procedures</term>
<term>Fabae</term>
<term>Fernandez</term>
<term>Fungal</term>
<term>Fungal contigs</term>
<term>Fungal origin</term>
<term>Fungal sequences</term>
<term>Fungal transcripts</term>
<term>Fungi</term>
<term>Fungus</term>
<term>Gene</term>
<term>Gene models</term>
<term>Genome</term>
<term>Genome sequences</term>
<term>Genomic</term>
<term>Glutamine hydrolysing</term>
<term>Graminis</term>
<term>Hacquard</term>
<term>Hahn</term>
<term>Haustorium</term>
<term>Hemileia</term>
<term>Hemileia vastatrix</term>
<term>Homologues</term>
<term>Homology</term>
<term>Homology searches</term>
<term>Hypothetical protein</term>
<term>Independent replicates</term>
<term>International databases</term>
<term>Intracellular secretion</term>
<term>Joint genome institute</term>
<term>Kemen</term>
<term>Laccaria</term>
<term>Laccaria bicolor</term>
<term>Late stage</term>
<term>Lini</term>
<term>Mannitol</term>
<term>Mannitol dehydrogenase</term>
<term>Melampsora</term>
<term>Mendgen</term>
<term>Mesophyll cells</term>
<term>Metabolism</term>
<term>Molecular plant pathology</term>
<term>National center</term>
<term>Nicole</term>
<term>Nonredundant nucleotide</term>
<term>Nucleic acids</term>
<term>Nucleotide</term>
<term>Order pucciniales</term>
<term>Oryza</term>
<term>Oryza sativa</term>
<term>Pathogen</term>
<term>Pathol</term>
<term>Petitot</term>
<term>Phakopsora pachyrhizi</term>
<term>Plant cell</term>
<term>Plant cells</term>
<term>Plant contigs</term>
<term>Plant host</term>
<term>Plant pathol</term>
<term>Plant pathology</term>
<term>Plant sequences</term>
<term>Poplar</term>
<term>Populus</term>
<term>Populus trichocarpa</term>
<term>Populus trichocarpa populus deltoides</term>
<term>Protein</term>
<term>Protein sequences</term>
<term>Public databases</term>
<term>Puccinia</term>
<term>Puccinia graminis tritici</term>
<term>Puccinia triticina</term>
<term>Pucciniales</term>
<term>Puthoff</term>
<term>Pyrosequencing</term>
<term>Ramiro</term>
<term>Relative abundance</term>
<term>Ribosomal structure</term>
<term>Rodrigues</term>
<term>Rtp1</term>
<term>Rust</term>
<term>Rust contigs</term>
<term>Rust effectors</term>
<term>Rust fungi</term>
<term>Rust fungus</term>
<term>Rust fungus hemileia vastatrix</term>
<term>Rust fungus uromyces fabae</term>
<term>Rust genes</term>
<term>Rust homologues</term>
<term>Rust species</term>
<term>Rust transcripts</term>
<term>Sativa</term>
<term>Secretion prediction</term>
<term>Sequence tags</term>
<term>Sequencing</term>
<term>Silva</term>
<term>Sporulation</term>
<term>Stringent criteria</term>
<term>Time course</term>
<term>Time point</term>
<term>Titanium pyrosequencing</term>
<term>Total number</term>
<term>Transcript</term>
<term>Transcript accumulation</term>
<term>Translation elongation factor</term>
<term>Transporter</term>
<term>Trichocarpa</term>
<term>Trinucleotide frequencies</term>
<term>Tritici</term>
<term>Uredinial stage</term>
<term>Uredinium</term>
<term>Uromyces</term>
<term>Uromyces appendiculatus</term>
<term>Uromyces fabae</term>
<term>Vastatrix</term>
<term>Vastatrix contigs</term>
<term>Vastatrix genes</term>
<term>Vastatrix races</term>
<term>Vastatrix transcripts</term>
<term>Vesicular transport</term>
<term>Vitis vinifera</term>
<term>Voegele</term>
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<front>
<div type="abstract" xml:lang="en">Coffee (Coffea arabica L.), one of the key export and cash crops in tropical and subtropical countries, suffers severe losses from the rust fungus Hemileia vastatrix. The transcriptome of H. vastatrix was analysed during a compatible interaction with coffee to obtain an exhaustive repertoire of the genes expressed during infection and to identify potential effector genes. Large‐scale sequencing (454‐GS‐FLEX Titanium) of mixed coffee and rust cDNAs obtained from 21‐day rust‐infected leaves generated 352 146 sequences which assembled into 22 774 contigs. In the absence of any reference genomic sequences for Coffea or Hemileia, specific trinucleotide frequencies within expressed sequence tags (ESTs) and blast homology against a set of dicots and basidiomycete genomes were used to distinguish pathogen from plant sequences. About 30% (6763) of the contigs were assigned to H. vastatrix and 61% (13 951) to C. arabica. The majority (60%) of the rust sequences did not show homology to any genomic database, indicating that they were potential novel fungal genes. In silico analyses of the 6763 H. vastatrix contigs predicted 382 secreted proteins and identified homologues of the flax rust haustorially expressed secreted proteins (HESPs) and bean rust transferred protein 1 (RTP1). These rust candidate effectors showed conserved amino‐acid domains and conserved patterns of cysteine positions suggestive of conserved functions during infection of host plants. Quantitative reverse transcription‐polymerase chain reaction profiling of selected rust genes revealed dynamic expression patterns during the time course of infection of coffee leaves. This study provides the first valuable genomic resource for the agriculturally important plant pathogen H. vastatrix and the first comprehensive C. arabica EST dataset.</div>
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<name sortKey="Duplessis, Sebastien" sort="Duplessis, Sebastien" uniqKey="Duplessis S" first="Sébastien" last="Duplessis">Sébastien Duplessis</name>
<name sortKey="Duplessis, Sebastien" sort="Duplessis, Sebastien" uniqKey="Duplessis S" first="Sébastien" last="Duplessis">Sébastien Duplessis</name>
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<name sortKey="Poulain, Julie" sort="Poulain, Julie" uniqKey="Poulain J" first="Julie" last="Poulain">Julie Poulain</name>
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