RNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.

Biotroph pathogens establish intimate interactions with their hosts that are conditioned by the successful secretion of effectors in infected tissues and subsequent manipulation of host physiology. The identification of early-expressed pathogen effectors and early-modulated host functions is current...

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Autores principales: Benjamin Petre, Emmanuelle Morin, Emilie Tisserant, Stéphane Hacquard, Corinne Da Silva, Julie Poulain, Christine Delaruelle, Francis Martin, Nicolas Rouhier, Annegret Kohler, Sébastien Duplessis
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:34e355dd5f52492ba2efca95fb437a5f2021-11-18T07:06:59ZRNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.1932-620310.1371/journal.pone.0044408https://doaj.org/article/34e355dd5f52492ba2efca95fb437a5f2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22952974/?tool=EBIhttps://doaj.org/toc/1932-6203Biotroph pathogens establish intimate interactions with their hosts that are conditioned by the successful secretion of effectors in infected tissues and subsequent manipulation of host physiology. The identification of early-expressed pathogen effectors and early-modulated host functions is currently a major goal to understand the molecular basis of biotrophy. Here, we report the 454-pyrosequencing transcriptome analysis of early stages of poplar leaf colonization by the rust fungus Melampsora larici-populina. Among the 841,301 reads considered for analysis, 616,879 and 649 were successfully mapped to Populus trichocarpa and M. larici-populina genome sequences, respectively. From a methodological aspect, these results indicate that this single approach is not appropriate to saturate poplar transcriptome and to follow transcript accumulation of the pathogen. We identified 19 pathogen transcripts encoding early-expressed small-secreted proteins representing candidate effectors of interest for forthcoming studies. Poplar RNA-Seq data were validated by oligoarrays and quantitatively analysed, which revealed a highly stable transcriptome with a single transcript encoding a sulfate transporter (herein named PtSultr3;5, POPTR_0006s16150) showing a dramatic increase upon colonization by either virulent or avirulent M. larici-populina strains. Perspectives connecting host sulfate transport and biotrophic lifestyle are discussed.Benjamin PetreEmmanuelle MorinEmilie TisserantStéphane HacquardCorinne Da SilvaJulie PoulainChristine DelaruelleFrancis MartinNicolas RouhierAnnegret KohlerSébastien DuplessisPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 8, p e44408 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Benjamin Petre
Emmanuelle Morin
Emilie Tisserant
Stéphane Hacquard
Corinne Da Silva
Julie Poulain
Christine Delaruelle
Francis Martin
Nicolas Rouhier
Annegret Kohler
Sébastien Duplessis
RNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.
description Biotroph pathogens establish intimate interactions with their hosts that are conditioned by the successful secretion of effectors in infected tissues and subsequent manipulation of host physiology. The identification of early-expressed pathogen effectors and early-modulated host functions is currently a major goal to understand the molecular basis of biotrophy. Here, we report the 454-pyrosequencing transcriptome analysis of early stages of poplar leaf colonization by the rust fungus Melampsora larici-populina. Among the 841,301 reads considered for analysis, 616,879 and 649 were successfully mapped to Populus trichocarpa and M. larici-populina genome sequences, respectively. From a methodological aspect, these results indicate that this single approach is not appropriate to saturate poplar transcriptome and to follow transcript accumulation of the pathogen. We identified 19 pathogen transcripts encoding early-expressed small-secreted proteins representing candidate effectors of interest for forthcoming studies. Poplar RNA-Seq data were validated by oligoarrays and quantitatively analysed, which revealed a highly stable transcriptome with a single transcript encoding a sulfate transporter (herein named PtSultr3;5, POPTR_0006s16150) showing a dramatic increase upon colonization by either virulent or avirulent M. larici-populina strains. Perspectives connecting host sulfate transport and biotrophic lifestyle are discussed.
format article
author Benjamin Petre
Emmanuelle Morin
Emilie Tisserant
Stéphane Hacquard
Corinne Da Silva
Julie Poulain
Christine Delaruelle
Francis Martin
Nicolas Rouhier
Annegret Kohler
Sébastien Duplessis
author_facet Benjamin Petre
Emmanuelle Morin
Emilie Tisserant
Stéphane Hacquard
Corinne Da Silva
Julie Poulain
Christine Delaruelle
Francis Martin
Nicolas Rouhier
Annegret Kohler
Sébastien Duplessis
author_sort Benjamin Petre
title RNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.
title_short RNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.
title_full RNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.
title_fullStr RNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.
title_full_unstemmed RNA-Seq of early-infected poplar leaves by the rust pathogen Melampsora larici-populina uncovers PtSultr3;5, a fungal-induced host sulfate transporter.
title_sort rna-seq of early-infected poplar leaves by the rust pathogen melampsora larici-populina uncovers ptsultr3;5, a fungal-induced host sulfate transporter.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/34e355dd5f52492ba2efca95fb437a5f
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