Cargando…

Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation

Cooperation involving Plant Growth-Promoting Rhizobacteria results in improvements of plant growth and health. While pathogenic and symbiotic interactions are known to induce transcriptional changes for genes related to plant defense and development, little is known about the impact of phytostimulat...

Descripción completa

Detalles Bibliográficos
Autores principales: Drogue, Benoît, Sanguin, Hervé, Chamam, Amel, Mozar, Michael, Llauro, Christel, Panaud, Olivier, Prigent-Combaret, Claire, Picault, Nathalie, Wisniewski-Dyé, Florence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222233/
https://www.ncbi.nlm.nih.gov/pubmed/25414716
http://dx.doi.org/10.3389/fpls.2014.00607
_version_ 1782342999436427264
author Drogue, Benoît
Sanguin, Hervé
Chamam, Amel
Mozar, Michael
Llauro, Christel
Panaud, Olivier
Prigent-Combaret, Claire
Picault, Nathalie
Wisniewski-Dyé, Florence
author_facet Drogue, Benoît
Sanguin, Hervé
Chamam, Amel
Mozar, Michael
Llauro, Christel
Panaud, Olivier
Prigent-Combaret, Claire
Picault, Nathalie
Wisniewski-Dyé, Florence
author_sort Drogue, Benoît
collection PubMed
description Cooperation involving Plant Growth-Promoting Rhizobacteria results in improvements of plant growth and health. While pathogenic and symbiotic interactions are known to induce transcriptional changes for genes related to plant defense and development, little is known about the impact of phytostimulating rhizobacteria on plant gene expression. This study aims at identifying genes significantly regulated in rice roots upon Azospirillum inoculation, considering possible favored interaction between a strain and its original host cultivar. Genome-wide analyzes of Oryza sativa japonica cultivars Cigalon and Nipponbare were performed, by using microarrays, seven days post-inoculation with Azospirillum lipoferum 4B (isolated from Cigalon) or Azospirillum sp. B510 (isolated from Nipponbare) and compared to the respective non-inoculated condition. A total of 7384 genes were significantly regulated, which represent about 16% of total rice genes. A set of 34 genes is regulated by both Azospirillum strains in both cultivars, including a gene orthologous to PR10 of Brachypodium, and these could represent plant markers of Azospirillum-rice interactions. The results highlight a strain-dependent response of rice, with 83% of the differentially expressed genes being classified as combination-specific. Whatever the combination, most of the differentially expressed genes are involved in primary metabolism, transport, regulation of transcription and protein fate. When considering genes involved in response to stress and plant defense, it appears that strain B510, a strain displaying endophytic properties, leads to the repression of a wider set of genes than strain 4B. Individual genotypic variations could be the most important driving force of rice roots gene expression upon Azospirillum inoculation. Strain-dependent transcriptional changes observed for genes related to auxin and ethylene signaling highlight the complexity of hormone signaling networks in the Azospirillum-rice cooperation.
format Online
Article
Text
id pubmed-4222233
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-42222332014-11-20 Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation Drogue, Benoît Sanguin, Hervé Chamam, Amel Mozar, Michael Llauro, Christel Panaud, Olivier Prigent-Combaret, Claire Picault, Nathalie Wisniewski-Dyé, Florence Front Plant Sci Plant Science Cooperation involving Plant Growth-Promoting Rhizobacteria results in improvements of plant growth and health. While pathogenic and symbiotic interactions are known to induce transcriptional changes for genes related to plant defense and development, little is known about the impact of phytostimulating rhizobacteria on plant gene expression. This study aims at identifying genes significantly regulated in rice roots upon Azospirillum inoculation, considering possible favored interaction between a strain and its original host cultivar. Genome-wide analyzes of Oryza sativa japonica cultivars Cigalon and Nipponbare were performed, by using microarrays, seven days post-inoculation with Azospirillum lipoferum 4B (isolated from Cigalon) or Azospirillum sp. B510 (isolated from Nipponbare) and compared to the respective non-inoculated condition. A total of 7384 genes were significantly regulated, which represent about 16% of total rice genes. A set of 34 genes is regulated by both Azospirillum strains in both cultivars, including a gene orthologous to PR10 of Brachypodium, and these could represent plant markers of Azospirillum-rice interactions. The results highlight a strain-dependent response of rice, with 83% of the differentially expressed genes being classified as combination-specific. Whatever the combination, most of the differentially expressed genes are involved in primary metabolism, transport, regulation of transcription and protein fate. When considering genes involved in response to stress and plant defense, it appears that strain B510, a strain displaying endophytic properties, leads to the repression of a wider set of genes than strain 4B. Individual genotypic variations could be the most important driving force of rice roots gene expression upon Azospirillum inoculation. Strain-dependent transcriptional changes observed for genes related to auxin and ethylene signaling highlight the complexity of hormone signaling networks in the Azospirillum-rice cooperation. Frontiers Media S.A. 2014-11-06 /pmc/articles/PMC4222233/ /pubmed/25414716 http://dx.doi.org/10.3389/fpls.2014.00607 Text en Copyright © 2014 Drogue, Sanguin, Chamam, Mozar, Llauro, Panaud, Prigent-Combaret, Picault and Wisniewski-Dyé. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Drogue, Benoît
Sanguin, Hervé
Chamam, Amel
Mozar, Michael
Llauro, Christel
Panaud, Olivier
Prigent-Combaret, Claire
Picault, Nathalie
Wisniewski-Dyé, Florence
Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation
title Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation
title_full Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation
title_fullStr Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation
title_full_unstemmed Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation
title_short Plant root transcriptome profiling reveals a strain-dependent response during Azospirillum-rice cooperation
title_sort plant root transcriptome profiling reveals a strain-dependent response during azospirillum-rice cooperation
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222233/
https://www.ncbi.nlm.nih.gov/pubmed/25414716
http://dx.doi.org/10.3389/fpls.2014.00607
work_keys_str_mv AT droguebenoit plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT sanguinherve plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT chamamamel plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT mozarmichael plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT llaurochristel plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT panaudolivier plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT prigentcombaretclaire plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT picaultnathalie plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation
AT wisniewskidyeflorence plantroottranscriptomeprofilingrevealsastraindependentresponseduringazospirillumricecooperation