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Transcriptional profile of sweet orange in response to chitosan and salicylic acid

BACKGROUND: Resistance inducers have been used in annual crops as an alternative for disease control. Wood perennial fruit trees, such as those of the citrus species, are candidates for treatment with resistance inducers, such as salicylic acid (SA) and chitosan (CHI). However, the involved mechanis...

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Autores principales: Coqueiro, Danila Souza Oliveira, de Souza, Alessandra Alves, Takita, Marco Aurélio, Rodrigues, Carolina Munari, Kishi, Luciano Takeshi, Machado, Marcos Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415254/
https://www.ncbi.nlm.nih.gov/pubmed/25887907
http://dx.doi.org/10.1186/s12864-015-1440-5
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author Coqueiro, Danila Souza Oliveira
de Souza, Alessandra Alves
Takita, Marco Aurélio
Rodrigues, Carolina Munari
Kishi, Luciano Takeshi
Machado, Marcos Antonio
author_facet Coqueiro, Danila Souza Oliveira
de Souza, Alessandra Alves
Takita, Marco Aurélio
Rodrigues, Carolina Munari
Kishi, Luciano Takeshi
Machado, Marcos Antonio
author_sort Coqueiro, Danila Souza Oliveira
collection PubMed
description BACKGROUND: Resistance inducers have been used in annual crops as an alternative for disease control. Wood perennial fruit trees, such as those of the citrus species, are candidates for treatment with resistance inducers, such as salicylic acid (SA) and chitosan (CHI). However, the involved mechanisms in resistance induced by elicitors in citrus are currently few known. RESULTS: In the present manuscript, we report information regarding the transcriptional changes observed in sweet orange in response to exogenous applications of SA and CHI using RNA-seq technology. More genes were induced by SA treatment than by CHI treatment. In total, 1,425 differentially expressed genes (DEGs) were identified following treatment with SA, including the important genes WRKY50, PR2, and PR9, which are known to participate in the salicylic acid signaling pathway, and genes involved in ethylene/Jasmonic acid biosynthesis (ACS12, AP2 domain-containing transcription factor, and OPR3). In addition, SA treatment promoted the induction of a subset of genes involved in several metabolic processes, such as redox states and secondary metabolism, which are associated with biotic stress. For CHI treatment, there were 640 DEGs, many of them involved in secondary metabolism. For both SA and CHI treatments, the auxin pathway genes were repressed, but SA treatment promoted induction in the ethylene and jasmonate acid pathway genes, in addition to repressing the abscisic acid pathway genes. Chitosan treatment altered some hormone metabolism pathways. The DEGs were validated by quantitative Real-Time PCR (qRT-PCR), and the results were consistent with the RNA-seq data, with a high correlation between the two analyses. CONCLUSIONS: We expanded the available information regarding induced defense by elicitors in a species of Citrus that is susceptible to various diseases and identified the molecular mechanisms by which this defense might be mediated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1440-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-44152542015-05-01 Transcriptional profile of sweet orange in response to chitosan and salicylic acid Coqueiro, Danila Souza Oliveira de Souza, Alessandra Alves Takita, Marco Aurélio Rodrigues, Carolina Munari Kishi, Luciano Takeshi Machado, Marcos Antonio BMC Genomics Research Article BACKGROUND: Resistance inducers have been used in annual crops as an alternative for disease control. Wood perennial fruit trees, such as those of the citrus species, are candidates for treatment with resistance inducers, such as salicylic acid (SA) and chitosan (CHI). However, the involved mechanisms in resistance induced by elicitors in citrus are currently few known. RESULTS: In the present manuscript, we report information regarding the transcriptional changes observed in sweet orange in response to exogenous applications of SA and CHI using RNA-seq technology. More genes were induced by SA treatment than by CHI treatment. In total, 1,425 differentially expressed genes (DEGs) were identified following treatment with SA, including the important genes WRKY50, PR2, and PR9, which are known to participate in the salicylic acid signaling pathway, and genes involved in ethylene/Jasmonic acid biosynthesis (ACS12, AP2 domain-containing transcription factor, and OPR3). In addition, SA treatment promoted the induction of a subset of genes involved in several metabolic processes, such as redox states and secondary metabolism, which are associated with biotic stress. For CHI treatment, there were 640 DEGs, many of them involved in secondary metabolism. For both SA and CHI treatments, the auxin pathway genes were repressed, but SA treatment promoted induction in the ethylene and jasmonate acid pathway genes, in addition to repressing the abscisic acid pathway genes. Chitosan treatment altered some hormone metabolism pathways. The DEGs were validated by quantitative Real-Time PCR (qRT-PCR), and the results were consistent with the RNA-seq data, with a high correlation between the two analyses. CONCLUSIONS: We expanded the available information regarding induced defense by elicitors in a species of Citrus that is susceptible to various diseases and identified the molecular mechanisms by which this defense might be mediated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1440-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-12 /pmc/articles/PMC4415254/ /pubmed/25887907 http://dx.doi.org/10.1186/s12864-015-1440-5 Text en © Coqueiro et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Coqueiro, Danila Souza Oliveira
de Souza, Alessandra Alves
Takita, Marco Aurélio
Rodrigues, Carolina Munari
Kishi, Luciano Takeshi
Machado, Marcos Antonio
Transcriptional profile of sweet orange in response to chitosan and salicylic acid
title Transcriptional profile of sweet orange in response to chitosan and salicylic acid
title_full Transcriptional profile of sweet orange in response to chitosan and salicylic acid
title_fullStr Transcriptional profile of sweet orange in response to chitosan and salicylic acid
title_full_unstemmed Transcriptional profile of sweet orange in response to chitosan and salicylic acid
title_short Transcriptional profile of sweet orange in response to chitosan and salicylic acid
title_sort transcriptional profile of sweet orange in response to chitosan and salicylic acid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415254/
https://www.ncbi.nlm.nih.gov/pubmed/25887907
http://dx.doi.org/10.1186/s12864-015-1440-5
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