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Transcriptomic dissection of the rice – Burkholderia glumae interaction
BACKGROUND: Bacterial panicle blight caused by the bacterium Burkholderia glumae is an emerging disease of rice in the United States. Not much is known about this disease, the disease cycle or any source of disease resistance. To understand the interaction between rice and Burkholderia glumae, we us...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165909/ https://www.ncbi.nlm.nih.gov/pubmed/25183458 http://dx.doi.org/10.1186/1471-2164-15-755 |
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author | Magbanua, Zenaida V Arick, Mark Buza, Teresia Hsu, Chuan-Yu Showmaker, Kurt C Chouvarine, Philippe Deng, Peng Peterson, Daniel G Lu, Shien |
author_facet | Magbanua, Zenaida V Arick, Mark Buza, Teresia Hsu, Chuan-Yu Showmaker, Kurt C Chouvarine, Philippe Deng, Peng Peterson, Daniel G Lu, Shien |
author_sort | Magbanua, Zenaida V |
collection | PubMed |
description | BACKGROUND: Bacterial panicle blight caused by the bacterium Burkholderia glumae is an emerging disease of rice in the United States. Not much is known about this disease, the disease cycle or any source of disease resistance. To understand the interaction between rice and Burkholderia glumae, we used transcriptomics via next-generation sequencing (RNA-Seq) and bioinformatics to identify differentially expressed transcripts between resistant and susceptible interactions and formulate a model for rice resistance to the disease. RESULTS: Using inoculated young seedlings as sample tissues, we identified unique transcripts involved with resistance to bacterial panicle blight, including a PIF-like ORF1 and verified differential expression of some selected genes using qRT-PCR. These transcripts, which include resistance genes of the NBS-LRR type, kinases, transcription factors, transporters and expressed proteins with functions that are not known, have not been reported in other pathosystems including rice blast or bacterial blight. Further, functional annotation analysis reveals enrichment of defense response and programmed cell death (biological processes); ATP and protein binding (molecular functions); and mitochondrion-related (cell component) transcripts in the resistant interaction. CONCLUSION: Taken together, we formulated a model for rice resistance to bacterial panicle blight that involves an activation of previously unknown resistance genes and their activation partners upon challenge with B. glumae. Other interesting findings are that 1) though these resistance transcripts were up-regulated upon inoculation in the resistant interaction, some of them were already expressed in the water-inoculated control from the resistant genotype, but not in the water- and bacterium-inoculated samples from the susceptible genotype; 2) rice may have co-opted an ORF that was previously a part of a transposable element to aid in the resistance mechanism; and 3) resistance may have existed immediately prior to rice domestication. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-755) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4165909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41659092014-09-19 Transcriptomic dissection of the rice – Burkholderia glumae interaction Magbanua, Zenaida V Arick, Mark Buza, Teresia Hsu, Chuan-Yu Showmaker, Kurt C Chouvarine, Philippe Deng, Peng Peterson, Daniel G Lu, Shien BMC Genomics Research Article BACKGROUND: Bacterial panicle blight caused by the bacterium Burkholderia glumae is an emerging disease of rice in the United States. Not much is known about this disease, the disease cycle or any source of disease resistance. To understand the interaction between rice and Burkholderia glumae, we used transcriptomics via next-generation sequencing (RNA-Seq) and bioinformatics to identify differentially expressed transcripts between resistant and susceptible interactions and formulate a model for rice resistance to the disease. RESULTS: Using inoculated young seedlings as sample tissues, we identified unique transcripts involved with resistance to bacterial panicle blight, including a PIF-like ORF1 and verified differential expression of some selected genes using qRT-PCR. These transcripts, which include resistance genes of the NBS-LRR type, kinases, transcription factors, transporters and expressed proteins with functions that are not known, have not been reported in other pathosystems including rice blast or bacterial blight. Further, functional annotation analysis reveals enrichment of defense response and programmed cell death (biological processes); ATP and protein binding (molecular functions); and mitochondrion-related (cell component) transcripts in the resistant interaction. CONCLUSION: Taken together, we formulated a model for rice resistance to bacterial panicle blight that involves an activation of previously unknown resistance genes and their activation partners upon challenge with B. glumae. Other interesting findings are that 1) though these resistance transcripts were up-regulated upon inoculation in the resistant interaction, some of them were already expressed in the water-inoculated control from the resistant genotype, but not in the water- and bacterium-inoculated samples from the susceptible genotype; 2) rice may have co-opted an ORF that was previously a part of a transposable element to aid in the resistance mechanism; and 3) resistance may have existed immediately prior to rice domestication. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-755) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-03 /pmc/articles/PMC4165909/ /pubmed/25183458 http://dx.doi.org/10.1186/1471-2164-15-755 Text en © Magbanua et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 Magbanua, Zenaida V Arick, Mark Buza, Teresia Hsu, Chuan-Yu Showmaker, Kurt C Chouvarine, Philippe Deng, Peng Peterson, Daniel G Lu, Shien Transcriptomic dissection of the rice – Burkholderia glumae interaction |
title | Transcriptomic dissection of the rice – Burkholderia glumae interaction |
title_full | Transcriptomic dissection of the rice – Burkholderia glumae interaction |
title_fullStr | Transcriptomic dissection of the rice – Burkholderia glumae interaction |
title_full_unstemmed | Transcriptomic dissection of the rice – Burkholderia glumae interaction |
title_short | Transcriptomic dissection of the rice – Burkholderia glumae interaction |
title_sort | transcriptomic dissection of the rice – burkholderia glumae interaction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165909/ https://www.ncbi.nlm.nih.gov/pubmed/25183458 http://dx.doi.org/10.1186/1471-2164-15-755 |
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