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Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics

Molecular changes elicited by plants in response to fungal attack and how this affects plant–pathogen interaction, including susceptibility or resistance, remain elusive. We studied the dynamics in root metabolism during compatible and incompatible interactions between chickpea and Fusarium oxysporu...

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Autores principales: Kumar, Yashwant, Zhang, Limin, Panigrahi, Priyabrata, Dholakia, Bhushan B., Dewangan, Veena, Chavan, Sachin G., Kunjir, Shrikant M., Wu, Xiangyu, Li, Ning, Rajmohanan, Pattuparambil R., Kadoo, Narendra Y., Giri, Ashok P., Tang, Huiru, Gupta, Vidya S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066658/
https://www.ncbi.nlm.nih.gov/pubmed/26801007
http://dx.doi.org/10.1111/pbi.12522
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author Kumar, Yashwant
Zhang, Limin
Panigrahi, Priyabrata
Dholakia, Bhushan B.
Dewangan, Veena
Chavan, Sachin G.
Kunjir, Shrikant M.
Wu, Xiangyu
Li, Ning
Rajmohanan, Pattuparambil R.
Kadoo, Narendra Y.
Giri, Ashok P.
Tang, Huiru
Gupta, Vidya S.
author_facet Kumar, Yashwant
Zhang, Limin
Panigrahi, Priyabrata
Dholakia, Bhushan B.
Dewangan, Veena
Chavan, Sachin G.
Kunjir, Shrikant M.
Wu, Xiangyu
Li, Ning
Rajmohanan, Pattuparambil R.
Kadoo, Narendra Y.
Giri, Ashok P.
Tang, Huiru
Gupta, Vidya S.
author_sort Kumar, Yashwant
collection PubMed
description Molecular changes elicited by plants in response to fungal attack and how this affects plant–pathogen interaction, including susceptibility or resistance, remain elusive. We studied the dynamics in root metabolism during compatible and incompatible interactions between chickpea and Fusarium oxysporum f. sp. ciceri (Foc), using quantitative label‐free proteomics and NMR‐based metabolomics. Results demonstrated differential expression of proteins and metabolites upon Foc inoculations in the resistant plants compared with the susceptible ones. Additionally, expression analysis of candidate genes supported the proteomic and metabolic variations in the chickpea roots upon Foc inoculation. In particular, we found that the resistant plants revealed significant increase in the carbon and nitrogen metabolism; generation of reactive oxygen species (ROS), lignification and phytoalexins. The levels of some of the pathogenesis‐related proteins were significantly higher upon Foc inoculation in the resistant plant. Interestingly, results also exhibited the crucial role of altered Yang cycle, which contributed in different methylation reactions and unfolded protein response in the chickpea roots against Foc. Overall, the observed modulations in the metabolic flux as outcome of several orchestrated molecular events are determinant of plant's role in chickpea–Foc interactions.
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spelling pubmed-50666582016-11-01 Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics Kumar, Yashwant Zhang, Limin Panigrahi, Priyabrata Dholakia, Bhushan B. Dewangan, Veena Chavan, Sachin G. Kunjir, Shrikant M. Wu, Xiangyu Li, Ning Rajmohanan, Pattuparambil R. Kadoo, Narendra Y. Giri, Ashok P. Tang, Huiru Gupta, Vidya S. Plant Biotechnol J Research Articles Molecular changes elicited by plants in response to fungal attack and how this affects plant–pathogen interaction, including susceptibility or resistance, remain elusive. We studied the dynamics in root metabolism during compatible and incompatible interactions between chickpea and Fusarium oxysporum f. sp. ciceri (Foc), using quantitative label‐free proteomics and NMR‐based metabolomics. Results demonstrated differential expression of proteins and metabolites upon Foc inoculations in the resistant plants compared with the susceptible ones. Additionally, expression analysis of candidate genes supported the proteomic and metabolic variations in the chickpea roots upon Foc inoculation. In particular, we found that the resistant plants revealed significant increase in the carbon and nitrogen metabolism; generation of reactive oxygen species (ROS), lignification and phytoalexins. The levels of some of the pathogenesis‐related proteins were significantly higher upon Foc inoculation in the resistant plant. Interestingly, results also exhibited the crucial role of altered Yang cycle, which contributed in different methylation reactions and unfolded protein response in the chickpea roots against Foc. Overall, the observed modulations in the metabolic flux as outcome of several orchestrated molecular events are determinant of plant's role in chickpea–Foc interactions. John Wiley and Sons Inc. 2016-01-23 2016-07 /pmc/articles/PMC5066658/ /pubmed/26801007 http://dx.doi.org/10.1111/pbi.12522 Text en © 2016 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Kumar, Yashwant
Zhang, Limin
Panigrahi, Priyabrata
Dholakia, Bhushan B.
Dewangan, Veena
Chavan, Sachin G.
Kunjir, Shrikant M.
Wu, Xiangyu
Li, Ning
Rajmohanan, Pattuparambil R.
Kadoo, Narendra Y.
Giri, Ashok P.
Tang, Huiru
Gupta, Vidya S.
Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics
title Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics
title_full Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics
title_fullStr Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics
title_full_unstemmed Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics
title_short Fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics
title_sort fusarium oxysporum mediates systems metabolic reprogramming of chickpea roots as revealed by a combination of proteomics and metabolomics
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066658/
https://www.ncbi.nlm.nih.gov/pubmed/26801007
http://dx.doi.org/10.1111/pbi.12522
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