Virus-Induced Alterations in Primary Metabolism Modulate Susceptibility toTobacco rattle virusin Arabidopsis
Author(s) -
Lourdes FernándezCalvino,
Sonia Osorio,
M. Luisa Hernández,
Ignacio B. Hamada,
Francisco J. del Toro,
Livia Donaire,
Agnès Yu,
Regla Bustos,
Alisdair R. Fernie,
José M. MartínezRivas,
César Llave
Publication year - 2014
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.114.250340
Subject(s) - arabidopsis , biology , tobacco rattle virus , virus , arabidopsis thaliana , metabolism , secondary metabolism , mutant , gene , lipid metabolism , fatty acid metabolism , biochemistry , biosynthesis , genetics , plant virus
During compatible virus infections, plants respond by reprogramming gene expression and metabolite content. While gene expression studies are profuse, our knowledge of the metabolic changes that occur in the presence of the virus is limited. Here, we combine gene expression and metabolite profiling in Arabidopsis (Arabidopsis thaliana) infected with Tobacco rattle virus (TRV) in order to investigate the influence of primary metabolism on virus infection. Our results revealed that primary metabolism is reconfigured in many ways during TRV infection, as reflected by significant changes in the levels of sugars and amino acids. Multivariate data analysis revealed that these alterations were particularly conspicuous at the time points of maximal accumulation of TRV, although infection time was the dominant source of variance during the process. Furthermore, TRV caused changes in lipid and fatty acid composition in infected leaves. We found that several Arabidopsis mutants deficient in branched-chain amino acid catabolism or fatty acid metabolism possessed altered susceptibility to TRV. Finally, we showed that increments in the putrescine content in TRV-infected plants correlated with enhanced tolerance to freezing stress in TRV-infected plants and that impairment of putrescine biosynthesis promoted virus multiplication. Our results thus provide an interesting overview for a better understanding of the relationship between primary metabolism and virus infection.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom