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First published online January 24, 2008; 10.1104/pp.107.111898 Plant Physiology 146:1440-1453 (2008) © 2008 American Society of Plant Biologists OPEN ACCESS ARTICLE
Metabolic Profiles of Lolium perenne Are Differentially Affected by Nitrogen Supply, Carbohydrate Content, and Fungal Endophyte Infection1,[W],[OA]AgResearch, Palmerston North 4442, New Zealand (S.R., A.J.P., K.F., H.X.); and Department of Environmental Biology, University of Guelph, Guelph, Ontario, Canada N1G 2W1 (J.A.N.)
Lolium perenne cultivars differing in their capacity to accumulate water soluble carbohydrates (WSCs) were infected with three strains of fungal Neotyphodium lolii endophytes or left uninfected. The endophyte strains differed in their alkaloid profiles. Plants were grown at two different levels of nitrogen (N) supply in a controlled environment. Metabolic profiles of blades were analyzed using a variety of analytical methods. A total of 66 response variables were subjected to a principle components analysis and factor rotation. The first three rotated factors (46% of the total variance) were subsequently analyzed by analysis of variance. At high N supply nitrogenous compounds, organic acids and lipids were increased; WSCs, chlorogenic acid (CGA), and fibers were decreased. The high-sugar cultivar AberDove had reduced levels of nitrate, most minor amino acids, sulfur, and fibers compared to the control cultivar Fennema, whereas WSCs, CGA, and methionine were increased. In plants infected with endophytes, nitrate, several amino acids, and, magnesium were decreased; WSCs, lipids, some organic acids, and CGA were increased. Regrowth of blades was stimulated at high N, and there was a significant endophyte x cultivar interaction on regrowth. Mannitol, a fungal specific sugar alcohol, was significantly correlated with fungal biomass. Our findings suggest that effects of endophytes on metabolic profiles of L. perenne can be considerable, depending on host plant characteristics and nutrient supply, and we propose that a shift in carbon/N ratios and in secondary metabolite production as seen in our study is likely to have impacts on herbivore responses.
1 This work was supported by the New Zealand Foundation of Research, Science and Technology (contracts C10X0203 and PROJ 10333–ECOS–AGR) and was conducted at AgResearch Grasslands, New Zealand. This work was also supported by grants from the Canadian Natural Sciences and Engineering Research Council (to J.A.N.) and the Ontario Ministry of Agriculture, Food and Rural Affairs (to J.A.N.). The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Susanne Rasmussen (susanne.rasmussen{at}agresearch.co.nz). [W] The online version of this article contains Web-only data. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.107.111898 * Corresponding author; e-mail susanne.rasmussen{at}agresearch.co.nz. Received October 28, 2007; accepted January 17, 2008; published January 24, 2008. This article has been cited by other articles:
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