Title
Rapid metabolic profiling of Nicotiana tabacum defence responses against Phytophthora nicotianae using direct infrared laser desorption ionization mass spectrometry and principal component analysis
Date Issued
09 June 2010
Access level
open access
Resource Type
journal article
Author(s)
Scharte J.
Bones P.
Pirkl A.
Meldau S.
Baldwin I.
Hillenkamp F.
Weis E.
Dreisewerd K.
Westfälische Wilhelms-Universität Münster
Abstract
Background: Successful defence of tobacco plants against attack from the oomycete Phytophthora nicotianae includes a type of local programmed cell death called the hypersensitive response. Complex and not completely understood signaling processes are required to mediate the development of this defence in the infected tissue. Here, we demonstrate that different families of metabolites can be monitored in small pieces of infected, mechanically-stressed, and healthy tobacco leaves using direct infrared laser desorption ionization orthogonal time-of-flight mass spectrometry. The defence response was monitored for 1 - 9 hours post infection.Results: Infrared laser desorption ionization orthogonal time-of-flight mass spectrometry allows rapid and simultaneous detection in both negative and positive ion mode of a wide range of naturally occurring primary and secondary metabolites. An unsupervised principal component analysis was employed to identify correlations between changes in metabolite expression (obtained at different times and sample treatment conditions) and the overall defence response.A one-dimensional projection of the principal components 1 and 2 obtained from positive ion mode spectra was used to generate a Biological Response Index (BRI). The BRI obtained for each sample treatment was compared with the number of dead cells found in the respective tissue. The high correlation between these two values suggested that the BRI provides a rapid assessment of the plant response against the pathogen infection. Evaluation of the loading plots of the principal components (1 and 2) reveals a correlation among three metabolic cascades and the defence response generated in infected leaves. Analysis of selected phytohormones by liquid chromatography electrospray ionization mass spectrometry verified our findings.Conclusion: The described methodology allows for rapid assessment of infection-specific changes in the plant metabolism, in particular of phenolics, alkaloids, oxylipins, and carbohydrates. Moreover, potential novel biomarkers can be detected and used to predict the quality of plant infections. © 2010 Ibáñez et al; licensee BioMed Central Ltd.
Volume
6
Issue
1
Language
English
OCDE Knowledge area
Ciencias de las plantas, Botánica
Química analítica
Scopus EID
2-s2.0-77953187838
Source
Plant Methods
ISSN of the container
17464811
Sponsor(s)
We are grateful to Stefan Berkenkamp and Sequenom GmbH for providing use of their oTOF instrument, Matthias Schöttner for his support with the LC-ESI-MS/MS phytohormone measurements, Jens Soltwisch for his support with the IR-LDI-oTOF MS measurements, Ina Schmitz-Thom for her support with the dead cell count measurements, Dr. Jutta Essmann and Dr. Aleš Svatoš for fruitful discussions and support of this project. AJI gratefully acknowledges financial support of the Alexander von Humboldt foundation.
Sources of information:
Directorio de Producción Científica
Scopus