Untargeted metabolomics analysis reveals dynamic changes in azelaic acid- and salicylic acid derivatives in LPS-treated Nicotiana tabacum cells
To counteract biotic stress factors, plants employ multilayered defense mechanisms responsive to pathogen-derived elicitor molecules, and regulated by different phytohormones and signaling molecules. Here, lipopolysaccharide (LPS), a microbe-associated molecular pattern (MAMP) molecule, was used to...
Saved in:
Published in | Biochemical and biophysical research communications Vol. 482; no. 4; pp. 1498 - 1503 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
22.01.2017
|
Subjects | |
Online Access | Get full text |
ISSN | 0006-291X 1090-2104 |
DOI | 10.1016/j.bbrc.2016.12.063 |
Cover
Summary: | To counteract biotic stress factors, plants employ multilayered defense mechanisms responsive to pathogen-derived elicitor molecules, and regulated by different phytohormones and signaling molecules. Here, lipopolysaccharide (LPS), a microbe-associated molecular pattern (MAMP) molecule, was used to induce defense responses in Nicotiana tabacum cell suspensions. Intracellular metabolites were extracted with methanol and analyzed using a liquid chromatography-mass spectrometry (UHPLC-qTOF-MS/MS) platform. The generated data were processed and examined with multivariate and univariate statistical tools. The results show time-dependent dynamic changes and accumulation of glycosylated signaling molecules, specifically those of azelaic acid, salicylic acid and methyl-salicylate as contributors to the altered metabolomic state in LPS-treated cells.
•LPS-induced changes in the metabolome of tobacco cells were investigated.•PCA plots revealed time-dependent metabolic perturbations.•OPLS-DA plots indicated signatory bio-markers.•Glycosides of azelaic acid, salicylic acid and methylsalicylate are biomarkers.•AzA and SA play a role in LPS-induced priming and defence activation. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/j.bbrc.2016.12.063 |