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. 2020 Feb 1;25:e00425. doi: 10.1016/j.btre.2020.e00425

Table 3.

Recent metabolomic elucidation of plant host metabolome changes during plant-microbes symbiosis.

Profiled metabolome: plant host Interactions and study conditions Significant metabolites identified Metabolomic analytical resource References
a. Wheat; a. Wheat+ beneficial microbes (AMF + PGPR); in planta field trial; a. Xilitol, carnitines, d-arabitol, pipecolic acid, 2-oxoglutarate, pyruvate, zymosterol, choline group, ethanolamines, and l-arabinose; a. GC-TOF-MS and HILIC-Q-TOF-MS; a. [72];
b. Grape berries; b. Grape berries + phytopathogen (B. cinerea, Penicillium expansum, Aspergillus niger and A. carbonarius); in vitro microplate and zip-lock plastic bag assay; b. 1,5-dimethylnaphthalene, unidentified sesquiterpenes, 2-(4-hexyl-2,5-dioxo-2,5-dihydrofuran-3-yl)acetic acid, m-cresol and γ-nonalactone; b. SPME-GC-QTOF-MS; b. [81];
c. Barley, wheat and rice; c. Barley, wheat and rice + pathogen cassette (Lr34 resistance gene); in planta hydroponic experiment; c. Gentisic acid O-glucoside, C-glycosylated flavones, isoorientin-7-2″-di-O- glucoside and hordatines; c. UHPLC-HR-MS; c. [73];
d. Potato leaf; d. Potato leaf + Phosphite; in planta field trial; d. Caffeic acid, salicylic acid, and chlorogenic acid; d. GC-TOF-MS; d. [90];
e. Apple fruit; e. Apple fruit + phytopathogen (P. expansum); in vitro growth chamber experiment; e. Fructose, malic acid, shikimic acid, ascorbic acid and glutathione; e. HPLC; e. [75];
f. A. thaliana cell; f. A. thaliana + phytopathogen (P. syringae); in vitro growth chamber experiment; f. Unspecified; f. FT-IR; f. [41];
g. Soybean; g. Soybean + phytopathogen (R. solani); in vitro growth chamber experiment g. Coumarins, phytoalexins, and flavonoids; g. GC-MS g. [32];
h. Tomato; h. Tomato + phytopathogen (B. cinerea and P. syringae) + beneficial compound (hexanoic acid); in planta controlled experiment; h. 1-methyltryptophan; h. UHPLC-MS/GC-MS; h. [37];
i. Sugarcane bud setts; i. Sugar cane bud setts + Sporisorium scitamineum; in planta (green-house); i. Lyxose, glycerate, raffinose, and phenylpropanoid; i. GC-TOF-MS and LC-ESI-MS/MS; i. [74];
j. Tomato; j. Tomato + Trichoderma metabolites (6-pentyl-2H-pyran-2-one and harzianic acid); in vitro plant growth assay; j. Alanine, arginine, asparagine, fructose galactose, glucose, glutamine, leucine, methionine, phenylalanine, sucrose, threonine, trigonelline, tyrosine, and valine; j. HRMAS-NMR; and j. [76];
k. Citrus leaves; and k. Citrus seeds + Candidatus Liberibacter asiaticus; in planta controlled experiment; and k. Asparagine, choline, glucose, malic acid, maltose, proline, sucrose, threonine, trigonelline, quinic acid, and uridine; and k. NMR; k. [77]; and
l. Maize root l. Wild type (WT) BX regulated maize (Zea mays cv.W22) root + BX deficient W22 mutant; in planta (green-house) l. Dihydroxy-7-methoxy-1,4-benzoxazin-3-one and 2,4-dihydroxy-1,4-benzoxazin-3-one l. UPLC-Q-TOF-MS l. [78]

Key: GC: Gas Chromatography; HRMAS: High-Resolution Magic-Angle-Spinning; HILIC: Hydrophilic interaction; QTOF: Quadruple Time of Flight; LC: Liquid Chromatography; HR: High Resolution; MS: Mass spectrometry; UHP: Ultra-High Performance; SPME: Solid Phase Microextraction; ESI: Electrospray ionization; and FT-IR: Fourier Transform Infra-Red Spectroscopy.