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. 2022 Jul 20;11:e79679. doi: 10.7554/eLife.79679

Figure 3. Rhizosphere bacteria and drought induce systemic metabolic changes in root exudates.

Metabolic profiles of root exudate solutions from roots of irrigated and drought-exposed Cupressus sempervirens saplings, with and without bacterial inoculations. Intact roots were incubated for 48 hr to collect exudates, which were analyzed by mass spectrometry. (DB) drought with bacteria, (D) drought w/o bacteria, (IB) irrigated with bacteria, (I) irrigated w/o bacteria. (A) Principal coordinate analysis of the polar metabolite profiles of exudates from drought-exposed saplings with and without bacterial inoculations (DB and D, respectively; left), and in combination with irrigated saplings (I; right; excluding the group of irrigated trees with bacteria for clarity). (B) Heat map analysis of the fold change of each of 149 identified metabolites (rows) relative to control level (at the beginning of the experiment). Columns represent means for each of the four saplings groups (n=4–6). (C) Same as in (B) for the re-irrigation phase. The nine metabolite names indicate metabolites which were tested in vitro for bacterial growth. For the list of metabolites, see Figure 3—source data 1.

Figure 3—source data 1. Data and statistical analysis of root exudates polar metabolites.
Figure 3—source data 2. Statistical analysis of root exudates semi-polar metabolites.

Figure 3.

Figure 3—figure supplement 1. Semi-polar metabolic profiles of root exudate solutions from roots of irrigated and drought-exposed Cupressus sempervirens saplings, with and without bacterial inoculations.

Figure 3—figure supplement 1.

Intact roots were incubated for 48 hr to collect exudates, which were analyzed by mass spectrometry. (A) Principal component analysis of the semi-polar metabolite profiles of exudates from exudates from irrigated saplings (I), and drought-exposed saplings with and without bacterial inoculations (DB and D, respectively). (B) Heat map analysis of the fold change of each of 2285 semi-polar metabolite markers (rows) relative to control level. Columns represent means for each of the four saplings groups (n=4–6). (C) Heat map analysis of the fold change of each of 12 semi-polar identified metabolites. The numbers indicate the number of material in Figure 3—source data 2.