Table 1.
Representative studies where plants under different stresses can select/modulate the assembly of the root-associated microbiome. For each study (when possible) the trigger leading to plant activity that modulates the microbiome, the identified mechanism of action, the effect on the microbiome, the host plant and the reference is mentioned.
Trigger | Mechanisms | Effect | Host | Reference |
---|---|---|---|---|
Pathogen-triggered | ||||
Fusarium oxysporum f. sp. lycopersici | Disease -induced recruitment from suppressive compost | Enrichment of Proteobacteria, Actinobacteria, and Firmicutes (Bacillus) | Tomato | Antoniou et al., 2017 |
Hyaloperonospora arabidopsidis/Pseudomonas syringae pv. tomato | Legacy-mediated development of soil suppressiveness | Assemblage of beneficial rhizosphere microbiome | Arabidopsis/Tomato | Berendsen et al., 2018/ Yuan et al., 2018 |
Rhizoctonia solani | Activation of bacterial stress responses and activation of antagonistic traits that restrict pathogen infection | Shifts in microbiome composition and enrichment of Oxalobacteraceae, Burkholderiaceae, Sphingobacteriaceae, and Sphingomonadaceae | Sugar beet | Chapelle et al., 2016 |
Botrytis cinerea | Chemoattraction induced by root-exuded peroxidases and oxylipins | Attraction of Trichoderma harzianum and inhibition of Fusarium oxysporum | Tomato; Cucumber | Lombardi et al., 2018 |
Rhizoctonia solani | Pathogen-induced taxa enrichment from suppressive soils | Recruitment of specific taxa from rhizosphere of sugar beet infected with Rhizoctonia solani | Sugar beet | Mendes et al., 2011 |
Pseudomonas syringae pv. tomato | Root-secreted malic acid | Recruitment of Bacillus subtilis FB17 | Arabidopsis | Rudrappa et al., 2008 |
Fusarium oxysporum f. sp. lini | Disease-induced recruitment of beneficial microbes from Fusarium suppressive soils | Increase of taxa associated to Fusarium wilt suppressiveness | Flax | Siegel-Hertz et al., 2018 |
Huanglongbing (HLB) caused by Candidatus Liberibacter spp. | Putative mechanisms: HLB significantly altered the structure or functional potential of the citrus endosphere | Decrease in abundance of taxa and loss of functions in the rhizoplane-rhizosphere enriched microbiome of HLB- infected citrus roots | Citrus | Zhang et al., 2017 |
Insects-triggered | ||||
Aphids | Elicitation of plant immunity via SA/JA systemic signaling and expression of pathogenesis-related (PR) proteins in roots | Recruitment of the beneficial bacteria Bacillus subtilis and decrease of the population of Ralstonia solanacearum | Pepper | Lee et al., 2012 |
Whitefly | Whitefly infestation elicited SA and JA signaling in above and below ground tissues and overexpression of PR genes in the roots resulting in a differential microbiome assembly | The differential microbiome assembly induced resistance against to Xanthomonas axonopodis pv. vesicatoria and Ralstonia solanacearum | Pepper | Yang et al., 2011 |
Abiotic stress/nutrient deficiency-triggered | ||||
Phosphate deficiency | Phosphate starvation response via PHR1 and PHL1 and PHO2 | Differential assemblage of bacterial and fungal microbiota | Arabidopsis | Castrillo et al., 2017/ Fabianska et al., 2019 |
Gradients of phosphate, salinity, pH, temperature | - | Assembly of different modules of co-occurring strains | Arabidopsis | Finkel et al., 2019 |
wounding; salt stress | Chemoattraction induced by root-exuded peroxidases and oxylipins | Exudates attracted Trichoderma harzianum and showed deterrent activity against Fusarium oxysporum | Tomato; Cucumber | Lombardi et al., 2018 |
Iron deficiency/colonization by PGPR | Increased accumulation and secretion of the coumarin scopoletin exerts selective antimicrobial activity in rhizosphere | Differential microbiome assembly, repelling potential against phytopathogens and thus, recruiting potential beneficial microbes | Arabidopsis | Stringlis et al., 2018b |
Iron deficiency | Catecholic coumarins show differential antimicrobial activity | Shift in microbial composition of SynCom in vitro | Arabidopsis | Voges et al., 2019 |
Endogenous/exogenous plant-derived molecules-triggered | ||||
- | Overexpression of genes involved biosynthesis and transport of root-exuded secondary metabolites | Greater abundance of potentially beneficial bacteria | Arabidopsis | Badri et al., 2009 |
- | Differential exudation of root secondary metabolites regulated by Benzoxazinoids (BXs) | Enrichment of Methylophilaceae, Nitrosomonadaceae, Oxalobactereraceae, Syntrophobacteriaceae, and Gaiellaceae | Maize | Cotton et al., 2019 |
- | Benzoxazinoids (BXs) drive plant-soil feedback | BXs shape the microbiota of the next generation of plants | Maize | Hu et al., 2018 |
- | Differential secretion of triterpene-derived metabolites by altering triterpene gene cluster | Differential assembly of Arabidopsis root microbiome | Arabidopsis | Huang et al., 2019 |
- | Microbial sulfatase cleaves root-exuded sulfate esters produced by the camalexin biosynthetic pathway | Stimulation of microbial sulfatase activity in soil and is required for the plant growth-promoting effects of several bacterial strains | Arabidopsis | Koprivova et al., 2019 |
- | Assembly of differential microbiome between tomato cultivars susceptible and resistant to Ralstonia solanacearum | Enrichment of Flavobacterium in the microbiome of tomato cultivars resistant to Ralstonia, Flavobacterium application confers resistance to susceptible cultivar | Tomato | Kwak et al., 2018 |
SA | Compromised innate immune system impairing SA biosynthetic pathway | SA-dependent modulation of root microbiome and enrichment of Flavobacterium, Terracoccus, and Streptomyces in SA-treated roots and bulk soils | Arabidopsis | Lebeis et al., 2015 |
- | DIMBOA Benzoxazinoids (BXs) induce chemotaxis-associated genes in Pseudomonas putida | Enhanced rhizosphere colonization by P. putida | Maize | Neal et al., 2012 |
ACC; JA | ACC and JA application, induced altered expression of PRR and RLK and cell wall biosynthesis and maintenance related genes | Inhibition of the secondary stage of root colonization by Laccaria bicolor | Poplar | Plett et al., 2014b |