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
|