|
Moniliophthora roreri and Trichoderma harzianum
|
Phytopathogen-endophyte |
T39 butenolide, harzianolide, sorbicillinol |
Production of the described compounds was dependent on the phytopathogen presence and was spatially localized in the interaction zone. |
61
|
|
Trichoderma atroviride and Arabidopsis sp. |
Endophyte-plant |
Indole-acetic acid-related indoles |
Colonization of plant roots by endophyte promotes growth and enhances systemic disease resistance in the plant. |
71
|
|
Xylella fastidiosa and Methylobacterium mesophilicum
|
Phytopathogen-endophyte |
|
Genes related to growth were down-regulated while genes related to energy production, stress, transport, and motility were up-regulated in the phytopathogen. |
74
|
|
Burkholderia gladioli, B. seminalis and orchid |
Phytopathogen-endophyte-plant |
Extracellular polysaccharides; altering hormone metabolism (suggested) |
The endophyte strain probably interacts with the plant by using extracellular polysaccharides and by altering hormone metabolism, as was suggested by genomic analysis. |
75
|
|
Bradyrhizobium diazoefficiens and Aeschynomene afraspera
|
Symbiont-plant |
C35 hopanoids |
C35 hopanoid are essential for symbiose and are related to evasion of plant defense, utilization of host photosynthates, and nitrogen fixation. |
86
|
|
Stachybotrys elegans and Rhizoctonia solani
|
Mycoparasite-host |
Trichothecenes and atranones |
The mycotoxins produced by the mycoparasite induced alterations in R. solani metabolism, growth, and development. The biosynthesis of many antimicrobial compounds by R. solani were down regulated. |
17
|
|
Streptomyces coelicolor and other actinomycetes |
Microbial community |
Prodiginines, actinorhodins, coelichelins, acyl-desferrioxamines, and many unknown compounds |
Most of the compounds produced in each interaction were unique; the study revealed 227 compounds differentially produced in the interactions. |
92
|
|
Aspergillus nidulans and Streptomyces rapamycinicus
|
Microbial community |
Aromatic polyketides |
An intimate physical interaction between the microorganisms leaded to the activation of fungal secondary metabolite genes which were otherwise silent. The actinomycete triggered alterations in fungal histone acetylation. |
14
,
93
|
|
Pseudomonas species |
Microbial community |
Pyoverdines (siderophore) |
Pyoverdines are essential to infection and biofilm formation and have been reported to act as signaling molecules triggering a cascade that results in the production of several virulence factors. |
95
,
96
|
|
Vibrio sp. and diverse marine bacteria strains |
Microbial community |
Exogenous siderophores, such as N,N′-bis (2,3 dihydroxybenzoyl)-O-serylserine |
Many marine bacteria strains were reported to produce siderophores and iron-regulated outer membrane proteins only in the presence of exogenous siderophores produced by other species. |
97
|
|
Burkholderia spp., Rhizopus spp. and rice |
Symbiont-phytopathogen-plant |
Rhizoxin, bongkrekic acid, and enacyloxins |
The fungus is not capable of formating spores in the absence of the endosymbiont. The endosymbiont is responsible for the production of the phytotoxin rhizoxin, the causal agent of rice seedling blight. The fungus induces the growth of the endosymbiont. |
98
,
99
,
101
|
|
Vibrio fischeri and fishes or squids |
Symbiont-fish |
Quorum sensing |
In the symbiotic association with fishes and squids the autoinducer molecule reaches a threshold and luminescence genes are activated. |
91
,
92
|
|
Rhizobium leguminosarum and plant |
Symbiont-plant |
Quorum sensing |
The quorum sensing system in these bacteria is related to different functions: nodulation efficiency, growth inhibition, nitrogen fixation and plasmid transfer. |
111
|
|
Xanthomonas or Xylella and grapevines or citrus |
Pathogen-host |
Quorum sensing |
Quorum sensing signaling molecules control the expression of virulence factor as well as biofilm formation. |
104
|
|
Pantoea stewartii and Zea mays
|
Pathogen-host |
Quorum sensing |
QS mutants of P. stewartii were not able to disperse and migrate in the vasculature, consequently decreasing the disease. |
114
|
|
Pseudomonas syringae and tabacco and bean
|
Phytopathogen-plant |
Quorum sensing |
QS system allows this bacterium to control motility and exopolysaccharide synthesis essential on biofilm formation and leaves colonization. |
115
|
|
Candida albicans and Pseudomonas aeruginosa
|
Microbial community |
Quorum sensing |
P. aeruginosa QS system may block the yeast-to-hypha transition or activates the hypha-to-yeast reversion of C. albicans. Farnesol produced by C. albicans downregulate the QS system of P. aeruginosa. |
123
-
125
|