2014
DOI: 10.1007/s10886-014-0432-2
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A Volatile Relationship: Profiling an Inter-Kingdom Dialogue Between two Plant Pathogens, Ralstonia Solanacearum and Aspergillus Flavus

Abstract: Microbes in the rhizosphere have a suite of extracellular compounds, both primary and secondary, that communicate with other organisms in their immediate environment. Here, we describe a two-way volatile interaction between two widespread and economically important soil-borne pathogens of peanut, Aspergillus flavus and Ralstonia solanacearum, a fungus and bacterium, respectively. In response to A. flavus volatiles, R. solanacearum reduced production of the major virulence factor extracellular polysaccharide (E… Show more

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Cited by 60 publications
(46 citation statements)
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“…We visualized in a Venn diagram the distribution of the VOCs produced by the treatments [5,34]. However, due to the complexity in the VOCs profiles induced by the experimental conditions, the results provided by the Venn diagram were difficult to describe.…”
Section: Discussionmentioning
confidence: 99%
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“…We visualized in a Venn diagram the distribution of the VOCs produced by the treatments [5,34]. However, due to the complexity in the VOCs profiles induced by the experimental conditions, the results provided by the Venn diagram were difficult to describe.…”
Section: Discussionmentioning
confidence: 99%
“…Endophytic fungi-microorganisms that live inside plant tissues without causing disease symptoms or displaying outward signs of habitation are capable to produce secondary metabolites with antibiotic activity, such as, nonvolatile and volatile compounds [2,3]. Fungal volatiles mediate ecological relationships such as intra and interspecific communication and as defense compounds [4,5]. In addition, endophytic fungi could protect the host plant by producing nonvolatile and volatile compounds with antifungal activity against plant pathogens, and by mycoparasitism and predation that limits the pathogen growth.…”
Section: Introductionmentioning
confidence: 99%
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“…The xylem of 2–3 cm from the stem was dissected and the sap was rubbed in CPG medium and inoculated for 48h at 28°C. Identification was done on the basis of the morphology of the colony on CPG medium, Gram staining and microscopic examination 25, 26 .…”
Section: Methodsmentioning
confidence: 99%