Metabolomic and transcriptomic analysis of the defensive role of Actinobacteria within the fungus-growing termite system
Fungiculture in Macrotermitinae evolved 30 Mio. years ago in Sub-Saharan Africa. Fungus farming is accomplished through an intricate mode of substrate incorporation and intensive maintenance of the fungus comb, in which the symbiotic fungus and the associated microbial community reside to degrade the pre-digested plant material. Fungal fruiting bodies are ultimately eaten by the termites to secure insect nutrition.
Once the termite colony dies, when comb material deteriorates or is incubated without termites, fruiting bodies of species of the ascomycete genus Pseudoxylaria appear and rapidly overgrow the comb material. While Termitomyces sp. is an obligatory mutualist the termites feed on, the ecological role of Pseudoxylaria sp. in fungus-growing termite nests is still under debate. Overall, the fungus comb harbors a complex microbial community that is governed by intricate relationships (e.g. synergistic, antagonistic, cheating, co-existing) and only the concerted actions of the community ensure the emergent properties that vary significantly from the combined effects of individual microorganisms. Secreted microbial metabolites mediate the interactions and are considered the “currency and/or language” of the microbial community.
Our general scientific activity focuses on the biochemical analysis of the secreted metabolites, which governs the multilateral symbiotic interactions between termites, fungal cultivar, fungal competitors and associated bacteria. In the outlined project, we want to biochemically analyse the defensive role of isolated Actinobacteria and their interaction with the co-evolved garden weed Pseudoxylaria to gain insights how the complex termite-fungus symbiosis has remained sustainable over evolutionary time. We hypothesize that Actinobacteria provide a third line of defence against invading species by secretion of antimicrobial secondary metabolites (in addition to immunity provided by the insects and the mutualist Termitomyces). To investigate the hypothesis, we will analyse the response mechanism of Actinobacteria upon the presence of mutualists or competitors on a genetic and metabolomic level.
(2022) Comparative Genomic and Metabolomic Analysis of Termitomyces Species Provides Insights into the Terpenome of the Fungal Cultivar and the Characteristic Odor of the Fungus Garden of Macrotermes natalensis Termites. mSystems , e0121421.
(2022) GNPS-Guided Discovery of Madurastatin Siderophores from the Termite-Associated Actinomadura sp. RB99. Chemistry 28(36), e202200612.
(2020) Nocardia macrotermitis sp. nov. and Nocardia aurantia sp. nov., isolated from the gut of the fungus-growing termite Macrotermes natalensis. Int J Syst Evol Microbiol ,
(2020) Gene Cluster Activation in a Bacterial Symbiont Leads to Halogenated Angucyclic Maduralactomycins and Spirocyclic Actinospirols. Org Lett 22(7), 2634-2638.
(2020) Polyhalogenation of Isoflavonoids by the Termite-Associated Actinomadura sp. RB99. J Nat Prod ,
(2020) Streptomyces smaragdinus sp. nov., isolated from the gut of the fungus growing-termite Macrotermes natalensis. Int J Syst Evol Microbiol ,
Start of PhD
April 16, 2018