4.6 Article

Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites

期刊

METABOLITES
卷 11, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/metabo11120839

关键词

GNPS; LC-MS; MS; Macrotermitinae; Macrotermes; Odontotermes; symbiosis; Termitomyces; metabolomics; gut; MolDiscovery

资金

  1. Deutsche Forschungsgemeinschaft (DFG) [239748522]
  2. Villum Kann Rasmussen Young Investigator Programme [VKR10101]
  3. European Research Council [771349]
  4. European Research Council (ERC) [771349] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Fungus-farming termites have gut metabolomes that vary between species and castes, with primary metabolites dominating and significant overlap with the fungal mutualist and plant material. The identification of bioactive compounds of microbial origin suggests potential for compound discovery and future studies on defensive roles.
Fungus-farming termites host gut microbial communities that contribute to the pre-digestion of plant biomass for manuring the fungal mutualist, and potentially to the production of defensive compounds that suppress antagonists. Termite colonies are characterized by complex division of labor and differences in diet between termite size (minor and major) and morphological (worker and soldier) castes, and this extends to the composition of their gut microbial communities. We hypothesized that gut metabolomes should mirror these differences and tested this through untargeted LC-MS/MS analyses of three South African species of fungus-farming termites. We found distinct metabolomes between species and across castes, especially between soldiers and workers. Primary metabolites dominate the metabolomes and the high number of overlapping features with the mutualistic fungus and plant material show distinct impacts of diet and the environment. The identification of a few bioactive compounds of likely microbial origin underlines the potential for compound discovery among the many unannotated features. Our untargeted approach provides a first glimpse into the complex gut metabolomes and our dereplication suggests the presence of bioactive compounds with potential defensive roles to be targeted in future studies.

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