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Updated: Mar 31, 2026

Extracting DNA from the Gut Microbes of the Termite Zootermopsis Angusticollis and Visualizing Gut Microbes
Published on: May 28, 2007
Bacterial communities in termite fungus combs are comprised of consistent gut deposits and contributions from the
Saria Otani1, Lars H Hansen2,3, Søren J Sørensen4
1Department of Biology, Section for Ecology and Evolution, Centre for Social Evolution, University of Copenhagen, Universitetsparken 15, Building 3, 2100, Copenhagen East, Denmark. Saria.Otani@bio.ku.dk.
Abstract:
Fungus-growing termites (subfamily Macrotermitinae) mix plant forage with asexual spores of their plant-degrading fungal symbiont Termitomyces in their guts and deposit this blend in fungus comb structures, within which the plant matter is degraded. As Termitomyces grows, it produces nodules with asexual spores, which the termites feed on. Since all comb material passes through termite guts, it is inevitable that gut bacteria are also deposited in the comb, but it has remained unknown which bacteria are deposited and whether distinct comb bacterial communities are sustained. Using high-throughput sequencing of the 16S rRNA gene, we explored the bacterial community compositions of 33 fungus comb samples from four termite species (three genera) collected at four South African geographic locations in 2011 and 2013. We identified 33 bacterial phyla, with Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, and Candidate division TM7 jointly accounting for 92 % of the reads. Analyses of gut microbiotas from 25 of the 33 colonies showed that dominant fungus comb taxa originate from the termite gut. While gut communities were consistent between 2011 and 2013, comb community compositions shifted over time. These shifts did not appear to be due to changes in the taxa present, but rather due to differences in the relative abundances of primarily gut-derived bacteria within fungus combs. This indicates that fungus comb microbiotas are largely termite species-specific due to major contributions from gut deposits and also that environment affects which gut bacteria dominate comb communities at a given point in time.
Insights
Fungus-growing termites cultivate symbiotic fungi in specialized combs. Their gut bacteria are deposited in these combs, influencing the microbial community composition over time and varying by termite species and environment.
Area of Science:
- Termite biology
- Microbial ecology
- Symbiotic relationships
Background:
- Fungus-growing termites (Macrotermitinae) cultivate symbiotic fungi (Termitomyces) in specialized combs for nutrition.
- Plant matter is degraded within these combs, and gut contents, including bacteria, are inevitably deposited.
- The specific bacterial communities within fungus combs and their origins have not been well-characterized.
Purpose of the Study:
- To investigate the bacterial community composition of termite fungus combs.
- To determine the origin of bacteria found in fungus combs.
- To explore how environmental factors and termite species influence comb bacterial communities.
Main Methods:
- High-throughput sequencing of the 16S rRNA gene was used to analyze bacterial communities.
- Fungus comb samples from 33 colonies of four termite species across four locations were analyzed.
- Termite gut microbiota from 25 colonies were also analyzed for comparison.
Main Results:
- 33 bacterial phyla were identified, with Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, and TM7 dominating (92% of reads).
- Dominant bacteria in fungus combs were found to originate from the termite gut.
- While gut bacterial communities remained consistent, comb communities showed temporal shifts in relative abundances, not taxa, influenced by termite species and environment.
Conclusions:
- Fungus comb microbiotas are largely determined by the termite host's gut bacteria.
- Environmental factors influence the relative abundance of gut-derived bacteria within the combs.
- This study elucidates the complex interplay between termites, their fungal symbionts, gut bacteria, and the environment in shaping fungus comb ecosystems.
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