Abstract

Simple SummaryFungus-growing termites cultivate monocultures of a specific fungi (of a genus called Termitomyces) for food in their colony, analogously to human farmers growing crops. The termites forage for dead plant material in the environment, bring this into the mound and provide it to the fungus as a growth substrate. After fungal growth, the termites use the mixture of fungus and degraded plant material and also the asexual spores produced by the fungus as food. They also use the spores to inoculate new fungus gardens. The termite-fungus symbiosis is obligatory for both partners, the termites provide growth substrate and a protected growth environment for the fungi in exchange for a nitrogen-rich food source. Termites and fungi have been partners for more than 30 million years and although the symbiosis looks harmonious, the partners have some hidden conflicts about reproduction and resource investment. These conflicts raise questions on how the symbiosis apparently has remained stable for such a long time. We summarize our current understanding on the short-term stability of a single generation of termites, and also the long-term stability of the symbiosis across multiple generations. We identify unsolved questions in the field and suggest possible avenues to address these questions.The agricultural mutualistic symbiosis between macrotermitine termites and Termitomyces fungi is obligate for both partners. The termites provide a protective growth environment for the fungus by cultivating it inside their colony and providing it with foraged plant material. The termites use the fungus for plant substrate degradation, and the production of asexual fruiting bodies for nourishment and re-inoculation of the fungus garden. The termite colony can reach an age of up to several decades, during which time it is believed that a single fungal monoculture is asexually propagated by the offspring of a single founding royal pair. The termite-fungus mutualism has a long evolutionary history dating back more than 30 million years. Both on the time-scale of a termite colony lifespan and that of the mutualistic symbiosis, questions arise about stability. We address the physical stability of the mound, the termite colony and the monoculture fungal garden during a colony’s lifetime. On the long-term evolutionary scale, we address the stability of the symbiosis, where horizontal transmission of the symbiotic fungus raises the question of how the mutualistic interaction between host and symbiont persists over generations.

Highlights

  • Simple Summary: Fungus-growing termites cultivate monocultures of a specific fungi for food in their colony, analogously to human farmers growing crops

  • This review focuses on the evolutionary stability of the obligatory mutualistic symbiosis between the fungus-growing termites and their fungal symbionts

  • This review focused on the evolutionary stability of the mutualistic symbiosis between the fungus-growing termites and the fungus Termitomyces

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Summary

Stability of Symbioses

Stability is the quality or state of being steady and not likely to change, fail or decay [1]. During the establishment of the colony, it is possible and likely compatible homokaryons of the same species meet, they can fuse to form heterokaryotic mycelium that more than one heterokaryon is present within the termite nest. Theastermites bring new substrate the nest and build new the propagation of asexual spores and positive frequency-dependent selection on the most dominant fungal combs. While the termite colony grows, the termites (I) propagate small amounts of asexual fungal genotype, the fungal mycelium is kept a monoculture, with no fungal genetic variation in the spores which are transferred within the nest to new fungal combs. This intranest transmission is a termite hill.

The Physical Structure of the Termite Mound
Erosion and Persistence
Reuse by New Termite Colonies
Ages of Termite Mounds
The Longevity of a Termite Colony
Symbiont Transmission and Dispersal
Selection of the “Right” Partner
Conflict Reduction between Termite Host and Fungal Symbiont
Conflict between Symbionts
Positive Frequency-Dependent Selection and Bottlenecks
Symbiont Turn-Over
Mutations and Cheaters
Termite Adaptations against Fungal Genetic Variation
Termitomyces Adaptations against Fungal Genetic Variation
Conclusions
Methods
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