The ancient and highly evolved mutualism between fungus-growing ants and th
eir fungi is a textbook example of symbiosis. The ants carefully tend the f
ungus, which serves as their main food source, and traditionally are believ
ed to be so successful at fungal cultivation that they are able to maintain
the fungus free of microbial pathogens. This assumption is surprising in l
ight of theories on the evolution of parasitism, especially for those speci
es of ants that have been clonally propagating their cultivars for millions
of years. Recent work has established that, as theoretically predicted, th
e gardens of fungus-growing ants are host to a specialized, virulent, and h
ighly evolved fungal pathogen in the genus Escovopsis. In addition, the ant
s have evolved a mutualistic association with filamentous bacteria (actinom
ycetes) that produce antibiotics that suppress the growth of Escovopsis. Th
us, the attine symbiosis appears to be a coevolutionary "arms race" between
the garden parasite Escovopsis on the one hand and the ant-fungus-actinomy
cete tripartite mutualism on the other. These recent findings indicate that
microbes may be key components in the regulation of other symbiotic associ
ations between higher organisms.