In social insects, alerting nestmates to the presence of a pathogen should be critical for limiting its spread and initiating social mechanisms of defense. Here we show that subterranean termites use elevated vibratory alarm behavior to help prevent fatal fungal infections. The elevated alarm leads to elevated social hygiene. This requires that termites coalesce so that they can groom each other’s cuticular surfaces of contaminating conidial spores. Groups of 12 Reticulitermes flavipes workers varied in their response when immersed in conidia solutions of nine different strains of Metarhizium. Pathogen alarm displays of short 2–7-second bursts of rapid longitudinal oscillatory movement (LOM), observed over 12 min following a fungal challenge, were positively correlated with the time that workers spent aggregated together grooming each other. The frequency of these LOMs was inversely correlated with fatal fungal infections. The variation in fatalities appeared to be largely attributable to a differential response to Metarhizium brunneum and Metarhizium robertsii in the time spent in aggregations and the frequency of allogrooming. Isolated workers challenged with conidia did not display LOMs, which suggests that the alarm is a conditional social response. LOMs appear to help signal the presence of fungal pathogens whose virulence depends on the level of this emergency alert.

Allogrooming appears to be essential in many social animals for protection from routine exposure to parasites. In social insects, it appears to be critical for the removal of pathogenic propagules from the cuticle before they can start an infectious cycle. For subterranean termites, this includes fungal spores commonly encountered in the soil, such as Metarhizium conidia, that can quickly germinate and penetrate the cuticle. We investigated whether there is a difference in reliance on social and innate immunity in two closely related subterranean termites for protection from fatal infections by two locally encountered Metarhizium species. Our results indicate that relatively weak innate immunity in one termite species is compensated by more sustained allogrooming. This includes enhanced allogrooming in response to concentrations of conidia that reflect more routine contamination of the cuticle as well as to heavy cuticular contamination that elicits a networked emergency response.