TY - JOUR
T1 - Getting lost
T2 - the fungal hijacking of ant foraging behaviour in space and time
AU - Trinh, Thienthanh
AU - Ouellette, Renee
AU - de Bekker, Charissa
N1 - Funding Information:
We thank Biplabendu Das, Ian Will, Jordan Dowell, Chase Mason and Josh King for providing insight and advice on experimental design, Timothy Lindner for help with 3D-printing the ant foraging mazes and Josh McFadden for his assistance with fieldwork. This work was supported by a U.S. National Science Foundation ( NSF ) Career Award 1941546 and start-up funds from the University of Central Florida made available to C.d.B.
Publisher Copyright:
© 2021 The Author(s)
PY - 2021/11
Y1 - 2021/11
N2 - Many parasites have evolved strategies to exploit host behaviour for successful transmission. Ophiocordyceps manipulations of carpenter ant behaviour represent an evident example. Manipulated ants are coerced to ascend vegetation and clamp down their mandibles in a stereotypical ‘death-grip’ bite. The fungus then kills the ant, sprouts a stalk and releases infective spores. Research has focused on this final manipulation, leaving the subtler behavioural changes prebiting largely unexplored. Field and transcriptome studies found that the host circadian clock, olfaction and communication may be disrupted, which suggests that the fungus is affecting ant foraging activity and effectivity. To test this hypothesis, we investigated if the foraging behaviour of Camponotus floridanus ants is notably affected during early stage Ophiocordyceps infection. Specifically, we used a maze to quantify foraging patterns and trail optimization. Moreover, by comparing infected individuals to healthy ants and those infected with nonmanipulating Beauveria bassiana, we aimed to distinguish between nonmanipulator-specific and manipulator-specific changes. We found that Ophiocordyceps-infected ants became arrhythmic in their activity patterns, were less likely to participate in effective foraging efforts and seemed less able to communicate with their nestmates compared to healthy ants. We hypothesize that these changes in behaviours are adaptive to Ophiocordyceps transmission since they reduce the chance of aggressive interference by nestmates. Indeed, Beauveria-infected individuals remained rhythmic; however, they also seemed to lose their ability to forage optimally, suggesting that, in part, these changes in behaviour might be mere general behavioural side-effects of infection. Overall, this study informs future work on parasitic strategies underlying host manipulation, other parasite–host interactions and the behavioural ecology of infectious diseases in general.
AB - Many parasites have evolved strategies to exploit host behaviour for successful transmission. Ophiocordyceps manipulations of carpenter ant behaviour represent an evident example. Manipulated ants are coerced to ascend vegetation and clamp down their mandibles in a stereotypical ‘death-grip’ bite. The fungus then kills the ant, sprouts a stalk and releases infective spores. Research has focused on this final manipulation, leaving the subtler behavioural changes prebiting largely unexplored. Field and transcriptome studies found that the host circadian clock, olfaction and communication may be disrupted, which suggests that the fungus is affecting ant foraging activity and effectivity. To test this hypothesis, we investigated if the foraging behaviour of Camponotus floridanus ants is notably affected during early stage Ophiocordyceps infection. Specifically, we used a maze to quantify foraging patterns and trail optimization. Moreover, by comparing infected individuals to healthy ants and those infected with nonmanipulating Beauveria bassiana, we aimed to distinguish between nonmanipulator-specific and manipulator-specific changes. We found that Ophiocordyceps-infected ants became arrhythmic in their activity patterns, were less likely to participate in effective foraging efforts and seemed less able to communicate with their nestmates compared to healthy ants. We hypothesize that these changes in behaviours are adaptive to Ophiocordyceps transmission since they reduce the chance of aggressive interference by nestmates. Indeed, Beauveria-infected individuals remained rhythmic; however, they also seemed to lose their ability to forage optimally, suggesting that, in part, these changes in behaviour might be mere general behavioural side-effects of infection. Overall, this study informs future work on parasitic strategies underlying host manipulation, other parasite–host interactions and the behavioural ecology of infectious diseases in general.
KW - Beauveria
KW - Camponotus floridanus
KW - fungus
KW - host manipulation
KW - Ophiocordyceps
KW - parasite
UR - http://www.scopus.com/inward/record.url?scp=85116916174&partnerID=8YFLogxK
U2 - 10.1016/j.anbehav.2021.09.003
DO - 10.1016/j.anbehav.2021.09.003
M3 - Article
AN - SCOPUS:85116916174
SN - 0003-3472
VL - 181
SP - 165
EP - 184
JO - Animal Behaviour
JF - Animal Behaviour
ER -