Bacterial exposure leads to variable mortality but not a measurable increase in surface antimicrobials across ant species

Social insects have co-existed with microbial species for millions of years and have evolved a diversity of collective defenses, including the use of antimicrobials. While many studies have revealed strategies that ants use against microbial entomopathogens, and several have shown ant-produced compounds inhibit environmental bacterial growth, few studies have tested whether exposure to environmental bacteria represents a health threat to ants. We compare four ant species’ responses to exposure to Escherichia coli and Staphylococcus epidermidis bacteria in order to broaden our understanding of microbial health-threats to ants and their ability to defend against them. In a first experiment, we measure worker mortality of Solenopsis invicta, Brachymyrmex chinensis, Aphaenogaster rudis, and Dorymyrmex bureni in response to exposure to E. coli and S. epidermidis. We found that exposure to E. coli was lethal for S. invicta and D. bureni, while all other effects of exposure were not different from experimental controls. In a second experiment, we compared the antimicrobial ability of surface extracts from bacteria-exposed and non-exposed S. invicta and B. chinensis worker ants, to see if exposure to E. coli or S. epidermidis led to an increase in antimicrobial compounds. We found no difference in the inhibitory effects from either treatment group in either species. Our results demonstrate the susceptibility to bacteria is varied across ant species. This variation may correlate with an ant species’ use of surface antimicrobials, as we found significant mortality effects in species which also were producing antimicrobials. Further exploration of a wide range of both bacteria and ant species is likely to reveal unique and nuanced antimicrobial strategies and deepen our understanding of how ant societies respond to microbial health threats.

Draft Aphaenogaster genomes expand our view of ant genome size variation across climate gradients

Given the abundance, broad distribution, and diversity of roles that ants play in many ecosystems, they are an ideal group to serve as ecosystem indicators of climatic change. At present, only a few whole-genome sequences of ants are available (19 of >16,000 species), mostly from tropical and sub-tropical species. To address this limited sampling, we sequenced genomes of temperate-latitude species from the genus Aphaenogaster, a genus with important seed dispersers. In total, we sampled seven colonies of six species: Aphaenogaster ashmeadi, Aphaenogaster floridana, Aphaenogaster fulva, Aphaenogaster miamiana, Aphaenogaster picea, and Aphaenogaster rudis. The geographic ranges of these species collectively span eastern North America from southern Florida to southern Canada, which encompasses a latitudinal gradient in which many climatic variables are changing rapidly. For the six genomes, we assembled an average of 271,039 contigs into 47,337 scaffolds. The Aphaenogaster genomes displayed high levels of completeness with 96.1% to 97.6% of Hymenoptera BUSCOs completely represented, relative to currently sequenced ant genomes which ranged from 88.2% to 98.5%. Additionally, the mean genome size was 370.5 Mb, ranging from 310.3 to 429.7, which is comparable to that of other sequenced ant genomes (212.8–396.0 Mb) and flow cytometry estimates (210.7–690.4 Mb). In an analysis of currently sequenced ant genomes and the new Aphaenogaster sequences, we found that after controlling for both spatial autocorrelation and phylogenetics ant genome size was marginally correlated with sample site climate similarity. Of all examined climate variables, minimum temperature, and annual precipitation had the strongest correlations with genome size, with ants from locations with colder minimum temperatures and higher levels of precipitation having larger genomes. These results suggest that climate extremes could be a selective force acting on ant genomes and point to the need for more extensive sequencing of ant genomes.

Mutualism between co-introduced species facilitates invasion and alters plant community structure

Generalized mutualisms are often predicted to be resilient to changes in partner identity. Variation in mutualism-related traits between native and invasive species however, can exacerbate the spread of invasive species (‘invasional meltdown’) if invasive partners strongly interact. Here we show how invasion by a seed-dispersing ant ( Myrmica rubra ) promotes recruitment of a co-introduced invasive over native ant-dispersed (myrmecochorous) plants. We created experimental communities of invasive ( M. rubra ) or native ants ( Aphaenogaster rudis ) and invasive and native plants and measured seed dispersal and plant recruitment. In our mesocosms, and in laboratory and field trials, M. rubra acted as a superior seed disperser relative to the native ant. By contrast, previous studies have found that invasive ants are often poor seed dispersers compared with native ants. Despite belonging to the same behavioural guild, seed-dispersing ants were not functionally redundant. Instead, native and invasive ants had strongly divergent effects on plant communities: the invasive plant dominated in the presence of the invasive ant and the native plants dominated in the presence of the native ant. Community changes were not due to preferences for coevolved partners: variation in functional traits of linked partners drove differences. Here, we show that strongly interacting introduced mutualists can be major drivers of ecological change.

Edge Effects on Community and Social Structure of Northern Temperate Deciduous Forest Ants

Determining how ant communities are impacted by challenges from habitat fragmentation, such as edge effects, will help us understand how ants may be used as a bioindicator taxon. To assess the impacts of edge effects upon the ant community in a northern temperate deciduous forest, we studied edge and interior sites in Jericho, VT, USA. The edges we focused upon were created by recreational trails. We censused the ants at these sites for two consecutive growing seasons using pitfall traps and litter plot excavations. We also collected nests of the most common ant species at our study sites,Aphaenogaster rudis, for study of colony demography. Significantly greater total numbers of ants and ant nests were found in the edge sites compared to the interior sites but rarefaction analysis showed no significant difference in species richness.Aphaenogaster rudiswas the numerically dominant ant in the habitats sampled but had a greater relative abundance in the interior sites than in the edge sites both in pitfall and litter plot data. Queen number ofA. rudissignificantly differed between the nests collected in the edge versus the interior sites. Habitat-dependent changes in social structure of ants represent another possible indicator of ecosystem health.

Bactericidal and Fungicidal Activity of Ant Chemicals on Feather Parasites: An Evaluation of Anting Behavior as a Method of Self-Medication in Songbirds

Songbirds apply ants to their feathers during anting behavior, possibly as a method of reducing feather parasites. We tested polar and nonpolar ant secretions and pure formic acid for bactericidal and fungicidal effects on microbial ectoparasites of feathers. Microbial inhibition trials were run with the bacteria Bacillus licheniformis (strains OWU 138B and OWU 1432B) and B. subtilis; and with the fungi Chaetomium globosum, Penicillium chrysogenum, and Trichoderma viride. Ant chemicals were derived from Camponotus pennsylvanicus, Pheidole dentata, Aphaenogaster rudis, Crematogaster lineolata, and Lasius flavus worker-caste ants. Although pure formic acid strongly inhibited all bacteria and fungal hyphae tested, concentrations of formic acid found in the bodies of formicine ants did not. Neither hexane ant-chemical extracts nor ant suspensions in deionized water inhibited the microbial species. Consequently, the hypothesis that birds apply ants to control feather parasites was not supported.