Identification and Diversity of Bacterial Communities Associated with the Venom Glands of the Fire Ant, Solenopsis invicta Buren (Hymenoptera: Formicidae)
Abstract Background Ant-microbe interactions that naturally occur in the venom microenvironment remain mostly unknown. To best of our knowledge, no research exists that shows the identity and diversity of bacterial communities in the fires ants, and what adaptive advantages that venom-associated microbes might offer to their hosts or that hosts might provide to venom-associated bacteria. This study assessed the diversity and identity of bacteria associated with the venom glands of Solenopsis invicta and compared this community with the bacterial communities of two other stinging ants, Solenopsis geminata and Diacamma rugosum. Results The major phylum associated with the venom glands of S. invicta (workers, alates, and queens) and S. geminata (workers) was Proteobacteria, while Firmicutes were abundant in the venom glands of D. rugosum (workers). Tenericutes were also more abundant in the venom glands of S. invicta queens than in those of workers and alates. The relative abundance of Spiroplasma in S. geminata was significantly higher than those in D. rugosum and S. invicta. A microbial diversity analysis of venom glands of worker ants of Solenopsis species showed that the relative abundances of Bacillus and Lactococcus were higher in Guangxi S. invicta workers than in workers collected from Guangzhou. However, the abundance of Lactococcus in workers of D. rugosum was higher than those in workers of S. geminata from Guangxi and S. invicta collected from Guangzhou. Conclusions This study provides the first insight into the microbiota in the venom glands of S. invicta, S. geminata, and D. rugosum, which might contribute to a more comprehensive view of the role of bacteria in the synthesis or degradation of active venom components in the host. We hypothesized that the differences in bacterial communities of three ant species could be due to the local adaptation of insects along with the coevolution of bacteria and hosts.