Coexistence of Three Dominant Bacterial Symbionts in a Social Aphid and Implications for Ecological Adaptation

Simple Summary Most insects are associated with a variety of symbionts that play a crucial role in insect life history. Symbiosis of aphids and their symbionts is a good model system to study insect-symbiont interactions. Pseudoregma bambucicola is a typical social aphid that lives parthenogenetically throughout the year on bamboos in subtropical areas, and it is the only aphid that exclusively feeds on the hard stalks of bamboo. In this study, we surveyed the symbiotic bacterial community associated with P. bambucicola. Our results showed that the diversity of P. bambucicola microbiome was low, but three symbionts, namely the primary endosymbiont Buchnera and two secondary symbionts (Pectobacterium and Wolbachia), were stable coexisting with a high infection rate. Combined with the biology of P. bambucicola, we speculate that Pectobacterium may help P. bambucicola feed on the stalks of bamboo, and Wolbachia may regulate the loss of sexual reproduction or has a nutritional role in P. bambucicola. These findings will advance our knowledge of the microbiomes of social aphids and set the foundation for further studies on the functional roles of P. bambucicola symbionts. Aphids are associated with an array of symbionts that have diverse ecological and evolutionary effects on their hosts. To date, symbiont communities of most aphid species are still poorly characterized, especially for the social aphids. In this study, high-throughput 16S rDNA amplicon sequencing was used to assess the bacterial communities of the social aphid Pseudoregma bambucicola, and the differences in bacterial diversity with respect to ant attendance and time series were also assessed. We found that the diversity of symbionts in P. bambucicola was low and three dominant symbionts (Buchnera, Pectobacterium and Wolbachia) were stably coexisting. Pectobacterium may help P. bambucicola feed on the hard bamboo stems, and genetic distance analysis suggests that the Pectobacterium in P. bambucicola may be a new symbiont species. Wolbachia may be associated with the transition of reproduction mode or has a nutritional role in P. bambucicola. Statistical tests on the diversity of bacterial communities in P. bambucicola suggest that aphid populations attended by ants usually have a significantly higher evenness than populations without ant attendance but there was no significant difference among aphid populations from different seasons.

Automated summary

Pseudoregma bambucicola, a social aphid, has a low diversity microbiome with stable coexistence of Buchnera, Pectobacterium, and Wolbachia. Pectobacterium may assist in feeding on bamboo stems, while Wolbachia may be involved in reproductive mode regulation or nutritional support. Ant attendance increases evenness in aphid populations, but there is no significant seasonal difference in bacterial diversity among aphid populations.