Gut microbes play an important role in the biology and evolution of insects. Australian native dung beetles (Scarabaeinae) present an opportunity to study gut microbiota in an evolutionary context as they come from two distinct phy-logenetic lineages and some species in each lineage have secondarily adapted to alternative or broader diets. In this study, we characterized the hindgut bacterial communities found in 21 species of dung beetles across two lineages, using 16S rRNA sequencing. We found that gut microbial diversity was more dependent on host phy-logeny and gut morphology than specific dietary preferences or environment. In particular, gut microbial diversity was highest in the endemic, flightless genus Cephalodesmius, which feeds on a broad range of composted organic matter. The hindgut of Cephalodesmius beetles harbors a highly conserved core set of bacteria, suggesting that the bacteria are symbiotic. Symbiosis is supported by the persistence of the core microbiota across isolated beetle populations and between species in the genus. A coevolutionary relationship is supported by the expansion of the hindgut to form a fermentation chamber and the fermentative nature of the core microbes. In contrast, Australian species of the widespread dung beetle genus Onthophagus that specialize on a single food resource, such as dung or fungus, exhibit minimal food processing behavior and have a short, narrow hindgut and a variable gut microbiota with relatively few core bacterial taxa. A conserved, complex gut microbiota is hypothesized to be unnecessary for this highly mobile genus. IMPORTANCE Dung beetles are a very important part of an ecosystem because of their role in the removal and decomposition of vertebrate dung. It has been suspected that symbiotic gut bacteria facilitate this role, a hypothesis that we have explored with high-throughput barcoding. We found that differences in hindgut morphology had the greatest effect on the bacterial community composition. Species with a hindgut fermentation chamber harbored a distinctly different hindgut community compared to those species with a narrow, undifferentiated hindgut. Diet and phylogeny were also associated with differences in gut community. Further understanding of the relationships between dung beetles and their gut microbes will provide insights into the evolution of their behaviors and how gut communities contribute to their fitness.
DOI
10.1128/AEM.02100-20
Publication Year
2021
Publication Site
Applied and Environmental Microbiology
Journal Volume
87
Page Numbers
e02100–20
Family
Scarabaeidae
General topic
Ecology
Physiology
Specific topic
biotic interactions
Abstract Note