No abstract

The first step in understanding gut microbial ecology is determining the presence and potential niche breadth of associated microbes. While the core gut bacteria of adult honey bees is becoming increasingly apparent, there is very little and inconsistent information concerning symbiotic bacterial communities in honey bee larvae. The larval gut is the target of highly pathogenic bacteria and fungi, highlighting the need to understand interactions between typical larval gut flora, nutrition and disease progression. Here we show that the larval gut is colonized by a handful of bacterial groups previously described from guts of adult honey bees or other pollinators. First and second larval instars contained almost exclusively Alpha 2.2, a core Acetobacteraceae, while later instars were dominated by one of two very different Lactobacillus spp., depending on the sampled site. Royal jelly inhibition assays revealed that of seven bacteria occurring in larvae, only one Neisseriaceae and one Lactobacillus sp. were inhibited. We found both core and environmentally vectored bacteria with putatively beneficial functions. Our results suggest that early inoculation by Acetobacteraceae may be important for microbial succession in larvae. This assay is a starting point for more sophisticated in vitro models of nutrition and disease resistance in honey bee larvae.

Many insects obtain gut microbes from their diet, but how a mother's foraging patterns influence the microbes found in her offspring's food remains an open question. To address this gap, we studied a bee that forages for pollen from multiple species of plants and may therefore acquire diverse bacteria from different plants. We tested the hypothesis that pollen diversity correlates with bacterial diversity by simultaneously characterizing these two communities in bee brood provisions for the first time. We used deep sequencing of the plant RBCL gene and the bacterial 16S rRNA gene to characterize pollen and bacterial diversity. We then tested for associations between pollen and bacterial species richness and community composition, as well as co-occurrence of specific bacteria and pollen types. We found that both pollen and bacterial communities were extremely diverse, indicating that mother bees visit a wide variety of flowers for pollen and nectar and subsequently bring a diversity of microbes back into their nests. Pollen and bacterial species richness and community composition, however, were not correlated. Certain pollen types significantly co-occurred with the most proportionally abundant bacteria, indicating that the plants these pollen types came from may serve as reservoirs for these bacteria. Even so, the overall diversity of these communities appears to mask these associations at a broader scale. Further study of these pollen and bacteria associations will be important for understanding the complicated relationship between bacteria and wild bees.

The evolution of eusociality is a perennial issue in evolutionary biology, and genomic advances have fueled steadily growing interest in the genetic changes underlying social evolution. Along with a recent flurry of research on comparative and evolutionary genomics in different eusocial insect groups (bees, ants, wasps, and termites), several mechanistic explanations have emerged to describe the molecular evolution of eusociality from solitary behavior. These include solitary physiological ground plans, genetic toolkits of deeply conserved genes, evolutionary changes in protein-coding genes, cis regulation, and the structure of gene networks, epigenetics, and novel genes. Despite this proliferation of ideas, there has been little synthesis, even though these ideas are not mutually exclusive and may in fact be complementary. We review available data on molecular evolution of insect sociality and highlight key biotic and abiotic factors influencing social insect genomes. We then suggest both phylogenetic and ecological evolutionary developmental biology (eco-evo-devo) perspectives for a more synthetic view of molecular evolution in insect societies.

To evaluate sociality in small carpenter bees (Ceratina Latreille), we studied the life history and nesting biology of a common eastern North American species, Ceratina (Zadontomerus) calcarata Robertson. Pan-trap and nest collections throughout the active season (May to September 2006) were used to assess seasonal phenology and nesting biology of C. calcarata in southern Ontario. Adults overwintered in their natal nests. Males emerged in early May and occupied preexisting hollows in twigs and stems. Females emerged from hibernacula 2 weeks later, founding new nests. Nest founding and provisioning occurred throughout the spring; females remained with developing brood through the summer. Complete nests contained, on average, 6.9 offspring, with egg-to-adult development averaging 46 days. Ceratina calcarata is subsocial rather than solitary: mothers are long-lived and nestloyal, and care for offspring from egg to adulthood. Subsociality is found in all behaviourally classified small carpenter bees, while some species cross the boundary into social life, making Ceratina an important genus for the study of the transition between solitary and social life.Résumé-Afin d'évaluer la socialité des petites fourmis charpentières (Ceratina Latreille), nous avons étudié le cycle biologique et la biologie de la nidification chez une espèce commune de l'est de l'Amérique du Nord, C. (Zadontomerus) calcarata Robertson. Nous avons utilisé des pièges à cuvette et des récoltes de nids durant toute la saison active (mai à septembre 2006) pour déterminer la phénologie saisonnière et la biologie de la nidification chez C. calcarata dans le sud de l'Ontario. Les adultes passent l'hiver dans le nid où ils sont nés. Les mâ les émergent au début de mai et occupent des cavités préexistantes dans les ramilles et les tiges. Les femelles émergent des hibernacles deux semaines plus tard et fondent de nouveaux nids. La fondation et l'approvisionnement des nids se poursuivent pendant tout le printemps et les femelles demeurent avec le couvain en développement pendant tout l'été. Les nids complets contiennent en moyenne 6,9 rejetons et le développement de l'oeuf à l'adulte prend en moyenne 46 jours. Ceratina calcarata est subsocial plutô t que solitaire; les femelles vivent longtemps, sont fidèles au nid et s'occupent des petits, de l'oeuf à l'adulte. On retrouve de la subsocialité chez toutes les fourmis classées comme petites charpentières d'après leur comportement, bien que certaines espèces passent la frontière vers la vie sociale, ce qui fait de Ceratina un taxon important pour l'étude des transitions de la vie solitaire à la vie sociale.[Traduit par la Rédaction]

No abstract

Social corbiculate bees such as honey bees and bumble bees maintain a specific beneficial core microbiome which is absent in wild bees. It has been suggested that maintaining this microbiome can prevent disease and keep bees healthy. The main aim of our study was to identify if there are any core bacterial groups in the noncorbiculate bees Ceratina and Megalopta that have been previously overlooked. We additionally test for associations between the core bee microbes and pollen provisions to look for potential transmission between the two. We identify three enterotypes in Ceratina samples, with thirteen core bacterial phylotypes in Ceratina females: Rosenbergiella,

The origin of sterile worker castes, resulting in eusociality, represents one of the major evolutionary transitions in the history of life. Understanding how eusociality has evolved is therefore an important issue for understanding life on earth. Here we show that in the large bee subfamily Xylocopinae, a simple form of sociality was present in the ancestral lineage and there have been at least four reversions to purely solitary nesting. The ancestral form of sociality did not involve morphological worker castes and maximum colony sizes were very small. True worker castes, entailing a life-time commitment to non-reproductive roles, have evolved only twice, and only one of these resulted in discrete queen-worker morphologies. Our results indicate extremely high barriers to the evolution of eusociality. Its origins are likely to have required very unusual life-history and ecological circumstances, rather than the amount of time that selection can operate on more simple forms of sociality.