ABSTRACT
Paenibacillus larvae, the causal agent of American Foulbrood disease (AFB), affects honey bee health worldwide. The present study investigates the effect of bodily fluids from honey bee larvae on growth velocity and transcription for this Gram-positive, endospore-forming bacterium. It was observed that larval fluids accelerate the growth and lead to higher bacterial densities during stationary phase. The genome-wide transcriptional response of in vitro cultures of P. larvae to larval fluids was studied by microarray technology. Early responses of P. larvae to larval fluids are characterized by a general down-regulation of oligopeptide and sugar transporter genes, as well as by amino acid and carbohydrate metabolic genes, among others. Late responses are dominated by general down-regulation of sporulation genes and up-regulation of phage-related genes. A theoretical mechanism of carbon catabolite repression is discussed.
Subject(s)
Bees/metabolism , Body Fluids/metabolism , Genome, Bacterial/genetics , Paenibacillus/growth & development , Paenibacillus/genetics , Transcription, Genetic , Animals , Bees/microbiology , Gene Ontology , Larva/metabolism , Phenotype , Virulence Factors/geneticsABSTRACT
Eusocial insect societies display a remarkable reproductive division of labor between a single fertile queen and thousands of largely sterile workers. In most species, however, the workers retain the capacity to reproduce, particularly in queenless colonies where typically many workers lay eggs. As yet, the molecular determinants that initiate this shift in worker fertility are still poorly documented. By using RNA interference we here demonstrate that the knockdown of epidermal growth factor receptor, a gene which was previously shown to be involved in queen-worker caste differentiation, also induces reproduction in worker honeybees (Apis mellifera). These data show that worker fertility and queen-worker caste determination partly rely on the same gene regulatory networks, thereby providing a major breakthrough in our understanding of the molecular determinants of the social insects' spectacular reproductive division of labor.