LAUSR

Simple Summary Insecticides are considered to be one of the major factors of bee decline. In this study, the potential sublethal effects of selected neonicotinoids on honey bee larvae were investigated by protein expression profiling for the first time. The total larval protein expression was investigated by 2D gel electrophoresis after exposure to the insecticides dimethoate, fenoxycarb and flupyradifurone. Protein spots whose concentrations differed significantly from the controls were sequenced and identified against known insect proteins. Although the treated larvae did not show increased mortality or an aberrant development, the proteome comparisons showed differences in the metabolism, immune response and energy supply of the bee larvae. The strongest influence was found for flupyradifurone, which activates various detoxification pathways, the immune response or tissue regeneration. Our results suggest that there may be a delayed larval development or possibly a reduced honey bee brood vitality at sublethal concentrations. Abstract The western honey bee Apis mellifera is globally distributed due to its beekeeping advantages and plays an important role in the global ecology and economy. In recent decades, several studies have raised concerns about bee decline. Discussed are multiple reasons such as increased pathogen pressure, malnutrition or pesticide use. Insecticides are considered to be one of the major factors. In 2013, the use of three neonicotinoids in the field was prohibited in the EU. Flupyradifurone was introduced as a potential successor; it has a comparable mode of action as the banned neonicotinoids. However, there is a limited number of studies on the effects of sublethal concentrations of flupyradifurone on honey bees. Particularly, the larval physiological response by means of protein expression has not yet been studied. Hence, the larval protein expression was investigated via 2D gel electrophoresis after following a standardised protocol to apply sublethal concentrations of the active substance (flupyradifurone 10 mg/kg diet) to larval food. The treated larvae did not show increased mortality or an aberrant development. Proteome comparisons showed clear differences concerning the larval metabolism, immune response and energy supply. Further field studies are needed to validate the in vitro results at a colony level.