In this review, we provide a current reference on disease resistance in insect societies. We start with the genetics of immunity in the context of behavioral and physiological processes and scale up levels of biological organization until we reach populations. A significant component of this review focuses on Apis mellifera and its role as a model system for studies on social immunity. We additionally review the models that have been applied to disease transmission in social insects and elucidate areas for future study in the field of social immunity.

No abstract

-Social immunity, which describes how individual behaviors of group members effectively reduce disease and parasite transmission at the colony level, is an emerging field in social insect biology. An understudied, but significant behavioral disease resistance mechanism in honey bees is their collection and use of plant resins. Honey bees harvest resins with antimicrobial properties from various plant species and bring them back to the colony where they are then mixed with varying amounts of wax and utilized as propolis. Propolis is an apicultural term for the resins when used by bees within a hive. While numerous studies have investigated the chemical components of propolis that could be used to treat human diseases, there is a lack of information on the importance of propolis in regards to bee health. This review serves to provide a compilation of recent research concerning the behavior of bees in relation to resins and propolis, focusing more on the bees themselves and the potential evolutionary benefits of resin collection. Future research goals are also established in order to create a new focus within the literature on the natural history of resin use among the social insects and role that propolis plays in disease resistance.Apis mellifera / social immunity / antimicrobial defense / ecological immunity

Israeli acute paralysis virus (IAPV) is a widespread RNA virus of honey bees that has been linked with colony losses. Here we describe the transmission, prevalence, and genetic traits of this virus, along with host transcriptional responses to infections. Further, we present RNAi-based strategies for limiting an important mechanism used by IAPV to subvert host defenses. Our study shows that IAPV is established as a persistent infection in honey bee populations, likely enabled by both horizontal and vertical transmission pathways. The phenotypic differences in pathology among different strains of IAPV found globally may be due to high levels of standing genetic variation. Microarray profiles of host responses to IAPV infection revealed that mitochondrial function is the most significantly affected biological process, suggesting that viral infection causes significant disturbance in energy-related host processes. The expression of genes involved in immune pathways in adult bees indicates that IAPV infection triggers active immune responses. The evidence that silencing an IAPV-encoded putative suppressor of RNAi reduces IAPV replication suggests a functional assignment for a particular genomic region of IAPV and closely related viruses from the Family Dicistroviridae, and indicates a novel therapeutic strategy for limiting multiple honey bee viruses simultaneously and reducing colony losses due to viral diseases. We believe that the knowledge and insights gained from this study will provide a new platform for continuing studies of the IAPV–host interactions and have positive implications for disease management that will lead to mitigation of escalating honey bee colony losses worldwide.

Summary— Hygienic and non-hygienic colonies from 'Starline' stock of Apis mellifera were tested for their ability to remove pupae infested with Varroa mites. The hygienic and non-hygienic lines were selected and bred on the basis of their removal response to freeze-killed brood. A Jenter Box® was used to test whether they would remove experimentally infested pupae following methods of Boecking and Drescher (1992). In 1994, the hygienic colonies removed significantly more pupae infested with one mite per cell than the non-hygienic colonies. In 1995, there was no significant difference between the hygienic and non-hygienic colonies when one or two mites were introduced per pupa due to variation in response among hygienic colonies. There was no significant difference between the rate of removal of infested pupae from the Jenter Box and from natural wax comb by the hygienic colonies. The number of mites damaged by grooming ranged from 6.0 to 42.3% among all colonies. The reproductive success of the mites not removed from the cells by the bees was low in both hygienic and non-hygienic colonies.

No abstract

-Honey bee colonies, selected for hygienic behavior on the basis of a freeze-killed brood assay, demonstrated resistance to American foulbrood disease. Over two summers in 1998 and 1999, 18 hygienic and 18 non-hygienic colonies containing instrumentally inseminated queens were challenged with comb sections containing spores of the bacterium Paenibacillus larvae subsp. larvae that causes the disease. The strain of bacterium was demonstrated to be resistant to oxytetracycline antibiotic. Seven (39%) hygienic colonies developed clinical symptoms of the disease but five of these recovered (had no visible symptoms) leaving two colonies (11%) with clinical symptoms. In contrast, 100% of the non-hygienic colonies that were challenged developed clinical symptoms, and only one recovered. All non-hygienic colonies had symptoms of naturally occurring chalkbrood disease (Ascosphaera apis) throughout both summers. In contrast 33% of the hygienic colonies developed clinical symptoms of chalkbrood after they were challenged with American foulbrood, but all recovered. The diseased non-hygienic colonies produced significantly less honey than the hygienic colonies.Apis mellifera / hygienic behavior / American foulbrood / disease resistance

Persistent exposure to mite pests, poor nutrition, pesticides, and pathogens threaten honey bee survival. In healthy colonies, the interaction of the yolk precursor protein, vitellogenin (Vg), and endocrine factor, juvenile hormone (JH), functions as a pacemaker driving the sequence of behaviors that workers perform throughout their lives. Young bees perform nursing duties within the hive and have high Vg and low JH; as older bees transition to foraging, this trend reverses. Pathogens and parasites can alter this regulatory network. For example, infection with the microsporidian, Nosema apis, has been shown to advance behavioral maturation in workers. We investigated the effects of infection with a recent honey bee pathogen on physiological factors underlying the division of labor in workers. Bees infected with N. ceranae were nearly twice as likely to engage in precocious foraging and lived 9 days less, on average, compared to controls. We also show that Vg transcript was low, while JH titer spiked, in infected nurse-aged bees in cages. This pattern of expression is atypical and the reverse of what would be expected for healthy, non-infected bees. Disruption of the basic underpinnings of temporal polyethism due to infection may be a contributing factor to recent high colony mortality, as workers may lose flexibility in their response to colony demands.