RESUMEN
Chemical communication is a widely used mode of communication for social insects and has been demonstrated to be involved in many behaviours and physiological processes such as reproduction, nutrition or the fight against parasites and pathogens. In the honey bee, Apis mellifera, the release of chemical compounds by the brood plays a role in worker behaviour, physiology, and foraging activities and colony health as a whole. Several compounds have already been described as brood pheromones, such as components of the brood ester pheromone and (E)-ß-ocimene. Several other compounds originating from diseased or varroa-infested brood cells have been described as triggering the hygienic behaviour of workers. So far, studies of brood emissions have focused on specific stages of development and little is known about the emission of volatile organic compounds by the brood. In this study, we investigate the semiochemical profile of worker honey bee brood during its whole developmental cycle, from egg to emergence, with a specific focus on volatile organic compounds. We describe variation in emissions of thirty-two volatile organic compounds between brood stages. We highlight candidate compounds that are particularly abundant in specific stages and discuss their potential biological significance.
Asunto(s)
Varroidae , Compuestos Orgánicos Volátiles , Abejas , Animales , Larva/fisiología , Feromonas , Conducta Animal , Varroidae/fisiologíaRESUMEN
Invasive species events related to globalization are increasing, resulting in parasitic outbreaks. Understanding of host defense mechanisms is needed to predict and mitigate against the consequences of parasite invasion. Using the honey bee Apis mellifera and the mite Varroa destructor, as a host-parasite model, we provide a comprehensive study of a mechanism of parasite detection that triggers a behavioral defense associated with social immunity. Six Varroa-parasitization-specific (VPS) compounds are identified that (1) trigger Varroa-sensitive hygiene (VSH, bees' key defense against Varroa sp.), (2) enable the selective recognition of a parasitized brood and (3) induce responses that mimic intrinsic VSH activity in bee colonies. We also show that individuals engaged in VSH exhibit a unique ability to discriminate VPS compounds from healthy brood signals. These findings enhance our understanding of a critical mechanism of host defense against parasites, and have the potential to apply the integration of pest management in the beekeeping sector.
Asunto(s)
Acetatos/aislamiento & purificación , Abejas/metabolismo , Conducta Animal/fisiología , Mezclas Complejas/química , Cetonas/aislamiento & purificación , Varroidae/química , Acetatos/química , Acetatos/farmacología , Animales , Abejas/citología , Abejas/efectos de los fármacos , Abejas/parasitología , Conducta Animal/efectos de los fármacos , Bioensayo , Mezclas Complejas/farmacología , Femenino , Interacciones Huésped-Parásitos , Cetonas/química , Cetonas/farmacología , Varroidae/patogenicidadRESUMEN
Social immunity forms an essential part of the defence repertoire of social insects. In response to infestation by the parasitic mite Varroa destructor and its associated viruses, honey bees (Apis mellifera L.) have developed a specific behaviour (varroa-sensitive hygiene, or VSH) that helps protect the colony from this parasite. Brood cells heavily infested with mites are uncapped, the brood killed, and the cell contents removed. For this extreme sacrifice to be beneficial to the colony, the targeting of parasitized brood for removal must be accurate and selective. Here we show that varroa-infested brood produce uniquely identifiable cues that could be used by VSH-performing bees to identify with high specificity which brood cells to sacrifice. This selective elimination of mite-infested brood is a disease resistance strategy analogous to programmed cell death, where young bees likely to be highly dysfunctional as adults are sacrificed for the greater good of the colony.
Asunto(s)
Abejas/fisiología , Conducta Animal/fisiología , Resistencia a la Enfermedad/fisiología , Animales , Abejas/parasitología , Abejas/virología , Higiene , Varroidae/patogenicidad , Varroidae/virologíaRESUMEN
BACKGROUND: Juvenile hormone (JH) plays an important role in honeybee development and the regulation of age-related division of labor. However, honeybees can be exposed to insect growth regulators (IGRs), such as JH analogs developed for insect pest and vector control. Although their side effects as endocrine disruptors on honeybee larval or adult stages have been studied, little is known about the subsequent effects on adults of a sublethal larval exposure. We therefore studied the impact of the JH analog pyriproxyfen on larvae and resulting adults within a colony under semi-field conditions by combining recent laboratory larval tests with chemical analysis and behavioral observations. Oral and chronic larval exposure at cumulative doses of 23 or 57 ng per larva were tested. RESULTS: Pyriproxyfen-treated bees emerged earlier than control bees and the highest dose led to a significant rate of malformed adults (atrophied wings). Young pyriproxyfen-treated bees were more frequently rejected by nestmates from the colony, inducing a shorter life span. This could be linked to differences in cuticular hydrocarbon (CHC) profiles between control and pyriproxyfen-treated bees. Finally, pyriproxyfen-treated bees exhibited fewer social behaviors (ventilation, brood care, contacts with nestmates or food stocks) than control bees. CONCLUSION: Larval exposure to sublethal doses of pyriproxyfen affected several life history traits of the honeybees. Our results especially showed changes in social integration (acceptance by nestmates and social behaviors performance) that could potentially affect population growth and balance of the colony.
Asunto(s)
Abejas/efectos de los fármacos , Conducta Animal/efectos de los fármacos , Hormonas Juveniles/efectos adversos , Distancia Psicológica , Piridinas/efectos adversos , Animales , Abejas/anatomía & histología , Abejas/crecimiento & desarrollo , Abejas/metabolismo , Hidrocarburos/metabolismo , Relaciones Interpersonales , Larva/efectos de los fármacos , Larva/crecimiento & desarrolloRESUMEN
BACKGROUND: Exclusion from a social group is an effective way to avoid parasite transmission. This type of social removal has also been proposed as a form of collective defense, or social immunity, in eusocial insect groups. If parasitic modification of host behavior is widespread in social insects, the underlying physiological and neuronal mechanisms remain to be investigated. We studied this phenomenon in honey bees parasitized by the mite Varroa destructor or microsporidia Nosema ceranae, which make bees leave the hive precociously. We characterized the chemical, behavioral and neurogenomic changes in parasitized bees, and compared the effects of both parasites. RESULTS: Analysis of cuticular hydrocarbon (CHC) profiles by gas chromatography coupled with mass spectrophotometry (GC-MS) showed changes in honey bees parasitized by either Nosema ceranae or Varroa destructor after 5 days of infestation. Levels of 10-HDA, an antiseptic important for social immunity, did not change in response to parasitism. Behavioral analysis of N. ceranae- or V. destructor- parasitized bees revealed no significant differences in their behavioral acts or social interactions with nestmates. Digital gene expression (DGE) analysis of parasitized honey bee brains demonstrated that, despite the difference in developmental stage at which the bee is parasitized, Nosema and Varroa-infested bees shared more gene changes with each other than with honey bee brain expression gene sets for forager or nurse castes. CONCLUSIONS: Parasitism by Nosema or Varroa induces changes to both the CHC profiles on the surface of the bee and transcriptomic profiles in the brain, but within the social context of the hive, does not result in observable effects on her behavior or behavior towards her. While parasitized bees are reported to leave the hive as foragers, their brain transcription profiles suggest that their behavior is not driven by the same molecular pathways that induce foraging behavior.
Asunto(s)
Abejas/parasitología , Encéfalo/metabolismo , Ácaros , Nosema , Conducta Social , Animales , Abejas/fisiología , Interacciones Huésped-Parásitos , Hidrocarburos/química , TranscriptomaRESUMEN
Parasites are known to cause the loss of individuals in social insects. In honey bee colonies the disappearance of foragers is a common factor of the wide extended colony losses. The emergent parasite of the European honey bee Nosema ceranae has been found to reduce homing and orientation skills and alter metabolism of forager bees. N. ceranae-infected bees also show changes in Ethyl Oleate (EO) levels, which is so far the only primer pheromone identified in workers that is involved in foraging behavior. Thus, we hypothesized that N. ceranae (i) modifies flight activity of honey bees and (ii) induces EO changes that can alter foraging behavior of nestmates. We compared flight activity of infected bees and non-infected bees in small colonies using an electronic optic bee counter during 28 days. We measured EO levels by gas chromatography-mass spectrometry and spore-counts. Bee mortality was estimated at the end of the experiment. Infected bees showed precocious and a higher flight activity than healthy bees, which agreed with the more elevated EO titers of infected bees and reduced lifespan. Our results suggest that the higher EO levels of infected bees might delay the behavioral maturation of same age healthy bees, which might explain their lower level of activity. We propose that delayed behavioral maturation of healthy bees might be a protective response to infection, as healthy bees would be performing less risky tasks inside the hive, thus extending their lifespan. We also discuss the potential of increased flight activity of infected bees to reduce pathogen transmission inside the hive. Further research is needed to understand the consequences of host behavioral changes on pathogen transmission. This knowledge may contribute to enhance natural colony defense behaviors through beekeeping practices to reduce probability of colony losses.
Asunto(s)
Abejas/microbiología , Conducta Animal , Fenómenos de Retorno al Lugar Habitual , Nosema/fisiología , Feromonas/metabolismo , Animales , Abejas/metabolismo , Abejas/fisiología , Colapso de Colonias , Vuelo Animal , Interacciones Huésped-Parásitos , Conducta SocialRESUMEN
Nosema ceranae, a microsporidian parasite originally described in the Asian honey bee Apis cerana, has recently been found to be cross-infective and to also parasitize the European honey bee Apis mellifera. Since this discovery, many studies have attempted to characterize the impact of this parasite in A. mellifera honey bees. Nosema species can infect all colony members, workers, drones and queens, but the pathological effects of this microsporidium has been mainly investigated in workers, despite the prime importance of the queen, who monopolizes the reproduction and regulates the cohesion of the society via pheromones. We therefore analyzed the impact of N. ceranae on queen physiology. We found that infection by N. ceranae did not affect the fat body content (an indicator of energy stores) but did alter the vitellogenin titer (an indicator of fertility and longevity), the total antioxidant capacity and the queen mandibular pheromones, which surprisingly were all significantly increased in Nosema-infected queens. Thus, such physiological changes may impact queen health, leading to changes in pheromone production, that could explain Nosema-induced supersedure (queen replacement).
Asunto(s)
Abejas/microbiología , Nosema/patogenicidad , Animales , Antioxidantes/metabolismo , Abejas/fisiología , Cuerpo Adiposo/microbiología , Femenino , Jerarquia Social , Interacciones Huésped-Patógeno , Feromonas/química , Feromonas/metabolismo , Reproducción/fisiología , Vitelogeninas/metabolismoRESUMEN
BACKGROUND: In honey bee colony, the brood is able to manipulate and chemically control the workers in order to sustain their own development. A brood ester pheromone produced primarily by old larvae (4 and 5 days old larvae) was first identified as acting as a contact pheromone with specific effects on nurses in the colony. More recently a new volatile brood pheromone has been identified: E-ß-ocimene, which partially inhibits ovary development in workers. METHODOLOGY AND PRINCIPAL FINDING: Our analysis of E-ß-ocimene production revealed that young brood (newly hatched to 3 days old) produce the highest quantity of E-ß-ocimene relative to their body weight. By testing the potential action of this molecule as a non-specific larval signal, due to its high volatility in the colony, we demonstrated that in the presence of E-ß-ocimene nest workers start to forage earlier in life, as seen in the presence of real brood. CONCLUSIONS/SIGNIFICANCE: In this way, young larvae are able to assign precedence to the task of foraging by workers in order to increase food stores for their own development. Thus, in the complexity of honey bee chemical communication, E-ß-ocimene, a pheromone of young larvae, provides the brood with the means to express their nutritional needs to the workers.
Asunto(s)
Alquenos/farmacología , Abejas/fisiología , Monoterpenos Acíclicos , Animales , Conducta Animal , VolatilizaciónRESUMEN
BACKGROUND: In social insects, the queen is essential to the functioning and homeostasis of the colony. This influence has been demonstrated to be mediated through pheromone communication. However, the only social insect for which any queen pheromone has been identified is the honey bee (Apis mellifera) with its well-known queen mandibular pheromone (QMP). Although pleiotropic effects on colony regulation are accredited to the QMP, this pheromone does not trigger the full behavioral and physiological response observed in the presence of the queen, suggesting the presence of additional compounds. We tested the hypothesis of a pheromone redundancy in honey bee queens by comparing the influence of queens with and without mandibular glands on worker behavior and physiology. RESULTS: Demandibulated queens had no detectable (E)-9-oxodec-2-enoic acid (9-ODA), the major compound in QMP, yet they controlled worker behavior (cell construction and queen retinue) and physiology (ovary inhibition) as efficiently as intact queens. CONCLUSIONS: We demonstrated that the queen uses other pheromones as powerful as QMP to control the colony. It follows that queens appear to have multiple active compounds with similar functions in the colony (pheromone redundancy). Our findings support two hypotheses in the biology of social insects: (1) that multiple semiochemicals with synonymous meaning exist in the honey bee, (2) that this extensive semiochemical vocabulary exists because it confers an evolutionary advantage to the colony.
RESUMEN
The behavioral and electroantennographic responses of Cydia pomonella (L.) to the ripe pear volatile ethyl (2E,4Z)-2,4-decadienoate (Et-E,Z-DD), were compared in insecticide-susceptible and -resistant populations originating from southern France. A dose-response relationship to this kairomonal attractant was established for antennal activity and did not reveal differences between susceptible and resistant strains. Conversely, males of the laboratory strains expressing metabolic [cytochrome P450-dependent mixed-function oxidases (mfo)] or physiological (kdr-type mutation of the sodium-channel gene) resistance mechanisms exhibited a significantly higher response to Et-E,Z-DD than those of the susceptible strain in a wind tunnel experiment. No response of the females to this kairomone could be obtained in our wind-tunnel conditions. In apple orchards, mfo-resistant male moths were captured at significantly higher rates in kairomone-baited traps than in traps baited with the sex pheromone of C. pomonella. Such a differential phenomenon was not verified for the kdr-resistant insects, which exhibited a similar response to both the sex pheromone and the kairomonal attractant in apple orchards. Considering the widespread distribution of metabolic resistance in European populations of C. pomonella and the enhanced behavioral response to Et-E,Z-DD in resistant moths, the development of control measures based on this kairomonal compound would be of great interest for the management of insecticide resistance in this species.
Asunto(s)
Resistencia a los Insecticidas/fisiología , Insecticidas/toxicidad , Mariposas Nocturnas/fisiología , Feromonas/farmacología , Animales , Conducta Animal , Estimulación Eléctrica , Vuelo Animal , Genotipo , Resistencia a los Insecticidas/efectos de los fármacos , Mariposas Nocturnas/efectos de los fármacos , Mariposas Nocturnas/genética , VientoRESUMEN
In the codling moth Cydia pomonella (L), insecticide resistance genes have been associated with pleiotropic effects affecting phenology. In this paper, we investigated whether an increase in the frequency of insecticide resistance in field populations of C pomonella was likely to entail significant divergences in the temporal occurrence of both susceptible and insecticide-resistant individuals. For this purpose, we built a phenological model that provided suitable predictions of the distinct and diverging seasonal evolutions of populations of a susceptible and two insecticide-resistant (at two and three loci) homozygous genotypes of C pomonella. Model simulations for each genotype were further compared with pheromone trap catches recorded in a field insecticide-treated population over an 8-year period (from 1992 to 2000), which reflected the progressive annual increase in the frequency of resistance in southeastern France. We found a significant delay in field adult emergence relative to those predicted by the homozygous susceptible model, and the magnitude of such a delay was positively correlated with increasing frequencies of insecticide resistance in the sampled field population of C pomonella. Adult emergence predicted in the theoretical population that was homozygous for resistance at two loci converged with those recorded in the field during the investigated 8-year period. This suggested that the pleiotropic effects of resistance were likely to result in a significant phenological segregation of insecticide-resistant alleles in the field. The results of this study emphasized the potential for pest populations exposed to chemical selection to evolve qualitatively with respect to phenology. This may raise critical questions regarding the use of phenological modelling as a forecasting tool for appropriate resistance management strategies that would take into account the diverging seasonal evolutions of both insecticide resistance and susceptibility.
Asunto(s)
Resistencia a los Insecticidas/genética , Mariposas Nocturnas/crecimiento & desarrollo , Mariposas Nocturnas/genética , Animales , Genotipo , Hibernación , Control de Insectos , Larva/crecimiento & desarrollo , Modelos Biológicos , Estaciones del Año , Temperatura , Factores de TiempoRESUMEN
Intrapopulation variability in the seasonal regulation of insect lifecycles has been shown to be due partly to genetic changes. Selection for insecticide resistance in the codling moth Cydia pomonella results from allelic substitution at two to three loci in south-eastern French populations of this species. However, such an adaptive process has been associated with an increased heterogeneity in the developmental responses to climatic factors such as temperature. In this paper, we investigate whether such pleiotropic effects of resistance on development induce a significant discrepancy in seasonal regulation in this species. The seasonal changes in a susceptible and two insecticide-resistant homozygous genotypes of C. pomonella, as well as their reciprocal F1 progeny, were followed under natural conditions during the reproductive season through the emergence events of adults, within-generation developmental rates and the number of generations. A significant delay in the occurrences of homozygous resistant genotypes resulted from significantly lower pre-imaginal developmental times relative to homozygous susceptible ones. Subsequent assessment of the number of generations indicated significantly higher diapause propensities in carriers of the resistance alleles (37.0-76.2%) than in susceptible homozygotes (6-7%), which mostly pupated towards a third generation of adults. In the light of these findings, pleiotropic effects of adaptive changes might be a crucial source of divergence in seasonal regulation at the population level, involving significant life-history trade-offs. In addition to man-made selective factors during the reproductive season, such an effect on the lifecycle could be a key component in the process of selection for resistance genes in south-eastern France C. pomonella populations.
Asunto(s)
Mariposas Nocturnas/genética , Selección Genética , Animales , Variación Genética , Resistencia a los Insecticidas/genética , Resistencia a los Insecticidas/fisiología , Mariposas Nocturnas/crecimiento & desarrollo , Mariposas Nocturnas/metabolismo , TemperaturaRESUMEN
Insecticide resistance in the codling moth, Cydia pomonella, partly results from increased metabolic detoxification. The aim of this study was to follow the age variations in larval susceptibility to deltamethrin and teflubenzuron in one susceptible (S) strain, and two resistant (Rv and Rt) ones selected for resistance to deltamethrin and diflubenzuron, respectively. The age variation of the activities of cytochrome P450-dependent monooxygenase (MFO), glutathione S-transferases (GST), and esterases in S and both resistant strains were simultaneously investigated. The highest levels of insecticide resistance were recorded in late instars in both resistant strains, although Rv neonates exhibited enhanced resistance to deltamethrin. The involvement of an additional deltamethrin-specific mechanism of resistance, which could be mainly expressed in early instars, was supported by previous demonstration of a kdr point mutation in the Rv strain. The cross-resistance between deltamethrin and teflubenzuron indicated the involvement of non-specific metabolic pathways in resistance to teflubenzuron, rather than target site modification. A positive correlation between enhanced GST activities and deltamethrin resistance suggested that this mechanism might take place into the adaptive response of C. pomonella to pyrethroids treatments. Enhanced MFO activity was recorded in each instar of the two resistant strains compared to the susceptible one. But these activities were not correlated to the responses to deltamethrin nor to teflubenzuron. In the light of these findings, studying age-dependence of responses to selection is central to the implementation of monitoring tests of resistances, especially if the target instars are difficult to collect in the field.