|Home | About | Journals | Submit | Contact Us | Français|
Disease is a major factor driving the evolution of many organisms. In honey bees, selection for social behavioral responses is the primary adaptive process facilitating disease resistance. One such process, hygienic behavior, enables bees to resist multiple diseases, including the damaging parasitic mite Varroa destructor. The genetic elements and biochemical factors that drive the expression of these adaptations are currently unknown. Proteomics provides a tool to identify proteins that control behavioral processes, and these proteins can be used as biomarkers to aid identification of disease tolerant colonies.
We sampled a large cohort of commercial queen lineages, recording overall mite infestation, hygiene, and the specific hygienic response to V. destructor. We performed proteome-wide correlation analyses in larval integument and adult antennae, identifying several proteins highly predictive of behavior and reduced hive infestation. In the larva, response to wounding was identified as a key adaptive process leading to reduced infestation, and chitin biosynthesis and immune responses appear to represent important disease resistant adaptations. The speed of hygienic behavior may be underpinned by changes in the antenna proteome, and chemosensory and neurological processes could also provide specificity for detection of V. destructor in antennae.
Our results provide, for the first time, some insight into how complex behavioural adaptations manifest in the proteome of honey bees. The most important biochemical correlations provide clues as to the underlying molecular mechanisms of social and innate immunity of honey bees. Such changes are indicative of potential divergence in processes controlling the hive-worker maturation.
Social insects such as the honey bee (Apis mellifera L.) derive great benefit from living in tight-knit groups that enable greater efficiencies in brood care, foraging and defense against predation. However, the high population densities and relatedness of individuals leave colonies susceptible to emerging infectious diseases . Varroa destructor, an ectoparasitic mite of the honey bee  causes varroasis, which is a leading contributor to ongoing colony losses in commercial apiculture worldwide . V. destructor feeds on the hemolymph of larval and adult bees, inflicting nutritional stress and immune suppression, as well as acting as a major vector for viral pathogen transmission .
In solitary insects, cellular or humoral-based defenses provide the only known system for immunity, but A. mellifera's genome reveals that while honey bees contain these systems for immunity, the number of immunity genes is lower than that of solitary insects such as flies, moths and mosquitoes . As an apparent compensation for this, social insects have evolved collective systems of behavior that provide defenses against disease and parasitism. Two related behaviors, hygienic behavior (HB) and Varroa sensitive hygiene (VSH), are highly variable among A. mellifera colonies and are seen as important traits in the development of disease and mite-resistant stock. HB is a well-documented protective behavior that involves nurse-aged worker bees uncapping brood cells and removing parasitized or diseased pupae . VSH is less well-understood but it encompasses a suite of behaviors that ultimately suppress mite reproduction by uncapping and/or removing mite-infested pupae from sealed brood resulting in a high proportion of non-reproductive mites in the brood that remains [7,8]. HB and VSH can be quantified using field assays and are heritable so, while both are now used in the selective breeding of Varroa-resistant bees [9,10], the genetic and biochemical mechanisms that drive them are poorly resolved.
To date, most selective breeding in commercial apiculture focuses on traits such as honey production, color, gentleness, winter survival or other economic parameters. When combined with continual dilution of the gene pool through importation of susceptible stock, these selections limit host adaptation to pathogens. In order to improve disease and mite tolerance, field assays for HB and VSH must be incorporated into the stock selection process [11,12]; however, these assays are resource intensive, lack sensitivity and may require closed breeding , limiting their suitability for widespread application. To support the creation of novel assays, a molecular-level mechanistic understanding of resistance traits is seen as a promising avenue to support commercial breeding and disease prevention through marker-assisted selection (MAS) . To date, low-resolution microsatellite-based quantitative trait loci (QTL) for HB have been reported , as have some of the biochemical consequences to the host of infection by V. destructor and associated viruses [16,17]. Transcriptome changes in A. mellifera and in Varroa's natural host A. cerana also pinpoint subtle changes in transcript expression for components responsible for neuronal rewiring, olfaction, metabolism and aspects of social behavior that may be critical components driving mechanisms of Varroa tolerance [18,19].
All the molecular investigations of HB and VSH have used well-controlled colonies or individual bees without examining the natural variation and distribution of both the traits and their molecular components. Thus, here we tested the hypothesis that inter-colony variation in disease resistance parameters is reflected by changes in the expression of specific proteins. Sampling from a large cohort of colonies, we measured the relative abundance of approximately 1,200 proteins from two bee tissues involved in interactions with the pathogens and correlated these with estimates for active bee behavioral phenotypes for HB and VSH, as well as host-pathogen population dynamics. Through meta-analysis of these data with other available information, proteins and biochemical processes most likely to be responsible for the observed disease resistance traits were identified.
To assess the expression of disease tolerant behaviors, colony-level measurements of various metrics of HB, VSH and mite-host population dynamics were made (Figure (Figure1),1), including phoretic infestation (PH, mites on adult bees), natural mite drop (ND, estimate of mite death rate), and levels of brood infestation (BI). HB was estimated by observing the proportion of a defined number of freeze-killed, sealed brood cells that bees first uncapped (uncapped, U) and then removed (removed, R) at 24 and 48 hours (Figure (Figure2a).2a). The hygienic response to freeze-killed brood was time dependent, with widely distributed levels of HB at 24 hours and the majority of hives achieving the accepted 95% threshold for the proportion of removed cells at 48 hours . Because colony scores in the other measured parameters were distributed roughly similarly to HB at 24 hours as indicated in the kernel density plot of Figure Figure2b,2b, we asked which of them were independent measures and which were interrelated. Pearson's product-moment correlation (PPMC) coefficient revealed a statistically significant negative pair-wise dependence between estimates for hygiene and mite infestation dynamics (PH, ND) (Figure (Figure2b).2b). Maximum dependence was observed between cell removal and PH (r = -0.54, P = 0.0007), confirming that colonies better able to detect and uncap cells with affected brood are able to reduce adult infestations more efficiently. Observing differences in density for temporal aspects of hygiene and interactions between disease-tolerant behaviors and infestation indicated we were detecting natural variation in the speed of HB removal that directly influenced the colonies' tolerance to Varroa mites.
While most of the parameters discussed above are known to have a genetic basis, all must ultimately manifest as the result of changes in protein expression and/or activity. To explore potential mechanisms underpinning natural variation in Varroa tolerance across these colonies, we examined the protein expression profiles of two tissues that play a critical role in the bee-Varroa interaction: antennae of brood-nest workers (that is, mostly nurse bees) and the integument from fifth instar worker larvae. Antennae were used because they are adult bees' primary sensory organs and many of the behaviors evaluated here involve bees being able to sense the presence of either the pathogen itself or a damaged/diseased nest-mate. Integument was chosen because it is the initial physical barrier to Varroa when they feed on larvae and as such the innate processes found here may be critical components in the response of hygienic adults and provide direct innate mechanisms of tolerance. It is possible that changes in the composition of larval proteins or the metabolites produced by these proteins during infection may trigger HB or VSH in adult nurses.
Using liquid chromatography-tandem mass spectrometry (LC-MS/MS) to analyze three independent samples of each tissue, we constructed protein expression profiles for approximately 1,200 proteins across all colonies as described previously . By centering and standardizing across labels and colonies, the relative expression ratios from individual LC-MS/MS experiments are converted into a roughly normalized distribution of protein effect, representing the expression level of each protein in each colony relative to the population average. These variables (response variable) were then regressed against the behavior and infestation estimates (predictor variable) measured for that colony. The direction of each regression was determined by the sign of the estimated regression coefficient and the significance of that effect was accessed using a mixed linear model with probability cut-off at Q <.2 adjusting for multiple comparisons or later P < .05 for explorative data analysis (see Figure Figure33).
To adjust significance levels to account for the multiple-testing hypothesis, proteins were filtered using Q <.2 cut-off; for HB one antennal protein and five larval proteins survived this additional filter (Tables (Tables1,1, ,2).2). In the antennae, the hypothetical protein 'LOC552009' of unknown function correlated with HB at 48 hours (Q = 0.09) for both 'uncapped' and 'removed' behaviors. Sequence analysis revealed that LOC552009 contains a conserved domain similar to the mammalian protein lipid transport protein Apolipoprotein O (ApoO) . Figure 4a, b shows the added variable plot for this protein correlating with HB (removed 48 hours), peptides identified and protein sequence containing the conserved domain for ApoE.
In larvae, several more candidate proteins were identified as strong positive and negative predictors for HB (Table (Table2),2), suggesting that events in the larvae may be able to influence HB of the adult. Further correlation analysis of mite infestation/fertility measures (PH, BI, ND and VSH) identified the hemocyte protein-glutamine gamma-glutamyltransferase-like (a putative transglutaminase) as highly significant (Q = 0.02) and positively correlated with ND (Figure (Figure4c4c).
To increase the specificity of our measures for infestation dynamics, we next calculated the ratio of mites observed phoretically to those found in brood cells (PH/BI). This adjustment enabled quantitation of the relationship between two important stages in the mite life cycle, where long phoretic phases may be indicative of poor reproductive success and the influence of adult bee behavior or larval attractiveness. After adjustment, several proteins (nine in antenna, four in larva) were highly significant (Q <.2) in both tissues. Importantly, the adjusted metric was also highly correlated with ND (Pearsons product correlation: t = 5.2211, df = 36, P = 7.633e-06) and in larva correlated with increased significance with the protein Tg (Q = 0.01), supporting the role of Tg as an accurate measure of Varroa resistance (Figure (Figure4,4, Tables Tables1,1, ,2).2). Tg also provides the clearest link to phenotype. In insects, Tg is the primary protein facilitating the crosslinking of the clotting factors, hemolectin and Eig71Ee. Tg drives clot formation, an important defensive process against ectoparasites such as the Varroa mite. Of the proteins correlating in the antenna, several form part of diverse metabolic pathways and are impossible to link to function at this point. However, calcyphosin-like protein and phenoloxidase subunit A3 are worthy of discussion. Calcyphosin (Q = 0.02) has been found expressed in olfactory cells in lobster and with a putative role in signal transduction in sensory cells. Phenoloxidases (Q = 0.1) are a critical part of insect immunity during the pathogen encapsulation response, but are also important in the ecdysteroid-dependent processes linked to polyphenism and caste differentiation.
The proteins discussed above that survive correction for multiple hypothesis testing should be excellent predictors of HB, perhaps even usable in marker-assisted selective breeding. To find so many highly significant proteins in a completely out-bred population is remarkable but the requirements that they must pass mean that it may be too restrictive a dataset to understand fully some of the molecular mechanisms underlying the relevant behaviors. To this end, we expanded the analysis to discover processes with mechanistic relevance for HB and VSH. Those proteins with a significant correlation (P < .05) to one or more behavioral traits were explored using ontological classifications provided by the honey bee refseq entry in the National Center for Biotechnology Information (NCBI) or the flybase homolog. The most significant of these enrichments (P < .05, Table Table3)3) largely tracked with the altered distributions for estimates of HB, suggesting some of the molecular mechanisms that may regulate this behavior. The set of proteins highly correlated with rapid HB (>95% removed by 24 hours) was particularly enriched for proteins involved in 'sensory development'. At 24 hours, both uncapping and removal traits correlated with the up-regulation of the secretory proteins windbeutel, amphiphysin (Amph) and [RefSeq:CG6259] which encodes the homolog to human CHMP5 protein. Proteins down regulated in rapid hygienic bees were ankyrin 2, laminin A, Zasp (Z band alternatively spliced PDZ-motif protein) and fasciclin 1 (Fas1) all involved in 'cell adhesion'. Proteins correlating with both elements of HB at 48 hours (>95% open/cleaned 48 h ours) were enriched in the ontology 'mitochondrial inner membrane'. This ontology was also identified for the rapid uncapping behavior and corresponds to reduction in primary metabolic pathways.
VSH and HB correlated strongly with some of the same proteins, even though there was no apparent interdependence between VSH and HB (Figure (Figure5).5). Proteins that correlated with VSH and HB included Fas1, which was negatively correlated with rapid HB and VSH, while Amph and helicase 25E (Hel25E) levels were significant positive predictors of both VSH and rapid HB (Figure (Figure5).5). In addition, several unique proteins with roles in synaptic function correlated only with VSH. VSH was negatively correlated with expression of the mushroom body protein (Mub), soluble NSF attachment protein (SNAP) and gammaCOP. Mub is involved in temperature preference in Drosophila,  while SNAP is a key pre-synaptic protein mediating synaptic vesicle fusion and gammaCOP is involved in vesicle trafficking at synapses and other vesicle sorting pathways . The protein with greatest change in expression with respect to VSH measurements was [RefSeq:LOC412768], a poorly annotated member of the take-out/juvenile hormone binding protein (To/JHBP) superfamily involved in chemoreception.
HB and VSH are considered to be specific behavioral adaptations of the adult honey bee to diseased brood. However, as our molecular understanding of these traits improves, it is possible that factors expressed within the larva in response to the pathogens may influence the manifestation of the relevant behaviors. Protein/behavior correlations of larval proteins revealed enrichment of chitin-based cuticle structural proteins, particularly cuticular proteins 3 and 13 (CRP3 and CRP13; Table Table4).4). Larval expression of the peptidyl-amino acid modifying enzymes Caf1 and [RefSeq:CG6370] was also positively correlated with HB. CG6370 encodes a dolichyl-diphosphooligosaccharide-protein glycosyltransferase involved in N-glycan biosynthesis in the lumen of the endoplasmic reticulum and, interestingly, four other lumenal proteins were also positively correlated. The larval protein/behavior correlation with the steepest slope was [RefSeq:CG1318-PA], a beta-N-acetyl-D-hexosaminidase with broad substrate specificity ranging from N-glycans to chitooligosaccharides. Three proteins clustered under the term carbohydrate metabolism were negatively correlated with VSH in larval tissue. Ecdysone-inducible gene (ImpL3), phosphoglucomutase (Pgm) and gene analogous to small peritrophins (Gasp) all process carbohydrates. Gasps specifically bind or regulate chitin structure in developing embryos, ImpL3 is a lactate dehydrogenase induced by the prohormone of 20-hydroxyecdysone that regulates insect molting, while Pgm is a glycolytic enzyme, a process vital for the biosynthesis of chitin from glycogen. Taken together, these observations suggest a role for larval chitin biosynthesis and/or structural regulation in hygienic and VSH behavior. In the proteins positively correlated with VSH, gene enrichment identified casein kinase II, alpha 1 polypeptide isoform 1 (CkIIapha1 or CK2) and peptidoglycan-recognition protein-SA (PGRP-SA). Both are components of the 'cell surface receptor linked signaling pathway' ontology and effectors of interferon and lipopolysaccharide (LPS) macrophage inflammatory signaling . PGRP-SA detects Lys-type peptidoglycan (PG) from gram-positive bacteria, leading to activation of the Toll receptor pathway and, ultimately, to increased expression of antimicrobial peptides [25,26]. The larval inflammatory response may serve not only as an individual defense mechanism but also as an initiator of social immunity behavior, that is, VSH.
We have described here the discovery of several proteins whose expression levels may impact honey bee resistance to infestation by the Varroa mite. Natural diversity in these behaviors was a prerequisite to this study and we observed that the levels of each behavior in any given colony were not random. As expected, there was a strong negative correlation between mite infestation levels and HB. At the expression level, several proteins were highly significant predictors of HB and mite infestation dynamics. Highlighted within these proteins were the putative ApoO homolog and a putative Tg. Apolipoproteins are called apolipophorins in insects, and they have diverse roles in lipid solubilization and the transport of small hydrophobic ligands [27-29]. In innate immunity the apolipophorin ApoLp-III stimulates antimicrobial activity in the hemolymph, acting as a pattern recognition system for LPS and lipoteichoic acid (LTA) . Lastly, the strong correlation of Tg with both NDs and an increase in the ratio of phoretic mites to brood mites suggests that Tg activity could provide a measure of resistance to Varroa reproduction.
V. destructor is an ecto-parasite feeding communally and repeatedly on hemolymph of the honey bee through a bite wound in the cuticle [30-32]. In insects' innate immunity the cuticle provides the first line of defense; once breeched, innate defense systems of the haemocoel cavity are orchestrated by hemocytes, the fat body and hemocoel . Normal wounds heal as hemocytes and plasmatocytes exocytose the clotting factors hemolectin and Eig71Ee . These molecules and other plasma-based factors such as fondue are cross-linked by Tgs in a Ca2+ dependent mechanism to form a primary clot. However, V. destructor transmits bio-active compounds that prevent healing and allow continued feeding to occur at the same wound . In the tick arthropod-mammalian ecto-parasitic systems, 18 known bio-active suppressants target innate antiseptic defenses, including several immune cells types, inflammatory and coagulatory cascades . In honeybees, the effect V. destructor elicits on the immune system is uncertain. Yang and Cox-Foster  demonstrated that Varroa parasitism increases the susceptibility of adult bees to bacterial infection, but no major immunosuppressive effects were revealed by transcriptomic studies on specific immune genes or in global analyses [38,39]. More recently a study has reveled that salivary secretions from the Varroa mite are able to damage hemocyte aggregation in the tomato moth, (Lacanobia oleracea)  but no known factors of either pathogen or host are identified. We report here that elevated expression of a putative key clotting factor (Tg) is found in the larva of Varroa resistant bee colonies. These data indicate that honey bees have adapted to Varroa, increasing the clotting capacity of hemolymph in order to limit mite reproduction.
While the experiments described here were clearly of sufficient power to permit the discovery of some correlations between protein expression and behavioral traits, the variability within such out-bred populations is very high. This is likely a significant limitation in fully defining the molecular mechanism of something as complex as a behavior. Practical limitations in the number of colonies that could be sampled and the depth to which the proteome could be measured across multiple samples were inherent problems here, as with any proteomics study. Even so, an exploratory approach was seen as an important step in generating new hypotheses in a currently poorly understood area of biology.
It is thought that the speed with which hygienic bees respond is driven by a lower limit of olfactory detection of the diseased brood odor , which is in turn influenced by the neuromodulator octopamine . In the antennal lobe, octopamine concentration varies between behavioral state, being low in nurse bees and high in foragers. Juvenile hormone and brood pheromone both modulate behavioral responses to octopamine  and both are involved in several aspects of behavioral maturation, with the best-understood system being the transition from nurse to forager. This maturation invokes physiological changes that are underpinned by increased neural processing which is required to interpret complex visual information for flight behavior. Anatomically, expansion of the mushroom body neurophil space in the brain and decrease in the volume of the olfactory glomeruli of the antennal lobes occurs during this transition . Olfactory sensory neurons from the antennae project onto the glomeruli of the antennal lobe via the antennal nerve, and olfactory information is processed and projected to higher-order brain centers such as the mushroom bodies or lateral protocerebrum.
The data presented here indicates that cells (most likely neurons with antennal axons) of bees performing rapid hygiene express different levels of proteins involved in adhesion and vesicle processing (Figure (Figure6a),6a), supporting the role of octopamine and maturation as an important control of this behavior. The cell adhesion proteins identified were all integrin proteins, some of which have been reported to regulate synaptic plasticity . Specifically, ankerin 2 stabilizes synaptic connections to the spectrin-actin cytoskeleton and laminin A, Zasp and Fas1 are involved in the assembly of functional integrin adhesion sites essential for growth cone extension in axon guidance during neurogensis . The increased expression of vesicle sorting proteins in hygienic bees indicates that while plasticity may be reduced, antennae of hygienic bees provide a strong input into higher brain function. These data could be explained by the environment of a hygienic nest bee, in which strong brood and queen-based olfactory cues are the major sensory inputs for bee development, behavior and social cohesion  (Figure (Figure6d).6d). Dimorphism in neural plasticity has been well characterized in the antennae of drones, where the antennal sensory nerves are thicker but project into a smaller number of glomeruli than in workers [46,47]. This configuration provides drones with the lower limit of detection for queen pheromone, enabling efficient queen finding during mating flights.
VSH limits mite reproductive success in the brood by specifically detecting the presence of a post-ovipositional mite. As part of the bees' response, a sensitive adult uncaps and re-caps the cell, effectively inhibiting mite reproduction . The signal being sensed in this process remains unknown, although it peaks between three and five days after the cell is initially capped, leading to speculation that VSH adult bees respond to temporal fluxes in pathology mediated by oviposition, wounding related stress responses, infections, and olfactory cues . Correlation between VSH scores and two proteins encoding divergent members of the To/JHBP super-family suggest they may be functionally linked to the behavior; To/JHBPs contain a conserved ligand binding domain with differing affinities to small lipophilic molecules such as JH and the N-terminal signal peptide indicates that they are probably secreted into the hemolymph where they act as soluble receptors for their ligands [49,50]. In the honey bee genome there are eight To/JHBP genes, located at two distinct loci, and we see one protein from each loci, one positively correlated with VSH and one negatively correlated (Figure (Figure6b).6b). Biologically, this separation in the genome suggests divergent functions and this is further supported by their differential regulation in our study. One of these proteins is completely uncharacterized but in Phormia regina the ortholog of the other To/JHBP is thought to be involved in chemosensation in antennal olfaction and taste  leading to the attractive hypothesis that it is playing a similar role in sensing brood.
That sensory and neuronal processes have a link to disease tolerant behavior may be expected but, intriguingly, a class of proteins involved in larval cuticle formation/structure also emerged as likely candidates. An arthropod's cuticle forms the primary physical barrier to the environment so while the cuticle plays an obvious role in pathogen defense, how it may contribute to social immunity mechanisms is less clear. Cuticular lipids differ between bees depending upon caste and attacks by V. destructor can alter the composition in adults and larvae [51,52]. The role of the cuticle in social immunity is supported by the data presented here, which indicates that several proteins involved in forming and maintaining the cuticle are significantly correlated with disease tolerance behaviors of nurse bees (Figure (Figure6c6c).
Our analysis of tissue proteomes from a large cohort of commercial honey bee colonies provides new clues to the evolution of biochemical components facilitating adaptation to disease. The control of behavior potentially represents the most complex paradigm in all living creatures so its study in natural, outbred systems is fraught with many difficulties, explaining the lack of coherent mechanisms describing these processes. Honey bees live in eusocial colonies and provide a scalable system for the study of developmental social biology and the divisions of labor it defines. Our results represent indications of molecular mechanisms underlying innate and social immunity behaviors in honey bees and build upon previous work demonstrating adaption involving neural remodeling and odorant recognition. A focused investigation of the processes identified here will provide an explanation of how host-pathogen interactions drive selection to generate disease tolerant colonies.
All chemicals used were of analytical grade or better and all solvents were of HPLC-grade or better; all were obtained from ThermoFisher-Scientific (St. Waltham, MA, USA).
We established 40 genetically heterogeneous honey bee colonies at a research apiary (Grand Forks, BC, Canada) in the spring of 2009 by shaking workers into a large cage and then portioning them back into single Langstroth box colonies with nine frames in each. Selected queens were then introduced into each new colony with initial populations of 1 kg of bees with relatively uniform V. destructor infestation rates, varying among colonies from 6.2% to 7.6% per 100 adult bees. Colonies were allowed to develop for six weeks to allow worker populations to turn over and be composed of the introduced queen's progeny, at which point we evaluated each for physiological V. destructor interactions and HB. HB was measured as the proportion of sealed brood cells uncapped (U) and removed of pupae (R) within 24 and 48 hours of freeze-killing defined patches brood with liquid nitrogen; PH and BI were estimated as described . The proportion of uncapped cells referred to all cells uncapped by nurse bees including those where the pupae had been removed and those where the pupae was still present at the time of the observation. To estimate the ND V. destructor in each colony we counted the number of mites captured on screened bottom boards over four 24-hour collection periods spanning a period of 10 days. The ND estimates were normalized by colony size using the total weight of bees to determine the number of bees in each colony. VSH was estimated as the production of sexually viable female offspring as described .
We used triplex dimethylation labeling and generated a D-optimal design matrix to group the samples in blocks of three and assigned a label to each sample as described . A randomized incomplete block design similar to what we have used previously was chosen to minimize the standard error of the estimate of the colony effect on protein expression level .
The antennae and larvae from colonies were sampled in triplicate. Ten pairs of antennae from nurse bees and three fifth instar larvae were removed in situ and frozen on dry ice. Larvae were further dissected to remove the digestive tracts and free-flowing hemolymph with stability maintained in PBS (50 mM K2HPO4, 150 mM NaCl, pH 7.4) containing complete, EDTA-free protease inhibitor cocktail (Roche, Mississauga, ON, Canada). Both samples were washed three times in PBS and prepared using essentially the same method. Both tissues were homogenized in 50 mM Tris-HCl, 150 mM NaCl, 1% NP-40, 20 mM dithiolthretitol in a Fast Prep bead mill with 2.8 mm ceramic beads (MP Biomedicals, Santa Ana, CA, USA) using 1 or 3 cycles of 20 s at 6.5 M/s with cooling for larvae or antennae, respectively. Tissue lysates were clarified at 5,000 relative centrifugal force (rcf) for 5 min at 4°C before ethanol/sodium acetate precipitation . Proteolytic digestion of 20 μg (antennal) and 50 μg (larval) total protein was carried out as described ) and samples were labeled by reductive dimethylation using formaldehyde isotopologues  with slight modifications . After labeling, each sample was pooled as required by the experimental design and each pool was separated into five fractions (antennae) using C18-SCX-C18 STAGE tips  or into six fractions (larvae) by isoelectric focusing with the OFFGEL system (Agilent Technologies, Santa Clara, CA, USA) .
Quantitative proteomic datasets were generated for antennae exactly as described in . For larval tissue, LC-MS was done on a 1200 Series nanoflow HPLC system (Agilent Technologies) interfaced with a chromatin immunoprecipitation (CHIP)-cube to a 6520 Q-TOF (Agilent Technologies). Peptide separation was performed by reversed phase chromatography using a micro-fluidic CHIP comprised of an analytical column (75 μm ID, 150 mm length with a 300 Å C18 stationary phase) and a 160 nL trap column of the same phase. Peptides were loaded in 5% (v/v) acetonitrile, 0.1% (v/v), formic acid at 0.3 μL/min and then resolved at 0.3 μL/min for 90 min, during which a linear gradient of acetonitrile was created from 5% to 50% in 0.1% (v/v) formic acid. Mass spectrometry: Operating in auto MS/MS acquisition mode, the Q-TOF was set up to acquire full scan data over a mass range of 350 to 2,000 m/z and MS2 for the six most intense, multiply-charged ions. Peak lists were created using Spectrum Mill extractor specifying fixed modification carboxyamidomethylation (C) and triplex dimethyl-mix (K,N-term) which accounts for all possible label moieties. Scans were merged within +/- 45 s elution time and maximum m/z window of 0.5 Da (usually 20 ppm). For database searching, oxidation (M) was added as a variable modification, peptide tolerance was +/- 20 ppm and fragment ion tolerance was 50 ppm, dynamic peak thresholding was switched on. Search results from Spectrum Mill were validated using autovalidation for protein score >20; (charge 2, Score >5, % SPI <50, Fwd - Rev Score >1, Rand 1-2 score >1), (charge 1, Score >6, % SPI <60, Fwd - Rev Score >1, Rand 1-2 score >1), (charge 3, Score >5, % SPI <50, Fwd - Rev Score >1, Rand 1-2 score >1) and for peptide hits (charge 2, Score >12, % SPI <60, Fwd - Rev Score >2, Rand 1-2 score >2), (charge 1, Score >8, % SPI <70, Fwd - Rev Score >2, Rand 1-2 score >2), (charge 2, Score >12, % SPI <60, Fwd - Rev Score >2, Rand 1-2 score >2). Both larvae and antennae datasets have peptide identification false discovery rates (FDR) well below 1% and were compiled into protein data arrays as described . All experimental design and proteomic results are listed in Additional files 1, 2, 3 and 4.
All MS/MS data used in this study have been made available in two locations: they have all been deposited into the Honey Bee PeptideAtlas [58,59] as processed spectra and the raw files themselves are available on our FTP site (ftp://foster.chibi.ubc.ca/Downloads/BeeBiomarkers/).
Logarithms of intensities were normalized by first subtracting the average of the three measurements in each block (for each protein independently) and then centering and standardizing within each label (across proteins) by the median and median absolute deviation . For each protein, a linear mixed effects model was used to estimate the effect of each predictor variable on the protein expression level, adjusting for block and label factors. Colony was treated as a random factor to control for the three repeated measures within each colony. For each predictor variable an estimated effect, standard error and P-value was computed for each protein response. FDRs (q-values) were computed for the set of P-values of a given predictor over all protein response variables to adjust for multiple comparisons. All calculations were performed in the R statistical language.
Analysis was performed using Exploratory Gene Association Networks (EGAN) software  with pre collated networks for Drosophila melanogaster (Dmel). A. mellifera (Amel) gene identifiers were mapped to Dmel orthologs using the Round-Up database  and any unmapped Amel identifiers were assigned functions based on their closest homolog in D. melanogaster using BLAST-P, resulting in a total of 90% coverage for all antennal proteins identified. The remaining 10% were dealt with manually by drawing information from several sources: 1) honey bee genes othologs implicated in immunity ; 2) proteins found significantly regulated in response to bacterial infection by Paenibacillus larvae ; 3) proteins regulated in response to V. destructor infestation ; and 4) proteins specific to colony collapse disorder (CCD) affected colonies . Enrichment analysis of proteins whose expression levels correlated (P < .05) with behavior and their direction of regulation was carried out by integrating these nodes with gene ontology nodes for component, function and process. For each node, over-representation or enrichment analysis was carried out employing a standard one-tailed Fisher's exact (hypergeometric) test using the entire gene list as background. Heat maps representing the interaction of important genes and their relationships by nodes were generated for both datasets independently.
Apo: apolipoprotein; BI: brood infestation; CCD: colony collapse disorder; CHIP: chromatin immunoprecipitation; Fas1: fasciclin 1; FDR: false discovery rate; Gasp: gene analogous to small peritrophins; HB: hygienic behavior; HPLC: high pressure liquid chromatography; JH: juvenile hormone; LC: liquid chromatography; LPS: lipopolysaccharide; LTA: lipoteichoic acid; MS: mass spectrometry; ND: natural drop; PBS: phosphate buffered saline; Pgm: phosphoglucomutase; PG: petidoglycan; PGRP-SA: peptidoglycan recognition protein SA; PH: phoretic; PPMC: Pearson's Product movement correlation; QTL: quantitative trait loci; RCF: relative centrifugal force; STAGE: stop and go extraction; To/JHBP: take-out/juvenile hormone binding protein; VSH: Varroa sensitive hygiene; Zasp: Z band alternately spliced PDZ-motif protein.
The authors declare that they have no competing interests.
APM, SFP, MMG, LH and LJF designed the experiments. LH maintained the bees and was assisted in performing behavioral assays by APM and SFP. LJF, KM, MMG and RP dissected the bees. RP and KM performed the biochemistry and mass spectrometry, as well as the functional bioinformatics. LJF authored the scripts for compiling proteomic data. RW designed and performed the statistical analyses. RP, LJF and MMG interpreted the results and wrote the initial version of the manuscript. All authors have read and approved the manuscript for publication.
Spreadsheet of five pages for larval dataset. Page 1, P values and protein annotation. For all proteins identified and quantitated the resultant P value from the correlation analysis with each trait and refseq annotation. Page 2, T statistic for each correlation provides a standardized value for the rate of change for each protein against per unit of each trait measured. Page 3, EGAN mapping, honey bee protein GI mapped to NCBI fly gene id. Page 4, P values for biological process gene enrichment for protein groups created by trait correlation and direction of correlation. Page 5, P values for global biological process gene enrichments.
Spreadsheet of five pages for antenna dataset. Page 1, P values and protein annotation. For each protein identified the resultant P value from the correlation analysis with each trait and refseq annotation is provided. Page 2, T statistic for each correlation provides a standardized value for the rate of change for each protein against per unit of each trait measured. Page 3, EGAN mapping, honey bee protein GI mapped to NCBI fly gene id. Page 4, P values for biological process gene enrichment for protein groups created by trait correlation and direction of correlation. Page 5, P values for global biological process gene enrichments.
Spreadsheet of five pages for processed antenna LC-MS data. Page 1 gives the experimental design designating used to generate LC-MS datasets. Each block is shown with colony numbers and the output file name generated for each block. Pages 2 to 4 are examples of the output from LC-MS and protein identification and quantitification result for each peptide used to generate proteins ratios. Page 5 is the result of rolling all peptide identification up into unique proteins using parsimony rules.
Spreadsheet of five pages for processed larval LC-MS data. Page 1 gives the experimental design designating used to generate LC-MS datasets. Each block is shown with colony numbers and the output file name generated for each block. Pages 2 to 4 are examples of the output from LC-MS and protein identification and quantitification result for each peptide used to generate proteins ratios. Page 5 is the result of rolling all peptide identification up into unique proteins using parsimony rules.
The authors wish to thank Nikolay Stoynov for technical assistance in LC/MS analysis, Julian Yiu and Tram Nguyen for help with sample collection, as well as members of our respective groups for advice and fruitful discussions. This work was supported by funding from Genome Canada, Genome British Columbia, the British Columbia Honey Producers Association through the Boone-Hodgson-Wilkinson Trust Fund, the Canadian Honey Council and Canadian Association of Professional Apiculturists through the Canadian Bee Research Fund, the British Columbia Blueberry Council and the British Columbia Cranberry Marketing Association. Mass spectrometry infrastructure used in this project was supported by the Canada Foundation for Innovation, the British Columbia Knowledge Development Fund and the British Columbia Proteomics Network (BCPN). LJF is the Canada Research Chair in Quantitative Proteomics.