- Research article
- Open Access
Differential gene expression of the honey bee Apis mellifera associated with Varroa destructor infection
- M Navajas1Email author,
- A Migeon†1,
- C Alaux†2,
- ML Martin-Magniette3, 4,
- GE Robinson2,
- JD Evans5,
- S Cros-Arteil1,
- D Crauser6 and
- Y Le Conte6
© Navajas et al; licensee BioMed Central Ltd. 2008
- Received: 21 December 2007
- Accepted: 25 June 2008
- Published: 25 June 2008
The parasitic mite, Varroa destructor, is the most serious pest of the western honey bee, Apis mellifera, and has caused the death of millions of colonies worldwide. This mite reproduces in brood cells and parasitizes immature and adult bees. We investigated whether Varroa infestation induces changes in Apis mellifera gene expression, and whether there are genotypic differences that affect gene expression relevant to the bee's tolerance, as first steps toward unravelling mechanisms of host response and differences in susceptibility to Varroa parasitism.
We explored the transcriptional response to mite parasitism in two genetic stocks of A. mellifera which differ in susceptibility to Varroa, comparing parasitized and non-parasitized full-sister pupae from both stocks. Bee expression profiles were analyzed using microarrays derived from honey bee ESTs whose annotation has recently been enhanced by results from the honey bee genome sequence. We measured differences in gene expression in two colonies of Varroa-susceptible and two colonies of Varroa-tolerant bees. We identified a set of 148 genes with significantly different patterns of expression: 32 varied with the presence of Varroa, 116 varied with bee genotype, and 2 with both. Varroa parasitism caused changes in the expression of genes related to embryonic development, cell metabolism and immunity. Bees tolerant to Varroa were mainly characterized by differences in the expression of genes regulating neuronal development, neuronal sensitivity and olfaction. Differences in olfaction and sensitivity to stimuli are two parameters that could, at least in part, account for bee tolerance to Varroa; differences in olfaction may be related to increased grooming and hygienic behavior, important behaviors known to be involved in Varroa tolerance.
These results suggest that differences in behavior, rather than in the immune system, underlie Varroa tolerance in honey bees, and give an indication of the specific physiological changes found in parasitized bees. They provide a first step toward better understanding molecular pathways involved in this important host-parasite relationship.
- Hygienic Behavior
- Varroa Destructor
- Deformed Wing Virus
- Varroa Mite
- Queen Mandibular Pheromone
The honey bee (Apis mellifera, Insecta: Hymenoptera) has become an important model for genetic study, especially as its genome has been sequenced . It is also an important economic insect as it is the world's principal crop pollinator and honey producer . These activities have been threatened by the spread of Varroa destructor (Acari: Parasitiformes) a parasite of honey bees that causes devastating harm in many countries . Varroa mites are ectoparasites of honey bees, parasitizing immature and adult bees and reproducing in cells in the honeycomb that contain brood . Varroa mites or virus associated to mites impair the honey bee immune system  and in some cases boost the amplification of bee viruses . The mechanisms underlying the mite's suppression of bee immunity and its impacts on pathogen virulence have not been elucidated.
There are genetic differences in the ability of honey bees to tolerate Varroa parasitism (tolerance is defined here as the capacity for the bees to survive when the parasite develops, preventing the demise of the hive). Some colonies of honey bees tolerate Varroa infection and survive despite the presence of the parasite in the hive [7–10]. These differences have been attributed to a variety of factors, including grooming and hygienic behavior , and differences in the timing of larval and pupal development that impact mite reproduction .
Colonies of the Asian honey bee Apis cerana (the original host of V. destructor) suffer less damage from this parasite than A. mellifera in spite of the presence of the mite in the hives, and these two factors have been implicated . The mechanisms underlying genetic differences for honey bee tolerance to Varroa mites are unknown. Insights into these mechanisms may lead to new molecular tools for both Varroa diagnosis and selective breeding of mite-tolerant honey bees for the bee industry. These issues are now amenable to study thanks to new genomic resources available for honey bees. Microarray analyses of differences in gene expression due to both mite parasitization and genotypic differences in bee tolerance are powerful approaches to explore the role of many genes in what are no doubt multifactorial resistance traits. Microarrays have proven to be useful in the study of host-pathogen interactions in other insects [14–18].
Differences in bee gene expression in response to Varroa infestation and bee genotype
Comparisons of Varroa-infected and non-infected pupae from the 4 colonies studied pinpointed the expression of 32 genes whose expression varied significantly between the two types of pupae. Among them, 15 (47%) of these cDNAs were significantly up-regulated and 17 (53%) down-regulated in bees exposed to Varroa. The magnitude of the difference of expression is small in all cases. The single exception was EST (BB160020A20G03) which was over-expressed 20-fold in bees infected with Varroa. BLAST searches indicated that this EST matches the honey bee virus (AY292384), deformed wing virus .
There were 116 cDNAs whose expression varied with bee genotype, 47 (40.5%) of them up-regulated and 69 (59.5%) down-regulated. Two genes were regulated both as a function of Varroa infection and bee genotype. Dlic 2 is down-regulated in Varroa-parasitized bees and up-regulated in tolerant bees, whereas Strn-Mlck is down-regulated both in Varroa-parasitized and tolerant bees. The full list of genes with significant differences in expression is presented in Additional file 1.
Identification of A. mellifera-regulated transcripts and assignment of biological functions
To add biological meaning to the relatively large amount of microarray-derived data, we searched the GeneOntology database for the putative biological processes and molecular functions for the genes that showed significant differences in expression. Among these 148 genes, 19 associated with the presence of Varroa and 68 associated with bee genotype had information in Gene Ontology.
Functional clustering based on Gene Ontology
Biological process (unknown)
cell organization and biogenesis
Molecular function (unknown)
(B) Bee phenotype
Biological process (unknown)
regulation of physiological process
regulation of transcription
cell organization and biogenesis
nervous system development
Molecular function (unknown)
nucleic acid binding
ion transporter activity
ubiquitin-protein ligase activity
transmembrane receptor protein kinase activity
cytoskeletal protein binding
signal transducer activity
Characteristics of the RT-qPCR analysis of differentially expressed genes of Apis mellifera
Honey bee ID
Forward primer sequences
Reverse primer sequence
Amplicon size (bp)
Previous gene expression studies concerning honey bee immunity have mainly investigated responses to microbial pathogens . Yet physiological responses to macroparasites such as Varroa are likely to be very different from microorganisms, as has been shown recently in a study on Drosophila revealing the ability of this species to activate a systemic immune response adapted to the invader . The results described here pinpoint several genes regulated by Varroa parasitism that can be linked to honey bee responses to the presence of Varroa or to differences in bee tolerance.
Honey bee biological response to Varroa parasitism
Varroa parasitism and deformed wing virus
One of the consequences of Varroa parasitism is a decline in immune capacity which appears to induce the proliferation of viruses such as deformed wings virus in bees . The down-regulation of the autophagic-specific gene 18 (Atg18) detected here is noticeable. Autophagy is an important mechanism for innate immunity against bacteria and viruses [21, 22]. The candidate innate immunity gene poly U binding factor 68 Kd (pUf68)  is also down-regulated in Varroa parasitized bees. By decreasing autophagy and immunity processes in bees, Varroa might favor the proliferation of DWV. Interestingly, the Varroa-parasitized bees displayed high levels of DWV viral RNA (about 20-fold; Additional file 1). The boost of DWV multiplication might cause cellular and molecular damage, and thus the observed production of genes for protein repair (Pcmt) , and the labeling of proteins for degradation (Nedd8) . In contrast to these findings, we did not see a decrease on transcript abundance of immune pathway members  (Evans et al., 2006) found on this array. In fact, transcripts for the gene Rab7, a plausible regulator of immunity, were up-regulated in Varroa-parasitized bees.
The most notable symptoms of Varroa-parasitized bees are disfigured, small adults with deformed legs and wings [4, 6]. Our results show that at the transcriptome level the presence of Varroa down-regulates two genes involved in developmental processes, slg and dlg1. It has been shown that the Drosophila sugarless (sgl) gene regulates wingless signaling , which has a critical role in developmental processes. The gene dlg1 has been implicated in the control of proliferation of Drosophila imaginal discs programmed to produce adult structures at metamorphosis . Although a down-regulation of these genes could have been induced by the presence of Varroa (via the DWV virus), a specific link with the development of deformed adults of virus-infected bees would need to be further investigated.
Cognitive impairment in bees parasitized by Varroa
Varroa infestation does not always cause wing deformity. Adults may sometimes appear to be normal morphologically, but there are mite effects on adult bee behavior. In particular, mite-parasitized foragers display a decrease in learning capability , prolonged absences from the nest and a lower rate of return to the colony . A decrease in neuronal capacities involved in learning and navigation is a possible cause. Although the physiological mechanisms underlying reduced performance by bees in the presence of Varroa remain unknown, our results show that, the gene pale encoding tyramine hydroxylase is down-regulated in pupae parasitized by Varroa. Interestingly, the gene pale is needed for dopamine synthesis, which stimulates the nervous system and has many functions in the brain, including important roles in neural development, behavior and cognition, motor activity, motivation and learning. It is also interesting to note that the Dlic2 and Atg18 genes, both down-regulated in Varroa-parasitized bees, are enhancers of the blue cheese gene (bchs), which is up-regulated in tolerant bees (see below). The bchs gene has been reported as preventing progressive neural degeneration in aged flies . It is plausible, if these changes are chronic (still expressed in adults), that infested bees have a higher rate of neuronal apoptosis when aging, which might explain why foragers (the oldest bees in the nest) have difficulties in learning and orientating in flight.
Behavioral resistance of bees to Varroa
Grooming behavior seems to be one of the main characters involved in the tolerance of bees to Varroa . Similarly, selection for tolerance to Varroa seems to be possible by selecting bees with a high level of hygienic behavior . Hygienic behavior is understood as the ability of bees to uncap and remove infected brood. Although the molecular mechanisms underlying this trait remain unknown, some insights are provided here based on the large-scale comparative analysis of transcriptome differences between Varroa-tolerant and sensitive bees.
A disproportionately high fraction of the genes differentially expressed between tolerant and susceptible bees are involved in the development of the nervous system (Fig. 2B). A large part of these genes are down-regulated in tolerant bees compared to sensitive bees, including the genes futsch, scratch (scrt), otk, Myosin heavy-chain-like (Mhcl), groucho (gro), kekkon-1 (kek1) [26, 33–38]. Fringe (fng), also down regulated in Varroa-tolerant bees, plays an important role in the positive regulation of Notch signalling pathway involved in the regulation of genes that control multiple cell differentiation processes during embryonic and adult life, such as neuronal function and development . Finally, a gene involved in locomotory behavior, single-minded (sim), is down-regulated in tolerant bees. Drosophila mutant sim flies are only able to walk in circles and this phenotype is due to defects in the central brain complex .
Several genes involved in neuron excitability are up-regulated in Varroa-tolerant bees compared to sensitive bees. Purity of essence (poe) (also named pushover) is involved in neuronal excitability and may play a role in responsiveness to environmental stimuli and behavior. For example, fly mutants display behavioral defects such as sluggishness, uncoordination and defective flight . This gene has been shown to be down-regulated in honey bees by the queen mandibular pheromone, which slows the behavioral maturation of workers, e.g. transition from inside hive work (nurse) to foraging activity(forager) . The GluClα gene, a glutamate-gated Cl- channel specific to arthropods, which is also up-expressed in tolerant bees, is known to modulate neuronal membrane excitability . The paralytic gene (para), known to be important in the conducting of nerve action potentials in flies , is also up-regulated. Seen together, these genes suggest a mechanism by which Varroa-tolerant bees are more sensitive to external stimuli than Varroa sensitive bees. Also, the Dynein heavy chain 64C gene (Dhc64c), up-regulated in tolerant bees, is required for proliferation of mushroom-body neuroblasts . Mushroom bodies have an important role in insect cognition and are known to be involved in learning and memory, particularly for smell.
Interestingly, several genes involved in olfaction (smell impaired 21F smi21F, suppressor of the white-apricot gene su(w a ), poe, para, Rogdi) are up-regulated in Varroa-tolerant bees compared to sensitive bees [46–50]. However, the Down syndrome cell adhesion molecule gene (Dscam) and four wheel drive (fwd) also have a role in olfaction, and they are down-regulated in Varroa-tolerant bees . The differential expression of this group of genes depending on bee genotype is of major importance considering that in the hive, olfaction and neuronal sensitivity together may play a major role in the detection of Varroa infested cells. Observations made on two earlier generations of the bee stocks here studied have been shown that Varroa-tolerant bees have better ability to detect the mite . Previous studies showed that hygienic bees have a higher olfactory sensitivity and responsiveness than non-hygienic bees [52–54]. They are notably able to discriminate between odors of healthy and diseased brood at a lower stimulus level, suggesting that olfaction and responsiveness play a key role in hygienic behavior. In addition, observations made on the behavior of the brood, have shown open cells containing destroyed parasitized bee pupae in tolerant experimental colonies, which is in agreement with a bee hygienic behavior against Varroa. If these gene candidate pathways for Varroa behavioral tolerance can be further confirmed, the results suggest that they already set up during the pupae stage.
There were differences in expression between tolerant and sensitive bees for genes involved in increased resistance to toxins like Ahcy13 (Adenosylhomocysteinase at 13) involved in detoxification , and para involved in resistance to insecticide pyrethroids and DDT (Dichloro-Diphenyl-Trichloroethane) . Two genes linked to immunity, Dsam and otk, members of the Immunoglobulin gene superfamily in Drosophila  were down-regulated in Varroa-tolerant bees, while one galectin-family gene (an apparent ortholog to Drosophila CG32226) appears to be upregulated.
Low fold differences in gene expression
For most of the genes showing significant differences in expression in the present study, the magnitude of these differences was small. Recent reports have shown that microarrays can significantly underestimate gene expression changes and therefore if a severe cut-off is applied, this approach might miss important changes in gene expression. Recent reports have validated the capability of a microarray approach to detect small gene expression differences ; 87% of a set of parasite-specific genes displayed changes 2-fold or less in D. melanogaster challenged to a protozoan parasite . Similarly, about 60% of genes of the lepidopteran, Spodoptera frugiperda, revealed around 0.5-fold changes in the transcript levels associated with virus infection . As one possible explanation for low level gene regulation, it has been suggested in Drosophila that much of the response to parasite attack probably does not involve de novo gene expression but post-transcriptional events . Another possibility is that many small differences in gene expression reflect subtle modulation by a large number of factors acting in cascade. The small changes reported here might also represent an underestimation of tissue-specific effects obscured by whole-body analysis. Future studies of Varroa effects on honey bees should analyze specific tissues, and our results suggest a focus on the brain would be fruitful. Previous studies have demonstrated extensive regulation of brain gene expression in conjunction with honey bee behaviour [42, 59–61].
This work is the first step towards understanding the genomic responses of honey bees to Varroa parasitism. It demonstrates that honey bee pupae exhibit differences in gene expression associated either with the presence of Varroa, or with tolerance to this parasite. These results highlight the potential importance of behavioral mechanisms of response to Varroa and suggest that a study focused on the brain is of importance for the future. For an economically important species such as the honey bee, the identification of parasite-specific response factors might ultimately serve to identify molecules that act on bee parasites. In addition, differences between tolerant and sensitive bees could lead to developing tools to select improved strains of honey bees for beekeepers.
Honey bee colonies and sample collection
Both, sensitive and tolerant honey bee colonies here studied, belong to non related local strains of the same A. mellifera population which is bred in the Laboratory of Bee Biology and Protection, Institut National de la Recherche Agronomique, Avignon, France. Four colonies were used for this study; two (T222 and T757) had survived for 11 years with no chemical treatment against Varroa despite the widespread presence of this parasite in the locale, and displayed a very low rate of parasitism . The other two colonies (S21 and S38) showed a very high level of parasitism. No acaricide treatment was applied to avoid pesticide bias. Parasitism intensity was determined by counting the number of mites that died naturally and accumulated on the floor of the hive in each colony during the year (method described in Ellis et.al. ). Estimations based on data for 5 years (4 measurements/year) showed that the infestation rate in colonies S21 and S38 was on average 10 times higher than in colonies T222 and T757.
The reproduction of Varroa mites can be affected by traits in developing bees [63, 64]. We therefore examined gene expression in pupae. Honey bee pupae were collected from the four bee colonies at the blue-eye stage at the start of cuticle pigmentation, making it possible to determine the bee developmental stage . Capped brood cells were opened and two samples of 50 parasitized and non-parasitized pupae were collected. A pupa was considered to be parasitized if a reproductive Varroa was found with it in the honeycomb cell. The pupae were collected and snap frozen using N2 and stored at -80°C until RNA extraction.
We compared parasitized and non-parasitized pupae from both susceptible and tolerant colonies. To minimize the effect of genetic variation, pools of full-sister pupae (related by 75% due to haplodiploidy ) were collected in equal numbers from each of the study colonies.
Sibling estimation by microsatellite genotyping
To identify full sisters, one hundred bees per colony were genotyped (50 parasitized and 50 not parasitized) using Ap53 and A107 microsatellite loci; these loci have been shown to be effective for this purpose . DNA was extracted from 2 legs/pupa, and DNA extraction and PCR amplification were as described , except that the PCR products were detected on a MegaBACE DNA Analysis System 1000 (Molecular Dynamics Inc., USA). The genotype data were used to assemble sets of 8 pupae belonging to the same full sibling group. For each of these, subsets of pupae of Varroa-parasitized and non parasitized bees were analyzed in microarray experiments. This procedure minimizes the effects of intra-colonial genetic variation on gene expression.
Microarray experimental design
The sets of bees were freeze-dried and ground in liquid nitrogen. 30 mg (about 3% of the powder obtained) was used for each RNA extraction using the RNeasy Plant Mini Kit (Qiagen, Courtaboeuf, France) following the manufacturer's protocol for animal tissues. The total RNA solution was treated in liquid by RNase-Free DNase I and purified on column RNA Cleanup (Qiagen, Courtaboeuf, France) according to the manufacturer's protocols. The purity and concentration of RNA were determined by OD measurements in a spectrophotometer. RNA extraction was validated by specific PCR amplifications following RT-PCR of both the glyceraldehyde 3 phosphate dehydrogenase 1 (XM_397363) and the epsilon-tubulin 1 (XM_394700) genes. The quality of the extracted RNA (integrity and size distribution of total RNA) was verified by 1.2% agarose gel electrophoresis in TAE buffer and ethidium bromide staining.
cDNA synthesis and array hybridizations
10 μg total RNA was used for cDNA synthesis using fluorescent Cy3-dCTP or Cy5-dCTP (Amersham Biosciences, Orsay, France) and the Pronto!TM plus System kit (Promega, Charbonnières, France) for labeling. Dye-labeled cDNAs were purified on cleanup columns (Promega, Charbonnières, France). 55 pmol of the labeled cDNA per dye was used per slide. Prehybridation, hybridization and washing steps were performed according to . The slides were hybridized at 42°C and air dried by centrifugation for 2 min at 800 rpm at room temperature.
Microarray data acquisition and statistical analysis
The arrays were scanned on a GenePix 4000A scanner (Axon Instruments, Foster City, USA) and images were analyzed by GenePix Pro 3.0 (Axon Instruments, Foster City, USA). For each array, the raw data comprised the logarithm (base 2) of median feature pixel intensity at wavelength 635 nm (red) and 532 nm (green). No background was subtracted. We excluded control spots (as described in ) and spots for which duplicates did not pass quality controls standards, cDNAs were not found by spot-finding software, or those determined to be irregular by visual inspection. Intensity signals for cDNAs passing these filters were normalized for intensity- and position-dependent bias. Array-by-array normalization was performed to remove systematic biases. Then, we replaced the value of the spots that were considered as badly formed features with the value of the duplicate. We averaged the two values from each duplicated feature to obtain one value of the gene per array in each condition.
A total of 4,795 cDNAs passed initial filters; 3,045 of these were collapsed to genes and 1,750 ESTs were unassigned. We refer to the combined set of genes and unassigned ESTs as genes, although some redundancy might exist. ANOVA analysis was used to classify the differentially expressed genes according with the different factors considered (P < 0.05 was used to denote statistical significance).
Statistical analyses were conducted using R version 2.2.0  and the R/maanova software package version 0.98.8 [61, 68]. The gene-by-gene mixed effect ANOVA model, Yijkvr = μ + Ai + Dj + (ST)k + Vv + Eijkvr, was applied. Observation Yijkvr is the expression value of the gene in the biological replicate r studied on array i when the condition is labelled with dye j. The condition is defined by a modality of the genotype, say k, and the modality of the Varroa, say v. The residual of the mode Eijkvr and the term Ai are treated as random effects and the others as fixed effects. Statistical tests were performed with R/Maanova using the hybrid variance model, Fs, based on a James-Stein estimator [69, 70]. To control the number of false-positives, the significance (nominal P-value) of genes was computed using a permutation test (pvalperm with 1000 permutations) . Permutation tests have the advantage of not assuming a parametric underlying distribution of expression values. A gene was declared differentially expressed if its adjusted P-value is lower than 0.05. The adjusted P-value used here made it possible to control the Family Wise Error Rate (FWER)
Functional analysis of gene expression
Microarray ESTs were annotated as described in [60, 71]. Briefly, ESTs corresponding to microarray cDNAs were tested for near-perfect matches (98% identity) to coding (protein) sequence or to genomic sequence within or immediately downstream (500 bp) of predicted genes (using release 1 of the honey bee Official Gene Set ). Redundant cDNA values were averaged (by using untransformedvalues), and resulting values were assigned to official gene names (which are all prefixed "GB"). Remaining cDNAs not associated with predicted sequences retained their EST identifiers and are presented here by EST accession number (prefixed "BB"). Genes were tentatively assigned molecular function terms based on annotation of the single best BLASTX match in Drosophila melanogaster.
We used Gene Ontology (GO) analysis to identify the biological function of the differentially expressed genes, as described in . We sought statistically overrepresented terms among the set of genes significantly regulated. This Enrichment of Gene Ontology (GO) category was tested with a Hypergeometric test followed by the Benjamini Hochberg correction for multiple testing using the analysis tool GOToolBox . Briefly, the analysis calculates the frequency of terms of a gene list (the significantly regulated genes) and compares these results with total frequencies of genes analyzed. We also grouped functionally related genes on the basis of their GO terms. Distances based on GO terms are calculated for all possible pairs from the gene list which are then used for clustering (e.g. the probability that they are functionally related). The functional clustering of genes was carried out in GOToolBox using the WPGMA algorithm. A minimum cluster size of 3 genes was applied.
Transcript quantification by RT-qPCR
The results of the microarray study were confirmed by measuring the expression of 4 differentially regulated genes (Table 2) using Real-Time quantitative PCR (RT-qPCR). Using an aliquot of the RNA extractions (pools of 8 bees) used for the microarray work, cDNAs were created using the ImProm-II™ Reverse Transcription System kit (Promega). This cDNA (three replicates) was used as template for the Real-Time PCR performed in a Roche LightCycler 480 Instrument platform. The reaction mix consisted of 10 μl of LightCycler 480 SYBR Green Supermix (Roche Laboratories), 5 μl (either 600 nM or 300 nM) of forward and reverse primers, 3 μl dH2O and 2 μl cDNA template. Three reactions were performed and means calculated for each locus and treatment. To standardize the results, a housekeeping gene (Rp49) that did not vary in expression was used as control. The forward/reverse primer sequences are indicated in Table 2. The efficiency for each locus was determined by running a dilution series (1000x, 100x, 10x, 1x) in triplicate. The results were standardized using the  method. Efficiency of the amplicons obtained for each locus was adequately high and at least 97% (Table 2).
We thank C. Whitfield for helpful discussion in a previous version of the experimental design, advice in hybridization protocols and earlier statistical analysis. We also thank A. Rieux for his input in the real-time PCR experiments and J-M Bécard and T. Newman for technical assistance. We thank B. Blondin and P. Delobel for help in array's scanning and for providing access to laboratory facilities at Montpellier SupAgro. This work was funded by a European grant for beekeeping, FEOGA-convention 07-17/2004-2007.
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