The Varroa mite, Varroa destructor, a parasitic mite that afflicts honey bees, has become increasingly resistant to acaricides like fluvalinate due to its widespread use. The target site insensitivity mechanism, mediated by the L925V/M/I mutations in the voltage-gated sodium channel, plays a major role in resistance. Additionally, cytochrome P450 monooxygenases (Cyp450s) appear to function as a metabolic resistance factor; however, no Cyp450-mediated resistance mechanism has been reported to date. The aim of this study was to identify and characterize Cyp450s associated with fluvalinate resistance. A synergistic bioassay confirmed the involvement of Cyp450s in conferring tolerance or resistance to fluvalinate. Correlation analysis between mortality data and the expression levels of Cyp450 genes led to the identification of several candidates that may play a crucial role in fluvalinate resistance. Analysis of tissue distribution patterns revealed that these genes were most abundantly expressed in the cuticle and synganglion. This suggests that, despite their relatively low expression level, they may play a critical role in protecting the target site from fluvalinate due to its predominant expression in neuronal tissues. Functional analysis, in conjunction with baculovirus expression, demonstrated that fluvalinate has high inhibition rates against the recombinant candidate Cyp450s, suggestive of their strong interaction with fluvalinate. We discussed the potential utilization of their expression levels as a molecular marker for diagnosing metabolic resistance in field-collected Varroa mites.

To control an external parasitic mite, a honey bee line possessing high hygienic behavior (HHB) against an external parasitic mite, Varroa destructor, has been bred in South Korea and an assessment method has been necessitated to diagnose HHB line from the low hygienic behavior (LHB) line. Thus, in this study, we developed single nucleotide polymorphism (SNP) markers from whole genome sequencing of each 20 worker bees from HHB and LHB lines of A. mellifera ligustica (Hymenoptera: Apidae). An average of 319,445,977 sequence reads was mapped to the known A. mellifera reference genome (an average of 87.46%). In 2,316,128 and 3,266,756 SNPs from each HHB and LHB line, an average of 93.6% and was located in the intergenic spacers and introns, whereas, the remaining 6.4% was located in the genic region, respectively. Among them 20 SNPs that were fixed at each line possessing within-individual homozygosity were selected and each four SNPs were used to diagnose the two honey bee lines either by typical PCR-restriction fragment length polymorphism method or allele-specific PCR. The remaining six SNPs had the size difference, enabling relatively easy differentiation between the two honey bee lines on typical agarose gel and another remaining six SNPs only has sequence difference including SNP sites. Thus, these SNP markers can be used to diagnose the honey bee line with HHB from LHB line against V. destructor.

The varroa mite, Varroa destructor, is a small ectoparasitic mite which attacks honeybee, Apis mellifera, and also known to harbor small RNA viruses which infect honeybees. To survey the transcriptome of varroa mite, total RNA of female adult mites was subjected to RNA-seq to construct an in silico cDNA library. 2 × 8.3 Gbase of quality filtered paired-end nucleotide sequences were obtained to construct 28,302 of protein-coding contigs by de novo assembly, and subsequent BLAST search revealed the viruses infect honeybee or associated with varroa mites. Six of the contigs showed high sequence identity to Iflavirus, picorna-like virus, rhabdovirus, and macula-like virus were discovered. It implies that the viral flora in varroa mites and honeybees might be more complex than previously studied, and suggests the importance of further virome studies for better understanding of honeybee health.

Varroa destructor is a devastating ectoparasitic mite which attacks Honeybee, Apis mellifera. V. destructor feeds on honeybee hemolymph, and often harbors small RNA viruses such as the deformed wing virus to transmit these viruses in the infested bee hive. To survey the genes of V. destructor, total RNA was subjected to high-throughput transcriptome sequencing to construct in silico cDNA library by using the Illumina HiSeq 2000 platform. Total of 2×107,748,792 paired-end short reads were obtained and quality filtered reads were subjected to Trinity de novo assembler followed by TransDecoder, and CD-HIT program to make a V. destructor reference cDNA library containing 28,023 of clustered contigs with protein coding capacity. These cDNA sequences will help us to understand the molecular biology of V. destructor.

Varroa destructor and Tropilaelaps mercedesae mites are ectoparasitic to honey bee having similar life cycle and damage symptoms. Both invade into the last instar larval cell and reproduce during capped brood period of honey bee development. Female adult mites escape from the comb cell on the back of the emerging adult bee (phoretic period) and invade another cell for reproduction. Objective of this study was to study the effect of competitive interaction on each parasitic mite species population. We assessed population monitoring of host and parasitic mites. Honey bee population was monitored by approximating sealed brood and adult bees based on the coverage of the combs. Parasitic mites were monitored by detection technique like sugar shake, stick board, and sealed brood. This monitoring continued at weekly interval during 2008, 2014, and 2015. Additionally Invasion distribution of each species was checked. We calculated carrying capacity, population growth rate, and competition parameter from population monitoring data. Single parasitic mite, Varroa occurred and infestation increased continuously throughout the year in 2008. Co-occurrence of Varroa and Tropilaelaps in honey bee colonies was studied in 2014 and 2015. Carrying capacity was higher in single parasite infesting honeybee than parasites in co-occurrence. While using sugar method, carrying capacity of Varroa alone was found higher than in its co-occurrence with Tropilaelaps. Population growth rate of Varroa when tested alone was higher than its co-occurrence with Tropilaelaps in sugar method. Population growth rate of Varroa and Tropilaepas was higher in sticky method than sugar methods when they were tested in co-occurrence. Population growth rate is higher in Tropilaelaps (0.09) than Varroa (0.05) when both are tested in co-occurrence. We calculated competition parameter of Varroa and Tropilaelaps which was 1.9 and 0.53, respectively. Negative effect on regulation of carrying capacity and population growth rate is due to interspecies competition. Varroa population was higher than Tropilaelaps because there was high intraspecies competition among Tropilaelaps. Single Varroa or its co-occurrence with Tropilaelaps both can destroy honeybee colonies.

Several Mites are currently the most serious threat to the world bee industry. The ectoparasitic honey bee mites was originally confined to the Asian honey bee(Apis cerana etc.). Varroa destructor and Tropilaelaps clareae has plagued European honey bees, Apis mellifera. Differences in mite tolerance are reported between two honey bee species A. mellifera and A. cerana. We were amplified antimicrobial peptide cDNA genes (Defencin, Abaecin, Royalisin, Apidaecin and Hymenoptaecin) by RT-PCR. We explored the transcriptional response to mite parasitism in A. mellifera 4th instars larvae which differ in susceptibility to V. destructor and T. clareae, comparing parasitized and non-parasitized 4th instars larvae (worker and Drone) from same hive. Differential gene expression of worker bees and Drone bees induced by mites (V. destructor and T. clareae) infection was investigated by northern blot. Mites (V. destructor and T. clareae) parasitism caused changes in the expression of genes related to sex distinction. Bees tolerant to mites (V. destructor and T. clareae) were mainly characterized by differences in the expression of genes regulating antimicrobial gene expression. It provides a first step toward better understanding molecular expression involved in this differential sex distinction host-parasite relationship. We were detected bee virus in A. mellifera, comparing parasitized and non-parasitized 4th instars larvae (worker and Drone). Therefore, this result was demonstrated that mites were another possible route of horizontal transmission, as several viruses were detected in mites and their hosts.

The ectoparasitic honey bee mites was originally confined to the Asian honey bee(Apis cerana etc.), mites had become widely established in the world and have continued to cause extensive bee colony deaths. Mites attach to adults and developing brood, where they feed on their blood. If left untreated, mites can deform bees and eventually kill the colony. Varroa destructor and Tropilaelaps clareae has plagued European honey bees, Apis mellifera. Differences in mite tolerance are reported between two honey bee species A. mellifera and A. cerana. We were counted number of mites(V. destructor and T. clareae) form 20 colonies. V. destructor and T. clareae has very similar behavior in honeybee colony. When behaviorally close, two competing species may populational interfere, and thereby affect their population dynamics. We tested for populational interference (PI) between two populational competing honeybee mites, V. destructor and T. clareae, by investigating their population dynamics when they competed on the same colony.

Modeling the complex system often provide better understanding of the behavior of the system given that parameters for the modeling are appropriate. The honeybee mite, Varroa destructor Anderson and Trueman, is one of the most serious pests of honeybees in Korea. Even with vast amount of ecological information of this parasite and its host, Apis mellifera, in the world, limited information is available in Korean environment. This paper provides some basic framework of the varroa mite population dynamics modified from published works in western world to adapt to Korean beekeeping environment. Overall population growth rate was in agreement to those previous published. However the detail behavior was quite different mainly because of splitting honeybee colony during the summer season. Although this framework provide reasonable, logical theoretical linkage to varroa mite population growth, implementation of the results provided from this model is not appreciated mainly because this paper is intended to show the basic framework, not the simulated results. Thus, further incorporation of realistic parameters from honey bee and its parasites in Korean environment would provide better insight of the population behavior and management options. Also, research gaps which need to be filled are further discussed.

Varroa destructor is an ecto-parasite mite and worldwide pest of the honey bee Apis mellifera L. The pyrethroid tau-fluvalinate (Apistan), an acaricide that is tolerated by honey bees, has been used for varroa mite control since the mid 1980s. Even though various resistances to tau-fluvalinate in varroa mites have been reported from Europe, Israel, and USA, the nature of tau-fluvalinate resistance in varroa mites in Korea has never been investigated. To investigate and understand tau-fluvalinate resistance in varroa mites in Korea, we conducted bioassay in several apiaries located different regions in Korea. To understand the molecular mechanisms underlying the difference of tau-fluvalinate resistances in varroa mites, partial genomic DNA fragments of a voltage-sensitive sodium channel gene from varroa mites were cloned and sequenced, since tau-fluvalinate is known to act on the sodium channels directly. Two novel mutations in sodium channels of varroa mites were present in eight apiaries. Two mutations might be a geographical polymorphism of sodium channel of varroa mites in Korea.

Varroa destructor Anderson & Trueman is the most injurious parasitic pest of honeybee in the world. Varroa mites had been originally external parasites of Asian honeybee (Apis cerana Fab.) in south eastern Asia. They jumped to European honeybees (Apis mellifera L.) by 1963. Since then they have killed millions of European honeybee colony, which might be susceptible to them, in Asia, Europe, America, and Africa. Also in Korea since Varroa mites were first found in 1968, they have been destructive pests in most of A. mellifera apiaries. Varroa destructor commonly infesting the European honeybees was classified in 2000 as a different species from the Varroa jacobsoni originally identified on Asian honeybees. Varroa mites not only feed the haemolymph of bees, but also introduce virulent viral diseases, and interrupt the development of bee colony. The other external parasitic mite, Tropilaelaps clarea Delfinado & Baker, which was introduced in 1994 from China, has widely spread and also brought damages on honeybees.