2013 Annual Report
1a.Objectives (from AD-416):
The parasitic mite Varroa destructor is the central pest of domesticated and free-living honey bee, causing direct impacts on bee health as well as indirect effects caused by vectoring viruses and other bee disease agents. We propose to use emerging high-throughput sequencing techniques to sequence, assemble and annotate the genome of this mite, and use the resulting insights to improve honey bee health and crop pollination. We will increase project impacts through a cost-effective partnership across existing academic sequencing and informatics centers and by choosing appropriate sequencing techniques for specific questions. We will leverage this project by engaging ca. 40 academic and governmental researchers in a volunteer consortium, 22 of whom met along with nine industry leaders for an initial ‘Varroa Genome Workshop’ in January, 2009, at the American Beekeeping Federation Annual Convention, Reno Nevada.
1b.Approach (from AD-416):
We will continue genomic sequencing to 20x coverage with an ‘optimal’ mix of straight and end-pair 454 reads, followed by genome assembly. Transcriptome surveys will be carried out using 454 pyrosequencing, focused on.
2)host finding (tarsal
3)immune responses (gut with and without virus infection), and.
SNPs and protein polymorphism will be discovered using the ABI SOLiD platform on the mite
transcriptome. These data will be aligned with homologous sequence data from the genome
reads and from the 454 transcriptome reads to give an abundance of SNPs. Development and testing of a canonical gene will be followed by Integration and posting of emerging data
via Beebase, NCBI, and other public databases.
Samples were collected from multiple life stages from both male and female varroa mites and ribonucleic acid (RNA) was extracted. These samples have been processed for RNA sequencing and sequences are currently being assembled with bioinformatic tools at the University of Maryland.