Source: GEORGETOWN UNIVERSITY submitted to
GENOME CHARACTERIZATION OF THE MITE VARROA DESTRUCTOR, THE PRIMARY PEST OF HONEY BEES
Sponsoring Institution
Agricultural Research Service/USDA
Project Status
TERMINATED
Funding Source
Reporting Frequency
Annual
Accession No.
0421249
Grant No.
(N/A)
Project No.
1275-21000-090-25G
Proposal No.
(N/A)
Multistate No.
(N/A)
Program Code
(N/A)
Project Start Date
May 2, 2011
Project End Date
Jan 31, 2013
Grant Year
(N/A)
Project Director
EVANS J D
Recipient Organization
GEORGETOWN UNIVERSITY
37th & O STREETS NW
WASHINGTON,DC 20057
Performing Department
(N/A)
Non Technical Summary
(N/A)
Animal Health Component
(N/A)
Research Effort Categories
Basic
40%
Applied
40%
Developmental
20%
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
21130101130100%
Goals / Objectives
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.
Project Methods
1) Continued genomic sequencing to 20x coverage with an ¿optimal¿ mix of straight and end-pair 454 reads, followed by genome assembly; 2) Transcriptome surveys using 454 pyrosequencing, focused on: a) nymphal development, b) host finding (tarsal library), c) immune responses (gut with and without virus infection), and d) gut microbes; 3) SNP and protein polymorphism discovery using the ABI SOLiD platform on the mite transcriptome. Mites will be from the Midwestern, Southern, mid-Atlantic and Western U.S. as well as ¿outgroups¿ from Australia and France. These data will be aligned with homologous sequence data from the genome reads (Maryland mite), and from the 454 transcriptome reads to give an abundance of SNPs; and 4) Development and testing of a canonical gene set and posting of emerging data via Beebase, NCBI, and other public databases.

Progress 05/02/11 to 01/31/13

Outputs
Progress Report 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. Approach (from AD-416): 1) Continued genomic sequencing to 20x coverage with an �optimal� mix of straight and end-pair 454 reads, followed by genome assembly; 2) Transcriptome surveys using 454 pyrosequencing, focused on: a) nymphal development, b) host finding (tarsal library), c) immune responses (gut with and without virus infection), and d) gut microbes; 3) SNP and protein polymorphism discovery using the ABI SOLiD platform on the mite transcriptome. Mites will be from the Midwestern, Southern, mid-Atlantic and Western U.S. as well as �outgroups� from Australia and France. These data will be aligned with homologous sequence data from the genome reads (Maryland mite), and from the 454 transcriptome reads to give an abundance of SNPs; and 4) Development and testing of a canonical gene set and posting of emerging data via Beebase, NCBI, and other public databases. In the current year, the collaborator relocated to the University of Missouri and this agreement has ended and has been reinitiated at the University of Missouri for the coming year. Progress was made on a gene set for mites that will provide tools for developing novel miter controls.

Impacts
(N/A)

Publications


    Progress 10/01/11 to 09/30/12

    Outputs
    Progress Report 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. Approach (from AD-416): 1) Continued genomic sequencing to 20x coverage with an �optimal� mix of straight and end-pair 454 reads, followed by genome assembly; 2) Transcriptome surveys using 454 pyrosequencing, focused on: a) nymphal development, b) host finding (tarsal library), c) immune responses (gut with and without virus infection), and d) gut microbes; 3) SNP and protein polymorphism discovery using the ABI SOLiD platform on the mite transcriptome. Mites will be from the Midwestern, Southern, mid-Atlantic and Western U.S. as well as �outgroups� from Australia and France. These data will be aligned with homologous sequence data from the genome reads (Maryland mite), and from the 454 transcriptome reads to give an abundance of SNPs; and 4) Development and testing of a canonical gene set and posting of emerging data via Beebase, NCBI, and other public databases. The subcontract has focused on bioinformatic analyses for this project. A second genome assembly was built and is now available for the public. The results from these analyses are shared with mite and honey bee researchers and are actively being used to resolve weak points in Varroa mites as well as the availabilities of mites to carry viruses and other bee disease organisms. The subcontractee has posted genomic assembly and annotation data on their own servers and made this information accessible to a wide community.

    Impacts
    (N/A)

    Publications


      Progress 10/01/10 to 09/30/11

      Outputs
      Progress Report 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. Approach (from AD-416) 1) Continued genomic sequencing to 20x coverage with an �optimal� mix of straight and end-pair 454 reads, followed by genome assembly; 2) Transcriptome surveys using 454 pyrosequencing, focused on: a) nymphal development, b) host finding (tarsal library), c) immune responses (gut with and without virus infection), and d) gut microbes; 3) SNP and protein polymorphism discovery using the ABI SOLiD platform on the mite transcriptome. Mites will be from the Midwestern, Southern, mid-Atlantic and Western U.S. as well as �outgroups� from Australia and France. These data will be aligned with homologous sequence data from the genome reads (Maryland mite), and from the 454 transcriptome reads to give an abundance of SNPs; and 4) Development and testing of a canonical gene set and posting of emerging data via Beebase, NCBI, and other public databases. This research contributes to the Build a Genome Project for Varroa mites, a central pest of honey bees worldwide, and a key research pest in the parent project. The results will enhance the bioinformatic analyses of this project. One genome assembly has been generated and the genes on this assembly have been described in Genbank and in one summary manuscript. Progress on further work is monitored by monthly phone calls and frequent e-mail communication with Georgetown University.

      Impacts
      (N/A)

      Publications