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Veterinary Pest Genomics Center Overview

The Veterinary Pest Genomics Center (VPGC) is an initiative within the US Department of Agriculture's Agricultural Research Service (ARS). The vision for this initiative is to leverage big data solutions to evaluate risk from, and develop mitigations for invasive and other economically important veterinary pests. The introduction of invasive veterinary pests is accelerated by global change, including anomalies related to climate variability. An important aspect of this effort is to foster an innovation ecosystem involving the network of laboratories directly linked to ARS National Program 104 (Veterinary, Medical, and Urban Entomology), and related locations, in a way that allows ARS to leverage its scientific talent and other research assets.

VPGC's mission is to:

  1. Utilize key biological resources, next generation sequencing technology, and state-of-the-art bioinformatics approaches to sequence and annotate the genomes, transcriptomes, proteomes and metagenomes of important and emerging arthropod pests of veterinary importance
  2. Develop and use molecular tools for population genomics studies of veterinary pests in their indigenous and invasive ranges to understand the role of different evolutionary forces in shaping phenotypic variation of high-consequence to agriculture
  3. Apply biogeographic, spatial, and temporal analyses to quantify and predict economically important or potential veterinary pest distributional changes, and integrate these analyses with genetic studies of rapid evolution and adaptation of pests to new or changing environments
  4. Conduct feasibility studies to evaluate advanced computing hardware and software systems for their ability to store and analyze large data sets on veterinary pests, and the capacity to integrate results from longitudinal
    environmental assessments

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VPGC Datasets

4 datasets

Data from: Deer keds and blacklegged ticks infesting ungulates in the United States: molecular detection of Bartonella spp., Rickettsia spp., Anaplasma spp., and Borrelia spp.

    Deer keds are blood-feeding flies from which several human and animal pathogens have been detected, including the causative agent of Lyme Disease (Borrelia burgdorferi). Cervids, which are the primary hosts of deer keds, are not natural reservoirs of B. burgdorferi, and it has been suggested that deer keds may acquire bacterial pathogens by co-feeding near ticks that are infected with the bacteria. We tested this hypothesis by using a molecular assay to screen for presence of Anaplasma spp., Bartonella spp., Borrelia spp., and Rickettsia spp. in specimens of European deer keds (n=306) and blacklegged ticks (n=315) collected from 38 individual white-tailed deer in Pennsylvania. There was limited similarity in the bacterial DNA detected between these ectoparasites per host, suggesting that co-feeding may not be a mechanism by which deer keds acquire these bacteria.

    Annotated reference transcriptome for female Culicoides sonorensis biting midges

      Unigene sequences were annotated by BlastX alignment to the non-redundant protein database (National Center for Biotechnology Information/GenBank) and the Aedes aegypti and Culex quinquefasciatus gene annotations (Vectorbase). This was done with a 1e-05 expectation value. Top hits are shown including accession numbers and description, if available. Unigene number and corresponding GenBank accession numbers are provided for all C. sonorensis genes.