<strong>2006</strong> MERCK/MERIALVETERINARY SCHOLARSYMPOSIUMABSTRACTS72
CLINICAL SCIENCES AND BEHAVIOR (SESSION 1)Prevalence and Risk Factors for Heartworm Infection in Dogs in the United <strong>State</strong>s, 2002-2005Evan N. Apotheker 1 , Nita W. Glickman 1 , Hugh B Lewis 2 , Larry T. Glickman 1Purdue University, West Lafayette, IN 1 , Banfield the Pet Hospital, Portland, OR 2Heartworm infection caused by Dir<strong>of</strong>ilaria immitis is widespread in dogs in the United <strong>State</strong>s and may result in apotentially fatal disease. Mosquitoes transmit D. immitis using dogs as both the definitive host and reservoir. Smallerregional studies have examined the epidemiology <strong>of</strong> heartworm disease but few national surveys have been conducted.Computerized medical records <strong>of</strong> dogs visiting >500 Banfield Pet Hospitals located in 44 states were analyzed to estimatethe prevalence <strong>of</strong> heartworm infection in dogs and to characterize risk factors for infection. Infection with D. immitis wasdetermined based on a positive heartworm antigen ELISA. The number <strong>of</strong> dogs tested, the total number <strong>of</strong> tests performed, aswell as the dog’s age sex, breed, weight and neuter status, and state <strong>of</strong> residence, were determined. The prevalence <strong>of</strong>heartworm infection was 1.46% in dogs tested between January 1, 2002 and December 31, 2005. The prevalence wassignificantly higher in the South Atlantic, Gulf Coast, and Mississippi River Valley regions. Host factors significantly (P1 year, weight >25 lbs, sexually intact, and being amixed breed versus a pure breed dog. These results suggest the amount <strong>of</strong> outdoor activity and level <strong>of</strong> owner care influencethe risk <strong>of</strong> heartworm infection in dogs. The geographical pattern <strong>of</strong> heartworm infection observed in this study was similarto findings reported by the American Heartworm Society based on questionnaires to veterinary practices. Findings <strong>of</strong>epidemiological studies using large computerized databases such as Banfield’s national pet practice can be used to improvethe quality <strong>of</strong> health care and disease prevention for all pets.Immunohistochemical analysis <strong>of</strong> cytochrome P4501A1 (CYP1A1) induction in the skin, blubber and liver<strong>of</strong> harbor seal pups (Phoca vitulina) stranded along the California coast.Trevor S. Arnold* 1 , Andrea L. Bogomolni 2 , Michael Ziccardi 1 , John J. Stegeman 2Wildlife Health Center, UC Davis <strong>School</strong> <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong>, Davis California 1Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 2Marine mammals are exposed to a variety <strong>of</strong> environmental contaminants which can increase their risk <strong>of</strong>developing several health problems such as immune suppression and reproductive complications. While direct measurement<strong>of</strong> contaminants in tissues is possible, the techniques are expensive and require specialized equipment. Also, directmeasurement does not indicate toxicity, as contaminants can be sequestered in tissues (e.g. adipose) and many only exerttheir toxicity via metabolites. Cytochrome P4501A1 (CYP1A1) is induced by certain organic pollutants and is essential forthe metabolism <strong>of</strong> many biologically important contaminants, such as polycyclic aromatic hydrocarbons (PAH), coplanarpolychlorinated biphenols (PCB), tetrachlorodibenodiozins (TCDD) and tetrachlorodibenz<strong>of</strong>urnans (TCDF). This studyemploys immunohistochemistry to determine the levels <strong>of</strong> CYP1A1 induction in neonatal harbor seals (Phoca vitulina). Amonoclonal antibody against scup (Stenotomus chrysops) Cytochrome P4501A (MAb 1-12-3) was used to stain CYP1A1protein in the skin/blubber and liver <strong>of</strong> harbor seal pups that stranded along the coast <strong>of</strong> California. By comparingskin/blubber CYP1A1 induction to liver induction this study is intended to add evidence towards validating the use <strong>of</strong>minimally invasive skin biopsies rather than liver biopsies to determine whole body CYP1A1 activity, and thereforesimultaneously assess contaminant load and toxicity. Preliminary data indicate that CYP1A1 activity is low in bothskin/blubber and liver tissues from the pups sampled. Analysis is currently underway to determine the degree <strong>of</strong> correlationbetween skin/blubber and liver CYP1A1 induction. Data also indicates the presence <strong>of</strong> a possible endogenous CYP1A1inducer in the sebaceous glands <strong>of</strong> harbor seals.Optimization and Validation <strong>of</strong> a Commercially Available Phagocytic Assay for Differentiation <strong>of</strong> AvianHeterophilsCatherine C. Ashe, B.A.*, Cheryl B.Greenacre, DVM, DAVBP (Avian), Stephen Kania, PhDUniversity <strong>of</strong> Tennessee College <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong>, Knoxville, TN 37996Department <strong>of</strong> Small Animal <strong>Medicine</strong> and the Department <strong>of</strong> Comparative <strong>Medicine</strong>Avian blood presents several problems for veterinary practitioners. Nucleated erythrocytes and thrombocytes makeautomated counting <strong>of</strong> white blood cells impossible. As a result, leukocyte counts must be generated manually. However,problems also exist with manual counts and differentials. Small lymphocytes and thrombocytes, as well as large lymphocytesand monocytes may appear morphologically similar. Thus, there exists no objective method for quantifying avian whiteblood cells. Preferred manual methods include the use <strong>of</strong> the Eosinophil Unopette 5877® system or Natt and Herrick’sSolution followed by counting <strong>of</strong> cells on a hemacytometer. These methods <strong>of</strong>fer neither the precision nor the ease <strong>of</strong> anautomated counter. This study seeks to find an objective method for identifying and segregating heterophil populations. Thefocus is tw<strong>of</strong>old. First, validation and optimization <strong>of</strong> a commercially available human phagocytosis assay was conducted.This assay uses fluorescently labeled (FITC), opsonized E. coli as a cell marker. Once validated and optimized, the assay was73
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2006 MERCK/MERIALNATIONAL VETERINAR
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3:00-3:30 pm BreakNovel therapy for
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KEYNOTE SPEAKERRonald Veazey, D.V.M
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Mini Symposium II:Fish Research: A
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David G. Baker, D.V.M., M.S., Ph.D.
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Konstantin G. Kousoulas, Ph.D.Profe
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Joseph Francis, B.V.Sc., M.V.Sc., P
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dogs with cancer, the potential rol
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2006 MERCK/MERIALVETERINARY SCHOLAR
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Adherent bacilli were present in th
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isolated to analyze cytokine gene e
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purified, viral RNA was extracted a
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The effects of co-engagement of TLR
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Occurrence of Leptospira Vaccine Fa
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undifferentiated catecholaminergic
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the concept that the greater detoxi
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quantitative PCR using gene targets
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Rotenone Induced Dopamine Neuron De
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decrease in serum cortisol, with a
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and detrimental impacts on the brai
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actions of cells prior to embryo de
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Utilizing cDNA Subtraction to Exami
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expression in unilaterally pregnant
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Salmonella is increased. Poultry sa
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exports. The estimated prevalence o
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eeding grounds near Minnedosa, MB s
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(PBMC) were isolated using commerci
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2006 MERCK/MERIALVETERINARY SCHOLAR
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Trainees acquire in-depth knowledge
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comparative pathology and/or resear
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Department of Veterinary Bioscience
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PhD, Director, Center for Comparati
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MICHIGAN STATEUNIVERSITYJames Crawf
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UNIVERSITY OFPENNSYLVANIALindsay Th