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2006 merck/merial - School of Veterinary Medicine - Louisiana State ...

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eeding grounds near Minnedosa, MB spring <strong>of</strong> 2004 and near St. Denis, SK spring <strong>of</strong> 2005 and <strong>2006</strong>. Fall samples werecollected from waterfowl trapped in large bait traps at banding stations south <strong>of</strong> Moose Jaw, SK in 2004 and 2005. Sampleswere also collected from hunter-killed ducks in fall <strong>of</strong> 2005. Blood samples (3 ml) were collected from the right jugular vein<strong>of</strong> live-caught birds and ducks were classified according to age, sex and species. Samples were centrifuged at 4000 rpm for 8minutes and serum was stored for further analysis at -80¨¬C. Serum samples were tested for presence <strong>of</strong> neutralizingantibodies using WNV-specific blocking ELISA. A sample was considered positive for WNV if the absorbance valuedetermined by ultraviolet spectrophotometry was ¡Â 70% <strong>of</strong> the absorbance value <strong>of</strong> the negative reference serum. Betweenspring <strong>of</strong> 2005 and <strong>2006</strong>, 440 samples were collected from Mallards (Anas platyrhynchos), Blue-winged Teal (Anas discors),Northern Pintails (Anas acuta) and Redheads (Aythya americana). Initial results have shown 18% prevalence <strong>of</strong> WNVantibodies in adult male mallards in fall <strong>of</strong> 2005 compared to 10% prevalence in spring <strong>of</strong> <strong>2006</strong>. Juvenile male mallards showthe reverse trend, 0% prevalence in fall <strong>of</strong> 2005 compared to 18.5% prevalence in spring <strong>of</strong> <strong>2006</strong>. Further analysis isunderway to compare trends <strong>of</strong> male mallard populations to prevalence <strong>of</strong> WNV antibody in different species, sexes, andages <strong>of</strong> waterfowl.An Epidemiological Study <strong>of</strong> Leptospirosis in Champaign County CaninesJacqueline Scapa*, Dr. Marylin Ruiz, Dr. NamJung Jung, and Dr. Carol Maddox<strong>Veterinary</strong> Diagnostic Laboratory/Department <strong>of</strong> <strong>Veterinary</strong> Pathobiology, College <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong> at theUniversity <strong>of</strong> Illinois at Urbana, Champaign.Leptospirosis is a bacterial disease caused by any one <strong>of</strong> sixteen species and 2,000 serovars <strong>of</strong> the spirocheteLeptospira. This study is designed to examine the correlation between cases <strong>of</strong> Leptospirosis in the canine population <strong>of</strong>Champaign County and ponds or other bodies <strong>of</strong> water containing Leptospira. Suburban retention ponds in the new housingdevelopments <strong>of</strong> Champaign County may serve as exposure sites for pets and pet owners who frequent the area on walks orduring other recreational activities. Advanced GIS s<strong>of</strong>tware and GPS mapping has permitted the selection <strong>of</strong> ponds based ontheir proximity to cases <strong>of</strong> canine Leptospirosis.Real-time Polymerase Chain Reaction was used to determine the presence <strong>of</strong> Leptospira in every pond sampled thusfar, providing evidence that these ponds, contaminated by wildlife with endemic Leptospira infections, may serve as thereservoirs responsible for the infection in canines. Investigation is currently underway to determine if these ponds containpathogenic Leptospira serovars.Epidemiology <strong>of</strong> feline pathogenic hemoplasma infectionsJeralyn Terry and Dr. Jane Sykes, BVSc(Hons), PhD, DACVIMDepartment <strong>of</strong> <strong>Medicine</strong> & Epidemiology<strong>School</strong> <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong>, University <strong>of</strong> California, DavisUntil recently, only two hemotropic mycoplasmas (hemoplasmas) were identified as causes <strong>of</strong> feline infectiousanemia: Mycoplasma haem<strong>of</strong>elis (Mhf) and Candidatus Mycoplasma haemominutum (Mhm). Recently, a third type <strong>of</strong>hemoplasma was identified as being prevalent in Swiss cats, which has been named Candidatus Mycoplasma turicensis(Mtc). In addition, an organism related to the newly discovered canine organism, Candidatus Mycoplasma haematoparvum(Mhp-like) was identified in two cats presenting to the UC Davis <strong>Veterinary</strong> Medical Teaching Hospital. Theseepierythrocytic bacteria are best diagnosed using the polymerase chain reaction (PCR), as cytological evaluation <strong>of</strong> bloodsmears has low sensitivity and specificity. Infection with Mhf or Mtc has been associated with anemia in immunocompetentcats, whereas Mhm appears only to cause anemia in immunosuppressed cats. In addition, Mhm has been described as havinga synergistic effect with underlying retroviral (FeLV) infections in causing anemia and possible progression <strong>of</strong>myeloproliferative disease.We hypothesize that other unidentified types <strong>of</strong> hemoplasmas may be prevalent in anemic cats throughout theUnited <strong>State</strong>s, and that in contrast to a recent study in Europe, hemoplasma infection is associated with retroviral infection inthe United <strong>State</strong>s. The purpose <strong>of</strong> this study is to evaluate the prevalence, risk factors, and hematologic variables associatedwith hemoplasma infection in cats suspected to have hemoplasmosis from throughout the United <strong>State</strong>s. Blood smears andEDTA blood samples have now been collected through IDEXX Laboratories from over 300 cats that have had completeblood counts performed from various parts <strong>of</strong> the United <strong>State</strong>s. All samples will be tested using ELISA assays for FeLV andFIV. DNA will be extracted from samples using automated (Corbett) extraction methods. Each sample will be subjected toboth conventional and real-time PCR for Mhm, Mhf, and Mtc. PCR products from samples testing positive with conventionalbut not real-time PCR will be sequenced to determine whether a novel organism is present. The relationship betweeninfection with each hemoplasma species, signalment, geographic location, CBC results, retroviral status, and whether or notbacteria were visualized on cytology will be determined using appropriate statistical analyses.154

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