used to label avian heterophils for identification by a Beckman Coulter Epics XL flow cytometer. The assay is optimized forhumans at 37°C and 10 minutes incubation time. Avian species have a higher average body temperature, ranging from 40-43°C. First, optimization <strong>of</strong> phagocytosis by heterophils was attempted by increasing the incubation temperature from 37°Cto 43°C. Secondly, the incubation time was manipulated from 5 minutes to 20 minutes. Preliminary results indicate that alonger incubation time at a higher temperature increases phagocytic activity <strong>of</strong> avian heterophils. Once the assay iscompletely adjusted for use in avian species, the mean number <strong>of</strong> phagocytizing cells will be determined in the control group(4°C) and the non-control group. In conclusion, we found that this assay can be used to differentiate heterophils using a flowcytometer. Evaluation <strong>of</strong> immune function is the next step.The Effect <strong>of</strong> Pilot Hole Drilling on Temperature <strong>of</strong> Cortical Bone and Drill Hole Accuracy in EquineCadaveric Third Metacarpal BonesElizabeth Barno*, Timothy LescunPurdue University <strong>School</strong> <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong>; Lafayette, INTransfixation casting is becoming a more widely and successfully used technique in the treatment <strong>of</strong> equine distallimb fractures. It is a modified form <strong>of</strong> external skeletal fixation which involves the placement <strong>of</strong> transcortical pins in intactbone proximal to the fracture site, which are then incorporated into a fiberglass cast. One <strong>of</strong> the major problems encounteredwith this type <strong>of</strong> casting is the loosening <strong>of</strong> these pins over time. Thermal bone damage that occurs at the time <strong>of</strong> pinplacement has been shown to contribute to premature pin loosening. This damage may also compound loosening attributedto infection or cyclic loading. It has been suggested that drilling sequentially larger holes to achieve a 6.2 mm hole for pininsertion may help to minimize heat generated in the cortical bone during drilling. It is unproven, however, that thistechnique actually reduces thermal damage. It is also unknown whether the drilling <strong>of</strong> pilot holes alters hole accuracy. Inthis study we will observe cortical bone temperatures in cadaveric equine cannon bones during the drilling <strong>of</strong> a 6.2 mm holewith and without pilot hole drilling. Temperature <strong>of</strong> the drill bit upon exiting will be also be recorded. The insertion torquerequired to place a transfixation pin will be observed as one measure <strong>of</strong> hole accuracy. Hole accuracy will also be measuredby the resultant hole diameter at three depths <strong>of</strong> the cortex as determined with digital calipers. We hypothesize that thedrilling <strong>of</strong> pilot holes will generate lower cortical temperatures immediately adjacent to the hole when compared to thedrilling <strong>of</strong> a single 6.2 mm hole. We also hypothesize that the accuracy <strong>of</strong> these holes will not be different when using eitherpilot hole drilling or a single 6.2 mm drill bit. The results obtained from this study may aid in developing an optimaltransfixation pin placement protocol which is vital to increase the success <strong>of</strong> transfixation casting.Evaluation <strong>of</strong> the Skelite Anterior Cervical Fusion Device in SheepRiccardo Beltramo*, Jason Hendry, Howard B Seim III D.V.M., Dipl ACVS, , A. Simon Turner, B.V.Sc., M.S.Dipl. ACVS.Small Ruminant Comparative Orthopaedic Laboratory, Colorado <strong>State</strong> University, Ft. Collins, CO 80523The objective <strong>of</strong> this study is to evaluate the Skelite Anterior Cervical Fusion Device in sheep. This device consistsin a ceramic cage made <strong>of</strong> calcium and phosphate that ultimately will be used to fuse one or more <strong>of</strong> the cervical vertebrae inhumans who have neck pain. Anterior cervical spine fusion surgery after discectomy in humans, frequently involves the use<strong>of</strong> bone graft and an anteriorly placed containment plate to improve stability, increase fusion rates, and prevent movement orsubsidence <strong>of</strong> the graft. Taking a bone graft from the iliac crest (pelvis) <strong>of</strong> a person is not without risks (postoperative painmonths later, nerve damage, infection). In an attempt to avoid complications from a bone graft, we are testing a new ceramicinterbody fusion device in the sheep cervical spine with a commercially available ventrally (“anteriorly”) placed plate toprevent extrusion <strong>of</strong> the device. During the surgery two discectomies are performed in each <strong>of</strong> ten sheep between vertebraeC2/C3 and C4/C5. The gaps between the vertebral bodies are filled with an autograft (previously taken from the sternum) orwith the Skelite Anterior Cervical Fusion Device. In this way, each sheep is treated with one control and one ceramicimplant. Our main objective is to determine if histological fusion occurs when the ceramic is used, and to determine theresultant biomechanical characteristics <strong>of</strong> the fusion mass. The fusion sites (autograft versus ceramic device) will becompared in each animal. Evaluations will be made at 3 months (6 sheep) and 12 months (4 sheep). Because <strong>of</strong> this delay theresults are not available now. This study is to assess the feasibility <strong>of</strong> eventually using this ceramic device in anterior cervicalspine fusion surgery in humans. Following Food and Drug Administration approval, this will be an important adjunct forspine surgery in the cervical vertebrae in people with neck pain.74
A study to evaluate plasma substance P, cortisol response and salicylate concentration in bulls followingcastration with or without non-steroidal anti-inflammatory drug analgesiaAngela Bettenhausen*, Johann CoetzeeDepartment <strong>of</strong> Clinical Sciences, College <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong>, Kansas <strong>State</strong> University. Manhattan, KS.Pain and distress inflicted by normal husbandry procedures such as castration are major animal welfare concerns inbeef cattle production. Acute cortisol response has been used to determine the extent and duration <strong>of</strong> distress associated withcastration in cattle. However, plasma cortisol measurement also measures homeostasis and cannot reliably discriminatebetween a painful and a stressful response. The need for a robust, repeatable physiological indicator <strong>of</strong> distress for use in theassessment <strong>of</strong> production procedures and environments has been recognized. A strong candidate is substance P and wehypothesize that the measurement <strong>of</strong> the plasma concentrations <strong>of</strong> this substance may be a robust, repeatable physiologicalindicator <strong>of</strong> pain and distress in cattle following castration. A study was conducted to evaluate the relationship betweenplasma substance P concentrations and cortisol response in association with plasma salicylate concentrations in twenty bullsthat were surgically castrated. The impact <strong>of</strong> administration <strong>of</strong> aspirin and sodium salicylate on animal well-being isincluded in this study as an alternative management technique to be considered by producers to alleviate pain at the time <strong>of</strong>castration. A group <strong>of</strong> five bulls served as intact controls, five bulls served as castrated controls, five bulls received oralaspirin at the dose <strong>of</strong> 50 mg/kg BW prior to castration and five bulls received an injection <strong>of</strong> sodium salicylate at the dose <strong>of</strong>50 mg/kg BW prior to castration. Blood samples for substance P, cortisol, and salicylate determination were collected priorto castration, immediately following castration and at 10, 20, 30, 40, 50 and 60 minutes and at 1.5, 2, 4, 6, 8, 10 and 12 hoursthereafter. Plasma substance P was determined by competitive immunoassay, cortisol by chemiluminescent enzymeimmunoassay, and plasma salicylate was determined by commercial immunoassay.Real-time monitoring <strong>of</strong> Salmonella poultry isolates on chicken skinT.D. Bodet*, M.L. Lawrence, A. Karsi, R.H. BaileyCollege <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong>, Mississippi <strong>State</strong> University, Mississippi <strong>State</strong>, MSSalmonella, a member <strong>of</strong> the family Enterobacteriaceae, is a gram-negative bacteria that causes enteric disease inmultiple animal species. Infection occurs as a result <strong>of</strong> ingestion <strong>of</strong> the bacteria, and salmonellosis may or may not occurdepending on the amount <strong>of</strong> bacteria ingested and host susceptibility. Human infection is highly associated with poultry byconsumption <strong>of</strong> undercooked meat or eggs or by consumption <strong>of</strong> cross contaminated food. Therefore, it is important tounderstand and further investigate the locations and quantities <strong>of</strong> Salmonella within the bird and possible interventions thatcould be used to reduce the risk <strong>of</strong> human infection. Ten Salmonella serovars have been identified as posing the greatest riskto humans from poultry products: Typhimurium, Kentucky, Montevideo, Mbandaka, Thompson, Schwarzengrund, Alachua,Seftenberg, Braenderup, and Heidelberg. pAKlux1 is a plasmid expressing bacterial luciferase that allows real-time detectionand quantification <strong>of</strong> Salmonella using luminescence. This plasmid was successfully transferred by electroporation intopoultry isolates from nine <strong>of</strong> the ten serovars (electroporation attempts into serovar Braenderup were unsuccessful), and itwas transferred into a non-pathogenic strain from serovar Typhimurium. The minimum number <strong>of</strong> detectable bioluminescentSalmonella was estimated using an IVIS imaging system. Plasmid stability was considered in a 15 day experiment measuringthe bacteria’s luminescence in broth with and without antibiotic. A model was also developed to monitor the amount <strong>of</strong>Salmonella on chicken skin. The process <strong>of</strong> rinsing the bird in the chicken plant was mimicked by submerging the skin inagitated cold water to test for the removal <strong>of</strong> Salmonella.A comparison <strong>of</strong> limb speed and trunk speed in dogs <strong>of</strong> varying sizeBottorff, B.S., Kim, J., Breur, G.J.Purdue University <strong>School</strong> <strong>of</strong> <strong>Veterinary</strong> <strong>Medicine</strong>Gait analysis is an <strong>of</strong>ten underutilized diagnostic tool that may be used to identify features <strong>of</strong> specific gaitabnormalities and make gait comparisons regarding different populations. Most commonly it is used as a non-invasive,objective, and quantitative method to evaluate orthopedic injury or measure functional return after treatment. Most researchon gait has been conducted on large breed dogs. Before gait analysis can be widely used for clinical patients, the techniquesused in larger dogs may have to be validated in smaller dogs. For instance, in large dogs, subject’s trunk velocity ismeasured, assuming it is an accurate representation <strong>of</strong> limb velocity. While in certain instances this assumption may be true,in others it may not be completely accurate. As a result, other measurements <strong>of</strong> gait may be miscalculated as variations inlimb velocity have been shown to affect vertical impulse and ground reaction force data, along with other variables.The objective <strong>of</strong> this study is to describe the discrepancy between limb velocity and trunk velocity during gait in small andlarge breed dogs. Five dogs in each <strong>of</strong> two size classifications (small, not exceeding 20 lbs; and large, over 55 lbs.) will becompared using kinetic and kinematic methods to analyze limb and trunk velocity. Measurements for trunk velocity will beobtained via analysis <strong>of</strong> time required for subject’s trunk to interrupt 9 photocells placed at 0.5 m interval, as well asdisplacement <strong>of</strong> a marker on the center <strong>of</strong> mass with 2-dimensional video analysis. Limb velocity measurements will be75
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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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YOUNG INVESTIGATOR AWARD HONORABLE
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Occurrence of Leptospira Vaccine Fa
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the concept that the greater detoxi
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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