The purposes of this study were to describe the clinical signs observed in PRRS positive herds during a porcine reproductive and respiratory syndrome (PRRS) outbreak in Ontario and to determine associations between these clinical signs and herd demographics and PRRS control strategies. All PRRS polymerase chain reaction-(PCR)-positive submissions to a diagnostic laboratory between September 1, 2004 and August 31, 2007 were identified (n = 1864). After meeting eligibility requirements and agreeing to voluntary study participation, producers from 455 of these submissions were surveyed for information on clinical signs observed in their herds, herd demographics, and PRRS control strategies used in their herds at the time that the PCR-positive samples were taken. Larger herd size was associated with an increased risk of reporting abortion, weakborn piglets, off-feed sows, and sow mortality in sow herds, and with an increased risk of reporting mortality in finishing herds. When disease control strategies were examined, use of a commercial PRRS vaccine in sows and gilts was associated with a decreased risk of reporting weakborn pigs and high pre-weaning mortality, while the use of serum inoculation in breeding animals was associated with an increased risk of reporting off-feed sows and sow mortality. Providing biofeedback of stillborn/mummified piglets, placenta or feces to gilts was associated with an increased risk of reporting respiratory disease and mortality in finishing pigs while all-in/all-out flow in farrowing rooms was associated with an increased risk of reporting sow mortality and weakborn piglets.

The objective of this project was to develop and implement an active surveillance program for the early and rapid detection of equine influenza viruses in Ontario. For this purpose, from October 2003 to October 2005, nasopharyngeal swabs and acute and convalescent serum samples were collected from 115 client-owned horses in 23 outbreaks of respiratory disease in Ontario. Sera were paired and tested for antibody to equine influenza 1 (AE1-H7N7), equine influenza 2 (AE2-H3N8), equine herpesvirus 1 and 4 (EHV1 and EHV4), and equine rhinitis A and B (ERAV and ERBV). Overall, the cause-specific morbidity rate of equine influenza virus in the respiratory outbreaks was 56.5% as determined by the single radial hemolysis (SRH) test. The AE2-H3N8 was isolated from 15 horses in 5 outbreaks. A 4-fold increase in antibody levels or the presence of a high titer against ERAV or ERBV was observed in 10 out of 13 outbreaks in which AE2-H3N8 was diagnosed as the primary cause of disease. In conclusion, AE2-H3N8 was found to be an important contributor to equine respiratory viral disease. Equine rhinitis A and B (ERAV and ERBV) represented an important component in the equine respiratory disease of performing horses.

Wound healing is a fundamental response to tissue injury and several natural products have been shown to accelerate the healing process. The present study was undertaken to determine the safety and efficacy of the topical treatment of acetone leaf extracts of Combretum imberbe, Combretum nelsonii, Combretum albopuntactum and Terminaliasericea based on their in vitro antimicrobial activity. Four circular full-thickness skin wounds were made on the backs of eight anaesthetised Wistar rats using aseptic techniques. The treatments were administrated topically using 10% and 20% concentrations of each extract in aqueous cream in separate treatments. Indications of erythema, exudate, crust formation, swelling and ulceration were used to determine the wound healing process. All of the wounds closed completely within 17 days. Throughout the experiment, a subcutaneous probe was used to determine that the body temperature and body weight of the rats were within the normal range. C. imberbe and C. nelsonii extracts accelerated wound healing, but there was no significant difference in wound contraction using 10% and 20% concentrations of the extracts in cream. The results also showed the potential usefulness of this model to measure accelerating wound healing. The extracts could perhaps overcome defects associated with healing failure in chronic wounds and prevent secondary bacterial and fungal infections.

Male Japanese black bears (Ursus thibetanus japonicus) have an explicit reproductive cycle. The objective of this study was to clarify the variation of plasma testosterone, FSH, inhibin, LH levels and testicular gonadotropin receptor mRNA expression of male bears associated with their testicular activity. Notably, this study investigated peripheral FSH concentration and localization of gonadotropin receptor mRNAs for the first time in male bears. Blood and testicular tissue samples were taken from captive, mature, male Japanese black bears during testicular active, regressive and recrudescent phases. Plasma hormone concentrations were measured by immunoassays, and gonadotropin receptor mRNA expression in the testis was investigated by in situ hybridization technique and also by real-time PCR. There were significant variations in plasma testosterone and inhibin concentrations. Changes in FSH concentration preceded these hormones with a similar tendency. Hormones started to increase during denning, and achieved the highest values at the end of the recrudescent phase for FSH and in the active phase for testosterone and inhibin. These changes in hormone concentrations were accompanied by testicular growth. In situ hybridization analysis revealed that FSH and LH receptor mRNA was possibly expressed in Sertoli cells and Leydig cells, respectively, as they are in other mammals. However, neither plasma LH concentration nor testicular gonadotropin receptor mRNA expression level varied significantly among the sampling months. These results suggest that FSH, inhibin and testosterone have roles in testicular activity in male bears. This study provides important endocrine information for comprehending seasonal reproductivity in male Japanese black bears.

The mRNA from distal ileum of Indian goat was cloned and characterized after purification. cDNA was synthesized using goat ileal epithelial RNA, omniscript and sensiscript reverse transcriptase and amplified by Hotstart Taq DNA polymerase with primers designed by taking conserved regions of cattle enteric _Ò-defensin, cattle lingual antimicrobial peptide(LAP) and goat _Ò-defensin-2 sequences. The amplified cDNA of 253bp was, ligated to linearised TA cloning vector and transformed into XLblue strain of E.coli which was grown overnight at 37oC in a LB plate containing ampicillin, IPTG and X-Gal. The recombinant plasmid was isolated and digested with NcoI. The white colonies showed a release of 253bp insert. The sequence analysis showed 26, 16 and 5-nucleotide substitution having 85.6%, 91.3%, 97.4% homology with reported cattle EBD, buffalo EBD and goat BD2 mRNA respectively. The deduced amino acid sequence encodes for a 64 amino acid precursor peptide showing 12,18 and 4 amino acid substitution having 80%, 70.8%, 93.8% homology with buffalo EBD, cattle EBD and goat BD2 peptide respectively. Both nucleotide and amino acid sequence homology showed that the cloned sequence was closer to goat BD2.

The effect of addition of Melia azedarach (fruit), Pimpinella anisum (seed), Cuminum cyminum linn (seed), Murraya koenigii (leaves), Emblica officinalis (fruit), Allium sativum linn (bulb), Terminalia arjuna (bark), Sapindus trifoliatus (seed), Zingiber officinale (rhizome), Trigonella foenun-graecum (seed) at three dose level (1.5%, 2.0% and 3.0% of DM) on pH, dry matter and organic matter digestibility of feed was studied with rumen liquor of goat. There was no significant change in the in vitro fluid pH, showing no adverse effect of herb addition. The addition of all the herbs at 1.5% level had no significant (P 0.05) effect on in vitro dry matter and organic matter digestibility. There was slight improvement in dry matter and organic matter digestibility with the addition of Trigonella foenungraecum at 2% level as compared to control. At 3% level of addition of this herb, there was significant (P 0.05) increase in the in vitro dry matter digestibility (%) with Trigonella foenun-graecum (51.97) as compared to control (43.95). Similarly there was significant (P 0.05) increase in the in vitro organic matter digestibility (%) with Trigonella foenun-graecum (54.95) as compared to control (46.87) having with no addition of herbs. So Trigonella foenun-graecum (seed) at 3% dose level can be further explored in in vivo experiment to utilize it as a feed additive to increase the digestibility of feed in goats.

Therapeutic and anti-oxidant potential of vitamin E and selenium was evaluated in mastitic cows. The CMT point score and milk somatic cell count (SCC) was significantly (P0.05) higher in mastitic cows prior to treatment. Reduced activity of enzymatic anti-oxidant catalase was observed in mastitic animals. The parameters studied in mastitic cows treated amoxicillin sulbactum (group II) and with amoxicillin sulbactum, vitamin E and selenium (group III) were compared with that of group I healthy cows. Significant reduction (P0.05) in CMT and SCC was observed in both the treated groups. However, reduction in CMT point score and SCC was more pronounced in group III than group II cows. Synergistic action of antibiotic and vitamin E selenium significantly (P0.05) enhanced the activity of catalase in group III mastitic animals on day 8 time period. Therefore, vitamin E and selenium supplementation could be advised in the therapy of mastitis.

Recombinant LipL32 and LipL41 outer membrane proteins of Leptospira interrogans serovar Canicola were produced, and used as a pooled antigen in enzyme-linked immunosorbent assay (ELISA) to detect leptospiral antibodies in bovine sera samples. The optimum concentration of the pooled antigen was found to be 50ng of each antigen per well by using known positive and negative cattle sera. Using a total of 500 bovine sera samples the sensitivity, specificity and accuracy of pooled antigen based ELISA as compared to microscopic agglutination test (MAT) were 100%, 88.1% and 91.6%, respectively. The results suggested that antigen in ELISA could be preferred for detection of all those cases, which might have remained undiagnosed by performing MAT.

Currently the diagnosis of renal diseases is based on thorough history, clinical examination, urinanalysis and investigation of hemato-biochemical profiles. But biochemical markers are not sensitive to detect early renal damage. Also usefulness of their estimation is limited in early renal failure when marked reduction of GFR may be associated with little change in their concentration. At present imaging is an important diagnostic tool for early precise diagnosis. Scintigraphy is a less known diagnostic imaging technique in veterinary medicine, although it is similar to competitive methods such as radiography, ultrasound and endoscopy. By all the other methods only morphological objects can be visualized whereas scintigraphy has the advantage of the so-called physiological imaging. Scintigraphy is able to visualize and quantitate distribution of different materials in living organisms indicating normal [physiological] or abnormal (pathological) processes of the object. This is a sensitive, specific and non-invasive diagnostic method supporting clinician's diagnosis, as a part of combined modality-imaging systems; it gives useful data for veterinary clinicians. Present study was planned to standardize the scintigraphic profile for healthy dogs. Perfusion index Mean ± S.D. for right kidneys and left kidney was 154.7 ± 40.05 and 169.0 ± 46.0. The mean percent uptake at 2-3 minutes was 53.56 ± 6.17 and 46.46 ± 6.17 for right and left kidney. Time taken to Peak (TPP) minute, which indicates efficiency of blood flow at both the kidneys, was 3.12 ± 1.21 and 3.03 ± 1.22 min for right and left kidney respectively. The T½ from peak count [min] for right and left kidney was 5.02 ± 2.24 and 5.15 ± 3.6 min. The GFR for right and left kidneys was 68.79 ± 33.67 and 61.62 ± 31.92, respectively and the normalized GFR when both the kidneys are considered together in healthy dogs was 439.48 ± 55.67.