The aim of this study was to evaluate the protective efficacy of the CIRCOQ porcine circovirus type 2 (PCV2) subunit vaccine in piglets with high maternally derived antibodies (MDAs) against disease caused by natural infection with PCV2d. A total of 130 weaned, 21-day-old healthy pigs was allocated into 3 trial groups. The signs of respiratory disorder were higher in unvaccinated pigs than in vaccinated pigs at 13 to 17 weeks old (P < 0.05), 18 to 22 weeks old (P < 0.001), and 23 to 27 weeks old (P < 0.01). The unvaccinated pigs had an early rate of dermatitis at 8 to 12 weeks old (10.0%), 13 to 17 weeks old (30.0%), 18 to 22 weeks old (46.7%), and 23 to 27 weeks old (33.3%), while there were no cases of dermatitis in vaccinated pigs. There was a significant difference (P < 0.05) in the mortality of pigs in the unvaccinated group and the 2-dosed vaccinated group. PCV2 viremia was detected in the blood and peaked at 105 days old in both unvaccinated pigs (Ct-adj = 8.40) and pigs vaccinated with 1 dose (Ct-adj = 6.37), while no detectable PCV2 virus was found in the blood of pigs vaccinated with 2 doses. At 77 and 105 days old, the PCV2 viremia load (Ct-adj) of unvaccinated pigs and those vaccinated with 1 dose was significantly higher (P < 0.05) than that of the 2-dosed vaccinated pigs. The body weight (BW), average weight gain (AWG), and average daily gain (ADG) in both groups of vaccinated pigs were significantly higher (P < 0.05) than those of unvaccinated pigs. The study vaccine was significantly efficacious in protecting vaccinated pigs against clinical symptoms, blood viral load, and mortality, as well as improving productivity, compared with unvaccinated pigs.

C-reactive protein (CRP) is an acute phase protein, which is used to evaluate and monitor the response of the innate immune system to a variety of inflammatory processes in the dog. The purpose of this study was to analytically validate a point-of-care assay (IDEXX Catalyst CRP Test) and an immunoturbidimetric assay (Gentian Canine CRP Immunoassay) for the measurement of serum CRP concentrations in dogs. These 2 assays (Catalyst, Gentian) were compared to a previously validated enzyme-linked immunosorbent assay (Tridelta Development EIA Canine CRP Assay). Linearity, precision, reproducibility, and accuracy were assessed using leftover serum samples. Agreement between assays was assessed using leftover serum samples and serum from clinically healthy dogs. Observed to expected ratios (O/E) for dilutional parallelism were 83.9 to 163.1% and 108.3 to 160.6% for the Catalyst and the Gentian assays, respectively. Coefficients of variation for intra-assay variability ranged from 6.4 to 9.5% for the Catalyst assay and 1.5 to 2.6% for the Gentian assay. Coefficients of variation for inter-assay variability ranged from 3.8 to 18.2% for the Catalyst assay and 4.5 to 5.8% for the Gentian assay. The mean O/E for recovery were 97.9% and 98.5% for the Catalyst and Gentian assays, respectively. Correlations between assays were as follows: Catalyst and Tridelta (R 2 = 0.76), Gentian and Tridelta (R 2 = 0.79), and Catalyst and Gentian (R (2) = 0.98). The Catalyst and Gentian assays are both acceptable for measuring CRP in dog serum, but their results are not directly comparable with the Tridelta assay.

Bone repair in horses implies invasive surgeries and increased cost. Research on musculoskeletal disorders therapy in horses includes cell-based therapy with mesenchymal stromal cells (MSCs). Mesenchymal stromal cells can be obtained from bone marrow (BMMSCs). Unfortunately, BMMSCs have limited cell replication in vitro. The objective of this study was to develop a biologically immortalized equine stem cell line derived from bone marrow, with unlimited in-vitro proliferation and the ability to differentiate into bone cells. Equine BMMSCs were transfected and immortalized with human telomerase reverse transcriptase (hTERT) gene. Cell passages from equine immortal BMMSCs were characterized by the presence of stemness CD markers and expression of multi-potent differentiation genes (OCT-4, SOX2, and NANOG). Equine immortal BMMSCs were incubated in osteogenic medium and bone cell differentiation was determined by alkaline phosphatase and von Kossa staining, and osteogenic gene expression (osteocalcin, Runx2, and osterix). Telomerase activity was determined by telomeric repeat amplification technique. Results showed that equine immortal BMMSCs were able to replicate in-vitro up to passage 50 and maintain stem cell characteristics by the presence of CD90 and expression of multi-potent genes. Equine immortal BMMSCs were able to differentiate into bone cells, which was confirmed by the positive osteogenic staining and gene expression. Equine BMMSCs were successfully immortalized and maintained characteristics of stem cells and readily differentiated into osteogenic cells. Extending the life span of equine BMMSCs by transfection of the hTERT gene will revolutionize the clinical use of MSCs by making them available to orthopedic surgeons "off the shelf."

Although glucocorticoid administration has produced impressive results in treating canine mast cell tumors (MCTs), in some cases, glucocorticoids fail to reduce the tumor volume, leading to tumor relapse even after treatment. To date, mechanisms involved in glucocorticoid resistance in canine MCTs remain poorly defined. The objective of this study was to establish glucocorticoid-resistant canine MCT cell lines derived from glucocorticoid-sensitive cell lines after prolonged treatment with dexamethasone (Dex). Real-time polymerase chain reaction (RT-PCR) revealed that elevation of glucocorticoid receptor (GR)-regulated gene expression was suppressed in Dex-resistant cell lines after Dex stimulation compared with parent Dex-sensitive cell lines. This indicated that GR-regulated transcription was suppressed in Dex-resistant cell lines. Insufficient expression of GRs was not detected in Dex-resistant cell lines. Possible inhibitors of GR-regulated transcription were increased in mRNA expression in Dex-resistant cell lines. In addition, it was determined that mRNA expression of drug efflux pumps and anti-apoptosis factors was higher in Dex-resistant cell lines. In conclusion, glucocorticoid-resistant canine MCT cell lines have been established that are derived from glucocorticoid-sensitive cell lines. These cell lines suggest that multiple mechanisms contribute to glucocorticoid resistance in canine MCT cells. The mechanisms of glucocorticoid resistance after long-term treatment can be further investigated using these cell lines and a novel therapeutic strategy for glucocorticoid-resistant canine MCT cells can be developed.

No abstract available.

The present study was conducted to investigate the effect of co-administration of zincsulfate with Carbimazole (CBZ) and, Levothyroxine (L-T4) on thyroid gland function inadult male rabbits. Fifty adult male rabbits, were divided randomly into five equal groups (6rabbits/group) as follows: The first group (control group): Rabbits were given oral doses ofdistilled water daily by gavage; second group (Hypothyroidism): Rabbits were given oraldoses of carbimazole (5 mg/kg. bw) daily by gavage; the third group; Rabbits were givenoral doses of carbimazole (5 mg/kg. bw) + zinc sulfate (20 mg/kg.bw); fourth group(Hyperthyroidism): Rabbits were given oral doses of L-T4 (100&micro;g/kg.bw) daily by gavage;Fifth group: Rabbits were given oral doses of L-T4(100&micro;g/kg.bw) + Zinc sulfate(20mg/kg.bw) daily by gavage. The treatment continued for 30 days. The results revealedthe following: A significant elevation in serum TSH level and a significant reduction inserum T4, T3 and, FT3 levels in CBZ treated rabbits group compared with the control group,while a significant reduction in serum TSH level and a significant elevation in serum levelsof T4, FT4 and FT3 in animals group treated with the L-T4 compared with the control groupHistopathological changes of hypothyroidism were observed in CBZ treated groupcharacterized by small thyroid follicles, increase the height of thyrocytes hyperplasia, andvacuolation of colloid. L-T4 and L-T4-Zinc treated groups showed large follicles distendedwith homogenous acidophilic colloid. No significant changes in thyroid architecture wereobserved in CBZ-Zinc treated group compared with the control group.

The focus of the present study was to characterize chimeric synthetic plantaricin F which naturally produced by Lactobacillus plantarum against zoonotic pathogenic bacteria Staphylococcus aureus and Escherichia coli as antibacterial peptide. The syntheticbacteriocin by bioinformatics revealed higher stability under studied parameter, hence was taken up for further investigation. The amino acids of bacteriocin from L. plantarum were analyzed by SnapGene. Further, synthetic PLNF was characterized in silico. The translated partial amino acid sequence of the synthetic PLNF gene displayed 253 amino acids for whole and 148 without tag. The predicted properties of the peptide included theoretical isoelectric point (pI) and hydrophobicity was highly acidic. Molecular weight was 27.2KDa for whole protein and 15.8 KDa for without tag. Predication the molecular approach of using SnapGene software and the protein was having antingcity against bacteria and has B-cell epitope on the surface of protein. Prediction data base on characterization of bacteriocin is novel and predicts synthetic PLNF to be a peptide responsible for antimicrobial activity. The study provides information about a broad spectrum bacteriocin in native probiotic culture and paves a way towards its application as alternative natural antimicrobial agent against zoonotic pathogenic bacteria. Finally, the 3D peptide structure analysis in present study showed that the predicted structure of model and has more functional properties and probably the form most suitable for binding to bacterial cell walls.

Turkey coronavirus (TCoV) is a Gammacoronavirus causing acute contagious enteritis in young turkeys, leading to impaired growth, low feed conversion, and increased mortality. The TCoV infections, in association/combination with other enteropathogenic viruses, bacteria & protozoa, are associated with poult enteritis-mortality syndrome (PEMS) in turkeys of 1-4 weeks age. In this review, classification & genotyping of TCoV, the implications of its recombination, and challenges to develop efficient vaccines against it are discussed. Though TCoV is monophyletic with infectious bronchitis virus (IBV) with a sequence similarity of &ge;86, however a classification scheme gathering all avian coronaviruses (ACoVs) is not established. Based on the N gene, ACoVs are classified into five clades. Clades 1 & 2 (chickens), Clade 3 (pigeon) Clade 4 (duck), and Clade 5 (goose). The Spike (S) gene of ACoVs has shown exceptional lability of being easily switched with multiple recombination events suggesting that TCoV may be an IBV recombinant. Recombination events altered the pathogenicity, host specificity, and tissue tropism of TCoVs. Attempts to develop attenuated, inactivated, DNA, and virus-vectored vaccines are ongoing. Experimentally, the attenuated TCoV strains induced strong humoral and cellular immune responses and completely protected against the homologous challenge but not heterologous TCoV challenge. Meanwhile, genetically engineered vaccines, either DNA or virus vectored vaccines, are limited with either late induction of a protective immune response and/or inability of the elicited antibody to neutralize virus infection and protect against virus challenge. Future research should focus on improving vaccine efficiency against TCoVs by developing more immunogenic vaccines, determining the appropriate dosing regimens, and include potent adjuvants

In the United States, non-typhoidal Salmonella causes over one million food-borne infections every year and turkey meat contaminated with Salmonella has been associated from the farm to the processing plant. These outbreaks emphasize efforts on decreasing and preventing human illness associated with live poultry contact through comprehensive interventions from farm-to-fork levels. This review article revises the role of the turkey upper respiratory tract, which is now known to play a crucial role in colonization and as a source of contamination, for this remarkable bacterium that has co-evolved to infect plants and animals. Because agriculture represents over 60 % of the economy of the state of Arkansas, the mission of our laboratory over the last 21 years has been to evaluate and develop applied research to help reduce the incidence of Salmonella spp. from commercial turkey operations. A summary of the published research is presented.

The aim of this study was to evaluate the anti-helminthic effect of a commercial formulation Bioverm® (Duddingtonia flagrans) in 28 sheep naturally infected with gastrointestinal nematodes. Animals were classified into two groups: G1 (n=14) treated with nematophagous fungi and G2 (n=14) untreated control. The efficacy of the anti-helminthic drug was assessed based on the egg count per gram of feces (EPG) of strongyles, larval culture, hemogram, leukogram, plasma protein levels, mucosal coloration using the FAMACHA© method, animals body weight, and evaluating the ocular mucosa for the FAMACHA© anemia guide were performed at days 0, 30, 60, 90, 120, 150, and 180. Additionally, the nematode larvae were quantified in the dry matter of the pastures of both groups. Results showed that the EPG was significantly decreased in animals receiving nematophagous fungi from D30 until the experiment end. The most common nematode genus was Haemonchus (63%), followed by Cooperia (23%) and Trichostrongylus (15%). Based on the fecal egg count reduction test (FECRT), treated animals showed a reduction of fecal egg count of 58.9%, 8.6%, 92.8%, 96.4%, and 96.2%, at D30, D60, D90, D120, and D180, respectively. The absolute values of red blood cells and leukocytes were significantly increased at D60 and D90, respectively, in the treated animals. A significant weight gain was observed in the treated ewes at the end of the experiment; however, there was no correlation between the EPGs values and hematocrit with the FAMACHA© degrees of animals in both experimental groups. The mean EPG of both groups and the number of infectious larvae in the pastures were not directly proportional. In conclusion, nematophagous fungi contributed to decreased parasitic load in sheep, and consequently, improve animal performance; they can be a suitable alternative to reduce problems associated with nematode infections.