Antagonism of detomidine with tolazoline in isoflurane-anaesthetised ponies

The effects of tolazoline (4.0 mg/kg iv) antagonism of detomidine (0.02 mg/kg iv) were evaluated in isoflurane-anaesthetised, ventilated ponies. Each of 6 ponies received both tolazoline and saline treatment during separate anaesthetic episodes only (no surgery was performed). Detomidine administration produced an increase in blood pressure, decrease in heart rate and decrease in P_aO₂ Tolazoline treatment transiently increased heart rate while blood pressure returned to baseline after both treatments. Arterial oxygenation decreased further after tolazoline treatment while oxgenation recovered towards baseline with saline treatment. No other cardiopulmonary effects were detected. Recovery from anaesthesia tended to be more rapid when detomidine was antagonized. The potential benefit of antagonizing detomidine-induced bradycardia with tolazoline, during isoflurane anaesthesia should be weighed against the potential to produce a decrease in arterial oxygenation. The mechanism for this effect is not clear.     

In vivo and in vitro genetic recombination between conventional and gene-deleted vaccine strains of pseudorabies virus

Pseudorabies virus (PRV), an alpha-herpesvirus, causes substantial economic losses in the swine industry and is currently the focus of eradication and control programs. Some of these programs rely on the ability of veterinarians to differentiate animals exposed to virulent strains of PRV from animals exposed to avirulent vaccine strains of PRV on the basis of a serologic response to nonessential glycoproteins that are deleted in some vaccine strains of PRV. Genetic recombination resulting in the creation of virulent strains of PRV with the same negative immunologic markers as vaccine strains could disrupt these programs. Two strains of PRV were coinoculated either into tissue culture or into sheep to facilitate recombination. Progeny viruses were selected to detect a specific recombinant phenotype. We were able to detect genetic recombination between vaccine strains of PRV following in vitro or in vivo coinoculation of 2 strains of PRV. The selected recombinants had marker-deleted phenotypes in strains with restored virulence genes. Increased virulence was observed in sheep after coinoculation of 2 avirulent vaccine strains of PRV.     

Monoclonal antibodies to lymphocyte surface antigens for cetacean homologues to CD2, CD19 and CD21.

CD2 is a pan-T cell marker, while CD19 and CD21 are important molecules in signal transduction of B lymphocytes. CD19 and CD21 are both present on mature B cells, while CD19 is also present in developing B cells and plasma cells. Monoclonal antibodies (mAbs) against cetacean lymphocyte putative homologues to CD2 (two different antibodies), CD19 and CD21 were characterized. The proteins immunoprecipitated were as follows: F21.I (putative anti-CD2), 43 and 59kDa; F21.B (putative anti-CD19), 83 and 127kDa; F21.F (putative anti-CD21), 144kDa. The second putative anti-CD2 (F21.C) selectively inhibited the binding of F21.I. Both the putative anti-CD2 (T cell markers) stained T-cell zones on lymph node sections, while both the B cell markers (putative CD19 and CD21) stained B-cell zones. F21.B and F21.F were absent from thymus single cell suspension but labeled 63 and 65% mesenteric lymph node lymphocytes, respectively, while both F21.C and F21.F were present on 100% thymocytes and fewer lymph node lymphocytes. B and T cell markers were mutually exclusive on double labeling using flow cytometry. These mAbs are foreseen as possible valuable diagnostic and research tools to assess immune functions of captive and wild cetaceans.     

Effect of compensatory growth on regulation of growth and lactation: response of dairy heifers to a stair-step growth pattern

The primary objective of this study was to improve the productive efficiency of growth via optimal use of both high fiber-low quality and high energy-high protein feeds in diets for growing dairy cattle. Twenty Holstein heifers were randomly assigned to either a control or treatment group. The control diet met the National Research Council (NRC) requirement for .45 kg/d gain, with heifers calving at 24 to 26 mo of age. The test groups were fed according to a 5-2-5-2 mo schedule in which the nutrient density was alternately 15% below or 40% above the NRC requirement. Results showed that the heifers on the test dietary regimen (compensatory growth) gained more and consumed less, resulting in significantly improved efficiency of growth (body gain/dry matter intake X 100), energy (body gain X 1,000/metabolizable energy (ME) intake) and protein utilization (body gain/protein intake X 100) in comparison to control animals (13.0 vs 7.3%; 57.9 vs 32.6 g/Mcal ME; 96.5 vs 54.2%, respectively). Marked changes in average concentration of urea-N, glucose, triglycerides, cholesterol and lecithin cholesterol acyltransferase activity in blood were seen for test heifers during the stair-step growth phase (i.e., alternating maintenance and compensatory). Evidence from this experiment suggests that the phased growth (stair-step) system offers a simple, practical and cost-effective method for raising dairy heifers.     

A national serological survey to verify Australia's freedom from porcine reproductive and respiratory syndrome

Objective To provide serological data to support Australia's claim of freedom from porcine reproductive and respiratory syndrome.
Design A national serological survey was designed to provide 99% confidence of detecting at least one infected pig herd in Australia, assuming that at least 5% of herds would have been exposed to porcine reproductive and respiratory syndrome virus and that at least 25% of the 'finisher' pigs in these herds would have antibodies to the virus.
Procedure A two-stage testing regime was used. All samples were tested with a commercially available enzyme-linked immunosorbent assay. If assay reactions were found, all samples from the herd were to be tested using the indirect immunofluorescence antibody assay.
Results Of the 875 samples from 163 herds from all States in Australia, there was some evidence of reactivity in only four samples from four herds on the enzyme-linked immunosorbent assay. Further testing using the indirect immunofluorescence antibody assay according to the study protocol demonstrated that the reactions were not due to the presence of specific porcine reproductive and respiratory syndrome virus antibodies in the sera.
Conclusion The results of this study support the view that Australian pigs are free of porcine reproductive and respiratory syndrome virus.     

THE TIME-OF-DAY GOLDFISH RECEIVE A SINGLE DAILY MEAL AFFECTS GROWTH

Six groups of goldfish, held on a 12L:12D photoperiod and 10°C, had access to food once daily at one of six different times of day. Appetite, somatic growth (weight and length), condition, and gonadal growth (females only) differed among the groups depending on the time-of-day of feeding.     

Effects of dried distillers grains and equivalent undegradable intake protein or ether extract on performance and forage intake of heifers grazing smooth bromegrass pastures

Crossbred heifers (n = 120; BW = 368 kg, SD = 39 kg) were used to determine effects of dried distillers grains (DDG) and relative contributions of undegradable intake protein (UIP) and fat (ether extract, EE) in DDG on ADG and forage intake (FI). Heifers rotationally grazed six 3.5-ha, smooth bromegrass paddocks (IVDMD = 65.7%, CP = 20.8%, UIP = 2.17%, DM basis). Heifers were blocked by previous ADG and allotted to treatments in a 3 x 3 + 1 factorial design. Factors were source and level of supplementation. Supplements were as follows: 1) DDG (UIP = 15.8%, EE = 9.67%), 2) corn gluten meal (CGM; UIP = 31.6%, EE = 0.83%), or 3) corn oil (OIL; UIP = 0.74%, EE = 19.3%). Amounts of DDG were 750, 1,500, or 2,250 g/d, whereas amounts of CGM and OIL were 375, 750, or 1,125 g/ d. Supplements containing CGM and OIL were fed in amounts that provided UIP and EE, respectively, equivalent to those of the DDG. Contrasts of interest were DDG vs. CGM and DDG vs. OIL. Control heifers were fed 250 g/d of a supplement containing corn bran and molasses (UIP = 0.92%, EE = 1.13%). Heifers were supplemented individually. Treatments were separated by regressing the response variables on grams of nutrient (DM, UIP, or EE) intake per kilogram of BW, because not all heifers consumed their allotment of supplement. Supplemental DDG resulted in a linear increase in ADG (P < 0.01), whereas CGM tended to increase ADG (P = 0.14) but at a rate that was 39% of that for DDG, representing a response to MP. Supplementation of OIL did not affect ADG (P = 0.25) and tended to result in ADG less than that of DDG (P = 0.09). Supplementation with DDG had no effect (P = 0.63) on FI when predicted by the use of chromic oxide but tended (P = 0.07) to decrease FI when it was predicted from ADG using NE equations. Despite the differences between methods in the significance of the effect of DDG, the rates of substitution agreed (-0.50 and -0.45 for chromic oxide and NE equations, respectively), suggesting that the chromic oxide method was less sensitive in assessing FI. Supplementation with CGM decreased FI (P < 0.01), but FI for CGM did not differ from that of DDG when the chromic oxide method was used (P = 0.19). Corn oil had no effect on FI (P = 0.42). Increased ADG and decreased FI observed from DDG supplementation is not independently explained by UIP or EE contained in DDG.     

Quantitative real-time polymerase chain reaction for detecting Mycoplasma hyosynoviae and Mycoplasma hyorhinis in pen-based oral,tonsillar, and nasal fluids

Mycoplasma (M.) hyorhinis and M. hyosynoviae are pathogens known to cause disease in pigs post-weaning. Due to their fastidious nature, there is increased need for culture-independent diagnostic platforms to detect these microorganisms. Therefore, this study was performed to develop and optimize quantitative real-time PCR (qPCR) assays to rapidly detect M. hyorhinis and M. hyosynoviae in pen-based oral fluids as well as nasal and tonsillar fluids as proxies for samples used in swine herd surveillance. Two methods of genomic DNA extraction, automated versus manual, were used to compare diagnostic test performance. A wean-to-finish longitudinal study was also carried out to demonstrate the reproducibility of using pen-based oral fluids. Overall, pen-based oral and tonsillar fluids were more likely to be positive for both types of bacteria whereas only M. hyorhinis was detected in nasal fluids. DNA extraction protocols were shown to significantly influence test result. Although the initial detection time somewhat differed, both organisms were repeatedly detected in the longitudinal study. Overall, this study evaluated two qPCR methods for rapid and specific detection of either mycoplasma. Results from the present investigation can serve as a foundation for future studies to determine the prevalence of the two microorganisms, environmental load, and effectiveness of veterinary interventions for infection control.