Evidence for absence of equine arteritis virus in the horse population of New Zealand

AIM: To summarise investigation and laboratory data collected between 2001 and 2011 to provide evidence that equine arteritis virus is not present in the horse population of New Zealand.

METHODS: Analysis was carried out on results from laboratory tests carried out at the Ministry for Primary Industries Animal Health Laboratory (AHL) for equine arteritis virus from horses tested prior to being imported or exported, testing of stallions as part of the New Zealand equine viral arteritis (EVA) control scheme and testing as part of transboundary animal disease (TAD) investigations for exclusion of EVA. Horse breeds were categorised as Thoroughbred, Standardbred or other.

RESULTS: A total of 7,157 EVA serological test records (from import and export testing, EVA control scheme testing and TAD investigations) were available for analysis between 2005 and 2011. For the three breed categories a seroprevalence of ≤1.6% at the 95% confidence level was determined for each category. Between 2001 and 2011, as part of the EVA control scheme, the EVA status of 465 stallions was determined to be negative. During 2005–2011 EVA was excluded from 84 TAD investigations.

CONCLUSIONS: There was no evidence of equine arteritis virus being present in the general horse population outside of carrier stallions managed under the EVA control scheme.

CLINICAL RELEVANCE: Equine arteritis virus is absent from the general horse population of New Zealand.     

Effects of Gonadotropins on In Vitro Maturation and of Electrical Stimulation on Parthenogenesis of Canine Oocytes

The objective of this study was to determine the effects of gonadotropins on in vitro maturation (IVM) and electrical stimulation on the parthenogenesis of canine oocytes. In experiment I, cumulus oocyte complexes were collected from ovaries at a random phase of the oestrus cycle and cultured on maturation medium treated with hCG or eCG for 48 or 72 h. There were no significant differences in the effects on the metaphase II (MII) rate between the hCG and eCG treatment groups over 48 h (5.4% vs 5.5%). The MII rate in the co-treatment group of hCG and eCG for 48 h was higher than in each hormone treated group (15.5%, p < 0.05). In experiment 2, the parthenogenetic effect on oocyte development, at various electrical field strengths (1.0, 1.5, 2.0 kV/cm DC) for 60 or 80 μs with a single DC pulse after IVM on the co-treatment of hCG and eCG, was examined. The rate of pronuclear formation (37.1%) in electrical activation at 1.5 kV/60 μs without cytochalasin B (CB) was higher than that of oocytes activated in the other groups (p < 0.05). However, we did not observe the cleavage stages. Also, CB did not influence parthenogenesis of canine oocytes. The results showed that the pronucleus formation rate, indicative of the parthenogenesis start point, could be increased by electrical stimulation. Therefore, these results can provide important data for the parthenogenesis of canine oocytes and suggest the probability of parthenogenesis in canines.     

The use of Vis-NIR spectral reflectance for determining root density: evaluation of ryegrass roots in a glasshouse trial

This paper reports the use of visible/near‐infrared reflectance spectroscopy (Vis‐NIRS) to predict pasture root density. A population of varying grass root densities was created by growing Moata ryegrass (Lolium multiflorum Lam.) for 72 days in pots of Ramiha silt loam (Allophanic) and Manawatu fine sandy loam (Recent Fluvial) (60 pots for each soil) differentially fertilized with nitrogen (N) and phosphorus (P) in a glass house experiment. At harvest, the reflectance spectra (350–2500 nm) from flat sectioned horizontal soil slices (1.3 cm depth), taken from 57 selected pots, were recorded using a portable spectroradiometer (ASD FieldSpec Pro, Boulder, CO). Root densities within each of the soil slices were measured using a wet sieving technique. A large variation in root densities (0.46–5.02 mg dry root cm^?3) was obtained from the glass house experiment as plant growth responded to the different soils and rates of N and P fertilizer treatment. Pots of the Manawatu soil contained greater ryegrass root densities (1.76–5.02 mg dry root cm^?3) than pots of the Ramiha soil (0.46–3.84 mg dry root cm^?3). Each soil had visually distinct reflectance spectra in the range 470–2440 nm, but different root masses produced relatively small differences in reflectance spectra. The first two principal components (PC1 and PC2) of a principal component analysis of the first derivative of the spectral reflectance accounted for 71.3% of the spectral variance and clearly separated the Ramiha and Manawatu soils. PC1, which accounted for 58.4% of the spectral variance, was also well correlated to root density. Partial least squares regression (PLSR) of the first derivative of the 10 nm spaced spectral data against measured root densities produced calibration models that allowed quantitative estimates of root densities (without removing outlier, r² cross‐validation = 0.78, ratio of prediction to deviation (RPD) = 2.14, root mean squares error of cross‐validation (RMSECV) = 0.60 mg cm^?3; with removing outliers, r² cross‐validation = 0.85, RPD = 2.63, RMSECV = 0.47 mg cm^?3). The study indicated that spectral reflectance measurement has the potential to quantify root density in soils.     

Differential expression of insulin‐like growth factor family members in immature cumulus–oocyte complexes from dairy cows with different genotypes

It has been evident the improvement of in vitro embryo production (IVEP) in dairy cows. Nevertheless, it is known that differences in the number and quality of oocytes between taurine and zebu females impact the efficiency and economic viability of IVEP. As the insulin‐like growth factor (IGF) system is related to follicular and oocyte development, we aimed to quantify mRNA abundance of IGF system members and pregnancy‐associated plasma protein‐A (PAPPA) in the cumulus–oocyte complexes (COCs) of Gir, 1/2 Holstein × 1/2 Gir and Holstein cows. Four pools of 30 immature COCs from Gir, 1/2 Holstein × 1/2 Gir and Holstein cows were obtained by ovum pickup (OPU), and the oocytes and cumulus cells (CC) were mechanically separated and stored at ?80°C. Total RNA was extracted from pools of 30 oocytes and their respective CC. Expression of target genes was assessed by real‐time RT‐PCR. In oocytes, the abundance of IGFR1 mRNA was higher (p < .05) in Gir cows compared with the other breeds. In contrast, in CC, mRNA encoding IGF2 (p < .05), IGFR2 (p < .05) and IGFBP4 (p < .01) was higher in Holstein donors compared with Gir and 1/2 Holstein × 1/2 Gir cows. Additionally, the abundance of PAPPA mRNA was higher in oocytes (p < .001) and CC (p < .01) in Gir and 1/2 Holstein × 1/2 Gir cows compared with the Holstein donors. In conclusion, the higher abundance of PAPPA mRNA in the oocytes and CC from Gir and cross‐breed donors combined with the low expression of IGFBP4 in the CC suggests an enhancement of the bioavailability of IGF‐free when compared with Holstein COCs.     

In vitro Capacitation and Acrosome Reaction of Dog Spermatozoa can be Feasibly Attained in a Defined Medium Without Glucose

Incubation of dog spermatozoa in a medium without glucose and in the presence of lactate and pyruvate (l-CCM) for 4 h at 38.5 degrees C in a 5% CO(2) atmosphere induced in vitro capacitation of these cells. This was verified after the combined specific capacitation-like changes in percentages of viability and altered acrosomes, motility characteristics, sperm location of reactivity against Pisum sativum, Arachis hypogaea and Helix pomatia lectins and the tyrosine phosphorylation pattern. Furthermore, a feasible acrosome reaction (AR) was induced when spermatozoa incubated in l-CCM for 4 h were further co-incubated for 1 h with canine oocytes. This was demonstrated by AR-like changes in percentages of viability, altered acrosomes, motility characteristics and sperm location of reactivity against P. sativum, A. hypogaea and H. pomatia lectins. All these results clearly indicate that in vitro capacitation, and subsequent AR, can be feasibly achieved without the presence of sugars. This ability can be related to the specific characteristics of energy-metabolism regulation reported in dog spermatozoa.     

Intracytoplasmic Glutathione Levels in Heifer Oocytes Cultured in different Maturation Media and its Effect on Embryo Development

The present study was carried out to study the effect of different maturation media on embryo development of heifer oocytes and on their glutathione (GSH) synthesis during in vitro maturation (IVM). Immature heifer oocytes were matured in parallel in one of four maturation media: (i) Tissue Culture Medium (TCM)-199 supplemented with 10 ng/ml of epidermal growth factor (EGF); (i) TCM-199 supplemented with 10 ng/ml of EGF plus 1 microg/ml of FSH; (iii) TCM-199 supplemented with 10% of foetal bovine serum (FBS) and (iv) TCM-199 supplemented with 10% of FBS plus 1 microg/ml of FSH. Cow oocytes were used as control and were matured in TCM-199 supplemented with 10 ng/ml of EGF. No differences were observed in blastocyst rate among the different heifer oocyte groups (8.8, 7.5. 8.4 and 6.8%, respectively) however, the percentage of blastocysts obtained from cow oocytes was significantly higher (30%; p < 0.01) than those obtained from heifer oocytes. De novo GSH synthesis during oocyte maturation of heifer and cow oocytes was detected. No significant differences in intracytoplasmic GSH levels were observed among the experimental heifer oocyte groups or between heifer and cow oocytes both before and after IVM. In conclusion, the blastocyst yield obtained from heifer oocytes was lower than that from cow oocytes and this fact could not be explained by significant differences in intracytoplasmic GSH contents of oocytes before or after IVM.     

恩拉霉素的研究进展

概述了恩拉霉素的理化特性、药效学、毒理学和临床应用研究进展,展望了今后恩拉霉素的研究方向.     

Soil water status mapping and two variable-rate irrigation scenarios

Irrigation is the major user of allocated global freshwaters, and scarcity of freshwater threatens to limit global food supply and ecosystem function—hence the need for decision tools to optimize use of irrigation water. This research shows that variable alluvial soil ideally requires variable placement of water to make the best use of irrigation water during crop growth. Further savings can be made by withholding irrigation during certain growth stages. The spatial variation of soil water supplied to (1) pasture and (2) a maize crop was modelled and mapped by relating high resolution apparent electrical conductivity maps to soil available water holding capacity (AWC) at two contrasting field sites. One field site, a 156-ha pastoral farm, has soil with wide ranging AWCs (116–230 mm m⁻¹); the second field site, a 53-ha maize field, has soil with similar AWCs (161–164 mm m⁻¹). The derived AWC maps were adjusted on a daily basis using a soil water balance prediction model. In addition, real-time hourly logging of soil moisture in the maize field showed a zone where poorly drained soil remained wetter than predicted. Variable-rate irrigation (VRI) scenarios are presented and compared with uniform-rate irrigation scenarios for 3 years of climate data at these two sites. The results show that implementation of VRI would enable significant potential mean annual water saving (21.8% at Site 1; 26.3% at Site 2). Daily soil water status mapping could be used to control a variable rate irrigator.     

Temperature and surface-ocean water balance of the mid-holocene tropical western pacific

Skeletal Sr/Ca and 18O/16O ratios in corals from the Great Barrier Reef, Australia, indicate that the tropical ocean surface approximately 5350 years ago was 1 degrees C warmer and enriched in 18O by 0.5 per mil relative to modern seawater. The results suggest that the temperature increase enhanced the evaporative enrichment of 18O in seawater. Transport of part of the additional atmospheric water vapor to extratropical latitudes may have sustained the 18O/16O anomaly. The reduced glacial-Holocene shift in seawater 18O/16O ratio produced by the mid-Holocene 18O enrichment may help to reconcile the different temperature histories for the last deglaciation given by coral Sr/Ca thermometry and foraminiferal oxygen-isotope records.