Effect of lasalocid on the GnRH-induced LH and testosterone release during puberal development in the Brahman bull

To determine the effect of lasalocid on endocrine patterns associated with puberty, 12 half-sib prepuberal Brahman bulls were allotted by age and weight (174 to 256 d of age; 141 to 243 kg) to control or lasalocid treatments. Bulls in the control treatment were fed a 4:1 corn:cottonseed meal concentrate plus Coastal bermudagrass hay to which the bulls were given ad libitum access. The lasalocid treatment was identical except for the addition of 200 mg of lasalocid.animal-1.d-1. Blood samples were collected frequently before and after GnRH (200 micrograms, i.m.) on d 7, at 28-d intervals thereafter, and within 14 d after puberty (defined as 50 x 10(6) sperm cells with 10% motility). By d 7, bulls fed lasalocid released more LH (P less than .05), but not testosterone (T;P greater than .10), in response to GnRH than controls. At the time that the first sperm cells were observed in an electroejaculate (FS), lasalocid-fed bulls released more (P less than .05) LH and T than controls. At puberty, there was no difference (P greater than .10) between treatments in amount of T released, although lasalocid-fed bulls released more LH (P less than .05). Before puberty, concentrations of LH were positively correlated with concentrations of T in samples collected 1 and 2 h later. Both groups of bulls exhibited a linear increase in T response with advancing age (P less than .005). Release of LH decreased with age in the control bulls (P less than .10) but was unaffected by age in lasalocid-fed bulls. Both groups showed a decreased (P less than .001) LH:T response ratio with advancing age. Results of this study with bulls confirm previous reports in heifers of the enhancing effect of an ionophore on reproductive function.     

Comparison of methods for the sampling and isolation of toxigenic Pasteurella multocida from the nasal cavity of pigs

The efficacy of detecting toxigenic Pasteurella multocida from nasal swabs of slaughtered and live pigs was assessed. The isolation of toxigenic P multocida from nasal cavities of slaughtered bacon pigs from two herds with atrophic rhinitis was reduced by immersion in the hot water tank by 25 per cent and 75 per cent. Individual sows from one of the infected herds were repeatedly swabbed to find the best method of isolating toxigenic P multocida. Toxigenic P multocida were isolated from 50 per cent of cotton swabs inoculated on to selective medium the same day. After 24 hours in the post, 45 per cent of cotton swabs placed in transport medium, 38 per cent of alginate swabs dissolved in transport medium and inoculated into mice, and 36 per cent of the dissolved swabs inoculated directly on to selective medium yielded toxigenic P multocida. These bacteria were isolated from only 25 per cent of cotton swabs held in transport medium at 10 degrees C for 48 hours to simulate prolonged postage times; from slaughtered pigs a similar reduction in isolation was seen with swabs kept for 24 or 48 hours. The reduced isolation caused by a delay before culture was associated with an overgrowth of other flora. The development of this flora was prevented by storage of swabs at 4 degrees C in the laboratory or by the use of cool boxes for postage.     

Presence of Maedi Visna Virus (MVV)‐Proviral DNA in the Genital Tissues of Naturally Infected Ewes

Maedi Visna virus (MVV) causes progressive degenerative inflammatory disease in multiple organs including the lungs (pneumonia, ‘maedi’), mammary gland, joints and nervous system (meningoencephalomyelitis, ‘visna’) in sheep. Maedi Visna Virus has been detected in macrophages of several tissues and epithelial cells in vivo: bone marrow, cells of the central nervous system, lung and bronchial tissues, milk epithelial cells recovered from milk samples and epithelial cells of mammary tissue. However, the presence of MVV in the genital tracts of naturally infected ewes has not previously been studied. The aim of this study was to use nested‐PCR, targeting the gag gene, to determine whether genital tissues (ovaries, oviducts and uterus) from 83 ewes originating from various breeding herds in the South‐East of France were positive for MVV‐proviral DNA. Peripheral blood mononuclear cells (PBMC) tested positive for MVV‐proviral DNA, using nested‐PCR analysis, in 57.8% of ewes (48/83). The provirus was also identified in 47% (78/166) of the ovaries, 38.6% (64/166) of the oviducts and 45.8% (38/83) of the uteri sampled. These findings clearly demonstrate, for the first time, that tissue samples from the genital tract of ewes (ovary, oviduct and uterus) can be infected with MVV. This suggests that there is a risk of vertical and/or horizontal transmission of MVV during embryo transfer from embryos produced in vivo or in vitro.     

Measurement of Parity Nonconservation and an Anapole Moment in Cesium

The amplitude of the parity-nonconserving transition between the 6S and 7S states of cesium was precisely measured with the use of a spin-polarized atomic beam. This measurement gives Im(E1pnc)/beta = -1.5935(56) millivolts per centimeter and provides an improved test of the standard model at low energy, including a value for the S parameter of -1.3(3)exp (11)theory. The nuclear spin-dependent contribution was 0.077(11) millivolts per centimeter; this contribution is a manifestation of parity violation in atomic nuclei and is a measurement of the long-sought anapole moment.     

Matching grass supply to grazing patterns for dairy cows

Four groups of five spring-calving Holstein–Friesian cows were given a daily grass allowance in a strip-grazing system after either morning (AM; two groups) or afternoon (PM; two groups) milking over a 10-week period. The dry-matter (DM) concentration of the grass tended to be higher after afternoon milking [AM, 178 vs. PM, 197 g DM (s.e.d. 5·32) kg^–1 fresh matter], and water-soluble carbohydrate concentrations were significantly higher [AM, 175 vs. PM, 204 g kg^–1 DM (s.e.d. 6·67)]. Although the total times spent grazing (AM, 461 vs. PM, 462 min day^–1) were similar for both groups, cows receiving their allocation in the afternoon had a longer evening meal (>4 h duration) compared with those receiving their allocation in the morning (2–3 h), which also spent more time ruminating [AM, 454 vs. PM, 433 min day^–1 (s.e.d. 1·80)]. This short-term study demonstrated how a relatively simple change in management practice in strip-grazing systems could benefit milk yield and pasture utilization. This is because the DM and water-soluble carbohydrate contents of the herbage are higher in the evening than in the morning, and this is when grazing animals concentrate much of their daily grazing activity.     

磷酸泰乐菌素颗粒剂生物效价测定方法的建立及验证

建立了磷酸泰乐菌素颗粒剂的生物效价测定方法，并对新建立的测定方法进行了验证，验证内容包括：方法对照试验、精密度试验、线性及线性范围试验、回收率试验。验证结果证明新方法能准确测定磷酸泰乐菌素颗粒剂的效价单位。     

Characterisation of porcine haemophili isolated from Australian pigs between 1988 and 1992

SUMMARY A total of 362 haemophili, isolated from pigs throughout Australia, were characterised by phenotypic properties. Most were identified as Actinobacillus pleuropneumoniae (296 isolates) or Haemophilus parasuis (52 isolates). The remaining isolates were identified as Haemophilus Taxon ‘minor group’ (12 isolates) and Haemophilus Taxon D (two isolates). All 296 A pleuropneumoniae isolates were serotyped by slide agglutination and/or gel diffusion, using rabbit antisera against all 12 recognised serovars. Of these, only 156 (52.7%) could be assigned to a single serovar as follows: serovar 1–85 isolates, serovar 2–4 isolates, serovar 3–2 isolates, serovar 5–10 isolates, serovar 7–51 isolates, serovar 11–2 isolates and serovar 12–2 isolates. Of the remaining 140 isolates, 91 gave cross-reactions with serovars 3 and 6, one cross-reacted with serovars 9 and 10, one cross-reacted with serovars 9 and 11 whereas 47 gave no reaction with any of the antisera.