Enterotoxemia in the goat: the humoral response and local tissue reaction following vaccination with two different bacterin-toxoids.

A vaccination trial involving 72 goats was designed to compare the epsilon antitoxin titres and local reactions at the injection sites, of two commercial enterotoxemia vaccines. Three dosage regimens were used for each vaccine (12 goats per group). Although no significant differences were noted in humoral immune response between the two vaccines (P = 0.05), one vaccine regime resulted in low titres (P = 0.05) on two occasions. Local tissue reactions at injection sites persisted for six months in 53% of the goats regardless of vaccine used or dosage administered. No immunological basis for the reported differences in vaccine efficacy between sheep and goats was observed in this trial.     

Dose-response shift in the ability of gilts to remain pregnant following exogenous estradiol-17 beta exposure

Sixty mated gilts were assigned to a 2 X 6 factorial arrangement (n = 5) of day of injection (d 9 and 10 vs 12 and 13; d 0 = first day of estrus) and dose of estradiol-17 beta (0, .125, .5, 2, 8 and 32 mg X gilt-1 X d-1). Gilts were subsequently slaughtered on d 30; pregnancy was verified and percent embryonic survival calculated. A 64-fold shift in the dose-response curve for percent embryonic survival illustrated that the adverse effects of exogenous estradiol-17 beta were less when administered on d 12 and 13 as compared with d 9 and 10 (day X dose, P less than .01). This experiment demonstrated that the uterine-embryonic environment of d 12 and 13 pregnant gilts was more tolerant of exogenous estrogen alterations than that of d 9 and 10 pregnant gilts.     

Experiments with the Bio-mittent lighting system for laying hens

1. Two experiments are described in which a system of intermittent lighting (15 min light followed by 45 min dark for 15 h, then 15 min light, 30 min dark, 15 min light and 8 h dark) was applied to laying pullets from 37 to 72 weeks of age. A step-up lighting programme was used as a control treatment (8L:16D from 0 to 18 weeks, photoperiod increased by 20 min each week from 18 to 41 weeks, 16L:8D from 41 to 72 weeks of age). 2. Food consumption was reduced by about 5% when intermittent lighting was in use and by 3.8% for the period from 18 to 72 weeks. 3. Rate of lay and egg weight were similar for intermittent lighting and the control treatment, provided that protein content of the diet was adjusted to maintain an adequate amino acid intake. 4. In the second trial 2 stocks, 2 stocking densities confounded with 2 temperatures and 2 types of food trough were used. Each of these factors affected food intake and it was found that more food was saved by intermittent lighting when intake was high and less when it was low. The proportion saved was approximately 5%. 5. Mortality was slightly but not significantly lower in both experiments where intermittent lighting was used. This may indicate that caged pullets are under less stress when intermittent lighting is used.     

Response of caeruloplasmin to Escherichia coli endotoxins and adrenal hormones in the domestic fowl

The injection of chickens with Escherichia coli endotoxins immediately produced a 50 per cent rise in plasma caeruloplasmin activity which was attributed to the release of the protein from liver cell. This was followed by a fall in activity, which was probably due to a fall in activity, which was probably due to a stabilising effect of adrenocortical hormones on the cell membranes, and then by a five-fold increase. The results of experiments with cycloheximide, adrenocorticotrophin, beta-methasone and reserpine indicated that the third phase of the response reflected increased synthesis in the liver which was partly induced by adrenal hormones. It increased with the dose and was not elicited by the particulate nature of the toxin preparation or by its lipid and polysaccharide components.     

Physicochemical properties of agrochemicals: Their effects on foliar penetration

Uptake and translocation of 26 chemicals (herbicides, fungicides, growth regulators, insecticides and model compounds), formulated with and without ‘Ethylan TU’ (NP8) surfactant, have been determined 24, 48 and 72 h after spraying onto leaves of maize, rape, strawberry and sugar beet. Eight of the chemicals may be classified as polar (log partition coefficient (P) < 0) and 18 as lipophilic (log P 0·8-4·6). Chemicals penetrated more readily into waxy leaves of rape and strawberry than into less-waxy sugar beet, whilst lowest rates were observed for maize. Rates of uptake varied from exceedingly low (< 2% 72 h after application) for uracil, maleic hydrazide, isoproturon and methyl phenylurea applied to maize, to rapid (>98% within 24 h of application) for acephate and triadimefon applied to strawberry leaves. The effects of NP8 on rates of chemical uptake were classified into 4 types, viz:-

• (i) low rates, with limited enhancement by NP8;
• (ii) high rates unaffected by NP8;
• (iiii) marked enhancement by NP8 within 24 h; and
• (iv) continuous enhancement by NP8 over 0-72 h.

Translocation into the tissues immediately adjacent to the target site was greater for waxy than less-waxy plants, enhancement by NP8 was attributed to its effects on penetration rather than to surfactant interactions at the sub-cuticular level. Logarithms of physicochemical properties (partition coefficient, water solubility S, molecular weight MW), together with deposit area and melting point (m.p.) values were used to investigate relationships with uptake and translocation. In most cases the variability could not be described adequately in a simple linear form. Regressions using the entire group of 26 chemicals also showed poor correlations between uptake patterns and individual variables. Polynomials in log S, log P, log MW and m.p. were used to test for complex relationships. A quadratic polynomial in log P, log S and m.p. accounted for slightly more (77%) of the variability between the means for total uptake than a cubic polynomial in log P and log S (75%). Although both regressions were significant, the ‘lack of fit’ indicated that other factors need to be included to account fully for the variability in rates of uptake and translocation.     

Development of the neonatal B and T cell repertoire in swine: implications for comparative and veterinary immunology

Birth in all higher vertebrates is at the center of the critical window of development in which newborns transition from dependence on innate immunity to dependence on their own adaptive immunity, with passive maternal immunity bridging this transition. Therefore we have studied immunological development through fetal and early neonatal life. In swine, B cells appear earlier in fetal development than T cells. B cell development begins in the yolk sac at the 20th day of gestation (DG20), progresses to fetal liver at DG30 and after DG45 continues in bone marrow. The first wave of developing T cells is gammadelta cells expressing a monomorphic Vdelta rearrangement. Thereafter, alphabeta T cells predominate and at birth, at least 19 TRBV subgroups are expressed, 17 of which appear highly homologous with those in humans. In contrast to the T cell repertoire and unlike humans and mice, the porcine pre-immune VH (IGHV-D-J) repertoire is highly restricted, depending primarily on CDR3 for diversity. The V-KAPPA (IGKV-J) repertoire and apparently also the V-LAMBDA (IGLV-J) repertoire, are also restricted. Diversification of the pre-immune B cell repertoire of swine and the ability to respond to both T-dependent and T-independent antigen depends on colonization of the gut after birth in which colonizing bacteria stimulate with Toll-like receptor ligands, especially bacterial DNA. This may explain the link between repertoire diversification and the anatomical location of primary lymphoid tissue like the ileal Peyers patches. Improper development of adaptive immunity can be caused by infectious agents like the porcine reproductive and respiratory syndrome virus that causes immune dysregulation resulting in immunological injury and autoimmunity.