Prospects for Plant Anthelmintics in Tropical Veterinary Medicine

Hammond, J.A., Fielding, D. and Bishop, S.C., 1997. Prospects for plant anthelmintics in tropical veterinary medicine. Veterinary Research Communications, 21 (3), 213-228The current use of anthelmintic plants in tropical veterinary medicine is reviewed and attention is drawn to the lack of scientific evidence for the effectiveness of many now in use. The case for anthelmintic plants as a means of overcoming some of the serious limitations of manufactured anthelmintics is outlined. Reasons why anthelmintic plants are not generally used in veterinary medicine, in contrast to their greater acceptance in human medicine, are considered. Strategies for their development and use are discussed, in particular the need for in vivo trials to identify those plants which are effective and suitable for general use: attention is drawn to possible candidates, including pyrethrum and papaya latex. Those helminths of most economic importance should be targeted first. Anthelmintic plants offer a traditional alternative to manufactured anthelmintics that is both sustainable and environmentally acceptable. Such plants could have a more important role in the future control of helminth infections in the tropics.     

Using genetic markers for disease resistance to improve production under constant infection pressure

Animals will show reduced production when exposed to a constant infection pressure unless they are fully resistant, the size of the reduction depending on the degree of resistance and the severity of infection. In this article, the use of QTL for disease resistance for improving productivity under constant infection pressure is investigated using stochastic simulation. A previously published model was used with two thresholds for resistance: a threshold below which production is not possible and a threshold above which production is not affected by the infection. Between thresholds, observed production under constant infection is a multiplicative function of underlying potential production and level of resistance. Some simplifications of reality were adopted in the model, such as no genetic correlation between potential production and resistance, the absence of influence of lack of resistance on reproductive capacity, and the availability of phenotypes in both sexes. Marker-assisted selection was incorporated by assuming a proportion of the genetic variance to be explained by the QTL, which thus is defined as a continuous trait. Phenotypes were available for production, not for resistance. The infection pressure may vary across time. Results were compared to mass selection on production under constant as well as intermittent infection pressure, where the infection pressure varied between but not within years. Selection started in a population with a very poor level of resistance. Incorporation of QTL information is valuable (i.e., the increase in observed production relative to mass selection) when a large proportion of the additive genetic variance is explained by the QTL (50% genetic variance explained) and when the heritability for resistance is low (h2R = 0.1). Under constant infection pressure, incorporating QTL information does not increase selection responses in observed production when the QTL effect explains less than 25% of the genetic variance. Under intermittent selection pressure, the use of QTL information gives a slightly greater increase in observed production in early generations, relative to mass selection on observed production, but still only when the QTL effect is large or the heritability for resistance is low. The additional advantage of incorporating QTL information is that use of (preventive) medical treatment is possible, or animals may be evaluated in uninfected environments.     

Modeling selection for production traits under constant infection pressure

This article presents a model describing the relationship between level of disease resistance and production under constant infection pressure. The model assumes that given a certain infection pressure, there is a threshold for resistance below which animals will stop producing, and that there is also a threshold for resistance above which animals produce at production potential. In between both thresholds animals will show a decrease in production, the size of decrease depending on the severity of infection and the level of resistance. The dynamic relationship between production and resistance when level of resistance changes, such as due to infection, is modeled both stochastically and deterministically. Selection started in a population with very poor level of resistance introduced in an environment with constant infection pressure. Mass selection on observed production was applied, which resulted in a nonlinear selection response for all three traits considered. When resistance is poor, selection for observed production results in increased level of resistance. With increasing level of resistance, selection response shifts to production potential and eventually selection for observed production is equivalent to selection for production potential. The rate at which resistance is improved depends on its heritability, the difference between both thresholds, and selection intensity. The model also revealed that when a zero correlation between resistance and production potential is assumed, the phenotypic correlation between resistance and observed production level increases for low levels of resistance and subsequently asymptotes to zero, whereas the phenotypic correlation between production potential and observed production asymptotes to 1.0. For most breeding schemes investigated, the deterministic model performed well in relation to the stochastic simulation results. Experimental results reported in literature support the model predictions.     

Prevalence of trichinosis in Canadian swine determined serologically by enzyme-linked immunosorbent assay.

Fifteen thousand three hundred and eighteen porcine sera from all regions of Canada were examined for the presence of anti-Trichinella antibodies using the enzyme-linked immunosorbent assay with an excretory-secretory antigen. Four sera (0.026%) revealed the presence of anti-Trichinella antibodies, with titers (optical density readings) that fell in the low positive or high negative range on repeated examinations. One animal originated in British Columbia and three in Ontario. Serological examination of swine in the herds at time of traceback did not reveal further animals with anti-Trichinella antibodies.     

The serological responses of chickens to mass vaccination with a live V4 Newcastle disease virus vaccine in the field and in the laboratory 1. Meat chickens

Meat chickens on commercial broiler farms were vaccinated once at 1 to 15 days of age with a live V4 Newcastle disease virus (NDV) vaccine administered by drinking water, aerosol or coarse spray. Hatchmates were housed and similarly vaccinated in laboratory isolation pens. Samples of birds were bled at weekly to fortnightly intervals and the serums tested for haemagglutination inhibiting antibody to NDV. Log2 mean titres of up to 6.26, and assumed protection levels (based on the percentage of birds with log2 titres of 4 or greater) of up to 89%, were obtained in field trials within 4 weeks of vaccination. Differences were observed between the results obtained from parallel field and laboratory trials. The presence of maternal NDV antibody reduced the response to vaccination. The results show that this V4 vaccine can produce an adequate serological response following mass administration to Australian meat chickens housed under commercial conditions.