The role of oral immunisation in stimulating Escherichia coli antibody of the IgM class in porcine colostrum.

Oral immunisation with Escherichia coli polysaccharide antigens provided a primary antigenic stimulus which facilitated the production of humoral IgM antibody following a single parenteral antigen dose. The peak antibody response of preparturient sows was manipulated to coincide with the period of colostrum formation so that high levels of IgM antibody were made available for neonatal defence. The characteristics of the immune response remained unchanged on reintroduction of the immunisation schedule for a second gestation period.     

Arbovirus isolations from mosquitoes in South Slovakia.

In the years 1973 and 1975 mosquitoes and some other Diptera (Tabanidae, Simuliidae, Hippoboscidae) were tested for virus. 13,924 mosquitoes, 75 horseflies and 60 blackflies were processed in 1973. Five strains of Tahyna virus were isolated from mosquito species Aedes vexans. 3,378 mosquitoes and 12 sheep keds were tested for virus in 1975. Twelve strains of Calovo virus were isolated from Anopheles maculipennis and one strain of Tahyna virus was obtained from Aedes vexans mosquitoes.     

Differentiation of strains of bean common mosaic virus

Pathogenicity and symptom expression of seventeen described isolates of bean common mosaic virus (BCMV) and five previously unreported isolates were compared on many bean cultivars (Phaseolus vulgaris L.). From these cultivars, a standard set of differentials were assigned to nine groups with different disease reactions. The twenty-two virus isolates comprised seven strain (pathotype) groups, three of which were divided into two subgroups each. To promote international standardization in BCMV research, recommendations are given for test conditions and procedures, criteria for strain differentiation, and maintenance of differential cultivars and virus strains.Samenvatting Zeventien beschreven stammen van het bonerolmozaïekvirus en vijf niet geïdentificeerde isolaten (Tabel 1) werden bestudeerd op een uitgebreide reeks van toetsrassen. De meeste van deze toetsrassen waren in de literatuur als zodanig vermeld, maar door de desbetreffende onderzoekers waren vaak verschillende series toetsrassen gebruikt, hetgeen de onderlinge vergelijking van de stammen bemoeilijkte.De bedoeling van dit onderzoek was: vergelijking en indeling van de virusstammen, samenstelling van een standaard-toetsrassenserie en het ontwerpen en beschrijven van werden zowel in Wageningen als in Prosser, Washington, USA, uitgevoerd met dezelfde virusisolaten en dezelfde zaadmonsters van de toetsrassen.De toetsrassen konden op grond van hun differentiële reacties na inoculatie met de virusstammen worden ingedeeld in negen groepen. De rassen binnen een groep hebben hetzelfde resistentiespectrum t.o.v. een standaardserie virusstammen. Uit elke groep werden op grond van hun geschiktheid (duidelijkheid en reproduceerbaarheid van de symptomen) één of meer vertegenwoordigers gekozen, waaruit een standaardserie van toetsrassen werd samengesteld (Tabel 2).De 22 stammen en isolaten werden op grond van hun pathogeniteitsspectrum t.o.v. de standaardserie van toetsrassen ingedeeld in tien groepen en subgroepen (Tabel 1). De stammen en isolaten binnen een groep of subgroep hebben eenzelfde pathogeniteitsspectrum (Tabellen 4 en 6) en worden op grond daarvan als identiek beschouwd. De differentiële reacties tussen de rassen van de standaardserie en de virusstammen en-isolaten zijn vermeld in de Tabellen 3 en 5. Voorgesteld wordt om de naam van de eerstbeschreven stam van iedere groep te handhaven en de andere stammen in een groep of subgroep op te vatten als isolaten daarvan.De toetsmethodiek wordt uitvoerig beschreven om standaardisatie van de stammenidentificatie te bevorderen. Ter verklaring van de in de literatuur gevonden tegenstrijdigheden in de differentiële reactie van de toetsrassen wordt een negental mogelijke oorzaken genoemd, o.a. het gebruik van planten van toetsrassen die reeds vanuit zaad met een onbekende stam waren besmet en het gebruik van onzuivere virusstammen (mengisolaten).De auteurs stellen zich verantwoordelijk voor het distribueren (op aanvraag) van kleine zaadhoeveelheden van de toetsrassen en, op beperkte schaal, van in zaad aanwezige zuivere virusstammen aan onderzoekers die betrokken zijn bij de identificatie van de stammen van dit virus. Bovendien zal zaad van de standaardserie van toetsrassen worden gedeponeerd in het National Seed Storage Laboratory te Fort Collins, Colorado, USA, terwijl de virusstammen (in zaad) in bewaring worden gegeven bij de American Type Culture Collection te Rockville, Maryland, USA, waar ze beschikbaar zullen blijven voor verder onderzoek.     

Studies on the chiral isomers of fonofos and fonofos oxon: II. In vitro metabolism

The in vitro metabolism of the chiral isomers of fonofos and fonofos oxon in the presence of mouse liver mixed-function oxidase and serum esterase was investigated. The metabolism of ³⁵S-labeled phenyl-(S)_P-fonofos mediated by mixed-function oxidase took place stereoselectively, resulting predominantly in (R)_P-fonofos oxon. Similarly, (R)_P-fonofos was converted to (S)_P-oxon. In each case, however, a significant amount of racemization occurred. Other products were diphenyl disulfide and diphenyl disulfide oxide. In addition to stereospecificity, the oxidative metabolism of (R)_P-fonofos proceeded at a rate faster than that of (S)_P-fonofos. Stereoselective rate differences also were observed in mouse or rat serum-catalzyed degradation of the fonofos oxon enantiomers, the (S)_P isomer being degraded about twofold faster than its enantiomer. The differences in toxicities of the isomers of fonofos and fonofos oxon were consistent with the in vitro metabolism data.     

Inhibition of chitin synthesis by two 1-(2,6-disubstituted benzoyl)-3-phenylurea insecticides. II

The knowledge of the biochemical mode of action of 1-(4-chlorophenyl)-3-(2,6-difluorobenzoyl)urea (diflubenzuron) is presented, explaining the insecticidal effect. Like its structural analog, 1-(2,6-dichlorobenzyl)-3-(3,4-dichlorophenyl)urea (Du 19111), it inhibits chitin synthesis in the cuticle of larvae. Virtually complete inhibition was demonstrable 15 min after the application of diflubenzuron. Neither diflubenzuron nor Du 19111 has any effect upon chitinase activity either in vivo or in vitro. The insecticidal effect upon the cuticle, therefore, must be explained as an inhibition of chitin synthesis and not as an activation of chitin degradation. In contrast to the action of Du 19111, no accumulation of N-acetylglucosamine occurs upon treatment of larvae with diflubenzuron. Similarities and differences in the mode of action of both compounds are discussed, together with other effects reported in the literature.     

Factors affecting the variability in cracked and dirty eggs and egg production profitability on an integrated poultry operation

1. A number of factors causing variability in the percentages of cracked, and dirty eggs and weekly standard margin (WSM) of returns from eggs over production costs were examined on an integrated commercial poultry plant in Scotland.

2. As the bird aged, the percentage of cracked eggs increased (P <0.01) and the percentage of grade A eggs and WSM decreased (P <0.01). Cracks in dirty eggs (10.1%) were more than double those in all eggs laid (4.9%).

3. Seasonal effects on percentage cracked eggs and percentage grade A eggs were one‐third the magnitude of those due to age but were significant (P <0.05).

4. Variability in percentage cracked eggs, dirty eggs and WSM accounted for by the factors measured, were 72, 64 and 92% respectively.

5. The variability in WSM was significantly affected by percentage lay, food consumption and age but not by percentage cracked eggs, originally dirty and grade A eggs.

6. Flock management and climate inside the laying house each increased the amount of variability accounted for in the percentage cracked eggs and dirty eggs by at least 10%.     

On estimating non‐additive genetic parameters in chickens 1

1. Several economically important traits in two Leghorn populations (over 9000 birds) were examined for additive and non‐additive components of genetic variance and sex‐linked effects. Data were analysed by two different statistical models based on least‐squares procedures.

2. Six different covariances were first calculated between relatives; i.e., full‐sibs, 3/4‐sisters, half‐sisters, dam‐daughters, grandam‐granddaughters and aunt‐nieces.

3. From the covariances, weighted least‐squares equations were used to obtain estimates of variance components for additive genetic, dominance, maternal and sex‐linkage effects.

4. The estimates of non‐additive components were highly variable but generally small compared with the additive genetic estimates.

5. In general this study suggests that for most traits, with the possible exception of rate of egg production, there is relatively little non‐additive genetic variation.

6. The consequences of possible negative correlations between additive effects and maternal effects are considered as they might apply to egg production in poultry.     

Broiler growth and feeding behaviour in three different lighting regimes

1. Female broiler chicks reared in a 12‐h photoperiod which included a simulated “dawn” and “dusk” grew slightly faster than those reared in a 12‐h photoperiod of uniform light and others kept in continuous light.

2. This was apparently because the chicks subjected to dawn and dusk ate more food than those subjected to 12‐h uniform light and converted food more efficiently than those in continuous light.     

The effect of soil aggregate size and water content on herbicide concentration in soil water

Suspensions of wettable powders of metribuzin and simazine were sprayed onto samples of two soils of two particle size grades, > 2.5 mm and <0.5 mm. The soils were either air-dry or at a water content of 12%. After either 1 h or 1 week, water was added to give a soil to water ratio of 1:1. Samples of solution were analysed after 1, 24 and 48 h. With metribuzin the intial concentration for both soils after wetting was greater from the >2.5 mm samples than the <0.5 mm samples, following application to dry soil, but by 48 h the differences were negligible. With simazine WRO soil did not show this effect at all and with Kirton soil only small differences were seen. If the soil was wet at the time of application, particle size had no effect except with simazine in Kirton soil. Generally metribuzin concentrations were higher after application to wet than to dry soils for at least 24 h after wetting whereas simazine concentrations were higher from initially dry soils and the differences had virtually disappeared 24 h after wetting. With the WRO soil herbicide concentrations in soil water were higher if the soil was wetted 1 h after spraying than if left for 1 week but the differences rarely persisted for 48 h. No such trend was observed with Kirton soil. It is concluded that the differences observed in these experiments could be responsible for variations in the performance of soil-applied herbicides.