Effect of different methods of maintenance on the development and morphology of Babesia bigemina in the gut of Boophilus microplus

The development and morphology of Babesia bigemina in the gut of Boophilus microplus ticks were studied during laboratory maintenance of the babesia by four methods: tick transmission in unsplenectomised (intact) calves; tick transmission in splenectomised calves; syringe passage at intervals of five days or less in splenectomised calves; and syringe passage at intervals of six weeks or more in intact calves. The first method had no apparent effect on the development of B bigemina in ticks compared to that of the original isolate. The other three methods had obvious effects, the most pronounced being increased numbers of babesial forms with processes, particularly during early stages of development. The findings emphasise the importance of maintaining laboratory strains of parasites by natural means in life cycle studies.     

Effect of trampling on the soils of the St James Walkway, New Zealand

Abstract. The influence of trampling on the soils of the St James Walkway was studied during 1985 by comparing 'on'- and off-track sites. Trampling increased the average soil bulk density by 0.3 g/cm³ at 0–5 cm depth and by 0.1 g/cm³ at 10–15 cm depth. Trampling increased the average soil shear strength by 11 kPa at 0–5 cm depth and by 6 kPa at 5–10 cm depth. All mineral soils were compacted to some extent by trampling. The podzolized high country yellow-brown earths (Dystrochrepts) were the most affected because their organic topsoil was truncated. Their exposed subsoil was however more resistant to further damage than their topsoil. Organic soils (Medihemists) were not compacted but their very low shear strength and high moisture content make them unsuitable for tracks. Untrampled soil bulk density and soil stone content were negatively correlated with the change in bulk density by trampling, and could be used to predict the risk of soil compaction by trampling.     

Determination of the source of relaxin immunoreactivity during pregnancy in the dog.

We investigated the source of immunoreactive relaxin (IR) in the dog during pregnancy using the following: (1) controls, (2) dogs ovariectomized during pregnancy and maintained on progesterone, (3) dogs hysterectomized during pregnancy or immediately postpartum, (4) corpora lutea, uteri, and placentas collected at various times during pregnancy for determination of IR, and (5) maternal (overian and uterine vein) and fetal (cardiac) blood and amniotic and allantoic fluid. Plasma IR patterns remained unchanged in animals subjected to ovariectomy, whereas in the controls IR was first detected at about Day 20 of pregnancy, peaked on Day 35, and was then remained at the same level until parturition. Hysterectomy, on the other hand, resulted in IR values becoming undetectable within 2 to 3 days. The highest tissue concentrations of IR were found in the placenta. These findings indicate that the source of relaxin in the pregnant dog is the placenta.     

Studies on the antigenic structure of Bacteroides nodosus.

The antigenic mosaics of three Bacteroides nodosus isolates (198, 199 and 127) were studied to elucidate the nature of the protective immunogen. In vaccinated sheep the three isolates induced high homologous serum agglutinin titres but it was also apparent that 198 and 199 shared a major surface antigen not present on 217. This major cross-reacting antigen was not detected with rabbit antisera. The fimbriae, consisting predominantly of protein, induced high homologous titres in rabbits and represented the type-specific antigen. Lipopolysaccharide (LPS) from each of the isolates induced low agglutinin titres and high 2-mercaptoethanol-sensitive indirect haemagglutinating antibody titres. The heat-stable LPS contained at least two common carbohydrate O antigen determinants but no type-specific O antigens were detected.     

Swine buffy coat culture: an aid to the laboratory diagnosis of hog cholera.

A 2-step technique for the isolation of hog cholera (HC) virus consisting of an initial culture on buffy coat (BC) cultures and subinoculation to a pig kidney cell line (PK-15) was described. By this technique, HC virus was confirmed in specimens from 65 herds in which the conventional cell culture isolation technique failed. The herds were located in 20 states and Puerto Rico. Specimens from 29 of the 65 herds were inoculated into specific-pathogen-free (SPF) pigs. Hog cholera virus was recovered from 27 of the test pigs. The 2 pigs from which virus was not recovered had signs of acute infection and, on necropsy, had gross lesions of HC infection.