J.D. Dunsmore

The accumulation of Toxocara canis larvae in the brains of mice

In a series of experiments it has been shown that larvae of Toxocara canis continue to accumulate in the brains of mice for many weeks after infection. This implies that the larvae, as long as they live, continue to circulate in the body until they reach the brain. Unlike other sites where they may be sequestered, in the brain they are not subject to encapsulation by a host reaction. The further implications of larval survival in the brain are discussed.

The ecology of Haemonchus contortus in a winter rainfall region in Australia: the development of eggs to infective larvae

The seasonal pattern of development of Haemonchus contortus eggs to infective larvae was investigated on the south coast of Western Australia. Sheep faeces containing H. contortus eggs were deposited on pasture plots at intervals over a 3-year period, and pasture grass and faeces were sampled periodically for infective larvae (L3). The maximum recoveries occurred in late autumn and in late spring, when adequate moisture coincided with warm temperatures. Larval development was low and sporadic over the hot and dry summer period, and depressed during winter, although most egg depositions in winter yielded L3 at some time. The proportion of L3 recovered was related to temperature and moisture parameters, and the major constraint appeared to be the availability of moisture at pasture level. The best indicator of the suitability of conditions for the development of H. contortus was the proportion of green pasture material present, based on a visual assessment.

Echinococcus granulosus: Secretory activity of the rostellum of the adult cestode in situ in the dog

Secretary activities associated with the rostellum of adult Echinococcus granulosus were studied using histological, histochemical, and ultrastructural techniques, following rapid fixation of the cestodes in situ in the small intestine of the anaesthetised dog. Studies concentrated on the host-parasite interface from 30 to 35 days postinfection. At this time, contraction of the muscular rostellar pad appeared to be associated with extension of the apical rostellum into a crypt of Lieberkuhn. Crypt invasion by the apical rostellum coincided with morphological changes and secretory activity in a group of modified tegumental cells, previously referred to as the rostellar gland. Secretory material, a cystine-rich protein, was observed in the nuclei and cytoplasm of the rostellar gland cells. Release of this material into the interface was seen only following crypt invasion by the apical rostellum. Although the mechanism of release is not clear, it may be analagous to holocrine secretory mechanisms, since apparent degeneration of the rostellar gland region was associated with secretion. Possible functional activities of the secretion associated with hook formation, nutrition, regulation, adhesion, and protection are discussed.

Comparative strobilar development of Echinococcus granulosus of sheep origin from different geographical areas of Australia in vivo and in vitro

Consistent differences in the growth, segmentation and maturation of Echinococcus granulosus in dogs were demonstrated between the parasite of Tasmanian sheep origin and that of Eastern and Western Australian sheep origin. These results were complemented by in vitro studies which found that Tasmanian E. granulosus produced eggs approx. 7 days earlier than the parasite of Eastern and Western Australian origin. These results support the suggestion that at least two distinct strains of E. granulosus of domestic animal origin exist in Australia. The significance of the differences in development demonstrated in this study is discussed.

The epidemiology of Sarcocystis spp. in cattle of Western Australia

Oesophagus samples from 714 cattle from Western Australia were examined by artificial digestion to detect the presence of Sarcocystis spp. The overall prevalence of infection was 52%. The prevalence of infection increased with age and was highest in the entire males (92%). The prevalence was lower in cattle which originated from arid and semiarid regions (9 and 31% respectively) than those from tropical (87%) and temperate (60%) regions. Possible reasons for these differences are discussed and it is concluded that environmental and management factors as well as host age and sex influence the prevalence of infection with Sarcocystis spp. in cattle.

The ecology of Haemonchus contortus in a winter rainfall climate in Australia: the survival of infective larvae on pasture.

At sites near Albany, on the south coast of Western Australia, sheep faecal pellets containing either eggs or infective larvae (L3) of Haemonchus contortus were deposited onto natural pasture plots at intervals over 3 years. Faecal and pasture samples were collected periodically and processed to detect L3. On annual pasture plots, L3 were recovered for from 10 to over 20 weeks from depositions made between autumn and early spring, at which time temperatures were mild or low, rainfall was frequent and the pasture was visibly green. During the hot and dry summer, when the pasture was completely dry, L3 often failed to develop or were recovered on only a single occasion, and the mean larval survival period on positive plots was less than 5 weeks. In contrast, L3 deposited on green perennial pasture plots in summer were recovered for up to 4 months in faecal pellets and on pasture. The longest periods of larval survival were associated with the lowest temperature and highest rainfall recordings, and with the greatest quantity of green plant material in the pasture. It is suggested that the poor survival of L3 during the dry summer period could be used in a strategic treatment programme to interrupt the transmission cycle of H. contortus in winter rainfall climates. However, areas of green pasture which persist in summer may provide a sufficiently moist microclimate to permit the survival of H. contortus L3 despite otherwise unfavourable environmental conditions.

Climate and the distribution of intestinal Trichostrongylus spp. of Sheep

The relative prevalences of Trichostrongylus vitrinus, T. colubriformis and T. rugatus in sheep in south-west Western Australia were examined for evidence of associations with climatic conditions in different localities. The region has a mediterranean-type climate with hot, dry summers and cool, wet winters. The intestinal Trichostrongylus spp. populations in sheep sampled comprised 50% T. vitrinus, 38% T. colubriformis and 12% T. rugatus. The prevalence of T. vitrinus was negatively correlated with mean autumn, winter and spring temperatures of a locality. The prevalence of T. colubriformis was positively correlated with mean autumn, winter and spring temperatures. The prevalence of T. rugatus was not correlated with temperature of any season, but was negatively correlated with mean annual rainfall and length of growing season of a locality. There were suggestions of association of amount of rainfall of a locality and prevalence of T. rugatus was not correlated with temperature of any season, but was negatively correlated with mean annual rainfall and length of growing season of a locality. There were suggestions of association of amount of rainfall of a locality and prevalence of T. colubriformis and of differences in seasonal prevalence of T. vitrinus, but the significance of these was obscured by confounding of some climatic factors. The differences in prevalence of the three Trichostrongylus spp. at different locations was attributed to differences in preferred ambient conditions for development and survival of the free-living stages.

Viability of the sporocysts of Sarcocystis cruzi after exposure to different temperatures and relative humidities

The effect of temperature and relative humidity (RH) on the survival of sporocysts of S. cruzi were investigated in vitro. Under all experimental conditions (temperature of 4 degrees C, 37 degrees C, or room temperature; RH of 18%, 75%, or 100%) some sporozoites retained their viability to excyst for at least 90 days. The best conditions for survival were 4 degrees C at 100% RH (more than 240 days) and 37 degrees C at 18% RH (more than 180 days). Sporocysts maintained at room temperature at all humidities had the lowest level of survival. It is concluded that sporocysts of S. cruzi are able to survive in most environments for several months and that the fluctuation of the daily ambient temperature is likely to influence the viability of the sporocysts.

STUDIES ON PATHOGENESIS, TISSUE INFECTION AND CONGENITAL TRANSMISSION IN COWS EXPERIMENTALLY INFECTED WITH SARCOCYSTIS CRUZI BY VARIOUS ROUTES

A group of nine cows, naturally infected with Sarcocystis, were challenged with Sarcocystis cruzi: three intrarumenally with sporocysts, two intrarumenally with water (controls), two intravenously with merozoites grown in vitro and two intravenously with saline solution (controls). The animals intrarumenally challenged with sporocysts developed acute sarcocystiosis and produced stillborn calves, whereas those intravenously challenged with merozoites suffered from subclinical sarcocystiosis with premature births. No parasites were found in calves from cows challenged with sporocysts; however, a meront of Sarcocystis was found within a macrophage in the cerebrospinal fluid of a calf from a cow intravenously inoculated with merozoites of S. cruzi. This is the first time that merozoites of S. cruzi grown in vitro have been demonstrated to retain the ability to infect their natural intermediate host and complete their life cycle.

Excystation rates and infectivity of sporocysts of Sarcocystis cruzi exposed to different treatments and storages

The effect of some chemical and anatomical factors on the excystability and infectivity in cell culture of sporocysts of Sarcocystis cruzi was investigated. A significantly (P < 0.001) higher excystation rate (ER) occurred when sodium bicarbonate was added to the excysting fluid at concentrations between 0.075 and 0.3 M. Sporocysts collected from different dogs had different ER. In contrast, although not uniformly distributed along the intestinal lumen, the sporocysts collected from the different tracts of the intestine showed similar ER. The period of storage did not affect the excystability of the sporocysts; however, it influenced the pattern of growth of the sporozoites in cell culture. Sporozoites excysted from sporocysts stored for approximately 2 years grew slower and produced significantly fewer merozoites compared to those excysted from sporocysts stored for 5-7 months.