Premature parturition in ewes inoculated with Sarcocystis ovicanis.

A dose of 6 X 10(4) Sarcocystis ovicanis sporocysts produced premature parturition in ewes and eventually proved fatal. The main pathological findings were myositis, myocarditis and encephalitis. Dose rates over the range of 2.5 X 10(3) to 6 X 10(4) depressed the haematocrit levels of pregnant ewes during the period 5-9 weeks after inoculation. Previous infection with S. gigantia did not protect from subsequent challenge with S. ovicanis.

Effects of different doses of dog-derived Sarcocystis sporocysts on growth rate and haematocrit in lambs.

Four-week-old lambs at pasture were dosed with dog-derived Sarcocystis sporocysts. No difference in growth rates was apparent at a dose of 1 X 10(3) sporocysts per lamb. The minimum dose required to depress growth rate was 2.5 X 10(3) sporocysts per lamb: at 4 weeks post-inoculation (w.p.i.) the weight gain of lambs infected with this dose was 0.6 kg less than the non-infected controls (P less than 0.05). At 11 w.p.i. the difference was 0.7 kg, but this was not significant because of the greater average body weights of both groups. Lambs given 5 X 10(3) sporocysts showed significant depression of weight gain at both 4 and 11 w.p.i. Haematocrit levels at 4-5 weeks post-inoculation were depressed by doses as low as 1 X 10(3) sporocysts.

Demonstration of viable Sarcocystis sporocysts in the faeces of a lamb dosed orally.

Faecal flotations prepared after dosing a lamb with 3.5 X 10(6) dog-derived Sarcocystis sporocysts proved infective for other lambs for at least 7 days post-dosing. This confirms observations suggesting faecal transfer of sporocysts from treated to control lambs.

The effect of Sarcocystis tenella on wool growth in sheep.

A dose of 1 X 10(4) Sarcocystis tenella sporocysts produced significant depression of wool growth in lambs dosed at 1 month of age. No significant effect on wool growth was produced when lambs were dosed at 5 months of age.

Demonstration of schizogonous stages of Sarcocystis gigantea in experimentally infected sheep.

Sarcocystis-free lambs were orally dosed with 1 X 10(6) sporocysts of Sarcocystis gigantea. Schizonts were found in endothelial cells of capillaries and arterioles of the brain, lung and kidney of lambs 7 and 14 days post-inoculation (d.p.i.). Between 21 and 35 d.p.i. there was extensive multi-focal encephalitis; however no organisms were detected in association with these lesions.

Experimental infection with Sarcocystis medusiformis in sheep.

The development of the parasite was studied in 48 sheep killed between 188 and 1132 days after experimental inoculation with Sarcocystis medusiformis sporocysts from cats. Immature sarcocysts were present at 188 days post inoculation (d.p.i.). At 331 d.p.i. macroscopic sarcocysts with an elongate fusiform appearance were seen in the laryngeal, abdominal and diaphragm musculature. The largest cyst measured 2 mm in length by 0.5 mm in width at 331 d.p.i.; histologically they contained metrocytes at the periphery of the cyst with more densely staining merozoites in the central region. By 443 d.p.i. typical 'thin' cysts 2-3.5 mm in length were seen in the flank and external thoracic muscles. By 765 d.p.i. sarcocysts were 5 mm in length. The ultrastructure of the cyst wall of these cysts resembled that of S. medusiformis. At 1132 d.p.i. sarcocysts measured 4 mm X 0.5 mm.

Morphology of Sarcocystis gigantea in experimentally-infected sheep.

The development of the parasite and lesions was studied in 32 sheep killed 10 days to 47 months after inoculation with Sarcocystis gigantea sporocysts from cats. At 21-42 days post-inoculation (d.p.i.), there was a mild encephalitis, but organisms were not seen in the brain. Immature sarcocysts were detected from 40-84 d.p.i. The cyst wall was not measurable by light microscopy at 40 d.p.i., but was 1.5-2 microns thick at 84 d.p.i. At 119 d.p.i. both immature cysts containing only metrocytes, and mature cysts containing both metrocytes and merozoites, were present. These mature cysts did not have a secondary cyst wall. A mature cyst, 350 microns in length, was found in a sheep killed at 8 1/2 months p.i. At 10 m.p.i. cysts were up to 0.5 mm long and a secondary cyst wall was present. At 47 m.p.i. cysts were 2-5 X 4.5-7.5 mm, and were found only in the muscles of tongue, oesophagus, pharynx and flank.

Development and growth of Sarcocystis gigantea in experimentally-infected sheep.

Immature, microscopic Sarcocystis gigantea sarcocysts were detected in experimental sheep from 1.3 to 4 months after dosing with sporocysts from cats. Mature, microscopic sarcocysts were also present at 4 months post-inoculation (p.i.). S. gigantea sarcocysts were 0.35 mm long at 8.5 months p.i. and gradually increased in size to 7.5 mm by 45 months p.i. Transmission back to cats was demonstrated at 14 months p.i.

Serodiagnosis of acute toxoplasmosis in macropods.

The sera of 34 Australian macropods, the brains of which had been bioassayed for Toxoplasma gondii, were used to establish that a titre greater than 1/32 was significant for a direct agglutination test against toxoplasmosis. In addition, the concentration of 2-mercaptoethanol required to destroy the IgM fraction of macropod serum was confirmed in a modified direct agglutination test. To further validate the tests, the serological responses of three eastern grey kangaroos (Macropus giganteus) dosed orally with T. gondii oocysts and one M. giganteus injected with T. gondii cysts were studied. The tests were then used to investigate a diagnosis of acute toxoplasmosis in four Tasmanian pademelons (Thylogale billardierii) clinically suspected of acquiring toxoplasmosis naturally. One hundred and fifty-one Bennett's wallabies (Macropus rufogriseus rufogriseus) and 85 T. billardierii were also tested to determine the prevalence of acute toxoplasmosis of macropods in the wild. Four percent of M. r. rufogriseus and 1.2% of T. billardierii possessed T. gondii-specific IgM in their sera.

Ovine sporozoan encephalomyelitis linked to Sarcocystis infection.

The unidentified sporozoan causing encephalomyelitis in sheep described by Hartley and Blakemore (1974) was restudied, and the parasite was identified as a Sarcocystis species based on its location and structure. The parasite was located free in the host-cell cytoplasm, divided by endopolygeny and mature merozoites lacked rhoptries.

Pathology produced by, prevalence, of, and probable life-cycle of a species of Sarcocystis in the domestic fowl.

Sarcosporidiosis was found to be the cause of a severe myositis in 3 fowls in Papua New Guinea and 2 in Australia. This represented 3.8% of a series of fowls examined in Papua New Guinea. The overall prevalence of infection in these birds was 45%. Both epidemiological and experimental evidence suggested that the dog was the definitive host for this particular type of sarcocyst.

Accumulation of persistent organic pollutants in Tasmanian platypus (Ornithorhynchus anatinus).

Tailfat samples were collected from 56 platypuses, 38 male and 18 female in Tasmania. No statistically significant, nor apparent, differences between the sexes were found for tailfat lipid levels and DDT and its metabolites. Lindane and PCB concentrations in tailfat lipid. Apparently--but not statistically--significantly different levels of DDT and its metabolites. Lindane and PCB concentrations were found in animals from different geographic regions of the State. Higher concentrations of DDT and its metabolites and Lindane were related to the intensity of agricultural activity and elevated PCB levels were mainly found in animals from zones with industrial and hydroelectric developments.

Environmental factors and chemical agents affecting the growth of the pathogenic marine ciliate Uronema nigricans.

The scuticociliate Uronema nigricans is an opportunistically parasitic marine ciliate known to cause disease in some aquacultural environments with epizootics documented from marine larval rearing systems, marine aquaria and in southern bluefin tuna Thunnus macoyii growout enclosures. This study examined growth responses of laboratory cultures of the ciliate and prey bacteria to variations in temperature and salinity, and the efficacy of potential chemotherapeutants for control of U. nigricans infections. Differences in ciliate growth responses were marginal at temperatures of 10 to 25 degrees C and at salinities between 15 and 35 ppt, though 3.5 ppt or less was lethal. Ciliates were found to be sensitive to fluctuations in bacterial densities, which may be a factor in the seasonal occurrence of the ciliate-related disease in tuna. Commonly used chemotherapeutants such as formalin, malachite green and hydrogen peroxide were all effective against the ciliate during in vitro trials.

Coccidia of wombats: correction of host-parasite relationships. Eimeria wombati (Gilruth and Bull, 1912) Comb. Nov. and Eimeria ursini Supperer, 1957 from the hairy-nosed wombat and Eimeria arundeli sp. n. from the common wombat.

Coccidial oocysts morphologically consistent with Eimeria ursini Supperer 1957, and E. tasmaniae Supperer 1957 were recovered from the feces of wild and captive hairy-nosed wombats (Lasiorhinus latifrons) in Australia. Eimeria arundeli so. n. was recovered from the feces of wild and captive common wombats (Vombatus ursinus). Eimeria arundeli oocysts are ellipsoidal to slightly ovoid 60.2--67.2 (63.7) X 40.6--47.6 (43.4); micropyle 3 in diameter usually visible; with oocyst wall granular, dark brown and occasionally opaque, 4--7 thick; inner oocyst wall clear, about 1.5 thick; small oocyst residuum present, four sporocysts ovoid 22.4--29.4 (25.8) X 12.6--15.4 (14.1) with protuberant Stieda body; opposite end of sporocyst also often slighly pointed; large granular sporocyst residuum obscuring sporozoites. Gametocytes of E. arundeli sp. n. and of an organism which is consistent with E. tasmaniae, are described developing in the lamina propria of villi in the small intestine. The stages in the hairy-nosed wombat are those described as Ileocystis wombati Gilruth and Bull 1912. It is suggested that the identification of the host of Supperer's E. ursini and E. tasmaniae as V. ursinus was in error and that the allopatric L. latifrons is the natural host. Eimeria tasmaniae Supperer 1957 is suppressed and E. wombati (Gilruth and Bull, 1912) comb. nov. is proposed and redescribed. No schizonts were identified among the endogenous stages, consistent with observations in the literature on other coccidia with similar gametocyte and oocyst structure.

Phylogeny of the multivalvulidae (Myxozoa: Myxosporea) based on comparative ribosomal DNA sequence analysis.

Fish parasites of the Multivalvulida (Myxozoa, Myxosporea) are widespread and can be associated with mortality or poor flesh quality in their commercially important marine hosts. Traditional classifications divide members of this order into families based on spore valve and polar capsule numbers. Analyses of the small-subunit (SSU) ribosomal DNA (rDNA) sequences from all representative families in the order (Trilosporidae, Kudoidae, Pentacapsulidae, Hexacapsulidae, and Septemcapsulidae) indicate that a revision of the taxonomy and nomenclature is warranted. In our phylogenetic analysis of (SSU and large subunit) rDNA sequences, members of Pentacapsula, Hexacapsula, and Septemcapsula root within a clade of Kudoa species with Unicapsula (Trilosporidae) as an outlier to these genera. Therefore, we propose to synonymize Pentacapsulidae, Hexacapsulidae, and Septemcapsulidae with Kudoidae alter the diagnosis of Kudoidae and Kudoa to accommodate all marine myxozoan parasites having 4 or more shell valves and polar capsules.

Immunoglobulin classes of antibodies produced against Toxoplasma gondii by ovine fetuses.

Sera from aborted or newborn lambs with congenital toxoplasmosis were fractionated on Sephadex G-200. Sera and fractions were tested for Toxoplasma antibodies using the indirect fluorescent antibody test. Most of the antibody was found to reside in the IgG fraction.

Placental transfer of specific antibodies during ovine congenital toxoplasmosis.

The passage of non-Toxoplasma antibodies from dam to fetus through damaged placenta was studied in sheep inoculated with Toxoplasma gondii. Six ewes were inoculated with chicken globulins and Leptospira bacterins 2 months before oral inoculation with Toxoplasma gondii oocysts. Ewes were euthanatized between 42 and 62 days after T gondii inoculation. Antibody titers against chicken globulins, Leptospira spp, Haemonchus contortus, Sarcocystis spp, and T gondii were measured in the maternal and fetal sera. All ewes became infected with T gondii and had grossly visible necrotic foci in the placentas, and T gondii antibodies were found in the fetuses and the ewes. Appreciable amounts of antibodies to Haemonchus contortus, Sarcocystis sp, Leptospira spp, and chicken globulins did not cross the placental barrier. Seemingly, serologic examination of the fetus was reliable for the diagnosis of ovine congential toxoplasmosis.

A species of Sarcocystis using owls as definitive hosts.

Sporulated oocysts found in the intestines of a Masked Owl (Tyto novaehollandiae) and a Barn Owl (T. alba) produced sarcocysts in mice. Schizonts were found in the livers of 3 mice that died at 7-8 days after dosing. Neither sarcocysts nor schizonts were found in chickens dosed with oocysts from a Masked Owl.

Sarcocystis and related organisms in Australian wildlife: III. Sarcocystis murinotechis sp.n. life cycle in rats (Rattus, Pseudomys and Mastocomys spp.) and tiger snakes (Notechis ater).

Sporocysts from tiger snakes (Notechis ater) produced thick-walled sarcocysts in laboratory rats (Rattus norvegicus). Ultrastructurally these organisms were identical with sarcocysts found in native rats, but were different from Sarcocystis singaporensis. Sarocystis murinotechis sp.n. is proposed for this parasite of rodents and tiger snakes. When naturally-infected rats were fed to kittens (Felis domestica), quolls (dasyurus viverrinus) and a masked owl (Tyto novaehollandiae) no sporocysts were detected in the faeces of these animals. Also, sporocysts from owls (T. novaehollandiae and Ninox novaeseelandiae) were not infective for rats (R. norvegicus).

Sarcocystis and related organisms in Australian Wildlife: IV. Studies on Sarcocystis cuniculi in European rabbits (Oryctolagus cuniculus).

The role of the cat (Felis domestica) as a definitive host for Sarcocystis cuniculi of European rabbits (Oryctolagus cuniculus) was confirmed. It was shown that after dosing with sporocysts from cats, rabbits developed sarcocysts and these became infective for cats at not less than 93 days post-infection (p.i.). The earliest infection detected was at 142 days p.i. Infected muscle from an experimental rabbit did not transmit Sarcocystis when fed to other rabbits. Microscopically, sarcocysts in European rabbits (O. cuniculus) were morphologically indistinguishable from those in cottontail rabbits (Sylvilagus floridanus).