Biomedical subjects
Publications and source records attributed to I K Barker.
A case of an ectopic mummified fetus in a Macaca assamensis is described. The condition was detected on routine clinical examination of a newly acquired monkey, and the mummified fetus was surgically removed.
A painted turtle (Chrysemys picta) which died in captivity had marked necrosis in the liver and lungs with numerous intranuclear inclusion bodies in hepatocytes and respiratory epithelial cells. Electron microscopy revealed herpesvirus-like particles in cells in affected tissues.
Lesions caused by an avian poxvirus were identified on the face and nares of fledgling white-tailed tropicbirds (Phaethon lepturus catesbyi) in the natural environment on Bermuda. Between 1958 and 1978, 6 of 81 fledglings found off the nest and unable to fly at departure time had lesions suggestive of poxvirus infection. More detailed nest-site surveys from 1974 to 1978 indicated an overall prevalence of less than 0.5%, involving the fledgling population only.
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.
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Klossiella spp. were found in kidneys of individuals from six genera in two of the three superfamilies of Australian marsupials. Klossiella quimrensis sp.n. is described in the bandicoots, Isoodon obesulus and Perameles gunnii (Peramelidae). K. convolutor sp.n. is described in the ringtail possum Pseudocheirus peregrinus (Petauridae). Three macropodid genera were infected. K.serendipensis sp.n. is described in the swamp wallaby, Wallabia bicolor, and K. callitris sp.n. is described in the western grey kangaroo, Macropus fuliginosus. Multinucleate bodies considered to be schizonts of a Klossiella sp. were observed in the kidneys of the potoroo, Potorous apicalis. Gametocytes only of K. serendipensis were seen, while gametogony and sporogony of K. convolutor and K. callitris were observed.
Twelve dogs were fed mutton containing small sarcocysts, and killed 1, 3, 4, 6, 7, 10, 15, 16, 17 days after infection (DAI). Beginning 13-15 DAI sporocysts 14.7 times 9.0 mum were passed in the faeces of the dogs killed 15-17 DAI. Histological examination showed that developing stages were most numerous in the subepithelial tissue at the tips of villi in the proximal third of the small intestine. Macrogametes containing tiny PAS + granules, and microgametocytes with peripheral developing microgametes were present 1 DAI. By 4 DAI oocysts, with a small nucleus and vacuolate cytoplasm were seen. Sporulation was observed 7-10 DAI. The first nuclear division resulted in 2 polar nuclei which divided laterally, resulting in 2 sporocysts each with 2 polar nuclei. This process was repeated once more to produce 4 nucleated sporozoites in each of 2 sporocysts. PAS + granules were seen at the periphery of sporulating oocysts and sporocysts. There was a large PAS + granule in the mid zone of sporozoites, with a smaller granule at one tip. Numerous sporulated sporocyst pairs were present beneath the epithelium at the tips of villi in dogs killed during patency. Four lambs were inoculated orally with sporocysts passed by dogs following feeding of infected mutton. Fifteen DAI schizonts were seen in the endothelium of arteries and arterioles in many organs, but not brain. Twenty-four DAI, smaller schizonts were seen in capillary endothelium in many organs, including brain. The two other lambs died 42 and 104 DAI, after an illness characterized by anaemia and ill-thrift. Mature schizonts were found in cells in the brain 42 DAI, associated with nonsuppurative meningoencephalitis. Developing sarcocysts were found in muscle, associated with myositis. Sarcocysts in muscle 104 DAI were mature. In the brain there were degenerate cysts and mature sarcocysts, and nonsuppirative meningoencephalitis.
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Stammerinema suffodiax sp. n. is described from the dasyurid marsupial Antechinus stuartii. It differs from S. soricis, the only other member of the genus, in lacking lateral body spines, as well as in the spicules and characters of the anterior extremity. As well as redescribing Synhimantus australiensis (Johnston and Mawson, 1952) now collected from the stomach of A. stuartii, a new capillariid, Capillaria rickardi from the stomach and two cestodes Hymenolepis aklei sp. n. and H. bradleyi sp. n. are described from the same host.
Observations were made on the histology of tissues from the first 6-10 m of the small intestine from both sheep infected with Trichostrongylus colubriformis and from uninfected controls. In uninfected animals, and in distal samples from infected lambs, villi were tall and covered by tall columnar epithelium, the intestinal crypts were convoluted and the lamina propria was only moderately cellular. In tissues with sub-total villus atrophy and a convoluted surface, the superficial epithelium was usually low columnar, often with an indistinct brush border. More severely affected mucosa was flat, with low surface epithelium and protruding crypt openings. The flat surfaces frequently had leaks of eosinophilic material and polymorphonuclear cells between enterocytes, or through erosions in the epithelium. Such defects were smaller and less frequent in mucosa with a convoluted surface. There were increased mitoses in intestinal crypts and a heavy inflammatory cell infiltrate in the lamina propria. Mast cell, globule leucocyte and theliolymphocyte numbers were not increased in infected sheep.
Increased permeability of capillaries and venules, labelled with colloidal carbon, was observed in the superficial mucosa of the small intestine of sheep infected with Trichostrongylus colubriformis. The labelled vessels were restricted to infected portions of the gut, and the intensity of labelling appeared to be related to density of the worm population. Open junctions were seen between endothelial cells in permeable vessels. In moderately atrophic infected intestine, enterocytes were domed, had sparse, short, distorted microvilli and many polyribosomes. Tight junctions between enterocytes seemed to be intact and distended intercellular spaces were seen. In more severely atrophic mucosa, enterocytes had distended mitochondria and endoplasmic reticulum, bizarre shapes, and the continuity of the epithelial sheet was occasionally disrupted. There was oedema in the lamina propria and neutrophils were seen in migration to the lumen of the gut. The possible mechanisms inducing these changes and their significance in terms of plasma protein loss and intestinal function are discussed.
Lesions, grossly and histologically typical of pox infection, occurred in a white-backed magpie from Melbourne, Australia. Electron microscopic examination revealed typical poxvirus particles in lesion material. The disease was experimentally transmitted to other magpies, but chickens, turkeys, pigeons, and canaries were refractory to experimental infection with magpie poxvirus. The epidemiology of magpie pox and the probable occurrence of pox-like disease in other native Australian birds are discussed.
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Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.