Biomedical subjects
Publications and source records attributed to G Uilenberg.
Cross immunity tests with strains of Cowdria ruminantium from South Africa, the Sudan, São Tomé and Nigeria failed to demonstrate antigenic differences. The antibiotic ampicillin showed no activity against heartwater.
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One pathogenic and 4 mild bovine Theileria strains from southern Africa, all transmitted by Rhipicephalus appendiculatus, were compared amongst themselves as well as to bovine and buffalo strains of the T. parva complex from eastern and southern Africa and to bovine strains of T. taurotragi from Tanzania considered to be derived from eland antelope. Criteria used were parasitological, clinical, serological and cross-immunity characters. The mild strains are similar to bovine T. taurotragi. Serological evidence suggested that T. taurotragi is also infective to sheep. The pathogenic strain belongs to the T. parva complex; the latter consists of a series of types with different behaviour ranging from the lawrencei-type (of buffalo) causing Corridor disease, through the bovis-type causing Rhodesian malignant theileriosis to the parva-type causing classical East Coat fever. Seven cattle-tick passages of a bovis-type strain did not result in transformation into a parva-type. Four species of bovine Theileriae are now known to occur in southern Africa: T. parva (lawrencei- and bovis-types) and T. taurotragi, both transmitted by R. appendiculatus, and T. mutans and T. velifera both with Amblyomma spp. as vectors.
Theileria parva infected lymphoblastoid bovine cells were grown in a medium based on HEPES-buffered RPMI 1640 with glutamine and antibiotics, supplemented with bovine serum. There were no significant differences in growth rate, viability, and percentage of infected cells when the substrate contained 10 or 20 per cent of either commercially available newborn calf serum of serum prepared from adult non-infected Friesian cattle or of serum prepared from a Friesian calf immunised against East Coast fever and having a high titre of antibodies to T. parva antigen in the indirect fluorescent antibody test. If studies showing that newborn calf serum gives results in the establishment and maintenance of T. parva cell culture similar to those of foetal calf serum are confirmed, this finding could mean an appreciable saving in the cost of in vitro work on this parasite.
The supernatant obtained after centrifugation of an emulsion of engorged female Amblyomma astrion ticks, collected from cattle on the West African island of São Tomé, was injected intravenously into a goat, which contracted heartwater. This confirmation of the existence of the disease on the island makes strict control measures necessary if present efforts at improving livestock production by imported exotic cattle are to be successful.
The tick Amblyomma maculatum proved to be an experimental vector of Cowdria ruminantium, the cause of heartwater of ruminants. Transstadial transmission from larva to nymph and from larva through nymph to adult was successful; however, an experiment on transovarial transmission gave negative results. Neither A americanum nor A cajennense transmitted the infection. There is a potential danger of the disease gaining access to the American mainland from the Caribbean where it is known to occur and of maintaining itself in areas where A maculatum occurs. Transstadial transmission experiments, using 3 American Amblyomma spp and an African strain of Theileria mutans, which is thought to occur in the Caribbean, were unsuccessful.
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Cattle living in a circumscribed area in Uganda, where both Theileria parva and T. mutans occurred naturally, were monitored for periods of up to 1 year by examination of blood and lymph node smears for parasites and the indirect fluorescent antibody test for antibodies to Theileria. Uninfected control cattle were added at intervals to ensure continuous challenge and to monitor the challenge. Although all 29 control animals became infected with T. parva, challenge was light at first as mortality from theileriosis only commenced in the 18 introduced after day 138 of the study; 14 of these died of the disease. Most of the 34 animals in the original group appeared to be susceptible to T. parva at the start of the study and 6 died of theileriosis. All animals were, or became, infected with T. mutans. Several animals exhibited patent T. parva infections on more than 1 occasion and 1 died from the second infection indicating the existence of immunologically different strains. Recovered animals appeared to acquire eventually a solid immunity to the local Theileria strains but 9 of the original animals and 7 of the controls died exhibiting massive tick and helminth burdens, sometimes aggravated by the effects of previous T. parva and/or T. mutans infections.
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A large Babesia sp., isolated from a sheep in Iran, provided to be serologically and morphologically different from B, motasi and B. ovis. The parasite, designated B. crassa n. sp., is characterized by the frequent occurrence of four organisms in one erythrocyte, which is the result of quadruple division and, in other cases, of two successive binary divisions. Parasited resulting from the first of two successive binary divisions are exceptionally broad. B. crassa appears to be of low pathogenicity for sheep and goats, to which it is also infective. The vector is unknown.
Bovine blood containing piroplasms of Theileria parva, as well as non-infected blood, was lysed and subjected to iso-electric focussing. Staining for 13 different enzymes revealed parasite-associated bands of glucose phosphate isomerase (GPI) activity, not of any of the other enzymes. There were no variations between individual donor animals in the host cell GPI bands and these bands did not interfere with the recognition of the parasite-associated bands, so that purification of the piroplasms was unnecessary. Blood from cattle infected with T. mutans also gave parasite-associated bands of GPI, but no such bands were seen in zymograms of blood from cattle infected with a Theileria sp. from Japan. Dependent on the level of parasitaemia, up to four parasite-associated bands were found in one strain of T. parva and up to three in two other strains. Among the disadvantages of using piroplasm material for the study of isoenzymes of T. parva is the fact that animals often die before their parasitaemia is sufficiently high, and that some strains never give rise to a high parasitaemia.
Eight dogs, given imidocarb dipropionate subcutaneously at a dose of 6 mg/kg, were challenged with a sporozoite stabilate of a French strain of Babesia canis, prepared from infected Dermacentor reticulatus ticks, 2, 3, 4 or 5 weeks after treatment. Three control dogs were similarly infected but not preventively treated. One of the controls and one of the dogs treated 5 weeks prior to challenge died of babesiosis. Prepatent and incubation periods were similar in treated and control dogs, and all dogs showed important reductions in the packed cell volume. Relapses were commonly seen after recovery from the initial reaction. Although further work is needed before a final conclusion can be drawn to whether imidocarb is suitable as a chemoprophylactic against B. canis infection, it can be used as a curative drug.
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A large Babesia species occurs in sheep on the North Sea islands of the Netherlands. The tick Haemaphysalis punctata is a vector. Its pathogenicity appears to be low. It is morphologically similar to a Turkish strain, considered to be B. motasi, which is also transmitted by Haemaphysalis ticks. It differs from the Turkish parasite serologically as well as in cross-immunity tests and in not being effective to goats. There may be a group of morphologically similar parasites with serological differences and different infectivity for sheep and goats. As it is impossible to know which one is to be considered as the original B. motasi, we designate the Dutch parasite as B. motase (Netherlands). Anaplasma mesaeterum was found to occur on the island of Texel as well as on Ameland, where it had been found initially.