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Bovine anaplasmosis, caused by the tick-borne rickettsia Anaplasma marginale, is endemic in South Africa and results in considerable economic loss to the cattle industry. This study was designed to characterize strains of A. marginale at the molecular level from cattle raised in communal and commercial farms in the north-eastern and south-western regions of the Free State Province, South Africa, that varied in rainfall and vegetation. Seroprevalence to A. marginale was determined in 755 cattle by an Anaplasma spp. competitive enzyme-linked immunosorbent assay and ranged from 44% to 98% and was similar in both regions. While Anaplasma centrale was not targeted in this study, A. marginale infections were identified by species-specific msp1alpha polymerase chain reaction in 129 of 215 of the samples studied. Similar genetic diversity of A. marginale strains was found in both the north-eastern and south-western regions. The sequences of 29 A. marginalemsp1alpha amplicons from South African strains revealed considerable genetic diversity providing 14 new repeat sequences. However, 42% of MSP1a repeat sequences were not unique to this region. These results indicated the presence of common genotypes between South African, American and European strains of A. marginale. Cattle movement between different parts of South Africa was suggested by the presence of identical A. marginale MSP1a genotypes in north-eastern and south-western regions of the Free State Province. Control strategies for anaplasmosis in South Africa should therefore be designed to be protective against genetically heterogeneous strains of A. marginale.

Vervet monkeys (Cercopithicus aethiops) were shown to give a positive delayed-type hypersensitivity (DTH) reaction to gp63, a major surface glycoprotein of Leishmania parasites, and also produce antibodies to the molecule following a triple vaccination with a total dose of 150 micrograms of recombinant gp63 mixed with Bacille Calmette Guerin (BCG). However,

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Summaryobjective To evaluate the repeatability and reproducibility of the serological direct agglutination test (DAT) for visceral leishmaniasis (VL) with aqueous antigen in a multi-centre study in VL-endemic areas in Sudan, Kenya and Nepal.methods Repeatability within each centre and reproducibility between the centres' results and an external reference laboratory (Belgium) was assessed on 1596 triplicate plain blood samples collected on filter paper.results High kappa values (range 0.86-0.97) indicated excellent DAT repeatability within the centres. The means of the titre differences between the reference laboratory and the centres in Sudan, Kenya and Nepal (2.3, 2.4 and 1.1, respectively, all significantly different from 0) showed weak reproducibility across centres. 95% of the titre differences between the reference laboratory and the respective centres were accounted for by large intervals: 0.6-9 fold titre variation for Sudan, 0.7-8 fold for Kenya and 0.26-4 fold for Nepal.conclusion High repeatability of DAT confirms its potential, but reproducibility problems remain an obstacle to its routine use in the field. Reproducibility was hindered by alteration of the antigen through temperature and shaking, especially in Kenya and Sudan, and by nonstandardization of the test reading. DAT handling procedures and antigen quality must be carefully standardized and monitored when introducing this test into routine practice. keywords reproducibility, direct agglutination test, visceral leishmaniasis, diagnosis, repeatability, agreement

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The purpose of the study was to record and determine intensities, seasonal incidence and distribution of helminth parasites of veterinary importance that occur in cattle, sheep and goats in the northeastern Free State. The study was conducted at Harrismith and Kestell and in Qwa-Qwa from March 2000 to May 2001. Cattle of various breeds (including Bonsmara, Simmentaler and Friesian), Merino sheep and Angora goats were sampled. Faecal samples were analysed using the McMaster and Visser sieve techniques for egg counts and faecal cultures for 3rd-stage nematode larvae identification. Haemonchus and Oesophagostomum were the dominant nematode genera found to be infecting the animals. The socioeconomic status of the farmers in the study area was determined through a questionnaire survey aimed at recording their management strategies. It indicated that 81 % of farmers take care of their livestock by feeding them with supplements. The low to moderate faecal egg counts from cattle showed that helminth infections in this region are still under control even though helminthosis seems to be a problem in small-stock, since EPG counts of more than >1000 were found. Cattle farmers in this region are encouraged to continue with good animal husbandry practices that have ensured that helminth infections rates are kept low. Small-stock farmers are, however, encouraged to control helminth infections in their sheep and goats by anthelmintic treatment