Two hundred and seventy-three elephant shrews, consisting of 193 Elephantulus myurus, 67 Elephantulus edwardii and 13 animals belonging to other species, were examined for ixodid ticks at 18 localities in South Africa and Namibia. The immature stages of Ixodes rubicundus, Rhipicentor nuttalli, Rhipicephalus warburtoni and a Rhipicephalus pravus-like tick were the most numerous of the 18 tick species recovered. Substantial numbers of immature Rhipicephalus arnoldi, Rhipicephalus distinctus and Rhipicephalus exophthalmos were also collected from elephant shrews at particular localities. Larvae of I. rubicundus were most numerous on E. myurus in Free State Province from April to July and nymphs from June to October. Larvae of R. nuttalli were most numerous on these animals during April, May, August and September, and nymphs in February and from April to August. The immature stages of R. warburton were collected from E. myurus only in Free State Province, and larvae were generally most numerous from December to August and nymphs from April to October.

Two hundred and seventy-three elephant shrews, consisting of 193 Elephantulus myurus, 67 Elephantulus edwardii and 13 animals belonging to other species, were examined for ixodid ticks at 18 localities in South Africa and Namibia. The immature stages of Ixodes rubicundus, Rhipicentor nuttalli, Rhipicephalus warburtoni and a Rhipicephalus pravus-like tick were the most numerous of the 18 tick species recovered. Substantial numbers of immature Rhipicephalus arnoldi, Rhipicephalus distinctus and Rhipicephalus exophthalmos were also collected from elephant shrews at particular localities. Larvae of I. rubicundus were most numerous on E. myurus in Free State Province from April to July and nymphs from June to October. Larvae of R. nuttalli were most numerous on these animals during April, May, August and September, and nymphs in February and from April to August. The immature stages of R. warburton were collected from E. myurus only in Free State Province, and larvae were generally most numerous from December to August and nymphs from April to October.

This paper focuses on the geographical distribution and habitats of Bulinus forskalii, the snail intermediate host of the conical fluke of equids, Gastrodiscus aegyptiacus as reflected by the 1 209 samples in the database of the National Freshwater Snail Collection of South Africa. The 362 different loci on record represent an extensive distribution in KwaZulu-Natal Province, the Limpopo Province, the coastal areas of the Eastern Cape Province and the south-eastern part of the North West Province. Although it was recorded from all types of water-body represented in the database, the highest percentages of samples were recovered from dams (30.4 %) and brooks (28.2 %). The majority of samples came from perennial habitats (59.1%), 60.7% from habitats with standing water, 54.0 % from habitats with clear water and 71.8 % from habitats of which the water was described as fresh. The majority of samples (39.5 %) were collected in habitats of which the substratum was recorded as muddy. The highest percentage of samples, by far (81.5 %), was collected in habitats that fell within the mean yearly temperature interval ranging from 15-20 C. An integrated decision tree constructed from the data in the database indicated that temperature and type of water-body played a decisive role in determining the presence of B. forskalii in a given area. The results of experimental exposure to miracidia of a local strain of both Schistosoma haematobium and Schistosoma mattheei in the laboratory indicated that a local strain of B. forskalii was incompatible with both these strains of parasite. Research to clarify the role of B. forskalii in the transmission of both Calicophoron microbothrium and G. aegyptiacus in South Africa, is recommended.

This paper focuses on the geographical distribution and habitats of Bulinus forskalii, the snail intermediate host of the conical fluke of equids, Gastrodiscus aegyptiacus as reflected by the 1 209 samples in the database of the National Freshwater Snail Collection of South Africa. The 362 different loci on record represent an extensive distribution in KwaZulu-Natal Province, the Limpopo Province, the coastal areas of the Eastern Cape Province and the south-eastern part of the North West Province. Although it was recorded from all types of water-body represented in the database, the highest percentages of samples were recovered from dams (30.4 %) and brooks (28.2 %). The majority of samples came from perennial habitats (59.1%), 60.7% from habitats with standing water, 54.0 % from habitats with clear water and 71.8 % from habitats of which the water was described as fresh. The majority of samples (39.5 %) were collected in habitats of which the substratum was recorded as muddy. The highest percentage of samples, by far (81.5 %), was collected in habitats that fell within the mean yearly temperature interval ranging from 15-20 °C. An integrated decision tree constructed from the data in the database indicated that temperature and type of water-body played a decisive role in determining the presence of B. forskalii in a given area. The results of experimental exposure to miracidia of a local strain of both Schistosoma haematobium and Schistosoma mattheei in the laboratory indicated that a local strain of B. forskalii was incompatible with both these strains of parasite. Research to clarify the role of B. forskalii in the transmission of both Calicophoron microbothrium and G. aegyptiacus in South Africa, is recommended.

A wild strain of Eimeria tenella was isolated and utilized for immunization studies. Its optimal sporulation was attained at room temperature 24-25 C after 24-48 h. Two groups of chicks were immunized by dosing a graded dose of five oocysts/chick/day for 6 days followed by 50 oocysts/chick/day for 7 days. A third group was not immunized and served as a negative control. Immunized chicks gained mass at the same rate as unimmunized ones, but when challenged with 200 000 oocysts/chick, mass gains declined in the unimmunized group. The growth rate of immunized chicks was not affected by challenge (P 0.05). Upon challenge, unimmunized chicks produced significantly more oocysts than immunized chicks (P 0.005). Immunized chicks withstood a challenged with 200 000 oocysts/chick without developing any clinical signs whereas the unimmunized chicks developed typical clinical signs of coccidiosis. Unimmunized chicks had significantly more severe lesions in the caecum than any other group (P 0.005) and also produced significantly more oocysts than any other group (P 0.005).

A wild strain of Eimeria tenella was isolated and utilized for immunization studies. Its optimal sporulation was attained at room temperature 24-25 °C after 24-48 h. Two groups of chicks were immunized by dosing a graded dose of five oocysts/chick/day for 6 days followed by 50 oocysts/chick/day for 7 days. A third group was not immunized and served as a negative control. Immunized chicks gained mass at the same rate as unimmunized ones, but when challenged with 200 000 oocysts/chick, mass gains declined in the unimmunized group. The growth rate of immunized chicks was not affected by challenge (P > 0.05). Upon challenge, unimmunized chicks produced significantly more oocysts than immunized chicks (P < 0.005). Immunized chicks withstood a challenged with 200 000 oocysts/chick without developing any clinical signs whereas the unimmunized chicks developed typical clinical signs of coccidiosis. Unimmunized chicks had significantly more severe lesions in the caecum than any other group (P > 0.005) and also produced significantly more oocysts than any other group (P > 0.005).

Seroprevalence rates of Toxoplasma gondii anti-antibodies in adult goats and sheep from different parts of Zimbabwe were determined. A total of 225 (67.9 %) of the 335 serum samples tested were positive for anti-T. gondii IgG antibodies with the indirect fluorescent antibody test. There were differences in antibody seroprevalences among communal land goats from the different agro-ecological zones (Natural regions IIb and III: 80 and 96.7 %, respectively; Natural region IV: 65.9 %; Natural region V: 45 %; and Natural region III had a significantly higher seroprevalence than IV and V. The highest seroprevalences found in Natural regions II b and III are likely to be linked to the existence of more households and hence the possibility of a higher concentration of domestic cats that increases the chances of environmental contamination with their faeces harbouring T. gondii oocysts. The seroprevalence rate in sheep from a large commercial farm (10 %) was significantly lower than that of sheep reared under the communal grazing system (80 %). Overall, significantly higher proportions of seropositive animals had antibody titres of 1:50 (34.2 % of 225) and 1:100 (44 % of 225) as compared to the 9.8 % and 12 % with antibody titres of 1:200 and 1:400, respectively.

Seroprevalence rates of Toxoplasma gondii anti-antibodies in adult goats and sheep from different parts of Zimbabwe were determined. A total of 225 (67.9 %) of the 335 serum samples tested were positive for anti-T. gondii IgG antibodies with the indirect fluorescent antibody test. There were differences in antibody seroprevalences among communal land goats from the different agro-ecological zones (Natural regions IIb and III: 80 and 96.7 %, respectively; Natural region IV: 65.9 %; Natural region V: 45 %; and Natural region III had a significantly higher seroprevalence than IV and V. The highest seroprevalences found in Natural regions II b and III are likely to be linked to the existence of more households and hence the possibility of a higher concentration of domestic cats that increases the chances of environmental contamination with their faeces harbouring T. gondii oocysts. The seroprevalence rate in sheep from a large commercial farm (10 %) was significantly lower than that of sheep reared under the communal grazing system (80 %). Overall, significantly higher proportions of seropositive animals had antibody titres of 1:50 (34.2 % of 225) and 1:100 (44 % of 225) as compared to the 9.8 % and 12 % with antibody titres of 1:200 and > 1:400, respectively.

Ticks were collected at approximately bi-monthly intervals between June 1996 and June 1997 from crested francolins, Francolinus sephaena, and from the vegetation on a mixed cattle and wildlife farm in Limpopo Province, South Africa. The birds were infested with the immature stages of 13 tick species, of which Amblyomma hebraeum, Amblyomma marmoreum and Hyalomma marginatumrufipes were the most numerous and prevalent. Ten ixodid tick species were collected from the vegetation, of which the immature stages of Rhipicephalus appendiculatus, Rhipicephalus (Boophilus) decoloratus and Rhipicephalus evertsi evertsi were the most numerous. No adult ticks were collected from the birds and only two from the vegetation. The restricted home range of crested francolins implies that they could serve as a source of tick infestation only for other animals within the same habitat as the birds.

Ticks were collected at approximately bi-monthly intervals between June 1996 and June 1997 from crested francolins, Francolinus sephaena, and from the vegetation on a mixed cattle and wildlife farm in Limpopo Province, South Africa. The birds were infested with the immature stages of 13 tick species, of which Amblyomma hebraeum, Amblyomma marmoreum and Hyalomma marginatumrufipes were the most numerous and prevalent. Ten ixodid tick species were collected from the vegetation, of which the immature stages of Rhipicephalus appendiculatus, Rhipicephalus (Boophilus) decoloratus and Rhipicephalus evertsi evertsi were the most numerous. No adult ticks were collected from the birds and only two from the vegetation. The restricted home range of crested francolins implies that they could serve as a source of tick infestation only for other animals within the same habitat as the birds.

Five species of ixodid ticks were found in a cross-sectional survey in which 200 sheep were examined for ticks in River Nile Province, Sudan. Hyalomma anatolicum anatolicum was the predominant species (73.6 %), whereas ticks belonging to the Rhipicephalus sanguineus group (14.7 %), Rhipicephalus evertsi evertsi (9.1 %), Rhipicephalus simus (2 %) and Hyalomma dromedarii (0.5 %) were also found. The mean tick load was 11.2 per animal. In a subsequent longitudinal survey ticks were collected on a monthly basis from eight sentinel sheep that were introduced into the area. It was found that H. a. anatolicum almost disappeared during the hot period between April and August, whereas it's highest numbers were present in winter between November and February. It is concluded that there is only one generation of H. a. anatolicum per year, which may explain the yearround appearance of clinical cases of malignant ovine theileriosis indicating endemic instability of this disease in River Nile Province.

Five species of ixodid ticks were found in a cross-sectional survey in which 200 sheep were examined for ticks in River Nile Province, Sudan. Hyalomma anatolicum anatolicum was the predominant species (73.6 %), whereas ticks belonging to the Rhipicephalus sanguineus group (14.7 %), Rhipicephalus evertsi evertsi (9.1 %), Rhipicephalus simus (2 %) and Hyalomma dromedarii (0.5 %) were also found. The mean tick load was 11.2 per animal. In a subsequent longitudinal survey ticks were collected on a monthly basis from eight sentinel sheep that were introduced into the area. It was found that H. a. anatolicum almost disappeared during the hot period between April and August, whereas it's highest numbers were present in winter between November and February. It is concluded that there is only one generation of H. a. anatolicum per year, which may explain the yearround appearance of clinical cases of malignant ovine theileriosis indicating endemic instability of this disease in River Nile Province.

Aqueous decoctions obtained from the galls of Guiera senegalensis were screened to determine their phytochemical composition and in vitro antiviral activity against fowlpox virus. In addition, we wanted to investigate the toxic effects, if any, of crude extracts in chickens. Steroids as well as cardiac glycosides not previously reported, an alkaloid, polyphenols and saponins were detected in the various fractions of organic solvents used for extracting the decoctions. Antiviral activity was determined by cytopathic effect inhibition assay in primary chicken embryo skin cells. The 50 % inhibitory concentration (EC50) was shown to be 15.6 g/ml. Toxicity for cells was established by determining the 50 % cytotoxic concentration (CCy50). A value of 90 g/ml and a selectivity index (CCy50/EC50) of 5.8 were obtained. In vivo studies of toxicity were performed in chickens that were dosed orally with decoctions of several concentrations for 2 weeks and then monitored for 3 months. No significant changes in several blood chemical parameters were obtained, except for a significant decline in SGOT levels in birds dosed with 100 mg/kg. These levels were nevertheless within the accepted normal range. The findings suggest that aqueous decoctions of galls from G. senegalensis are non-toxic for chickens when administered orally, even at a daily dose of 100 mg/kg for 14 days.

Aqueous decoctions obtained from the galls of Guiera senegalensis were screened to determine their phytochemical composition and in vitro antiviral activity against fowlpox virus. In addition, we wanted to investigate the toxic effects, if any, of crude extracts in chickens. Steroids as well as cardiac glycosides not previously reported, an alkaloid, polyphenols and saponins were detected in the various fractions of organic solvents used for extracting the decoctions. Antiviral activity was determined by cytopathic effect inhibition assay in primary chicken embryo skin cells. The 50 % inhibitory concentration (EC50) was shown to be 15.6 µg/ml. Toxicity for cells was established by determining the 50 % cytotoxic concentration (CCy50). A value of 90 µg/ml and a selectivity index (CCy50/EC50) of 5.8 were obtained. In vivo studies of toxicity were performed in chickens that were dosed orally with decoctions of several concentrations for 2 weeks and then monitored for 3 months. No significant changes in several blood chemical parameters were obtained, except for a significant decline in SGOT levels in birds dosed with 100 mg/kg. These levels were nevertheless within the accepted normal range. The findings suggest that aqueous decoctions of galls from G. senegalensis are non-toxic for chickens when administered orally, even at a daily dose of 100 mg/kg for 14 days.

A total of 17 commercially reared ostriches (Struthio camelus) from Msengi farm, Chinhoyi, Zimbabwe, observed with swollen eyes, severe conjunctivitis and constant lacrimation accompanied by a purulent exudate, were restrained for further clinical examination. Some of the birds were semi-blind with severe loss of body condition. When examined, tiny organisms were observed attached to the nictitating membranes and the conjuctival sacs of both eyes. The organisms were identified as Philophthalmus gralli, the "oriental eye-fluke" and Melanoides tuberculata, a prosobranch snail, was confirmed as the intermediate host through natural and experimental infection. To the best of our knowledge this is the first record of the oriental eye-fluke infection in birds in Zimbabwe and Africa and extends its known geographical range.

A total of 17 commercially reared ostriches (Struthio camelus) from Msengi farm, Chinhoyi, Zimbabwe, observed with swollen eyes, severe conjunctivitis and constant lacrimation accompanied by a purulent exudate, were restrained for further clinical examination. Some of the birds were semi-blind with severe loss of body condition. When examined, tiny organisms were observed attached to the nictitating membranes and the conjuctival sacs of both eyes. The organisms were identified as Philophthalmus gralli, the "oriental eye-fluke" and Melanoides tuberculata, a prosobranch snail, was confirmed as the intermediate host through natural and experimental infection. To the best of our knowledge this is the first record of the oriental eye-fluke infection in birds in Zimbabwe and Africa and extends its known geographical range.

Ingestion of the plant Nolletia gariepina was confirmed as the cause of acute mortalities in cattle in the Kuruman area of the Northern Cape Province of South Africa. The aim of this trial was to investigate the toxic effects of this plant with respect to clinical signs, pathophysiology and pathology using the sheep as a model. At dosages of 1.5 g dried, milled plant material/kg body mass there were no detectable abnormal findings, while at dosages of 2.8-3.0 g/kg most of the animals died acutely. In subacutely affected sheep, depression, inappetance, teeth grinding, tachycardia, weak ruminal movements and recumbency were noticed. The most prominent pathophysiological changes observed, included a sharp rise in non-protein nitrogen substances in the plasma, remarkable decline in glomerular filtration rate, increase in sodium and potassium excretion, and a rise in urine gamma glutamyltransferase activity. Macroscopically a severe nephrosis was present in all the animals. The most important findings detected histologically were necrosis of the proximal convoluted tubular epithelium and large numbers of protein casts in the lumens.

Ingestion of the plant Nolletia gariepina was confirmed as the cause of acute mortalities in cattle in the Kuruman area of the Northern Cape Province of South Africa. The aim of this trial was to investigate the toxic effects of this plant with respect to clinical signs, pathophysiology and pathology using the sheep as a model. At dosages of 1.5 g dried, milled plant material/kg body mass there were no detectable abnormal findings, while at dosages of 2.8-3.0 g/kg most of the animals died acutely. In subacutely affected sheep, depression, inappetance, teeth grinding, tachycardia, weak ruminal movements and recumbency were noticed. The most prominent pathophysiological changes observed, included a sharp rise in non-protein nitrogen substances in the plasma, remarkable decline in glomerular filtration rate, increase in sodium and potassium excretion, and a rise in urine gamma glutamyltransferase activity. Macroscopically a severe nephrosis was present in all the animals. The most important findings detected histologically were necrosis of the proximal convoluted tubular epithelium and large numbers of protein casts in the lumens.

A single-tube duplex nested polymerase chain reaction (sdn-PCR) was developed for the detection of and discrimination between ovine herpesvirus-2 (OvHV-2) and alcelaphine herpesvirus-1 (AlHV-1). These viruses respectively cause sheep- and wildebeest-associated malignant catarrhal fever (SAMCF and WA-MCF). In the first step of the sdn-PCR, two primers with high annealing temperatures based on conserved regions of the tegument genes were used for DNA amplification. In the second step, two primer sets based on variable regions of the respective OvHV-2 and AlHV-1 genes and with annealing temperatures 11 C below the primers used in the first step, were used. Internal regions of different sizes from amplicons produced in the first step were amplified. This single-tube test obviates the need for two separate assays to detect both viral types, thereby reducing time, labour and cost.

A single-tube duplex nested polymerase chain reaction (sdn-PCR) was developed for the detection of and discrimination between ovine herpesvirus-2 (OvHV-2) and alcelaphine herpesvirus-1 (AlHV-1). These viruses respectively cause sheep- and wildebeest-associated malignant catarrhal fever (SAMCF and WA-MCF). In the first step of the sdn-PCR, two primers with high annealing temperatures based on conserved regions of the tegument genes were used for DNA amplification. In the second step, two primer sets based on variable regions of the respective OvHV-2 and AlHV-1 genes and with annealing temperatures > 11 °C below the primers used in the first step, were used. Internal regions of different sizes from amplicons produced in the first step were amplified. This single-tube test obviates the need for two separate assays to detect both viral types, thereby reducing time, labour and cost.