Taurotragus Oryx Research Articles

PHARMACOKINETICS AND PHARMACODYNAMICS OF CARFENTANIL AND NALTREXONE IN FEMALE COMMON ELAND (TAUROTRAGUS ORYX)

The pharmacokinetic parameters of carfentanil and naltrexone were determined in the common eland (Taurotragus oryx). Six adult females were immobilized with xylazine (0.23 +/- 0.03 mg/kg i.m.) and carfentanil (0.0169 +/- 0.0005 mg/kg i.m.) for a 45-min period, during which time routine health care procedures were performed. Heart and respiration rates and body temperatures were monitored throughout the immobilization period. A single intramuscular injection of naltrexone (1.66 +/- 0.08 mg/kg i.m.) was sufficient for reversal. The eland were intermittently restrained in a hydraulic squeeze chute for serial blood sample collection via jugular venipuncture during immobilization and up to 48 hr post-immobilization. The quantification of carfentanil and naltrexone in the plasma was performed by liquid chromatography and mass spectroscopy methods. Carfentanil was rapidly absorbed following administration, with the peak plasma concentration (C(max)) at 13.8 min. Naltrexone was readily absorbed and reached C(max) at 23.4 +/- 16.8 min after administration. All animals stood 2.7 +/- 2.2 min after naltrexone administration. Carfentanil has a half-life of 7.7 hr, whereas naltrexone has a much shorter half-life of 3.7 hr. Although respiratory rates appeared to fluctuate widely among animals, heart rates and body temperature remained stable throughout the immobilization. Renarcotization was not noted as a major complication.

Potential risks of olfactory signaling: the effect of predators on scent marking by beavers

Mammals scent mark their territories to advertise occupancy and ownership. However, signaling with scent for territorial defense can have a negative effect by advertising an individual’s presence and location to predators. In this study, we measured responses to a simulated territorial intrusion by conspecific adult male Eurasian beavers (Castor fiber) either in the localized presence or in the absence of odor of a predator to test the hypothesis that the territorial defense of free-living beavers would be disrupted by the presence of predation risk in their natural environment. We predicted that beavers would significantly reduce their willingness to countermark intruder’s scent in the presence of the scent of predators (wolf [Canis lupus] and lynx [Lynx lynx]), compared with a control (no odor), as responses are in general stronger to predator scent marks than nonpredator scent. Therefore, we also predicted that the effects of nonpredatory mammal scent (neophobic control) (eland [Taurotragus oryx] and horse [Equus cabalus]) are to be expected somewhere in between the effects of the predator odor and a control. Our results suggest that both predator and nonpredator scents reduce beavers response to a simulated intruder’s scent mounds and therefore disrupt their territorial defense. However, predator scent had a stronger effect than nonpredator scent. Beavers may therefore be at great risk on territories with predators present because of the trade-off between predator avoidance and territorial defense. Our study demonstrates the potential of predation risk as a powerful agent of counterselection on olfactory signaling behavior.

Physical organization of the 1.709 satellite IV DNA family in Bovini and Tragelaphini tribes of the Bovidae: sequence and chromosomal evolution

Repetitive DNA in the mammalian genome is a valuable record and marker for evolution, providing information about the order and driving forces related to evolutionary events. The evolutionarily young 1.709 satellite IV DNA family is present near the centromeres of many chromosomes in the Bovidae. Here, we isolated 1.709 satellite DNA sequences from five Bovidae species belonging to Bovini: Bos taurus (BTA, cattle), Bos indicus (BIN, zebu), Bubalus bubalis (BBU, water buffalo) and Tragelaphini tribes: Taurotragus oryx (TOR, eland) and Tragelaphus euryceros (TEU, bongo). Its presence in both tribes shows the sequence predates the evolutionary separation of the two tribes (more than 10 million years ago), and primary sequence shows increasing divergence with evolutionary distance. Genome organization (Southern hybridization) and physical distribution (in situ hybridization) revealed differences in the molecular organization of these satellite DNA sequences. The data suggest that the sequences on the sex chromosomes and the autosomes evolve as relatively independent groups, with the repetitive sequences suggesting that Bovini autosomes and the Tragelaphini sex chromosomes represent the more primitive chromosome forms.

Comparative tick counts on game, cattle and sheep on a working game ranch in Kenya

The main objective of the study was to determine the possible influence of host species on the maintenance of ticks in the field by determining the relative contribution of game animals compared to domestic animals. The study was carried out on a game ranch 32 km south-east of Nairobi. Tick counts were carried out on 30 Zebu cattle (Bos indicus) aged 1 to 3 years and 20 red Maasai sheep (Ovis aries) aged 6 months to 1 year grazing with game animals in a common area for a period of 2 years and these counts were compared with those on eland and Thomson's gazelle. Half-body counts were carried out on the cattle and sheep once every week. To avoid excessive stress, the animals were dipped in amitraz whenever the half body counts exceeded 50 fully engorged female ticks of any species. Tick counts on two wild animal species (eland (Taurotragus oryx) and Thomson's gazelle (Gazella thomsonii)) were carried out during the weekly culling of the herbivores. The results revealed that there was no significant difference in the number ticks per square metre between the wild ungulates and the domestic animals.

115 SPERM CRYOPRESERVATION IN TRAGELAPHINE ANTELOPES

As an integral aspect of our program to develop assisted reproductive technologies in tragelaphine antelopes, we have been evaluating the effects of various extenders on cryosurvival of spermatozoa. Semen was collected by electroejaculation (EEJ) from an eland (Taurotragus oryx, n = 14 EEJs) and a bongo (Tragelaphus euryceros, n = 7 EEJs) male during sedation and standing restraint in a hydraulic chute. Epididymal spermatozoa were collected from the proximal vas deferens, and distal epididymides recovered from four common eland bulls after elective castration at the Hattiesburg Zoo, Mississippi (age = 46 months) and the San Diego Wild Animal Park, California (ages = 18, 20, and 23 months). Testes from a bongo (age = 6.5 yr) and a greater kudu bull (Tragelaphus strepsiceros, age = 7.5 yr) at the Audubon Nature Institute were recovered and processed immediately postmortem. Kudu, bongo, and the Hattiesburg eland testes were transported at ambient temperature whereas the testes from San Diego elands were shipped overnight in a cold-pack container. Sperm processing was done at room temperature (RT = 23°C) in HEPES-buffered Tyrode's solution. Four extenders containing 7% glycerol were evaluated: Biladyl®, TEST Yolk buffer (TYB), Beltsville extender (BF5F), and skim milk. For freezing, sperm samples were initially extended and gradually cooled to 4°C before sequential addition of extender containing glycerol at 4°C; the procedure was then modified by addition of the glycerol fraction at RT before the sample was cooled to 4°C. Spermatozoa were vapor-frozen in 0.5 mL straws placed 5 cm above liquid nitrogen before storage at −196°C. Straws were thawed in a water bath (38°C, 30 s) to evaluate cryosurvival. All eland and bongo electroejaculation procedures produced spermatozoa, although sperm quality varied. Ejaculate volume averaged 5.4 ± 1.2 mL and 3.7 ± 1.1 mL in the bongo and the eland, respectively. Sperm motility at collection, after cooling, and after freezing in the different extenders is presented in Table 1. No immediate decline in sperm motility was observed after adding glycerol to samples, whether at 23°C or 4°C. Bongo spermatozoa lost more motility during freezing than during cooling (15.0 ± 4.4 vs. 5.8 ± 2.0%; P = 0.006); whereas, in eland, motility loss during cooling and freezing was similar (25.3 ± 16.2 vs. 21.1 ± 7.7; P = 0.44). The present results indicate that cooling and freezing tolerance of spermatozoa in tragelaphine antelopes is influenced by species, extender type, and temperature at which a cryoprotectant is added. Table 1. Cryosurvival of ejaculated or epididymal spermatozoa of three antelope species in different extenders

Parâmetros cinéticos da degradação in vitro de alimentos incubados com inóculo microbiano de diferentes espécies de ruminantes

Parâmetros cinéticos da degradação ruminal de alguns alimentos utilizados para ruminantes de zoológicos foram estimados mediante incubação in vitro com líquido ruminal de audade (Ammotragus lervia), cervo sambar (Cervus unicolor), elande (Taurotragus oryx), bovino (Bos taurus), bubalino (Bubalus bubalis), caprino (Capra hircus) e ovino (Ovis aries). Os parâmetros cinéticos foram estimados pela técnica da produção de gás, cujos dados foram ajustados pelos modelos de um e de duplo compartimento. Não foram detectadas diferenças nos parâmetros cinéticos que permitissem agrupar os alimentos (fibrosos × não fibrosos) e os animais (domésticos × silvestres). O modelo de duplo compartimento foi o mais adequado para a estimação dos parâmetros cinéticos da degradação ruminal. Inóculo microbiano oriundo de ruminantes domésticos não é recomendado para estimar parâmetros cinéticos da degradação ruminal de alimentos utilizados para ruminantes silvestres de zoológicos.

Detection of bovine and human tuberculosis in cattle and other animals in six Central European countries during the years 2000-2004

During a five year period (2000–2004), the incidence of bovine and human tuberculosis in cattle and other animals from six Central European countries was evaluated: Croatia (HRV), the Czech Republic (CZE), Hungary (HUN), Poland (POL), Slovakia (SVK), and Slovenia (SVN). These countries, lying between the Baltic and the Adriatic seas, cover an area of 610 402 km<sup>2</sup> and had more than 68 million inhabitants and 9 330 264 cattle in 2003. Successful national control programmes against bovine tuberculosis in cattle were carried out up until 1980: HRV (1953–1966), CZE (1959–1968), HUN (1962–1980), POL (1959–1975) SVK (1959–1968), and SVN (1962–1973). During the entire monitored period skin testing with bovine tuberculin in all cattle older than two years was carried out regularly either once a year or every second year. Five of these countries (CZE, HUN, POL, SVK, and SVN) joined the EC on May 1<sup>st</sup>, 2004. CZE and SVK were officially declared free of bovine tuberculosis in cattle on March 31<sup>st</sup>, 2004 (Commission Decision No. 2004/320/EC) and March 4<sup>th</sup>, 2005 (Commission Decision No. 2005/179/EC), respectively. Bovine tuberculosis was diagnosed in a total of 188 cattle herds in the study area: 145 (77.1%) outbreaks in small herds (< 10 cows) and 43 (22.9%) outbreaks in large herds (≥ 10 cows). The last cases of bovine tuberculosis in cattle in SVK and in the CZE were diagnosed in 1993 and 1995, respectively. During the monitored period, bovine tuberculosis was diagnosed in animal species other than cattle found in zoological gardens: in two Bactrian camels (Camelus ferus) in the CZK, in one Siberian tiger (Panthera tigris f. altaica) in HUN, in one bison (Bison bison) and one eland (Taurotragus oryx) in POL, and in one dromedary camel (Camelus dromedarius) and two bison in SVN. In wild animals, bovine tuberculosis was diagnosed in wild boar (Sus scrofa) in HUN (n = 14) and HRV (n = 1), in six red deer (Cervus elaphus) in HUN, in 14 European bison (Bison bonasus f. bonasus) and two roe deer (Capreolus capreolus f. capreolus) in POL. Infections caused by Mycobacterium tuberculosis were also diagnosed in four cattle and two pigs in POL, in one cattle in SVN, in one dog (Canis lupus f. familiaris) in the CZE and in one dog in HUN. M. africanum was diagnosed in one hyrax (Procaria habessinica) in a zoological garden in HRV.

BEHAVIORAL TRAINING AND HYDRAULIC CHUTE RESTRAINT ENABLES HANDLING OF ELAND ANTELOPE (TAUROTRAGUS ORYX) WITHOUT GENERAL ANESTHESIA

Difficulties and risks associated with restraining large nondomestic ungulates are limiting factors toward developing and applying assisted reproductive technologies, such as artificial insemination and embryo transfer. In this study on 10 female eland (Taurotragus oryx), we evaluated the use of behavioral training and handling handling in a hydraulic chute to perform transvaginal ultrasound-guided oocyte retrieval and other clinical procedures. Nine females were conditioned to associate specific sound cues with food treats. The interval from the audio cue until acceptance of handheld treats varied among females (1.8-58.3 min). Animals also differed in their response to training for voluntary entry into the chute. Handling eland for oocyte retrieval in the hydraulic chute required xylazine sedation. During sedation and handling, eland undergoing oocyte retrieval procedures had higher blood glucose levels (14.4 +/- 3.1) than females handled similarly but without oocyte retrieval (9.3 +/- 2.7 mmol/L). Plasma osmotic pressure, hematocrit, and creatine phosphokinase activity were similar between these two groups. Females that were more difficult to train had higher blood glucose levels than the more cooperative animals. Cooperative females had fewer vertical stripes on their sides. More than 40 procedures were conducted without complications or mortality. The combination of behavioral conditioning-training and restraint of sedated eland in a hydraulic chute was a reliable and repeatable method for performing minimally invasive assisted reproductive techniques.

The effect of prolonged cold storage of eland ( Taurotragus oryx) cauda epididymides on the spermatozoa: possible implications for the conservation of biodiversity

The objectives of this study were to investigate the effects of prolonged storage of cauda epididymides at 4 °C on spermatozoa, and to determine the practicality of utilising epididymal sperm, harvested from testes collected during routine culling of game animals, in assisted reproductive technologies. Testes from eland ( Taurotragus oryx) were collected and epididymides removed and maintained at 4 °C. Sperm motility, viability, morphology and membrane integrity were examined at 12 h intervals for 108 h. Sperm motility and viability were significantly lower at the end of the experiment than at the start ( P < 0.05) and there was individual variation in the rate at which motility and viability declined. The total number of normal sperm decreased significantly with prolonged storage at 4 °C. Midpiece defects were the most common and head and tail abnormalities were rare. A significant decrease in acrosomal and nuclear membrane integrity was observed with prolonged cold storage but there was no significant change in cell membrane integrity. However, about 30% of epididymal sperm survived for 3 days at 4 °C and more than 10% survived for 4 days, and it should be possible to use sperm from culled animals in some assisted reproductive technologies.

63 IMPROVEMENT OF SEMEN-DERIVED EPITHELIAL CELL PROLIFERATION BY FIBROBLAST CO-CULTURE

We previously isolated epithelial-like cells (ELC) from sheep (Ovis aries) and eland (Taurotragus oryx) semen (Nel-Themaat et al. 2004 Reprod. Fertil. Dev. 16, 152) and subsequently developed a system to separate ELC before plating (Nel-Themaat et al. 2005 Reprod. Fertil. Dev. 17, 314). Cells attached and proliferated in only 50% and 31% of the attempts, respectively. Therefore, the purposes of the present study were to improve ELC proliferation by co-culture with inactivated 3T3 mouse fibroblasts and to characterize the obtained cells. Semen fractions from two mature Gulf Coast Native rams (n = 20 ejaculates) and one common eland bull (n = 2 ejaculates) were plated on feeder layers (A), on collagen with feeder cell inserts (B), or on collagen alone (C). For B and C, cell attachment and division were assessed; proliferation and passage 1 (P1) confluence were evaluated for A, B, and C. No difference in attachment rates between B (80%) and C (70%) were found for ovine cells, but (P &lt; 0.05) cells divided more times in B (80%) than in C (35%). All colonies in A (60%) and B (70%) reached P1 confluence and no difference was detected between A and B, but less proliferation (10%) and P1 confluence (5%) were observed in C. Therefore, contact between epithelial cells and feeders was not necessary for growth stimulation by the feeder cells. No difference among A, B, and C was detected for eland ELC proliferation (100%), but no P1 confluence was observed in C. Ram cells were subsequently characterized by immunohistochemical detection of keratin and vimentin, as well as morphology. The 3T3 cells cross-reacted with keratin, and characterization was thus performed mainly on morphology and vimentin expression. Distribution of vimentin microfilaments differed between different epithelial morphologies and fibroblasts. Expression in epithelial cells was faint and patchy in confluent colonies and located around cytoplasmic extremities in semi-confluent colonies. In 3T3 cells, expression was very prominent throughout the cytoplasm and around the nucleus. For treatments A and B, 63 and 57%, respectively, were characterized as only epithelial cells; 25 and 36%, respectively, appeared to contain a mixture of epithelial and fibroblast cells; and 13 and 7%, respectively, contained only fibroblast cells. Only one sample was evaluated from treatment C and only keratin was detected in the epithelial-like colony. We conclude that culture of semen-derived ELC is markedly improved by 3T3 fibroblast co-culture. Further research on conditioned media may simplify the system and reduce chances of 3T3 cell contamination.

328 SOMATIC CELL ISOLATION FROM SEMEN BY PERCOLL GRADIENTS

We previously isolated epithelial-like cells (ELC) from sheep (Ovis aries) and eland (Taurotragus oryx) ejaculates (Nel-Themaat et al. 2004 Reprod. Fertil. Dev. 16, 152). Success rates were low, and the presence of live sperm during initial culture may have altered medium properties, physically prevented contact between cells and the substrate, and/or damaged somatic cell membranes. Using the complete semen sample requires the sacrifice of valuable live spermatozoa without the certainty of obtaining a somatic cell population. Therefore, the purpose of the present study was to develop a method for isolating somatic cells from semen before culture. Separation by discontinuous Percoll gradient centrifugation was performed. Ejaculates obtained by electro-ejaculation from two Louisiana Native rams and rectal massage of one eland bull were washed, layered on columns of 2.5 mL each of 20% (P-20), 50% (P-50), and 90% (P-90) Percoll in 15-mL conical tubes, and centrifuged for 20 min at 400g. Bands were obtained at the three interfaces, as well as a pellet in the P-90 fraction. Each Percoll layer plus the interface band immediately below it was collected by aspiration. Cells from each fraction were re-suspended in serum-supplemented Minimum Essential Medium Alpha containing 500 IU/mL of penicillin, 0.5 mg/mL of streptomycin and 250 g/mL of gentamycin, and were plated on collagen-1 coated dishes. Trypan blue staining was used to determine cell viability in each fraction. After 24 h, dishes were washed and the culture continued until cells attached and proliferated. For both species, the surface fraction yielded primarily dead ELC that were morphologically flat and angular in shape. In the P-20 band, more viable cells were isolated compared with other fractions, although dead cells were also present. In the P-50 and P-90 fractions, few ELC were observed compared with the surface and P-20 fractions. A negligible number of sperm was observed in the surface and P-20 fractions. In contrast, mostly dead sperm were found at the P-50 and P-90 interface band, whereas live spermatozoa were detected in the P-90 pellet. Epithelial-like cells isolated from semen of both species attached (A, initial 24 h of culture), divided (D, within 3 days after plating), and proliferated (P, after 1 week of culture) (see Table). Ram ELC derived from the surface and from the P-20 and P-50 layers attached, but proliferation was detected only with cells collected in the P-20 fraction. In contrast, eland cells collected from the surface and P-20 layers readily attached and proliferated. In summary, a technique has been developed for the isolation of somatic cells from semen using a three-layer Percoll gradient. This method also allows the isolation of motile spermatozoa, hich are available for further use.

Helminth parasites of antelope in Zimbabwe: An update

An updated list of helminth parasites of impala ( Aepyceros melampus ), blue wildebeest ( Connochaetes taurinus ), sable antelope ( Hippotragus niger ), waterbuck ( Kobus ellipsiprymnus ), common duiker ( Sylvicapra grimmia ), eland ( Taurotragus oryx ), tsessebe ( Damaliscus lunatus ) and bushbuck ( Tragelaphus scriptus ) is given based on the results of a study of helminths of antelope reared with cattle. The helminths are listed according to host species. The list will constitute an update of the helminth checklist reported by Jooste (1989). New helminth species were recorded in impala, tsessebe, sable antelope, waterbuck, common duiker and bushbuck. Zimbabwe Vet. J. Vol.33(2) 2002: 109-115

A 12-month survey of the gastro-intestinal helminths of antelopes, gazelles and giraffids kept at two zoos in Belgium

Faecal egg count patterns and clinical signs associated with gastro-intestinal (GI) nematodes of 107 zoo ruminants were monitored at fortnightly intervals for 1 year. The ruminants in this study were kept under different husbandry conditions at two sites of the Royal Zoological Society of Antwerp, the Antwerp Zoo and the Animal Park Planckendael. Artiodactylids involved were Arabian oryx ( Oryx leucoryx), scimitar-horned oryx ( Oryx dammah), bongos ( Tragelaphus euryceros isaaci), sitatungas (Tragelaphus spekii gratus), common eland ( Taurotragus oryx), impala ( Aepyceros melampus), slender-horned gazelles, ( Gazella leptoceros), blue wildebeest ( Connochaetes taurinus taurinus), Kordofan giraffes ( Giraffe camelopardalis antiquorum) and okapi ( Okapia johnstoni). Nematode eggs were recovered from 586 of 1606 (36.5%) individual faecal samples, using flotation techniques. Infection levels were distinctly low at Antwerp Zoo, probably due to zero grazing and daily dung removal. At Planckendael, the herds of Arabian oryx, scimitar-horned oryx and slender-horned gazelles showed markedly higher egg counts than the other herds, with more than 10% of the faecal egg counts having more than 100 eggs per gram (epg) and maximum faecal egg counts of 600, 750 and 1350 epg, respectively. Faecal egg counts increased during the mid-grazing season (July) and peaked at the end of the grazing season (October). No clinical signs, such as loss of faecal consistency, could be correlated with faecal egg counts ( P > 0.05). With the exception of significantly more Nematodirus spp. eggs that were present in juvenile eland, no differences in faecal egg counts could be found between the sexes and different age groups. Abomasa and intestines of 17 animals that died during the survey were available for total worm counts. In one Arabian oryx, four slender-horned gazelles and one sitatunga low burdens ranging from 200 to 14,300 were found. Nematode species recovered were Camelostrongylus mentulatus from the abomasa and Trichostrongylus retortaeformis, Nematodirus fillicollis, Capillaria spp. and Trichuris spp. from the intestines. Our findings suggest different nematode infection levels between herds, which are mainly due to husbandry conditions but to a lesser extent to species- or individual susceptibility. Identification of ungulates that are highly infected and knowledge of the seasonal variation of their helminths can contribute greatly to a well-adjusted species-specific management and helminth control program.

Dominance hierarchy in a herd of female eland antelope (Taurotragus oryx) in captivity

AbstractThe dominance hierarchy of a group of adult female elands (n=10) kept in captivity was followed for 34 months. Outcomes of dominance relationships at the beginning and end of the study were compared. A clear dominance hierarchy existed in the herd. The dominance pattern was complex, but triads were predominantly (95%) transitive or linear. Reversal of dominance occurred in 12 dyads (27%), of which eight (67%) involved a single female. Two females shared the most dominant rank at the beginning of the study. One of these two females and another female later assumed the highest dominance rank on different occasions. A single female remained most subordinate throughout the study period. The correlation between body weight and dominance rank was not significant (r=0.46; P=0.21). Similarly, dominance rank was not associated with the taming potential of the females. However, the median dominance value increased in females with good taming potential, while it decreased in those with poor taming potential. In conclusion, captive eland antelope have a dynamic and complex dominance hierarchy that is predominantly linear. Zoo Biol 23:323–333, 2004. © 2004 Wiley‐Liss, Inc.

57EMBRYO DEVELOPMENT FOLLOWING INTERSPECIES NUCLEAR TRANSFER OF AFRICAN BUFFALO (SYNCERUS CAFFER), BONTEBOK (DAMALISCUS DORCUS DORCUS) AND ELAND (TAUROTRAGUS ORYX) SOMATIC CELLS INTO BOVINE CYTOPLASTS

Wildlife conservation requires traditional as well as innovative conservation strategies in order to preserve gene and species diversity. Interspecies nuclear transfer has the potential to conserve genes from critically endangered wildlife species where few or no oocytes are available from the endangered species, and where representative cell lines have been established for the wildlife population while numbers were still abundant. The purpose of this study was to investigate the developmental ability of embryos reconstructed with transfer of somatic cells from the African buffalo (Syncerus caffer), bontebok (Damaliscus dorcus dorcus) and eland (Taurotragus oryx) to enucleated domestic cattle (Bos taurus) oocytes. Skin tissue from the three wildlife species were collected by surgically removing approx. 1.0×1.0cm ear skin notches from animals immobilized with a combination of etorphine hydrochloride (M99; South Africa) and azaperone (Stressnil, South Africa). The biopsies were placed into physiological saline and transported to the laboratory at 4°C within 2h, cleaned with chlorohexidine gluconate and sliced finely in Minimal Essential Medium supplemented with 10% fetal calf serum. The resultant tissue explants were treated as previously described (Baumgarten and Harley 1995 Comp. Biochem. Physiol. 110B, 37–46) and actively growing fibroblast cultures made available for the nuclear transfer process. Nuclear transfer was performed using the HMC technique (Vajta et al., 2003 Biol. Reprod. 68, 571–578) using slaughterhouse-derived bovine oocytes. Culture was performed in SOFaaci (Vajta et al., 2003 Biol. Reprod. 68, 571–578) medium supplemented with 5% cattle serum using WOWs (Vajta et al., Mol. Reprod. Dev. 50, 185–191). Two identical replicates were made with somatic cells of each species. After successful reconstruction, 57, 42 and 48 nuclear transferred and activated buffalo, bontebok and eland embryos were cultured, respectively. All except for 2 buffalo embryos cleaved; 22 (39%) developed to or over the 8-cell stage, and 2 (3.5%) of them to the blastocyst stage. All but 3 bontebok embryos cleaved, 17 (40%) developed to or over the 8-cell stage, but none of them reached the compacted morula or blastocyst stage. Sixteen (33%) of the eland embryos developed to or over the 8-cell stage with one (2%) reaching the blastocyst stage. In conclusion, buffalo, bontebok and eland embryos developed from reconstruction using their respective somatic cells combined with bovine cytoplasts, however, in vitro developmental ability to the blastocyst stage was limited. Additional basic research that establishes the regulative mechanisms involved with early preimplantation development together with optimising nuclear transfer techniques may have the potential to one day play a role in the conservation of critically endangered wildlife species.

Antibodies to Neospora caninum in wild animals from Kenya, East Africa

The prevalence of antibodies to Neospora caninum was examined in six wild Artiodactyla species, and in five wild Carnivora species from Kenya. Blood sera (104 wild ungulates from Marula Estates (MEs), and 31 wild carnivores from Masai-Mara reserve and from other wildlife areas in northern and Southern Kenya), were screened using a Neospora agglutination test (NAT), with a twofold dilution (1:40–1:320 titres). Presence of NAT antibodies to N. caninun is reported here for the first time in zebra ( Equus burchelli), eland ( Taurotragus oryx), African buffalo ( Syncerus caffer), Thompson gazelle ( Gazella thompsoni), impala ( Aepyceros melampus), warthog ( Phacochoerus aethiopicus), spotted hyena ( Crocuta crocuta) and in free-ranging cheetah ( Acinonyx jubatus). At 1:80 dilution, prevalence was 61.5% in eland, 58.5% in zebra, 19.2% in Thompson gazelle, 33.3% in warthog, 50% in African buffalo, 30% in lion ( Panthera leo), 20% in cheetah, and 33.3% in spotted hyena. Antibodies up to 1:320 titre were detected in eland (38.4%), zebra (19.5%), Thompson gazelle (3.8%) and lion (5%). Amongst herbivores, sero-prevalence was significantly ( P<0.05) higher, at all dilutions, in “grazer/digger” species (e.g. eland and zebra) than in non-“grazer/digger” species (e.g. impala and Thompson gazelle). No antibodies to N. caninum were found in two leopards ( Panthera pardus) and one serval ( Felis serval). Our results indicates a steady presence of N. caninum in wild mammals from Kenya. The hypothesis of a sylvatic cycle of N. caninum could be suggested, but more data are needed to verify the hypothesis, as to evaluate the role of N. caninum infection on the dynamics of wild animals population in the study area.

Phylogenetic analysis of the microbial populations in the wild herbivore gastrointestinal tract: insights into an unexplored niche.

At present, there is little information on the phylogenetic diversity of microbial species that inhabit the gastrointestinal tracts of wildlife. To increase understanding in this area, we initiated a characterization of the bacterial diversity in the digestive tracts of three wild African ruminant species namely eland (Taurotragus oryx), Thompson's gazelle (Gazella rufifrons) and Grant's gazelle (Gazella granti), together with a domesticated ruminant species, zebu cattle (Bos indicus), and a non-ruminant species, zebra (Equus quagga). Bacterial diversity was analysed by PCR amplification, sequencing and phylogenetic analysis of 16S ribosomal DNA (rDNA) sequences. A total of 252 full-length 16S rDNA sequences averaging 1,500 base pairs (bp) in length, and an additional 27 partial sequences were obtained and subject to phylogenetic analysis. Using a 98% criterion for similarity, all except for one of the sequences were derived from distinct phylotypes. At least 24 distinct operational taxonomic units (OTU's) could be identified, with the majority of these sequences representing hitherto uncharacterized species and genera. The sequences were generally affiliated with four major bacterial phyla, the majority being members of the Firmicutes (low G+C Gram-positives) related to the genera Clostridium and Ruminococcus. By contrast, with earlier studies using 16S rDNA sequences to assess biodiversity in Bos taurus dairy cattle, Gram-negative bacteria in the Bacteroidales (Prevotella-Bacteroides group) were poorly represented. The lack of redundancy in the 16S rDNA dataset from the five African ungulate species, and the presence of novel sequences not previously described from the gastrointestinal tract of any animal species, highlights the level of diversity that exists in these ecosystems and raises the question as to the functional role of these species in the gastrointestinal tract.

DIETS OF SOUTHERN AFRICAN BOVIDAE: STABLE ISOTOPE EVIDENCE

Although bovids have been studied for decades, debate still exists about their diets. To address this problem, we examined bovid dietary ecology through analysis of stable carbon isotopes. We analyzed tooth enamel, bone collagen, and hair from 312 individual bovids, representing 27 species from southern Africa. Although dietary information from the literature is usually supported by this technique, our results and the literature are sometimes highly divergent. For instance, our results indicate that Taurotragus oryx and Raphicerus campestris eat less grass than is widely believed. Furthermore, contrary to most theoretical expectations, our data indicate no relationship between body size and percentage of monocots consumed by southern African Bovidae. Although many researchers have abandoned the idea that bovid soft-tissue anatomy is strongly indicative of diet, we demonstrate a strong relationship between the percentage of grass in a bovid's diet and several hard-tissue craniodental indices.

Redescriptions of Haemonchus mitchelli and Haemonchus okapiae (Nematoda: Trichostrongyloidea) and description of a unique synlophe for the haemonchinae.

In the course of a revision of Haemonchus Cobb, 1898 (Nematoda), commonly referred to as large stomach worms, significant new morphological information was discovered that allows the recognition of 2 species believed for more than 50 yr to be synonymous. Both species, Haemonchus mitchelli Le Roux, 1929, from the eland Taurotragus oryx and other African ruminants and H. okapiae van den Berghe, 1937, from the okapi Okapia johnstoni, have a synlophe of 42 ridges, but the synlophe of H. mitchelli is longer than that of H. okapiae. The distal tip of the left spicule of H. mitchelli bears a barb that is about twice as long as the short barb and half as long as the long barb on the right spicule. In contrast, the barb on the left spicule of H. okapiae is similar in size to the short barb and about 25% as long as the long barb of the right spicule. The dorsal ray of H. mitchelli is bifurcated distally for 25-39% (32%) of its length and its stem is expanded proximally, but the dorsal ray of H. okapiae is bifurcated 37-50% (42%) and its stem is of uniform thickness.

A questionnaire survey of the management and use of anthelmintics in cattle and antelope in mixed farming systems in Zimbabwe.

A survey of the management of mixed farming of cattle and antelope and use of anthelmintics was conducted on eleven farms between August and December 1999 by a self-administered questionnaire. Seventeen antelope species ranging from grey duikers (Sylvicapra grimmia) to eland (Taurotragus oryx) occurred on the farms. Impala (Aepyceros melampus) was the most abundant antelope on the farms. Seventy-five per cent of the antelope species on the farms were grazers and mixed feeders and shared grazing with cattle. Most farmers (n = 8) did not consider the stocking density for cattle and antelope as an important management factor. Fifty-four per cent of the farmers (n = 6) routinely dewormed both cattle and antelopes. Albendazole and fenbendazole were the most commonly used drugs for deworming cattle (72.7%) and antelope species (54.5%). The deworming of antelope was carried out during the dry season, using albendazole-, fenbendazole-and rafoxanide-medicated supplementary feed blocks. Doramectin injections were given to antelopes on two farms. Cattle were dewormed preventively and according to the general body condition of the animal. Few farmers (n = 4) followed the recommended deworming programme for cattle in Zimbabwe and only one farmer followed a specified dosing programme for game. However, results from the survey on the deworming of game indicate that farmers perceived helminth infections in antelope to be important.