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Dive into the research topics where B.L. Penzhorn is active.

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Featured researches published by B.L. Penzhorn.


Journal of Clinical Microbiology | 2005

Molecular Characterization of Theileria Species Associated with Mortality in Four Species of African Antelopes

Ard M. Nijhof; V. Pillay; Johan Christian Abraham Steyl; L. Prozesky; Wilhelm Heinrich Stoltsz; J. A. Lawrence; B.L. Penzhorn; Frans Jongejan

ABSTRACT Pathogen DNA was isolated from roan antelope (Hippotragus equinus), sable antelope (Hippotragus niger), greater kudu (Tragelaphus strepsiceros), and common gray duiker (Sylvicapra grimmia) in South Africa whose deaths were attributed to either theileriosis or cytauxzoonosis. We developed Theileria species-specific probes used in combination with reverse line blot hybridization assays and identified three different species of Theileria in four African antelope species. The close phylogenetic relationship between members of the genera Theileria and Cytauxzoon, similarities in the morphologies of developmental stages, and confusion in the literature regarding theileriosis or cytauxzoonosis are discussed.


Veterinary Parasitology | 2009

Sequence heterogeneity in the 18S rRNA gene within Theileria equi and Babesia caballi from horses in South Africa

Raksha Bhoora; Linda Franssen; Marinda C. Oosthuizen; Alan John Guthrie; Erich Zweygarth; B.L. Penzhorn; Frans Jongejan; Nicola E. Collins

A molecular epidemiological survey of the protozoal parasites that cause equine piroplasmosis was conducted using samples collected from horses and zebra from different geographical locations in South Africa. A total of 488 samples were tested for the presence of Theileria equi and/or Babesia caballi using the reverse line blot hybridization assay. Ten percent of the samples hybridized to the Theileria/Babesia genus-specific probe and not to the B. caballi or T. equi species-specific probes, suggesting the presence of a novel species or genotype. The small subunit of rRNA gene (18S; approximately 1600bp) was amplified and sequenced from 33 of these 488 samples. Sequences were compared with published sequences from the public sequence databases. Twelve distinct T. equi and six B. caballi 18S rRNA sequences were identified. Alignments demonstrated extensive sequence variation in the V4 hypervariable region of the 18S rRNA gene within T. equi. Sequence variation was also found in B. caballi 18S rRNA genes, although there was less variation than observed for T. equi. Phylogenetic analysis based on 18S rRNA gene sequences revealed three T. equi clades and two B. caballi clades in South Africa. The extent of sequence heterogeneity detected within T. equi and B. caballi 18S rRNA genes was unexpected since concerted evolution is thought to maintain homogeneity within repeated gene families, including rRNA genes, in eukaryotes. The findings reported here show that careful examination of variants of the 18S rRNA gene of T. equi and B. caballi is required prior to the development of molecular diagnostic tests to detect these parasites in horses. Species-specific probes must be in designed in regions of the gene that are both conserved within and unique to each species.


Veterinary Parasitology | 2008

Molecular detection of tick-borne protozoal and ehrlichial infections in domestic dogs in South Africa.

Paul Tshepo Matjila; Andrew L. Leisewitz; Frans Jongejan; B.L. Penzhorn

A total of 1,138 blood specimens were collected over a 6-year period (2000-2006) from domestic dogs in South Africa. Specimens from domestic dogs were obtained from the Onderstepoort Veterinary Academic Hospital (OVAH) in Pretoria, the Society for the Prevention of Cruelty to Animals (Johannesburg, Durban, East London and Bloemfontein) and private practices from four provinces (Gauteng, Mpumalanga, KwaZulu-Natal and Western Cape). All specimens were screened for Babesia, Theileria, Hepatozoon and Ehrlichia/Anaplasma species using PCR and Reverse Line Blot (RLB) assays. On RLB, 560/1,137 domestic dog-specimens were positive for one or more parasites. Of the positive domestic dog-specimens, 420 (75%) were infected with Babesia rossi; 82 (15%) dogs were infected with Theileria sp. (dog); 18 (3%) dogs were infected with Babesia vogeli; 14 (3%) specimens were infected with Ehrlichia canis. Mixed infections were also found: B. rossi and E. canis were detected in 12 (2%) specimens; B. vogeli and E. canis occurred in 7 (1%) specimens; Theileria sp. (dog) and E. canis in 3 (0.5%) specimens; B. rossi and B. vogeli in one specimen. B. rossi, B. vogeli and E. canis occurred simultaneously in one dog. There was also one incidental finding of a dog positive for Trypanosoma congolense. The results indicate that a wide range of tick-borne pathogens are circulating in the canine populations in South Africa.


Journal of Clinical Microbiology | 2008

Identification of a Novel Babesia sp. from a Sable Antelope (Hippotragus niger Harris, 1838)

Marinda C. Oosthuizen; Erich Zweygarth; Nicola E. Collins; Milana Troskie; B.L. Penzhorn

ABSTRACT Babesiosis in a sable antelope (Hippotragus niger Harris, 1838) was first reported in 1930; the parasite was named Babesia irvinesmithi. Recently, specimens from an adult sable that presented with a sudden onset of disease and that subsequently died during immobilization were submitted for molecular characterization. Microscopic examination of thin blood smears revealed the presence of small piroplasms. DNA was extracted from blood samples; the V4 variable region of the 18S rRNA gene was amplified and analyzed using the reverse line blot (RLB) assay. Amplicons did not hybridize with any of the Babesia or Theileria species-specific probes present on the blot and hybridized only with a Babesia or Theileria genus-specific probe, suggesting the presence of a novel species. The full-length 18S rRNA gene sequence was obtained and aligned with published sequences of related genera, and phylogenetic trees were constructed. Sequence similarity analyses indicated that a Babesia species, designated Babesia sp. (sable), was present. The sequence showed its highest similarity to B. orientalis and to an unnamed Babesia species previously detected in bovine samples. The latter was later established to be Babesia occultans. A Babesia sp. (sable)-specific RLB oligonucleotide probe was designed and used to screen 200 South African sable samples, but so far, no other sample has been found to be positive for the presence of Babesia sp. (sable) DNA. In summary, we identified a novel piroplasm parasite from a sable antelope that died from an unknown illness. While the parasite was observed in blood smears, there is no direct evidence that it was the cause of death.


Experimental and Applied Acarology | 2004

Displacement of Boophilus decoloratus by Boophilus microplus in the Soutpansberg region, Limpopo Province, South Africa.

M.H. Tønnesen; B.L. Penzhorn; N.R. Bryson; Wilhelm Heinrich Stoltsz; T. Masibigiri

Boophilus ticks (n = 25,987) were collected from cattle at 30 communal dip tanks and five commercial farms in the Soutpansberg region, Limpopo Province, South Africa, between May 1999 and December 2001. Only 6.6% were Boophilus decoloratus, while 93.4% were Boophilus microplus, a tick that had not been reported from this area previously. B. microplus was the most common Boophilus tick on communal dip tank cattle, while B. decoloratus was more commonly found on commercial farms. Where the two species occurred together, B. microplus tended to displace B. decoloratus. The displacement was almost complete at the communal dip tanks, while on the commercial farms the population change was still in progress at the end of the survey. The present study demonstrated that a postulated reproductive interference was insufficient in preventing B. microplus from spreading when the climatic conditions were favourable to this species, as the displacement in most of the areas appeared to be rapid and complete.


Veterinary Parasitology | 2008

Detection of a Theileria species in dogs in South Africa.

Paul Tshepo Matjila; Andrew L. Leisewitz; Marinda C. Oosthuizen; Frans Jongejan; B.L. Penzhorn

A Theileria species was detected by PCR in blood samples collected from dogs in the Pietermaritzburg area and was also found in dogs presented at the Outpatients Clinic of the Onderstepoort Veterinary Academic Hospital (OVAH), in the Pretoria area, South Africa. In the Pietermaritzburg area, 79 of the 192 samples were positive, while 3 out of 1137 of the Onderstepoort samples were positive. Three positive samples from Pietermaritzburg were co-infected with Ehrlichia canis. PCR positive samples were further analysed by the Reverse Line Blot (RLB) and sequence analysis. Phylogenetic analysis of the 18S rRNA full-length gene sequences of one sample (VT12) from Pietermaritzburg and two samples from OVAH (BC281 and BC295) revealed a close relationship with sequences of Theileria species (sable). Clinical signs of the dogs that were examined at Pietermaritzburg and OVAH included an immune-mediated condition with severe thrombocytopenia. These findings identify a Theileria sp. in dogs for the first time in South Africa and add yet another microorganism to the growing list of haemoprotozoan parasites infecting dogs worldwide. The clinical significance of this infection in dogs is poorly resolved.


Veterinary Parasitology | 2009

Identification of novel Babesia and Theileria species in South African giraffe (Giraffa camelopardalis, Linnaeus, 1758) and roan antelope (Hippotragus equinus, Desmarest 1804).

Marinda C. Oosthuizen; Basil A. Allsopp; Milana Troskie; Nicola E. Collins; B.L. Penzhorn

Blood specimens were received from five cases in which young adult giraffe, from different geographic origins in South Africa, showed sudden onset of disease and subsequently died. Additional specimens from two translocated giraffe, as well as one specimen from a roan antelope, were also included in the study. Blood slides from some of these animals showed the presence of piroplasms. DNA was extracted; the V4 hypervariable region of the 18S rRNA gene amplified and analyzed using the Reverse Line Blot (RLB) hybridization assay. PCR products failed to hybridize with any of the Babesia or Theileria species-specific probes, and only hybridized with the Babesia/Theileria genus-specific probe suggesting the presence of a novel species or variant of a species. Full-length 18S rDNA was amplified, cloned and the recombinants were sequenced. 18S rRNA gene sequence similarity analysis revealed the presence of novel piroplasm species in both healthy giraffe and a roan antelope and clinically sick or dead giraffe. Phylogenetic analysis grouped five of these organisms in the Babesia sensu stricto clade and three in the Theileria sensu stricto clade. Although parasites were observed in blood smears, there is no direct evidence that piroplasmosis caused the death of five giraffe, although it certainly seems to be likely.


Journal of Parasitology | 2001

BABESIA LEO N. SP. FROM LIONS IN THE KRUGER NATIONAL PARK, SOUTH AFRICA, AND ITS RELATION TO OTHER SMALL PIROPLASMS

B.L. Penzhorn; Anne M. Kjemtrup; Laura M. López-Rebollar; Patricia A. Conrad

Babesia leo, a small piroplasm isolated from lions in South Africa is described as a distinct species based on a phylogenetic analysis of the 18S rRNA gene. Intraerythrocytic trophozoite and merozoite stages of B. leo are morphologically indistinguishable from other small piroplasms of felids. Previous studies showed that B. leo was biologically and antigenically distinct from B. felis, which is known to infect wild and domestic felids in South Africa. Molecular characterization showed strong support for the phylogenetic seperation of B. leo as a distinct species from B. felis and other felid piroplasms. Phylogenetic analysis also showed that Babesia microti and all of the felid piroplasms from Africa with known 18S rRNA gene sequences available, including B. leo, formed a single, separate clade, sister to the other babesial and theilerial piroplasm parasites.


Veterinary Parasitology | 1999

Occurrence and diversity of coccidia in indigenous, Saanen and crossbred goats in South Africa

C.K. Harper; B.L. Penzhorn

Occurrence and diversity of Eimeria species in two groups of indigenous South African goats kept under traditional management systems, as well as in a mixed herd of Saanen, indigenous and crossbred goats kept under an intensive management system were examined. Infection rates ranged from 88.7 to 100% in the various groups. Mean OPG of immature goats (< 1 year old) exceeded that of adult goats at all three sites. There was no consistent difference between adult OPG counts at the three sites. Under the intensive system, adult crossbred goats had significantly higher OPG counts than adult Saanen or indigenous goats. Overall, OPG counts of immature goats were significantly higher during the dry season (winter) than during the wet season (summer). Ten Eimeria species were identified, Eimeria arloingi being the most prevalent species at all three sites, followed by Eimeria hirci. Up to seven Eimeria species were recovered from individual specimens.


Veterinary Parasitology | 2010

Extracts of Calpurnia aurea leaves from southern Ethiopia attract and immobilise or kill ticks

A. Zorloni; B.L. Penzhorn; Jacobus Nicolaas Eloff

Calpurnia aurea extracts are used in southern Ethiopia to protect stock against ticks. Acetone, hexane and water leaf extracts of C. aurea collected in southern Ethiopia were tested for repellent/attractant and acaricidal properties on unfed adult Rhipicephalus pulchellus ticks. In contrast to many other plant species evaluated, C. aurea extracts did not have repellent properties, but rather had a slight attractant capacity. With 20% and 10% acetone extracts, all ticks were either killed or their mobility severely compromised after 1microl of extract was topically applied on the abdomen. At a 5% concentration, 85% of ticks were still affected. A 10% aqueous solution also had a marked effect. The results prove the efficacy of the traditional use of this extract and may lead to a product that can be used commercially to protect animals against tick infestation, under subsistence as well as industrialized conditions.

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B.D. Lewis

University of Pretoria

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