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PubMed1995

ITS2 ribosomal RNA indicates Schistosoma hippopotami is a distinct species.

The internal transcribed spacer region of the ribosomal RNA, ITS2, was sequenced from a single specimen of S. hippopotami collected from a pulmonary artery of the hippopotamus, Hippopotamus amphibius in South Africa. The nucleotide sequence was aligned with those of S. mansoni, S. rodhaini, S. haematobium, S. intercalatum, S. curassoni, S. bovis and S. japonicum. Both maximum parsimony and genetic distance analyses were performed on these data sets. Using S. japonicum as outgroup to the African schistosomes, a single most-parasmonious tree was obtained of length 64 steps with a consistency index of 1-S. hippopotami was the sister-group to the remaining African species. This species has lateral-spined eggs and its basal position in the tree suggests that this condition is primitive and that terminal-spined eggs developed secondarily. Molecular data clearly show that S. hippopotami cannot be considered synonymous with S. mansoni. Assuming the hippopotamus is the normal host of S. hippopotami, phylogenetic analysis is consistent with an ancient association between schistosomes and ungulates.

Animals↗
PubMed1989

Scaling of long bone fracture strength with animal mass.

Most long bone fractures are the result of bending and/or torsional loading. To allometrically relate bone torsional and bending strength to animal mass (M), we define the bone strength index SB = J/dl where J = midshaft cross section polar moment of inertia, d = diameter, and l = length. In geometrically similar scaling, one would expect SB alpha M2/3. In this study, long bone geometric parameters were measured for 12 species of Artiodactyls. The relationships determined for length and diameter are similar to those reported by previous investigators (l alpha d3/4, l alpha M1/4). For the Artiodactyls studied, we found that SB alpha M0.82. Data previously collected by Biewener on a wide range of mammals (non-Artiodactyls) showed different scaling characteristics (l alpha d0.89, l alpha M0.31). However, our analysis of his data suggests roughly similar scaling of the torsional and bending strength index, SB alpha M0.77. It therefore appears that, in spite of differences in scaling of length and external diameter, the bending and torsional strengths scale similarly across a broad range of animals.

Animals↗
PubMed1988

Transmission of wildebeest-associated and sheep-associated malignant catarrhal fever to hamsters, rats and guinea-pigs.

Wildebeest-derived malignant catarrhal fever (WD-MCF) was transmitted to hamsters, rats and guinea-pigs by inoculation of rabbit lymphoid cells infected with alcelaphine herpesvirus-1, strain C-500. Sheep-associated MCF (SA-MCF) was transmitted to hamsters by inoculation of lymphoid cells from rabbits affected with SA-MCF derived from deer. Mice were refractory to both forms of the disease. With both forms of MCF, the incubation period during initial transmission varied from 21 to 90 days and disease was readily passaged in rodents by inoculation of live lymphoid cells. Clinical signs in hamsters most closely resembled those described for naturally occurring MCF. Results given here and in two following papers indicate that rodents are useful models to study the aetiology and pathogenesis of both forms of MCF.

Animals↗
PubMed1988

The pathology of wildebeest-associated malignant catarrhal fever in hamsters, rats and guinea-pigs.

Lesions typical of malignant catarrhal fever were found in hamsters, rats and guinea-pigs inoculated with a rabbit-passaged strain (C-500) of alcelaphine herpesvirus-1. Lesions found during primary passage included proliferation of lymphoid tissues, multisystemic mononuclear cell infiltrates, vasculitis and necrosis, especially in the alimentary tract. The character, severity and distribution of lesions remained stable in affected hamsters during serial passage of disease, whereas lympho-proliferation became dominant in rats. The lesions in rats typically affected lymph nodes, heart and kidney and appear similar to those caused by oncogenic herpesviruses. Because rodents are susceptible to malignant catarrhal fever, the prospect is advanced that they can be used to elucidate the pathogenesis of both lymphoproliferative and cytolytic aspects of the disease.

Animals↗