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Biomedical subjects

Louis H Du Preez

Publications and source records attributed to Louis H Du Preez.

3 recordsLinked to original sources

Quantitative measurement of Batrachochytrium dendrobatidis in amphibian skin.

The ability to quantify infections provides a tool with which to perform comparative pathological research. The need exists for a simplistic standard method to compare infection levels of Batrachochytrium dendrobatidis, a major cause of global amphibian declines. Through examination of skin sloughs of the Cape river frog Afrana fuscigula, we present an accessible method that not only provides quantitative measurements of B. dendrobatidis, but also provides information that increases the confidence of detection through histological surveys. The method relies on the availability of live animals that are actively shedding skin. By employing a direct microscopic count of sporangia, it is possible to express infection in terms of density. Micro-spatial infection in the skin of A. fuscigula is characterised by significant differences in sporangium density among the different components of the foot, and by similar differences in site infection frequency. Notably, toe tips and tubercles contain higher infection densities and are more often infected than webbing or the base of the foot. This pattern of infection might facilitate disease transmission due to the increased exposure of these components to abrasion. Density data can be used with the Poisson frequency function to approximate binomial probabilities of detecting B. dendrobatidis through histology. The probability matrix produced for A. fuscigula indicated that foot-site selection for histology markedly influenced the number of sections required to detect B. dendrobatidis at a specific level of probability. Thus, examination of a test sample of skin tissue with direct-count quantification can help in planning the sampling of tissues for histological surveys.

Animals↗

Demonstrating morphometric protocols using polystome marginal hooklet measurements.

The flexible body structure of polystomes (Monogenea: Polystomatidae) encumbers taxonomic classification and species identification. Large intraspecific and limited interspecific variation in the morphology of polystomes further complicates the identification of species. Apart from employing the host-specific nature of the polystomes, taxonomic characterisation relies heavily on the sclerotised skeletal structures, such as the hamuli and the marginal hooklets. The currently accepted measurement system for marginal hooklets appears to be non-optimal and an improved protocol is needed. This paper describes in detail how such a protocol is found by evaluating various sets of measurements statistically in order to identify the most informative combination of parameters. Thirteen measurements of marginal hooklets from 11 different Southern African Polystoma species were taken and evaluated. A new protocol for discriminating between species of Polystoma Zeder, 1800, that employs only three measurements, is proposed. The value of the processes to derive morphometric protocols, as described, is that it is not restricted to a specific taxon, but that it can be amended and applied to any taxonomic grouping.

Animals↗

Gonadal development of larval male Xenopus laevis exposed to atrazine in outdoor microcosms.

The potential effects of atrazine on gonadal development in metamorphs and subadults of the African clawed frog (Xenopus laevis) were studied under conditions of natural photoperiod and temperatures in outdoor microcosms from August 2002 to June 2003 in South Africa. Triplicate 1100 L microcosms for each nominal concentration of 0.0, 1, 10, and 25 microg of atrazine/L were used. Measured atrazine concentrations varied <25% throughout the study, and no atrazine was detected in the control microcosms. Tadpoles developed well at all concentrations. On the basis of histological examination of testes of recently metamorphosed stage 66 frogs, 57% of the individuals in the reference group exhibited testicular oocytes as compared with 57, 59, and 39% of the 1, 10, and 25 microg/L atrazine groups, respectively. The average prevalence of testicular oocytes for all of the treatments including the controls was 54% in a single testis, while, in 35% of individuals, testicular oocytes were observed in both testes. The number of testicular oocytes per individual ranged from 0 to 58 with means of 9.5, 9.8, 8.5, and 11.1 forthe 0.0, 1, 10, and 25 microg of atrazine/L groups, respectively. Ten months after metamorphosis, another subset of juveniles was examined, and the maximum number of testicular oocytes observed was five in one animal. The presence of testicular oocytes was not related to exposure to atrazine and may be a natural phenomenon during ontogeny.

Animals↗