RESUMEN
The classification and description of digenean trematodes are commonly accomplished by using morphological features, especially in adult stages. The aim of this study was to provide an analysis of the genetic composition of larval digenean trematodes using polymerase chain reaction (PCR) and sequence analysis. Deoxyribonucleic acid (DNA) was extracted from clinostomatid metacercaria, 27-spined echinostomatid redia, avian schistosome cercaria and strigeid metacercaria from various dams in the proximity of Tshwane metropolitan, South Africa. Polymerase chain reaction was performed using the extracted DNA with primers targeting various regions within the larval digenean trematodes' genomes. Agarose gel electrophoresis technique was used to visualise the PCR products. The PCR products were sequenced on an Applied Bioinformatics (ABI) genetic analyser platform. Genetic information obtained from this study had a higher degree of discrimination than the morphological characteristics of seemingly similar organisms.
Asunto(s)
Interacciones Huésped-Parásitos , Reacción en Cadena de la Polimerasa/veterinaria , Trematodos/clasificación , Animales , Peces/parasitología , Metacercarias/clasificación , Metacercarias/genética , Metacercarias/crecimiento & desarrollo , Metacercarias/aislamiento & purificación , Filogenia , Reacción en Cadena de la Polimerasa/métodos , Caracoles/parasitología , Sudáfrica , Trematodos/genética , Trematodos/crecimiento & desarrollo , Trematodos/aislamiento & purificaciónRESUMEN
The metacercarial (larval) stages of diplostomid digeneans are known to inhabit freshwater fish, causing tissue damage in the process. Due to their widespread diversity, little is known about their life cycle. The classification of these parasitic stages to the species level using only the morphology is very challenging due to the lack of genitalia; they are regarded to be the most important structures in the identification of these organisms. In this study, additional morphological information through light and scanning electron microscopy is given for two different diplostomids found in the cranial cavity of Clarias gariepinus and the vitreous chambers of Tilapia sparrmanii and Pseudocrenilabrus philander. The diplostomid metacercaria inhabiting the cranial cavity of Clarias gariepinus was morphologically identified as Diplostomulum (Tylodelphys) mashonense and an unknown metacercaria of the genus Diplostomum was found in the vitreous chambers of Pseudocrenilabrus philander and Tilapia sparrmanii. Both parasitic species' 28S recombinant deoxyribonucleic acid genomic regions were successfully amplified using Dig 125/1500R primer pairs. The assay yielded a product of approximately 1300 base pairs as seen on the gel images. There were 14 nucleotide differences over the entire analysed sequences resulting in a 1.1% (14/1273) nucleotide difference. In line with the morphological characteristics of these parasites, there seemed to be a slight difference in their genetic make-up. The application of molecular techniques on digenetic trematodes seems very promising and may yield great potential in future descriptions of morphologically similar parasitic species.
Asunto(s)
Enfermedades de los Peces/parasitología , Filogenia , Trematodos/clasificación , Trematodos/aislamiento & purificación , Infecciones por Trematodos/veterinaria , Animales , Femenino , Peces , Larva , Masculino , Metacercarias , Microscopía Electrónica de Rastreo/veterinaria , Trematodos/genética , Infecciones por Trematodos/parasitologíaRESUMEN
Freshwater snails are known to serve as first intermediate hosts for various parasitic diseases such as schistosomosis, amphistomosis and fasciolosis. Two freshwater snail species, Lymnaea natalensis, Krauss 1848 and Bulinus tropicus, Krauss 1848 were sampled from five localities in Gauteng and one locality in the North West Province from 2007 to 2010. These snails were collected in order to study their cercarial sheddings. They were found to be infected with three different types of strigea cercariae, of which the morphology was studied using standard light and scanning electron microscopy techniques.