Schistosomiasis control programs in Brazil have helped reduce prevalence and the severe forms of the disease, but have failed to prevent new foci from appearing, especially on the periphery of large cities. The current article aims to assess the prevalence of schistosomiasis and the presence of intermediates hosts for Schistosoma mansoni in the district of Ravena, Municipality of Sabará, Minas Gerais State, Brazil, 27 years after implementing water treatment and specific treatment for infected individuals. Ravena responded positively to schistosomiasis control measures, with a prevalence of 2.
View Article and Find Full Text PDFActa Trop
March 2006
In Brazil, Lymnaea columella is the most important intermediate host of Fasciola hepatica, the etiological agent of fasciolosis, which is a parasitic disease of veterinarian and human importance. Random amplified polymorphic DNA (RAPD) was used to investigate the genetic variability within and among nine Brazilian populations of L. columella comprising 205 individuals.
View Article and Find Full Text PDFThe specific identification of Lymnaeid snails is based on a comparison of morphological characters of the shell, radula, renal and reproductive organs. However, the identification is complicated by dissection process, intra and interspecific similarity and variability of morphological characters. In the present study, polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) techniques targeted to the first and second internal transcribed spacers (ITS1 and ITS2) rDNA and to the mitochondrial 16S ribosomal gene (16S rDNAmt) were used to differentiate the species Lymnaea columella, L.
View Article and Find Full Text PDFSimple sequence repeat anchored polymerase chain reaction amplification (SSR-PCR) is a genetic typing technique based on primers anchored at the 5' or 3' ends of microsatellites, at high primer annealing temperatures. This technique has already been used in studies of genetic variability of several organisms, using different primer designs. In order to conduct a detailed study of the SSR-PCR genomic targets, we cloned and sequenced 20 unique amplification products of two commonly used primers, CAA(CT)6 and (CA)8RY, using Biomphalaria glabrata genomic DNA as template.
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