Publications by authors named "Deuvania C da Silva"

Article Synopsis
  • The study focuses on detecting Cryptosporidium serpentis, a parasite causing gastritis in snakes, using real-time PCR, which targets the Hsp70 gene.
  • Fecal samples from 503 asymptomatic adult snakes were analyzed, revealing 60 positive cases of Cryptosporidium sp. using nested PCR, with specific species identified through sequencing.
  • Real-time PCR showed a 93.8% sensitivity and 99.5% specificity for detecting C. serpentis, confirming its effectiveness compared to the traditional nested PCR method.
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Infection by Cryptosporidium serpentis is one of the most important diseases in reptiles and is characterized by chronic clinical or subclinical infection and the presence of hypertrophic gastritis, food regurgitation, progressive weight loss, mortality, and intermittent or continuous shedding of oocysts in the feces. The objectives of this study were to standardize an indirect enzyme-linked immunosorbent assay (ELISA) to detect antibodies against C. serpentis and to evaluate the clinical, parasitological, and humoral immune response in snakes naturally infected with C.

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Due to the scarcity of information related to the epidemiology of Cryptosporidium infection in passerine birds, this study aimed to determine the periodicity of fecal shedding of Cryptosporidium spp. oocysts, after natural infection, and its clinical signs, mortality, and molecular characterization. Four hundred eighty fecal samples were collected from 40 birds, including 372 samples from 31 adult birds and 108 samples from nine young birds (up to 12 months old), housed in five aviaries, monthly from September 2007 to September 2008, with the exception of April.

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The aim of this study was to determine the prevalence of Cryptosporidium species and genotypes in birds kept in captivity in Brazil. A total of 966 samples from 18 families of birds was collected and stored in 5% potassium dichromate solution at 4 degrees C until processing. Oocysts were purified in Sheather sugar solution following extraction of genomic DNA.

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