2008
DOI: 10.1016/j.meegid.2007.10.001
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First phenotypic description of Fasciola hepatica/Fasciola gigantica intermediate forms from the human endemic area of the Nile Delta, Egypt

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Cited by 127 publications
(99 citation statements)
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“…1 In Egypt, intermediate hybrid forms exist together with Fasciola hepatica and F. gigantica. 2 The wide range of egg-size variability makes it difficult to determine species from eggs found in stool analysis. 3,4 Fascioliasis has been endemic in certain villages in the Nile Delta, but overall prevalence in Egypt is unknown because reports show wide variations in infection rates.…”
Section: Introductionmentioning
confidence: 99%
“…1 In Egypt, intermediate hybrid forms exist together with Fasciola hepatica and F. gigantica. 2 The wide range of egg-size variability makes it difficult to determine species from eggs found in stool analysis. 3,4 Fascioliasis has been endemic in certain villages in the Nile Delta, but overall prevalence in Egypt is unknown because reports show wide variations in infection rates.…”
Section: Introductionmentioning
confidence: 99%
“…Groups based on maximum and minimum values of the morphological measurements of Fasciola hepatica, Fasciola gigantica or Fasciola sp. (intermediate/hybrid forms) have been proposed for populations from Egypt and Iran [18], whereas, some authors have outlined some useful morphometric descriptions for the specific differentiation of the two species [21]. The basis of grouping was initially performed according to BL/ BW, and, secondarily, according to Distance between ventral sucker and posterior end of the body (VS-P).…”
Section: Discussionmentioning
confidence: 99%
“…Flukes were extensively washed with distilled water and identified morphologically as Fasciola gigantica according to existing keys (body length (BL), body width (BW), body length to width ration (BL/BW); Cone Length (CL); appearance of body sides and shoulder characteristics) as described by other authors [17,18] and stored at -70°C until extraction of genomic DNA. Total genomic DNA extraction: Body portions (the conical anterior end) from individual trematodes were each placed in 200 µl of sterile lysis buffer, containing 0.4 M NaCl, 10 mM Tris-HCl (pH 8) and 2 mM EDTA (pH 8) and crushed using a sterile pestle and mortar.…”
Section: Methodsmentioning
confidence: 99%
“…Worms were washed thoroughly with PBS, pH7.2, identified morphologically according to (Periago et al 2008) and kept frozen -20°C until use.…”
Section: Parasitesmentioning
confidence: 99%