2012
DOI: 10.1638/2011-0150.1
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Low Sensitivity of Antemortem Gill Biopsies For the Detection of SubclinicalPseudodactylogyrus biniInfestations in American Eels (Anguilla rostrata)

Abstract: The objectives of this study were twofold: to determine the sensitivity of gill biopsies used for the screening of Pseudodactylogyrus bini in subclinically infested American eels (Anguilla rostrata) and to evaluate the effect of bath anesthesia on the proportion of infested eels. Fifty-four eels were euthanized following either intracoelomic injection of T61 or deep anesthesia with tricaine methanesulfonate. Proportions of eels infested by P. bini diagnosed by gill biopsies taken through the gill slit and by m… Show more

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Cited by 4 publications
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“…In the case of Pseudodactylogyrus sp., the classical approach consists of microscopic observations of the gill filaments and the parasites themselves (morpho‐anatomical recognition on the sclerotized parts involved in their fixation) (Monni & Cognetti‐Varriale, 2002). Gill biopsies can also be performed but the prevalence of parasites using this technique was lower (20%) than the prevalence found by complete microscopic observation of the entire gill arches (70%) (Larrat et al., 2012). For A. crassus , its morphological identification is quite easy, the only tricky point being the identification of L3 and L4 larval stages, very difficult to distinguish, and which is often done only according to their size (Blanc et al., 1992; Sures et al., 1999).…”
Section: Causative Agent Identificationmentioning
confidence: 99%
“…In the case of Pseudodactylogyrus sp., the classical approach consists of microscopic observations of the gill filaments and the parasites themselves (morpho‐anatomical recognition on the sclerotized parts involved in their fixation) (Monni & Cognetti‐Varriale, 2002). Gill biopsies can also be performed but the prevalence of parasites using this technique was lower (20%) than the prevalence found by complete microscopic observation of the entire gill arches (70%) (Larrat et al., 2012). For A. crassus , its morphological identification is quite easy, the only tricky point being the identification of L3 and L4 larval stages, very difficult to distinguish, and which is often done only according to their size (Blanc et al., 1992; Sures et al., 1999).…”
Section: Causative Agent Identificationmentioning
confidence: 99%