1996
DOI: 10.1051/kmae:1996001
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Nécrose pancréatique infectieuse des salmonidés : évaluation de méthodes destinées à couper la transmission par l'oeuf

Abstract: RÉSUMÉDes ovules de truites Arc-en-Ciel ont été fécondés par des spermatozoïdes de la même espèce traités par l'iode suivant différents protocoles afin de couper la transmission de la nécrose pancréatique infectieuse (NPI) des salmonidés. L'efficacité de l'iode a été évaluée en parallèle par neutralisation du virus en 1 mn. Le protocole conseillé pour la solution d'iode disponible dans le commerce (ovules égouttés, puis recouverts de solution-iodée et sperme ajouté immédiatement) a d'abord été utilisé. A pH co… Show more

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“…rVHSV-Tomato was propagated in EPC cells (multiplicity of infection (MOI) of 1); briefly, the virus was adsorbed onto the cells for 1 h at 14 °C with regular gentle shaking; L-15 supplemented with 2% heat-inactivated FBS was added afterwards and the supernatants were collected at 5 days post-infection, 0.2 µm-filtered, aliquoted and stored at -80 °C. Infectious pancreatic necrosis virus (IPNV), isolate 31.75 [ 43 ], was propagated in CHSE-214 (MOI 0.001) at 14 °C in GMEM supplemented with 2% FBS, as described above for rVHSV-Tomato. The supernatants were collected at 3–4 days post-infection, 0.2 µm-filtered, diluted 1:5 (v/v) in TEN buffer (10 mM Tris, 1 mM EDTA, 150 mM NaCl, pH 7.1) and mixed again 1:1 (v/v) in glycerol 100%, aliquoted and stored at -20 °C.…”
Section: Methodsmentioning
confidence: 99%
“…rVHSV-Tomato was propagated in EPC cells (multiplicity of infection (MOI) of 1); briefly, the virus was adsorbed onto the cells for 1 h at 14 °C with regular gentle shaking; L-15 supplemented with 2% heat-inactivated FBS was added afterwards and the supernatants were collected at 5 days post-infection, 0.2 µm-filtered, aliquoted and stored at -80 °C. Infectious pancreatic necrosis virus (IPNV), isolate 31.75 [ 43 ], was propagated in CHSE-214 (MOI 0.001) at 14 °C in GMEM supplemented with 2% FBS, as described above for rVHSV-Tomato. The supernatants were collected at 3–4 days post-infection, 0.2 µm-filtered, diluted 1:5 (v/v) in TEN buffer (10 mM Tris, 1 mM EDTA, 150 mM NaCl, pH 7.1) and mixed again 1:1 (v/v) in glycerol 100%, aliquoted and stored at -20 °C.…”
Section: Methodsmentioning
confidence: 99%