Putative antiviral activity in hemolymph from adult Pacific oysters, Crassostrea gigas

International audience Innate, non-specific resistance mechanisms are important to pathogens, particularly for delaying virus replication at the onset of infection. Innate immunity constitutes the first line of defense in vertebrates and is the only one in invertebrates. Little is known about possib...

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Bibliographic Details
Published in:Antiviral Research
Main Authors: Olicard, Cécile, Renault, Tristan, Torhy, Corinne, C., Benmansour, Abdenour, A., Bourgougnon, Nathalie
Other Authors: Université de Bretagne Sud (UBS), Unité Amélioration génétique, Santé animale et Environnement (AGSAE), Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER), La Rochelle Université (ULR), Unité de recherche Virologie et Immunologie Moléculaires (VIM (UR 0892)), Institut National de la Recherche Agronomique (INRA)
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 2005
Subjects:
CRASSOSTREA GIGAS
ANTIVIRAL DEFENSE
HSV-1
HEMOLYMPH
OYSTER
IPNV
VHSV
[SDV]Life Sciences [q-bio]
Crassostrea gigas
Online Access:https://hal.inrae.fr/hal-02681265
https://doi.org/10.1016/j.antiviral.2005.03.003
Description
Summary:International audience Innate, non-specific resistance mechanisms are important to pathogens, particularly for delaying virus replication at the onset of infection. Innate immunity constitutes the first line of defense in vertebrates and is the only one in invertebrates. Little is known about possible antiviral substances in invertebrates. The present work concerns a study of antiviral substances in hemolymph from adult Crassostrea gigas oysters. Despite the detection of cytotoxicity in fresh filtered hemolymph for both mammalian (CC50: 750_g/ml) and fish cells (CC50: >2000_g/ml for EPC cells and 345 _g/ml for RTG-2 cells), an antiviral substance was detected. Fresh filtered hemolymph was capable of inhibiting the replication of herpes simplex virus type 1 in vitro at an EC50 of 425_g/ml (total proteins) and the replication of infectious pancreatic necrosis virus in EPC and RTG-2 cells at 217 and 156 _g/ml (total proteins), respectively.

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