FN Archimer Export Format PT J TI Virus-like particles associated with brown muscle disease in Manila clam, Ruditapes philippinarum, in Arcachon Bay (France) BT AF DANG, C. GONZALEZ, P. MESMER-DUDONS, N. BONAMI, J-R CAILL-MILLY, Nathalie DE MONTAUDOUIN, X. AS 1:1;2:1;3:1;4:2;5:3;6:1; FF 1:;2:;3:;4:;5:PDG-DOP-DCN-HGS-LRHAQ;6:; C1 Univ Bordeaux 1, CNRS, EPOC, Stn Marine Arcachon,UMR 5805, F-33120 Arcachon, France. Univ Montpellier, UMR Pathogen & Immun 5119, ECOLAG, CNRS UM2, F-34059 Montpellier, France. IFREMER, Lab Ressources Halieut Aquitaine, Anglet, France. C2 UNIV BORDEAUX, FRANCE UNIV MONTPELLIER, FRANCE IFREMER, FRANCE SI ANGLET SE PDG-DOP-DCN-HGS-LRHAQ IN WOS Ifremer jusqu'en 2018 copubli-france copubli-univ-france IF 1.697 TC 9 UR https://archimer.ifremer.fr/doc/00000/11130/7991.pdf LA English DT Article CR EVALUATION STOCK PALOURDES BASSIN D'ARCACHON DE ;adductor muscle;apoptosis;brown muscle disease;necrosis;Ruditapes philippinarum;transmission electron microscopy AB Recently, Manila clam, Ruditapes philippinarum, populations have suffered mortalities in Arcachon Bay (SW France). Mortality was associated with extensive lesions of the posterior adductor muscle, which become progressively brown and calcified. Ultrastructural observations by transmission electron microscopy revealed tissue degradation with necrotized muscle fibres and granulocytomas. Unenveloped virus-like particles (VLPs) were detected in muscle, granulocytic, epithelial and rectal cells. VLPs were abundant in the extracellular space, in the cytoplasm (free or enclosed in vesicles) and in the nucleoplasm of granulocytes. Nuclei and mitochondria of granulocytes displayed changes which suggested reactive oxygen species production and apoptosis induction. VLPs exhibited an icosahedral structure with a diameter of 25 to 35 nm. These observations suggest that the VLPs could belong to the family Picornaviridae or the Parvoviridae. PY 2009 PD JUN SO Journal Of Fish Diseases SN 0140-7775 PU Wiley-blackwell Publishing, Inc VL 32 IS 7 UT 000267071800002 BP 577 EP 584 DI 10.1111/j.1365-2761.2009.01019.x ID 11130 ER EF