FN Archimer Export Format PT J TI Unraveling concordant and varying responses of oyster species to Ostreid Herpesvirus 1 variants BT AF Friedman, Carolyn S. Reece, Kimberly S. Wippel, Bryanda J.T. Agnew, M. Victoria Dégremont, Lionel Dhar, Arun K. Kirkland, Peter MacIntyre, Alanna Morga, Benjamin Robison, Clara Burge, Colleen A. AS 1:1;2:2;3:1;4:3;5:4;6:5;7:6;8:2;9:4;10:2;11:3; FF 1:;2:;3:;4:;5:PDG-RBE-SGMM-LGPMM;6:;7:;8:;9:PDG-RBE-SGMM-LGPMM;10:;11:; C1 School of Aquatic & Fishery Sciences, University of Washington, Box 355020, Seattle, WA 98105, USA Virginia Institute of Marine Sciences, William & Mary, P.O. Box 1346, Gloucester Point, Virginia 23062, USA Institute of Marine and Environmental Technology, University of Maryland Baltimore County, 701 E Pratt Street, Baltimore, MD 21202, USA Ifremer, SG2M-LGPMM, Station La Tremblade, 17390 La Tremblade, France Aquaculture Pathology Laboratory, Animal and Comparative Biomedical Sciences, The University of Arizona, 1117 E Lowell Road, Tucson, AZ 85721, USA Elizabeth Macarthur Agricultural Institute, NSW Department of Primary Industries, Menangle, NSW 2568, Australia C2 UNIV WASHINGTON, USA VIRGINIA INST MARINE SCI, USA UNIV MARYLAND BALTIMORE CTY, USA IFREMER, FRANCE AQUACULTURE PATHOLOGY LABORATORY, USA EMAI, AUSTRALIA SI LA TREMBLADE SE PDG-RBE-SGMM-LGPMM IN WOS Ifremer UPR copubli-int-hors-europe IF 7.963 TC 8 UR https://archimer.ifremer.fr/doc/00631/74341/73993.pdf LA English DT Article DE ;OsHV-1;Crassostrea gigas;Crassostrea sikamea;Crassostrea virginica;Mortality;Viral load AB The Ostreid herpesvirus 1 (OsHV-1) and variants, particularly the microvariants (μVars), are virulent and economically devastating viruses impacting oysters. Since 2008 OsHV-1 μVars have emerged rapidly having particularly damaging effects on aquaculture industries in Europe, Australia and New Zealand. We conducted field trials in Tomales Bay (TB), California where a non-μVar strain of OsHV-1 is established and demonstrated differential mortality of naturally exposed seed of three stocks of Pacific oyster, Crassostrea gigas, and one stock of Kumamoto oyster, C. sikamea. Oysters exposed in the field experienced differential mortality that ranged from 64 to 99% in Pacific oysters (Tasmania>Midori = Willapa stocks), which was much higher than that of Kumamoto oysters (25%). Injection trials were done using French (FRA) and Australian (AUS) μVars with the same oyster stocks as planted in the field and, in addition, two stocks of the Eastern oyster, C. virginica. No mortality was observed in control oysters. One C. virginica stock suffered ~10% mortality when challenged with both μVars tested. Two Pacific oyster stocks suffered 75–90% mortality, while one C. gigas stock had relatively low mortality when challenged with the AUS μVar (~22%) and higher mortality when challenged with the French μVar (~72%). Conversely, C. sikamea suffered lower mortality when challenged with the French μVar (~22%) and higher mortality with the AUS μVar (~44%). All dead oysters had higher viral loads (~1000×) as measured by quantitative PCR relative to those that survived. However, some survivors had high levels of virus, including those from species with lower mortality. Field mortality in TB correlated with laboratory mortality of the FRA μVar (69% correlation) but not with that of the AUS μVar, which also lacked correlation with the FRA μVar. The variation in response to OsHV-1 variant challenges by oyster species and stocks demonstrates the need for empirical assessment of multiple OsHV-1 variants. PY 2020 PD OCT SO Science Of The Total Environment SN 0048-9697 PU Elsevier BV VL 739 UT 000561794200020 DI 10.1016/j.scitotenv.2020.139752 ID 74341 ER EF