FN Archimer Export Format PT J TI The mass mortality of blue mussels (Mytilus spp) from the Atlantic coast of France is associated with heavy genomic abnormalities as evidenced by flow cytometry BT AF BENABDELMOUNA, Abdellah LEDU, Christophe AS 1:1;2:1; FF 1:PDG-RBE-SG2M-LGPMM;2:PDG-RBE-SG2M-LGPMM; C1 IFREMER, RBE, SG2M, LGPMM,Stn La Tremblade, Ave Mus Loup, F-17390 La Tremblade, France. C2 IFREMER, FRANCE SI LA TREMBLADE SE PDG-RBE-SG2M-LGPMM IN WOS Ifremer jusqu'en 2018 IF 2.379 TC 25 UR https://archimer.ifremer.fr/doc/00341/45171/44566.pdf LA English DT Article DE ;Mussels;Mortality;Cytogenetic quality;Hemocytes;Ploidy AB Since 2014, France’s blue mussel industry has been facing heavy mortality outbreaks (90-100%) affecting both juveniles and adults. This report presents evidence of heavy genomic abnormalities associated with mortality outbreaks in blue mussels, Mytilus edulis-galloprovincialis, from the Atlantic coast of France. In this study, ploidy characteristics of hemic cells were investigated using Flow CytoMetry (FCM), revealing an unusual, broad continuum of ploidy distribution from hypodiploidy to tetraploidy. FCM was additionally used to evaluate, at individual and populations levels, different thresholds of genomic abnormality (GA%) using the percentage of non-diploid nuclei. Individual mussels were considered to be abnormal when more than 10% of hemocytes in S–G2/M phase were present. At the population level, a threshold of 6% for the mean intensity of the abnormality is proposed, which means in the population, more than 6% of individual mussels have to present with more than 10% of their hemocytes in S–G2/M phase. GA% was found to be significantly predictive of the final mortality. Based on the established thresholds, only two mussel stocks analyzed in this study were considered to have good cytogenetic quality, while all other stocks appeared to be affected. FCM offers a very powerful tool to help manage current blue mussel mortality in France. We also believe that annual and extensive determination of cytogenetic quality of wild and cultivated mussel beds along with exclusive use of FCM-qualified mussel seeds should be a priority. PY 2016 PD JUN SO Journal Of Invertebrate Pathology SN 0022-2011 PU Academic Press Inc Elsevier Science VL 138 UT 000380385000005 BP 30 EP 38 DI 10.1016/j.jip.2016.06.001 ID 45171 ER EF