FN Archimer Export Format
PT J
TI Development of a duplex Taqman real-time PCR assay for rapid identification of Vibrio splendidus -related and V. aestuarianus strains from bacterial cultures
BT 
AF SAULNIER, Denis
   DE DECKER, Sophie
   TOURBIEZ, Delphine
   TRAVERS, Marie-Agnes
AS 1:1;2:2;3:2;4:2;
FF 1:PDG-RBE-RMPF;2:;3:PDG-RBE-SG2M-LGPMM;4:PDG-RBE-SG2M-LGPMM;
C1 IFREMER, UMR EIO 241, UPF ILM IRD, BP 49, F-98719 Tahiti, French Polynesi, France.
   IFREMER, RBE SG2M, Lab Genet & Pathol Mollusques Marins, Av Mus de Loup, F-17390 La Tremblade, French Polynesi, France.
C2 IFREMER, FRANCE
   IFREMER, FRANCE
SI TAHITI
   LA TREMBLADE
SE PDG-RBE-RMPF
   PDG-RBE-SG2M-LGPMM
UM EIO
IN WOS Ifremer jusqu'en 2018
IF 1.701
TC 23
UR https://archimer.ifremer.fr/doc/00392/50308/51077.pdf
LA English
DT Article
DE ;Multiplex real-time PCR;Gene sequencing;Molluscs;Splendidus Glade;Vibrio aestuarianus
AB To enable the rapid and accurate identification of Vibrio splendidus-related and V. aestuarianus strains associated with Pacific cupped oyster Crassostrea gigas mortality, we developed a duplex Taqman real-time PCR assay and evaluated its efficacy. This technique proved to be rapid, sensitive, and specific and will be particularly valuable for epidemiologic studies. 
PY 2017
PD SEP
SO Journal Of Microbiological Methods
SN 0167-7012
PU Elsevier Science Bv
VL 140
UT 000407982100011
BP 67
EP 69
DI 10.1016/j.mimet.2017.07.002
ID 50308
ER

EF