FN Archimer Export Format
PT J
TI Analysis of Clinical Ostreid Herpesvirus 1 (Malacoherpesviridae) Specimens by Sequencing Amplified Fragments from Three Virus Genome Areas
BT 
AF RENAULT, Tristan
   MOREAU, Pierrick
   FAURY, Nicole
   PEPIN, Jean-Francois
   SEGARRA, Amelie
   WEBB, Stephen
AS 1:1;2:1;3:1;4:1;5:1;6:2;
FF 1:PDG-RBE-AGSAE-LGP;2:PDG-RBE-AGSAE-LGP;3:PDG-RBE-AGSAE-LGP;4:PDG-RBE-AGSAE-LGP;5:PDG-RBE-AGSAE-LGP;6:;
C1 IFREMER, Lab Genet & Pathol, Ronce Bains, Ronce Les Bains, La Tremblade, France.
   Cawthron Inst, Nelson, New Zealand.
C2 IFREMER, FRANCE
   CAWTHRON INST, NEW ZEALAND
SI LA TREMBLADE
SE PDG-RBE-AGSAE-LGP
IN WOS Ifremer jusqu'en 2018
   copubli-int-hors-europe
IF 5.08
TC 103
UR https://archimer.ifremer.fr/doc/00083/19445/17221.pdf
LA English
DT Article
AB Although there are a number of ostreid herpesvirus 1 (OsHV-1) variants, it is expected that the true diversity of this virus will be known only after the analysis of significantly more data. To this end, we analyzed 72 OsHV-1 "specimens" collected mainly in France over an 18-year period, from 1993 to 2010. Additional samples were also collected in Ireland, the United States, China, Japan, and New Zealand. Three virus genome regions (open reading frame 4 [ORF4], ORF35, -36, -37, and -38, and ORF42 and -43) were selected for PCR analysis and sequencing. Although ORF4 appeared to be the most polymorphic genome area, distinguishing several genogroups, ORF35, -36, -37, and -38 and ORF42 and -43 also showed variations useful in grouping subpopulations of this virus.
PY 2012
PD MAY
SO Journal Of Virology
SN 0022-538X
PU Amer Soc Microbiology
VL 86
IS 10
UT 000303787100052
BP 5942
EP 5947
DI 10.1128/JVI.06534-11
ID 19445
ER

EF