FN Archimer Export Format PT J TI Aichi Virus, Norovirus, Astrovirus, Enterovirus, and Rotavirus Involved in Clinical Cases from a French Oyster-Related Gastroenteritis Outbreak BT AF LE GUYADER, Soizick LE SAUX, Jean-Claude AMBERT-BALAY, Katia KROL, Joanna SERAIS, Ophelie PARNAUDEAU, Sylvain GIRAUDON, Helene DELMAS, Gilles POMMEPUY, Monique POTHIER, Pierre ATMAR, Robert L. AS 1:1;2:1;3:2;4:1;5:3;6:1;7:2;8:4;9:1;10:2;11:5; FF 1:PDG-DOP-DCN-EMP-MIC;2:PDG-DOP-DCN-EMP-MIC;3:;4:PDG-DOP-DCN-EMP-MIC;5:PDG-DOP-LER-LERLR;6:PDG-DOP-DCN-EMP-MIC;7:;8:;9:PDG-DOP-DCN-EMP;10:;11:; C1 IFREMER, Microbiol Lab, F-44311 Nantes 03, France. Ctr Hosp Univ, Reference Lab Enter Viruses, Lab Virol & Microbiol Med & Mol, Dijon, France. IFREMER, Lab Environm Ressources, Sete, France. Inst Veille Sanitaire, Dept Malad Infect, Unit Infect Enter, St Maurice, France. Baylor Coll Med, Dept Mol Virol & Microbiol, Houston, TX 77030 USA. C2 IFREMER, FRANCE CHU DIJON, FRANCE IFREMER, FRANCE INVS, FRANCE BAYLOR COLL MED, USA SI NANTES BREST SETE SE PDG-DOP-DCN-EMP-MIC PDG-DOP-LER-LERLR PDG-DOP-DCN-EMP IN WOS Ifremer jusqu'en 2018 copubli-france copubli-univ-france copubli-int-hors-europe IF 3.945 TC 213 UR https://archimer.ifremer.fr/doc/2008/publication-6099.pdf LA English DT Article AB Following a flooding event close to a shellfish production lagoon, 205 cases of gastroenteritis were linked to oyster consumption. Twelve stool samples from different individuals were collected. Analysis showed that eight samples were positive for multiple enteric viruses, and one stool sample had seven different enteric viruses. Analysis of shellfish implicated in the outbreak allowed detection of the same diversity of enteric viruses, with some viral genomic sequences being identical to those obtained from stool sample analysis. Shellfish were contaminated by as many as five different enteric viruses. For the first time in Europe, Aichi virus was identified in oyster samples. Shellfish samples collected over 3 weeks following the outbreak showed a progressive decline in the level of virus contamination as measured by the virus diversity detected and by quantitative reverse transcription-PCR. PY 2008 PD DEC SO Journal of Clinical Microbiology SN 0095-1137 PU American Society for Microbiology. VL 46 IS 12 UT 000261247900022 BP 4011 EP 4017 DI 10.1128/JCM.01044-08 ID 6099 ER EF