JCM Figure table search 04
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ambert-Balay, K.
Right arrow Articles by Kohli, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ambert-Balay, K.
Right arrow Articles by Kohli, E.
Journal of Clinical Microbiology, October 2005, p. 5179-5186, Vol. 43, No. 10
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.10.5179-5186.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Characterization of New Recombinant Noroviruses

K. Ambert-Balay,1,2* F. Bon,1,2 F. Le Guyader,3 P. Pothier,1,2 and E. Kohli1,2

Laboratoire de Virologie, Reference Laboratory for Enteric Viruses, Centre Hospitalier Universitaire, 21079 Dijon,1 Microbiologie Médicale et Moléculaire, UFRs Médecine et Pharmacie, 21079 Dijon,2 Laboratoire de Microbiologie, IFREMER, BP 21105, 44311 Nantes Cedex 03, France3

Received 16 December 2004/ Returned for modification 31 January 2005/ Accepted 20 June 2005

Noroviruses are important etiologic agents of acute gastroenteritis and show great genetic diversity. To characterize more fully previously detected strains that could not be assigned unequivocally to one particular genotype based on the RNA polymerase, we have sequenced a region in the capsid gene and, in some cases, in the junction between open reading frame 1 (ORF1) and ORF2. The results allowed us to identify several recombinant noroviruses: GGIIb viruses were detected for the first time in France in August 2000 and then spread through France and to Europe during the following winter. Here we present the characterization of three other probable GII recombinants which showed different phylogenetic positions depending on their ORF1 and ORF2 sequences. Analysis of the region located between ORF1 and ORF2 by a nucleotide identity window search showed a sudden shift in similarities. Moreover, recombination breakpoints were identified upstream and downstream of the beginning of ORF2 by using a statistical test, thus confirming the involvement of this region in recombination. Unlike GGIIb, the three recombinants described here do not seem to have diffused widely in the community: one was found in a waterborne outbreak, and the other two were found in sporadic cases. Recombination is important for the evolution of RNA viruses and has already been described for noroviruses. Our results suggest that recombination is not a rare phenomenon among noroviruses, but not all these presumed recombinants that formed during RNA replication are able to spread widely.


* Corresponding author. Mailing address: Laboratoire de Virologie, 2 boulevard Maréchal de Lattre de Tassigny, 21079 Dijon, France. Phone: 33 3 80 29 34 37. Fax: 33 3 80 29 36 04. E-mail: katia.balay{at}chu-dijon.fr.


Journal of Clinical Microbiology, October 2005, p. 5179-5186, Vol. 43, No. 10
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.10.5179-5186.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Antimicrob. Agents Chemother. Clin. Microbiol. Rev.
Clin. Vaccine Immunol. ALL ASM JOURNALS

Copyright © 2005 by the American Society for Microbiology. All rights reserved.