J Gen Virol Try IJSEM Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 88 (2007), 3347-3359; DOI 10.1099/vir.0.83321-0

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
Right arrow Citation Map
Services
Right arrow Email this article to a friend
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 reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bull, R. A.
Right arrow Articles by White, P. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bull, R. A.
Right arrow Articles by White, P. A.
Agricola
Right arrow Articles by Bull, R. A.
Right arrow Articles by White, P. A.

Norovirus recombination

Rowena A. Bull, Mark M. Tanaka and Peter A. White

School of Biotechnology and Biomolecular Sciences, Faculty of Science, University of New South Wales, Sydney 2052, Australia

Correspondence
Peter A. White
p.white{at}unsw.edu.au

RNA recombination is a significant driving force in viral evolution. Increased awareness of recombination within the genus Norovirus of the family Calicivirus has led to a rise in the identification of norovirus (NoV) recombinants and they are now reported at high frequency. Currently, there is no classification system for recombinant NoVs and a widely accepted recombinant genotyping system is still needed. Consequently, there is duplication in reporting of novel recombinants. This has led to difficulties in defining the number and types of recombinants in circulation. In this study, 120 NoV nucleotide sequences were compiled from the current GenBank database and published literature. NoV recombinants and their recombination breakpoints were identified using three methods: phylogenetic analysis, SimPlot analysis and the maximum {chi}2 method. A total of 20 NoV recombinant types were identified in circulation worldwide. The recombination point is the ORF1/2 overlap in all isolates except one, which demonstrated a double recombination event within the polymerase region.




This article has been cited by other articles:


Home page
J. Virol.Home page
K. Bok, E. J. Abente, M. Realpe-Quintero, T. Mitra, S. V. Sosnovtsev, A. Z. Kapikian, and K. Y. Green
Evolutionary Dynamics of GII.4 Noroviruses over a 34-Year Period
J. Virol., November 15, 2009; 83(22): 11890 - 11901.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
R. I. Glass, U. D. Parashar, and M. K. Estes
Norovirus Gastroenteritis
N. Engl. J. Med., October 29, 2009; 361(18): 1776 - 1785.
[Full Text] [PDF]


Home page
J. Virol.Home page
J. L. Hyde, S. V. Sosnovtsev, K. Y. Green, C. Wobus, H. W. Virgin, and J. M. Mackenzie
Mouse Norovirus Replication Is Associated with Virus-Induced Vesicle Clusters Originating from Membranes Derived from the Secretory Pathway
J. Virol., October 1, 2009; 83(19): 9709 - 9719.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
B. Carlsson, A. M. Lindberg, J. Rodriguez-Diaz, K.-O. Hedlund, B. Persson, and L. Svensson
Quasispecies dynamics and molecular evolution of human norovirus capsid P region during chronic infection
J. Gen. Virol., February 1, 2009; 90(2): 432 - 441.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
H. Almanza, C. Cubillos, I. Angulo, F. Mateos, J. R. Caston, W. H. M. van der Poel, J. Vinje, J. Barcena, and I. Mena
Self-Assembly of the Recombinant Capsid Protein of a Swine Norovirus into Virus-Like Particles and Evaluation of Monoclonal Antibodies Cross-Reactive with a Human Strain from Genogroup II
J. Clin. Microbiol., December 1, 2008; 46(12): 3971 - 3979.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
A. Kroneman, L. Verhoef, J. Harris, H. Vennema, E. Duizer, Y. van Duynhoven, J. Gray, M. Iturriza, B. Bottiger, G. Falkenhorst, et al.
Analysis of Integrated Virological and Epidemiological Reports of Norovirus Outbreaks Collected within the Foodborne Viruses in Europe Network from 1 July 2001 to 30 June 2006
J. Clin. Microbiol., September 1, 2008; 46(9): 2959 - 2965.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
F. Bucardo, J. Nordgren, B. Carlsson, M. Paniagua, P.-E. Lindgren, F. Espinoza, and L. Svensson
Pediatric Norovirus Diarrhea in Nicaragua
J. Clin. Microbiol., August 1, 2008; 46(8): 2573 - 2580.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
T. Okabayashi, S.-i. Yokota, Y. Ohkoshi, H. Ohuchi, Y. Yoshida, M. Kikuchi, K. Yano, and N. Fujii
Occurrence of Norovirus Infections Unrelated to Norovirus Outbreaks in an Asymptomatic Food Handler Population
J. Clin. Microbiol., June 1, 2008; 46(6): 1985 - 1988.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2007 by the Society for General Microbiology.