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Journal of Virology, April 2007, p. 4315-4322, Vol. 81, No. 8
0022-538X/07/$08.00+0     doi:10.1128/JVI.02458-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Antigenic and Genetic Evolution of Swine Influenza A (H3N2) Viruses in Europe{triangledown}

J. C. de Jong,1,2* D. J. Smith,1,3 A. S. Lapedes,4 I. Donatelli,5 L. Campitelli,5 G. Barigazzi,6 K. Van Reeth,7 T. C. Jones,3 G. F. Rimmelzwaan,1 A. D. M. E. Osterhaus,1,2 and R. A. M. Fouchier1

National Influenza Center, Department of Virology, Erasmus Medical Center, Rotterdam, The Netherlands,1 ViroClinics BV, Rotterdam, The Netherlands,2 Department of Zoology, University of Cambridge, Cambridge, United Kingdom,3 Theoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico,4 Division of Virology, Istituto Superiore di Sanità, Rome, Italy,5 Istituto Zooprofilattico Sperimentale, Parma, Italy,6 Laboratory of Virology, Faculty of Veterinary Medicine, Ghent University, Ghent, Belgium7

Received 8 November 2006/ Accepted 31 January 2007

In the early 1970s, a human influenza A/Port Chalmers/1/73 (H3N2)-like virus colonized the European swine population. Analyses of swine influenza A (H3N2) viruses isolated in The Netherlands and Belgium revealed that in the early 1990s, antigenic drift had occurred, away from A/Port Chalmers/1/73, the strain commonly used in influenza vaccines for pigs. Here we show that Italian swine influenza A (H3N2) viruses displayed antigenic and genetic changes similar to those observed in Northern European viruses in the same period. We used antigenic cartography methods for quantitative analyses of the antigenic evolution of European swine H3N2 viruses and observed a clustered virus evolution as seen for human viruses. Although the antigenic drift of swine and human H3N2 viruses has followed distinct evolutionary paths, potential cluster-differentiating amino acid substitutions in the influenza virus surface protein hemagglutinin (HA) were in part the same. The antigenic evolution of swine viruses occurred at a rate approximately six times slower than the rate in human viruses, even though the rates of genetic evolution of the HA at the nucleotide and amino acid level were similar for human and swine H3N2 viruses. Continuous monitoring of antigenic changes is recommended to give a first indication as to whether vaccine strains may need updating. Our data suggest that humoral immunity in the population plays a smaller role in the evolutionary selection processes of swine H3N2 viruses than in human H3N2 viruses.

* Corresponding author. Mailing address: National Influenza Center, Department of Virology, Erasmus Medical Center, P.O. Box 1738, 3000 DR Rotterdam, The Netherlands. Phone: 31 (10) 408 8067. Fax: 31 (10) 408 9485. E-mail: jc.de.jong{at}wxs.nl

{triangledown} Published ahead of print on 7 February 2007.

Journal of Virology, April 2007, p. 4315-4322, Vol. 81, No. 8
0022-538X/07/$08.00+0     doi:10.1128/JVI.02458-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.





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