Previous Article | Next Article ![]()
Journal of Virology, September 2008, p. 8927-8932, Vol. 82, No. 17
0022-538X/08/$08.00+0 doi:10.1128/JVI.00239-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Unité de Biologie des Virus Entériques,1 Unité de Pharmacoépidémiologie et Maladies Infectieuses, Institut Pasteur, Paris, France,2 Unité de Virologie Médicale, Institut Pasteur de Madagascar, Antananarivo, Madagascar3
Received 2 February 2008/ Accepted 9 June 2008
Pathogenic circulating vaccine-derived polioviruses (cVDPVs) have become a major obstacle to the successful completion of the global polio eradication program. Most cVDPVs are recombinant between the oral poliovirus vaccine (OPV) and human enterovirus species C (HEV-C). To study the role of HEV-C sequences in the phenotype of cVDPVs, we generated a series of recombinants between a Madagascar cVDPV isolate and its parental OPV type 2 strain. Results indicated that the HEV-C sequences present in this cVDPV contribute to its characteristics, including pathogenicity, suggesting that interspecific recombination contributes to the phenotypic biodiversity of polioviruses and may favor the emergence of cVDPVs.
Published ahead of print on 25 June 2008.
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»