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1 Enterovirus Laboratory and Molecular Biology Programme, National Public Health Institute, Mannerheimintie 166, FIN-00300 Helsinki, Finland
and2 Department of Microbiology, State University of New York, Stony Brook, NY, USA
We constructred a hybrid type 1/type 3 poliovirus comprising the BC-loop of capsid protein VP1 of PV3/Finland/60212/84 and the rest derived from PV1/Mahoney, and cultured the virus in the presence of diluted rabbit antiserum to PV3/Finland/60212/84. Several strains isolated under this selection showed point mutations in the inserted type 3 poliovirus sequence but only in one case in the flanking PV1/Mahoney-derived RNA. These results indicate that, with the use of recombinant cDNA technology, it may be possible to study molecular interactions of defined regions of virus capsid proteins with neutralizing polyclonal antibodies.
* Author for correspondence. Fax +358-0-4744355. e-mail Tapani.Hovi@ktl.fi
Present address: Connaught Laboratories Ltd, Willowdale, Ontario, Canada.
Received 19 October 1994;
accepted 16 March 1995.
This article has been cited by other articles:
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T. Hovi, N. Lindholm, C. Savolainen, M. Stenvik, and C. Burns Evolution of wild-type 1 poliovirus in two healthy siblings excreting the virus over a period of 6 months J. Gen. Virol., February 1, 2004; 85(2): 369 - 377. [Abstract] [Full Text] [PDF] |
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