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Journal of Virology, April 1999, p. 2710-2716, Vol. 73, No. 4
Department of Exotic Disease, National Institute of Animal
Health, 6-20-1, Josuihoncho, Kodaira, Tokyo 187-0022, Japan,1 and Institute for Animal
Health, Pirbright Laboratory, Pirbright, Woking, Surrey GU24 0NF,
United Kingdom2
Received 7 October 1998/Accepted 28 December 1998
A series of recombinant viruses were constructed using infectious
cDNA clones of the virulent J1'73 (large plaque phenotype) and the
avirulent H/3'76 (small plaque phenotype) strains of swine vesicular
disease virus to identify the genetic determinants of pathogenicity and
plaque phenotype. Both traits could be mapped to the region between
nucleotides (nt) 2233 and 3368 corresponding to the C terminus of VP3,
the whole of VP1, and the N terminus of 2A. In this region, there are
eight nucleotide differences leading to amino acid changes between the
J1'73 and the H/3'76 strains. Site-directed mutagenesis of individual
nucleotides from the virulent to the avirulent genotype and vice versa
indicated that A at nt 2832, encoding glycine at VP1-132, and G at nt
3355, encoding arginine at 2APRO-20, correlated with a
large-plaque phenotype and virulence in pigs, irrespective of the
origin of the remainder of the genome. Of these two sites,
2APRO-20 appeared to be the dominant determinant for the
large-plaque phenotype but further studies are required to elucidate
their relative importance for virulence in pigs.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Mapping the Genetic Determinants of Pathogenicity
and Plaque Phenotype in Swine Vesicular Disease Virus

*
Corresponding author. Mailing address: Department of
Exotic Disease, National Institute of Animal Health, 6-20-1, Josuihoncho, Kodaira, Tokyo 187-0022 Japan. Phone: 42-321-1441. Fax:
42-325-5122. E-mail: kannot{at}ed.affrc.go.jp
Present address: Department of Virology, National Institute of
Animal Health, 3-1-1, Kannondai, Ibaraki 305-0856, Japan.
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