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J. Virol., Jan 1998, 170-179, Vol 72, No. 1
D Boulanger, P Green, T Smith, CP Czerny and MA Skinner
The immunodominant, 39,000-molecular weight core protein (39K protein) of
fowlpox virus (FP9 strain), equivalent to the vaccinia virus A4L gene
product, contains highly charged domains at each end of the protein and
multiple copies of a 12-amino-acid serine-rich repeat sequence in the
middle of the protein. Similar repeats were also detected in other fowlpox
virus strains, suggesting that they might confer a selective advantage to
the virus. The molloscum contagiosum virus homolog (MC107L) also contains
repeats, unlike the vaccinia virus protein. The number of repeats in the
fowlpox virus protein does not seem to be crucial, since some strains have
a different number of repeats, as shown by the difference in the size of
the protein in these strains. The repeat region could be deleted,
indicating that it is not essential for replication in vitro. It was not
possible to delete the entire 39K protein, indicating that it was essential
(transcriptional control signals for the flanking genes were left intact).
The repeat region is partly responsible for the immunodominance of the
protein, but the C-terminal part of the protein also contains highly
antigenic linear epitopes. A role for the 39K protein in immune system
modulation is discussed.
Copyright © 1998, American Society for Microbiology
The 131-amino-acid repeat region of the essential 39-kilodalton core protein of fowlpox virus FP9, equivalent to vaccinia virus A4L protein, is nonessential and highly immunogenic
Department of Molecular Biology, Institute for Animal Health, Compton Laboratory, United Kingdom.
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