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Journal of Virology, January 2000, p. 272-280, Vol. 74, No. 1
0022-538X/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Foot-and-Mouth Disease Virus 3C Protease Induces
Cleavage of Translation Initiation Factors eIF4A and eIF4G within
Infected Cells
Graham J.
Belsham,*
Gerald M.
McInerney, and
Natalie
Ross-Smith
BBSRC Institute for Animal Health, Pirbright,
Woking, Surrey GU24 0NF, United Kingdom
Received 21 May 1999/Accepted 20 September 1999
Infection of cells by foot-and-mouth disease virus (FMDV) results
in the rapid inhibition of host cell protein synthesis. This process is
accompanied by the early cleavage of the translation initiation factor
eIF4G, a component of the cap-binding complex eIF4F. This cleavage is
mediated by the leader (L) protease. Subsequently, as the virus
proteins accumulate, secondary cleavages of eIF4G occur. Furthermore,
eIF4A (46 kDa), a second component of eIF4F, is also cleaved in these
later stages of the infection cycle. The 33-kDa cleavage product of
eIF4A has lost a fragment from its N terminus. Transient-expression
assays demonstrated that eIF4A was not cleaved in the presence of FMDV
L or with the poliovirus 2A protease (which also mediates eIF4G
cleavage) but was cleaved when the FMDV 3C protease was expressed. The
FMDV 3C protease was also shown in such assays to induce cleavage of
eIF4G, resulting in the production of cleavage products different from
those generated by the L protease. Consistent with these results,
within cells infected with a mutant FMDV lacking the L protease or
within cells containing an FMDV replicon lacking L-P1 coding sequences
it was again shown that eIF4A and eIF4G were cleaved.
*
Corresponding author. Mailing address: BBSRC Institute
for Animal Health, Pirbright Laboratory, Ash Rd., Pirbright, Woking, Surrey GU24 0NF, United Kingdom. Phone: 44 1483 232441. Fax: 44 1483 232448. E-mail: graham.belsham{at}bbsrc.ac.uk.
Journal of Virology, January 2000, p. 272-280, Vol. 74, No. 1
0022-538X/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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