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Journal of Virology, October 1999, p. 8448-8456, Vol. 73, No. 10
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Decreased Processivity of Human Immunodeficiency Virus Type 1 Reverse Transcriptase (RT) Containing Didanosine-Selected Mutation
Leu74Val: a Comparative Analysis of RT Variants Leu74Val and
Lamivudine-Selected Met184Val
Prem L.
Sharma* and
Clyde S.
Crumpacker
Division of Infectious Disease, Beth Israel
Deaconess Medical Center, Boston, Massachusetts 02215
Received 1 February 1999/Accepted 12 July 1999
We previously showed that a didanosine-selected mutation in pNL4-3
background conferred a replication disadvantage on human immunodeficiency virus type 1, resulting in a loss of replication fitness. This work has been extended by showing that a recombinant virus with the HXBc2 backbone and reverse transcriptase (RT) fragments from pNL4-3 containing the Leu74Val mutation produce decreasing amounts
of p24 antigen over a 3-week period. The HXBc2 recombinant containing
the wild-type RT from pNL4-3 replicated efficiently. When the
virion-associated RT containing the Leu74Val mutation was used in an RT
processivity assay with homopolymer RNA template-primer, poly(A), and
oligo(dT), the RT with altered Leu74Val mutation was less processive,
generating fewer cDNA products in comparison to wild-type pNL4-3 RT.
The replication kinetics and RT processivity of the mutant with the
Leu74Val mutation were compared to those of a lamivudine-selected
mutant Met184Val. In replication kinetics assays, mutant Leu74Val
replicated slower than the mutant Met184Val. In a processivity assay,
the mutant RTs from both viruses show comparable decreases in
processivity. These observations provide biochemical evidence of
decreased processivity to support the decrease in replication fitness
observed with the Leu74Val or Met184Val mutations.
*
Corresponding author. Mailing address: Division of
Infectious Disease, Beth Israel Deaconess Medical Center, 330 Brookline Ave., Boston, MA 01225. Phone: (617) 667-4355. Fax: (617)
667-5541. E-mail: psharma{at}caregroup.harvard.edu.
Journal of Virology, October 1999, p. 8448-8456, Vol. 73, No. 10
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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