Previous Article | Next Article 
Journal of Virology, June 2004, p. 5835-5847, Vol. 78, No. 11
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.11.5835-5847.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Human Immunodeficiency Virus Type 1 (HIV-1) Integrase: Resistance to Diketo Acid Integrase Inhibitors Impairs HIV-1 Replication and Integration and Confers Cross-Resistance to L-Chicoric Acid
Deborah J. Lee1 and W. E. Robinson Jr.1,2,3*
Departments of Microbiology and Molecular Genetics,1
Medicine,2
Pathology, University of California, Irvine, California 92697-48003
Received 13 October 2003/
Accepted 27 January 2004
The diketo acids are potent inhibitors of human immunodeficiency virus (HIV) integrase (IN). Mutations in IN, T66I, S153Y, and M154I, as well as T66I-S153Y and T66I-M154I double mutations, confer resistance to diketo acids (D. J. Hazuda et al., Science 287:646-650, 2000). The effects of these IN mutations on viral replication, enzymatic activity, and susceptibility to other HIV inhibitors are reported herein. By immunofluorescence assay and real-time PCR, all mutant viruses demonstrated a modest delay in viral spread compared to that of reference HIV. These viruses also showed a statistically significant defect in integration without defects in reverse transcription. Recombinant IN containing S153Y, T66I, and M154I-T66I mutations had an approximately twofold decrease in both disintegration and 3'-end-processing-strand transfer activities in vitro. In contrast, IN containing M154I demonstrated a greater than twofold increase in specific activity in both reactions. All mutant HIVs were resistant to L-chicoric acid, a dicaffeoyltartaric acid IN inhibitor, both in tissue culture and in biochemical assays, yet remained susceptible to the reverse transcriptase inhibitors zidovudine and nevirapine. Thus, IN mutations conferring resistance to the diketo acids can yield integration defects, attenuated catalysis in vitro, and cross-resistance to L-chicoric acid.
* Corresponding author. Mailing address: Department of Pathology, D440 Med. Sci. I, University of California, Irvine, CA 92697-4800. Phone: (949) 824-3431. Fax: (949) 824-2505. E-mail: ewrobins{at}uci.edu.
Journal of Virology, June 2004, p. 5835-5847, Vol. 78, No. 11
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.11.5835-5847.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Dicker, I. B., Terry, B., Lin, Z., Li, Z., Bollini, S., Samanta, H. K., Gali, V., Walker, M. A., Krystal, M. R.
(2008). Biochemical Analysis of HIV-1 Integrase Variants Resistant to Strand Transfer Inhibitors. J. Biol. Chem.
283: 23599-23609
[Abstract]
[Full Text]
-
Chen, A., Weber, I. T., Harrison, R. W., Leis, J.
(2006). Identification of Amino Acids in HIV-1 and Avian Sarcoma Virus Integrase Subsites Required for Specific Recognition of the Long Terminal Repeat Ends. J. Biol. Chem.
281: 4173-4182
[Abstract]
[Full Text]
-
Lee, D. J., Robinson, W. E. Jr.
(2006). Preliminary Mapping of a Putative Inhibitor-Binding Pocket for Human Immunodeficiency Virus Type 1 Integrase Inhibitors. Antimicrob. Agents Chemother.
50: 134-142
[Abstract]
[Full Text]
-
Winters, M. A., Merigan, T. C.
(2005). Insertions in the Human Immunodeficiency Virus Type 1 Protease and Reverse Transcriptase Genes: Clinical Impact and Molecular Mechanisms. Antimicrob. Agents Chemother.
49: 2575-2582
[Full Text]
-
Brigo, A., Lee, K. W., Iurcu Mustata, G., Briggs, J. M.
(2005). Comparison of Multiple Molecular Dynamics Trajectories Calculated for the Drug-Resistant HIV-1 Integrase T66I/M154I Catalytic Domain. Biophys. J
88: 3072-3082
[Abstract]
[Full Text]
-
Olszewski, A., Sato, K., Aron, Z. D., Cohen, F., Harris, A., McDougall, B. R., Robinson, W. E. Jr., Overman, L. E., Weiss, G. A.
(2004). Guanidine alkaloid analogs as inhibitors of HIV-1 Nef interactions with p53, actin, and p56lck. Proc. Natl. Acad. Sci. USA
101: 14079-14084
[Abstract]
[Full Text]
Copyright © 2004 by the American Society for Microbiology. All rights reserved.