Previous Article | Next Article 
Journal of Virology, March 2004, p. 2601-2605, Vol. 78, No. 5
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.5.2601-2605.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Human Immunodeficiency Virus Type 1 Escapes from RNA Interference-Mediated Inhibition
Atze T. Das,1,
Thijn R. Brummelkamp,2,
Ellen M. Westerhout,1 Monique Vink,1 Mandy Madiredjo,2 René Bernards,2 and Ben Berkhout1*
Department of Human Retrovirology, Academic Medical Center, University of Amsterdam,1
Division of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, The Netherlands2
Received 3 September 2003/
Accepted 14 October 2003
Short-term assays have suggested that RNA interference (RNAi) may be a powerful new method for intracellular immunization against human immunodeficiency virus type 1 (HIV-1) infection. However, RNAi has not yet been shown to protect cells against HIV-1 in long-term virus replication assays. We stably introduced vectors expressing small interfering RNAs (siRNAs) directed against the HIV-1 genome into human T cells by retroviral transduction. We report here that an siRNA directed against the viral Nef gene (siRNA-Nef) confers resistance to HIV-1 replication. This block in replication is not absolute, and HIV-1 escape variants that were no longer inhibited by siRNA-Nef appeared after several weeks of culture. These RNAi-resistant viruses contained nucleotide substitutions or deletions in the Nef gene that modified or deleted the siRNA-Nef target sequence. These results demonstrate that efficient inhibition of HIV-1 replication through RNAi is possible in stably transduced cells. Therefore, RNAi could become a realistic gene therapy approach with which to overcome the devastating effect of HIV-1 on the immune system. However, as is known for antiviral drug therapy against HIV-1, antiviral approaches involving RNAi should be used in a combined fashion to prevent the emergence of resistant viruses.
* Corresponding author. Mailing address: Department of Human Retrovirology, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands. Phone: 31 20 566 4822. Fax: 31 20 691 6531. E-mail:
b.berkhout{at}amc.uva.nl.
A.T.D. and T.R.B. contributed equally to this work.
Journal of Virology, March 2004, p. 2601-2605, Vol. 78, No. 5
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.5.2601-2605.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Liu, Y. P., Gruber, J., Haasnoot, J., Konstantinova, P., Berkhout, B.
(2009). RNAi-mediated inhibition of HIV-1 by targeting partially complementary viral sequences. Nucleic Acids Res
37: 6194-6204
[Abstract]
[Full Text]
-
Sugiyama, R., Habu, Y., Ohnari, A., Miyano-Kurosaki, N., Takaku, H.
(2009). RNA Interference Targeted to the Conserved Dimerization Initiation Site (DIS) of HIV-1 Restricts Virus Escape Mutation. J Biochem
146: 481-489
[Abstract]
[Full Text]
-
Zinke, M., Kendl, S., Singethan, K., Fehrholz, M., Reuter, D., Rennick, L., Herold, M. J., Schneider-Schaulies, J.
(2009). Clearance of Measles Virus from Persistently Infected Cells by Short Hairpin RNA. J. Virol.
83: 9423-9431
[Abstract]
[Full Text]
-
Yeung, M. L., Houzet, L., Yedavalli, V. S. R. K., Jeang, K.-T.
(2009). A Genome-wide Short Hairpin RNA Screening of Jurkat T-cells for Human Proteins Contributing to Productive HIV-1 Replication. J. Biol. Chem.
284: 19463-19473
[Abstract]
[Full Text]
-
Umbach, J. L., Cullen, B. R.
(2009). The role of RNAi and microRNAs in animal virus replication and antiviral immunity. Genes Dev.
23: 1151-1164
[Abstract]
[Full Text]
-
Shin, D., Lee, H., Kim, S. I., Yoon, Y., Kim, M.
(2009). Optimization of linear double-stranded RNA for the production of multiple siRNAs targeting hepatitis C virus. RNA
15: 898-910
[Abstract]
[Full Text]
-
Liu, Y. P., Haasnoot, J., ter Brake, O., Berkhout, B., Konstantinova, P.
(2008). Inhibition of HIV-1 by multiple siRNAs expressed from a single microRNA polycistron. Nucleic Acids Res
36: 2811-2824
[Abstract]
[Full Text]
-
von Eije, K. J., Brake, O. t., Berkhout, B.
(2008). Human Immunodeficiency Virus Type 1 Escape Is Restricted When Conserved Genome Sequences Are Targeted by RNA Interference. J. Virol.
82: 2895-2903
[Abstract]
[Full Text]
-
Shao, Y., Chan, C. Y., Maliyekkel, A., Lawrence, C. E., Roninson, I. B., Ding, Y.
(2007). Effect of target secondary structure on RNAi efficiency. RNA
13: 1631-1640
[Abstract]
[Full Text]
-
Gimenez-Barcons, M., Clotet, B., Martinez, M. A.
(2007). Endoribonuclease-Prepared Short Interfering RNAs Induce Effective and Specific Inhibition of Human Immunodeficiency Virus Type 1 Replication. J. Virol.
81: 10680-10686
[Abstract]
[Full Text]
-
Liu, Y. P., Haasnoot, J., Berkhout, B.
(2007). Design of extended short hairpin RNAs for HIV-1 inhibition. Nucleic Acids Res
35: 5683-5693
[Abstract]
[Full Text]
-
Westerhout, E. M., Berkhout, B.
(2007). A systematic analysis of the effect of target RNA structure on RNA interference. Nucleic Acids Res
35: 4322-4330
[Abstract]
[Full Text]
-
Yamamoto, T., Miyoshi, H., Yamamoto, N., Yamamoto, N., Inoue, J.-i., Tsunetsugu-Yokota, Y.
(2006). Lentivirus vectors expressing short hairpin RNAs against the U3-overlapping region of HIV nef inhibit HIV replication and infectivity in primary macrophages. Blood
108: 3305-3312
[Abstract]
[Full Text]
-
Bennasser, Y., Yeung, M. L., Jeang, K.-T.
(2006). HIV-1 TAR RNA Subverts RNA Interference in Transfected Cells through Sequestration of TAR RNA-binding Protein, TRBP. J. Biol. Chem.
281: 27674-27678
[Abstract]
[Full Text]
-
Nishitsuji, H., Kohara, M., Kannagi, M., Masuda, T.
(2006). Effective Suppression of Human Immunodeficiency Virus Type 1 through a Combination of Short- or Long-Hairpin RNAs Targeting Essential Sequences for Retroviral Integration.. J. Virol.
80: 7658-7666
[Abstract]
[Full Text]
-
Eberhardy, S. R., Goncalves, J., Coelho, S., Segal, D. J., Berkhout, B., Barbas, C. F. III
(2006). Inhibition of Human Immunodeficiency Virus Type 1 Replication with Artificial Transcription Factors Targeting the Highly Conserved Primer-Binding Site. J. Virol.
80: 2873-2883
[Abstract]
[Full Text]
-
Unwalla, H. J., Li, H.-T., Bahner, I., Li, M.-J., Kohn, D., Rossi, J. J.
(2006). Novel Pol II Fusion Promoter Directs Human Immunodeficiency Virus Type 1-Inducible Coexpression of a Short Hairpin RNA and Protein. J. Virol.
80: 1863-1873
[Abstract]
[Full Text]
-
Sabariegos, R., Gimenez-Barcons, M., Tapia, N., Clotet, B., Martinez, M. A.
(2006). Sequence Homology Required by Human Immunodeficiency Virus Type 1 To Escape from Short Interfering RNAs. J. Virol.
80: 571-577
[Abstract]
[Full Text]
-
Piva, R., Chiarle, R., Manazza, A. D., Taulli, R., Simmons, W., Ambrogio, C., D'Escamard, V., Pellegrino, E., Ponzetto, C., Palestro, G., Inghirami, G.
(2006). Ablation of oncogenic ALK is a viable therapeutic approach for anaplastic large-cell lymphomas. Blood
107: 689-697
[Abstract]
[Full Text]
-
Konstantinova, P., de Haan, P., Das, A. T., Berkhout, B.
(2006). Hairpin-induced tRNA-mediated (HITME) recombination in HIV-1.. Nucleic Acids Res
34: 2206-2218
[Abstract]
[Full Text]
-
Sanchez, A. B., Perez, M., Cornu, T., de la Torre, J. C.
(2005). RNA Interference-Mediated Virus Clearance from Cells both Acutely and Chronically Infected with the Prototypic Arenavirus Lymphocytic Choriomeningitis Virus. J. Virol.
79: 11071-11081
[Abstract]
[Full Text]
-
Lee, S.-K., Dykxhoorn, D. M., Kumar, P., Ranjbar, S., Song, E., Maliszewski, L. E., Francois-Bongarcon, V., Goldfeld, A., Swamy, N. M., Lieberman, J., Shankar, P.
(2005). Lentiviral delivery of short hairpin RNAs protects CD4 T cells from multiple clades and primary isolates of HIV. Blood
106: 818-826
[Abstract]
[Full Text]
-
Wilson, J. A., Richardson, C. D.
(2005). Hepatitis C Virus Replicons Escape RNA Interference Induced by a Short Interfering RNA Directed against the NS5b Coding Region. J. Virol.
79: 7050-7058
[Abstract]
[Full Text]
-
Lecellier, C.-H., Dunoyer, P., Arar, K., Lehmann-Che, J., Eyquem, S., Himber, C., Saib, A., Voinnet, O.
(2005). A Cellular MicroRNA Mediates Antiviral Defense in Human Cells. Science
308: 557-560
[Abstract]
[Full Text]
-
Godfrey, A., Anderson, J., Papanastasiou, A., Takeuchi, Y., Boshoff, C.
(2005). Inhibiting primary effusion lymphoma by lentiviral vectors encoding short hairpin RNA. Blood
105: 2510-2518
[Abstract]
[Full Text]
-
Omoto, S., Fujii, Y. R.
(2005). Regulation of human immunodeficiency virus 1 transcription by nef microRNA. J. Gen. Virol.
86: 751-755
[Abstract]
[Full Text]
-
Westerhout, E. M., Ooms, M., Vink, M., Das, A. T., Berkhout, B.
(2005). HIV-1 can escape from RNA interference by evolving an alternative structure in its RNA genome. Nucleic Acids Res
33: 796-804
[Abstract]
[Full Text]
-
Leonard, J. N., Schaffer, D. V.
(2005). Computational Design of Antiviral RNA Interference Strategies That Resist Human Immunodeficiency Virus Escape. J. Virol.
79: 1645-1654
[Abstract]
[Full Text]
-
Soldan, S. S., Plassmeyer, M. L., Matukonis, M. K., Gonzalez-Scarano, F.
(2005). La Crosse Virus Nonstructural Protein NSs Counteracts the Effects of Short Interfering RNA. J. Virol.
79: 234-244
[Abstract]
[Full Text]
-
Dave, R. S., Pomerantz, R. J.
(2004). Antiviral Effects of Human Immunodeficiency Virus Type 1-Specific Small Interfering RNAs against Targets Conserved in Select Neurotropic Viral Strains. J. Virol.
78: 13687-13696
[Abstract]
[Full Text]
-
Lu, X., Yu, Q., Binder, G. K., Chen, Z., Slepushkina, T., Rossi, J., Dropulic, B.
(2004). Antisense-Mediated Inhibition of Human Immunodeficiency Virus (HIV) Replication by Use of an HIV Type 1-Based Vector Results in Severely Attenuated Mutants Incapable of Developing Resistance. J. Virol.
78: 7079-7088
[Abstract]
[Full Text]