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Journal of Virology, January 2008, p. 495-502, Vol. 82, No. 1
0022-538X/08/$08.00+0     doi:10.1128/JVI.01096-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Novel Cytotoxic T-Lymphocyte Escape Mutation by a Three-Amino-Acid Insertion in the Human Immunodeficiency Virus Type 1 p6Pol and p6Gag Late Domain Associated with Drug Resistance{triangledown}

Jianhong Cao,1,2,{dagger} John McNevin,1 Matthew McSweyn,1 Yi Liu,4 James I. Mullins,2,3,4 and M. Juliana McElrath1,2,3*

Program in Infectious Diseases, Clinical Research Division, Fred Hutchinson Cancer Research Center,1 Department of Medicine,2 Department of Laboratory Medicine,3 Department of Microbiology, University of Washington, Seattle, Washington4

Received 21 May 2007/ Accepted 4 October 2007

Cytolytic T lymphocytes (CTL) play a major role in controlling human immunodeficiency virus type 1 (HIV-1) infection. To evade immune pressure, HIV-1 is selected at targeted CTL epitopes, which may consequentially alter viral replication fitness. In our longitudinal investigations of the interplay between T-cell immunity and viral evolution following acute HIV-1 infection, we observed in a treatment-naïve patient the emergence of highly avid, gamma interferon-secreting, CD8+ CTL recognizing an HLA-Cw*0102-restricted epitope, NSPTRREL (NL8). This epitope lies in the p6Pol protein, located in the transframe region of the Gag-Pol polyprotein. Over the course of infection, an unusual viral escape mutation arose within the p6Pol epitope through insertion of a 3-amino-acid repeat, NSPT(SPT)RREL, with a concomitant insertion in the p6Gag late domain, PTAPP(APP). Interestingly, this p6Pol insertion mutation is often selected in viruses with the emergence of antiretroviral drug resistance, while the p6Gag late-domain PTAPP motif binds Tsg101 to permit viral budding. These results are the first to demonstrate viral evasion of immune pressure by amino acid insertions. Moreover, this escape mutation represents a novel mechanism whereby HIV-1 can alter its sequence within both the Gag and Pol proteins with potential functional consequences for viral replication and budding.

* Corresponding author. Mailing address: Fred Hutchinson Cancer Research Center, D3-100, 1100 Fairview Avenue North, Seattle, WA 98109. Phone: (206) 667-6704. Fax: (206) 667-4411. E-mail: jmcelrat{at}fhcrc.org

{triangledown} Published ahead of print on 17 October 2007.

{dagger} Present address: Immune Monitoring Lab, Fred Hutchinson Cancer Research Center, Seattle, WA.

Journal of Virology, January 2008, p. 495-502, Vol. 82, No. 1
0022-538X/08/$08.00+0     doi:10.1128/JVI.01096-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



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