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Journal of Virology, January 2009, p. 1156-1160, Vol. 83, No. 2
0022-538X/09/$08.00+0     doi:10.1128/JVI.01734-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Differential Sensitivity of "Old" versus "New" APOBEC3G to Human Immunodeficiency Virus Type 1 Vif{triangledown}

Ritu Goila-Gaur, Mohammad A. Khan, Eri Miyagi, and Klaus Strebel*

Laboratory of Molecular Microbiology, Viral Biochemistry Section, National Institute of Allergy and Infectious Diseases, NIH, Building 4, Room 310, 4 Center Drive, MSC 0460, Bethesda, Maryland 20892-0460

Received 15 August 2008/ Accepted 31 October 2008

HIV-1 Vif counteracts the antiviral activity of APOBEC3G by inhibiting its encapsidation into virions. Here, we compared the relative sensitivity to Vif of APOBEC3G in stable HeLa cells containing APOBEC3G (HeLa-A3G cells) versus that of newly synthesized APOBEC3G. We observed that newly synthesized APOBEC3G was more sensitive to degradation than preexisting APOBEC3G. Nevertheless, preexisting and transiently expressed APOBEC3G were packaged with similar efficiencies into vif-deficient human immunodeficiency virus type 1 (HIV-1) virions, and Vif inhibited the encapsidation of both forms of APOBEC3G into HIV particles equally well. Our results suggest that HIV-1 Vif preferentially induces degradation of newly synthesized APOBEC3G but indiscriminately inhibits encapsidation of "old" and "new" APOBEC3G.


* Corresponding author. Mailing address: NIH, NIAID, 4/312, 4 Center Drive MSC 0460, Bethesda, MD 20892-0460. Phone: (301) 496-3132. Fax: (301) 402-0226. E-mail: kstrebel{at}nih.gov

{triangledown} Published ahead of print on 12 November 2008.


Journal of Virology, January 2009, p. 1156-1160, Vol. 83, No. 2
0022-538X/09/$08.00+0     doi:10.1128/JVI.01734-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

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