David M. Rekosh, PhD

David M. Rekosh, PhD

David  M.  Rekosh
Degree(s): PhD
Graduate School: MIT
Primary Appointment: Professor, Microbiology, Immunology, and Cancer Biology
Research Interests:
Human Immunodeficiency; Virus Gene Expression
Website: http://www.healthsystem.virginia.edu/internet/thaler/home.cfm
Email Address: dr4u@virginia.edu

Research Description

HIV is an important virus , not only because it is the cause of AIDS , but also because its study has led to the discovery of novel basic mechanisms that operate in eukaryotic cells. Over the past two decades , the study of HIV replication has provided insight into fundamental processes operating within the cell. Elucidating these processes provides information for the design of the next generation of anti-HIV drugs and also basic knowledge that will help us understand other disease processes unrelated to AIDS.

HIV Rev:  The centerpiece of our HIV research is focused on the elucidation of the function of the HIV Rev protein. A primary function of this protein is to facilitate the nucleo-cytoplasmic export of mRNAs that retain complete introns. Cellular mRNAs with retained introns are usually restricted by the cell from exiting the nucleus and since many HIV mRNAs have this property , Rev is essential for HIV replication. To perform its export function , Rev binds to a specific element present in some HIV mRNAs called the Rev Response Element. This RNA-protein complex then interacts , through the leucine-rich nuclear export signal in Rev , with cellular factors such as CRM1 and Ran-GTP to facilitate mRNA export. In addition , we have recently shown that Rev promotes the translation of intron-containing RNA.

Many details about Rev function remain unexplored , and our recent experiments focus on some of these issues. In particular , we are studying how small variations in the sequence of Rev and the RRE can modulate HIV infection. We also are studying the basis for the efficient inhibition of HIV replication by an antisense RNA that is directed against the HIV env gene region. An RNA , very similar to the one we are studying , is in clinical trials , and our recent studies show that the trafficking of this molecule through the Rev pathway is essential for it to be a potent inhibitor of HIV replication.

We are also using cell-based screening assays to identify compounds that specifically target HIV Rev function. A recent screen of 40 ,000 compounds has led to the identification of two small molecules that inhibit HIV replication and by interfering with Rev function. These compounds provide proof of principle that the targeting of Rev by a small molecules could lead to the development of a novel class of HIV therapeutics.

The Emergence of Drug Resistance among non Clade B Human Immunodeficiency Viruses:  HIV-1 drug resistance assays have become essential parts of monitoring in antiretroviral therapy , as they are useful in designing the selection of appropriate treatment regiments for AIDS patients. The genotypic DNA sequencing method has its limitation in that the algorithms defining drug resistance have only been developed for HIV clade B non-complex mutations and they are only an indrect measure of resistance. However , direct phenotypic methods overcome this problem. Based on a lentivirus Gag-Pol packaging system , we are developing systems using a luciferase reporter gene , to easily allow drug resistance to be measured in non Clade B viruses.

Using these assays , as well as genotypic sequencing methods , in collaboration with Dr. Pascal Bessong , of the University of Venda in South Africa we have been defining the prevalence of HIV resistance in the non-treated population in selected areas in Limpopo Province , a rural province in northern South Africa. We are also are investigating the impact of polymorphisms on baseline resistance , resistance development and the resistance evolutionary patterns in HIV-1-C infected patient who are undergoing treatment.

Selected Publications

Hammarskjold MH, Rekosh D.  A long-awaited structure is rev-ealed. Viruses. 2011 May;3(5):484-92. doi: 10.3390/v3050484.

Coyle JH, Bor YC, Rekosh D, Hammarskjold ML.  The Tpr protein regulates export of mRNAs with retained introns that traffic through the Nxf1 pathway. RNA. 2011 Jul;17(7):1344-56. doi: 10.1261/rna.2616111. Epub 2011 May 25.

Shuck-Lee D, Chang H, Sloan EA, Hammarskjold ML, Rekosh D.  Single-nucleotide changes in the HIV Rev-response element mediate resistance to compounds that inhibit Rev function. J Virol. 2011 Apr;85(8):3940-9. doi: 10.1128/JVI.02683-10. Epub 2011 Feb 2.

Ward AM, Rekosh D, Hammarskjold ML.  Trafficking through the Rev/RRE pathway is essential for efficient inhibition of human immunodeficiency virus type 1 by an antisense RNA derived from the envelope gene. J Virol. 2009 Jan;83(2):940-52. doi: 10.1128/JVI.01520-08. Epub 2008 Oct 29.

Shuck-Lee D, Chen FF, Willard R, Raman S, Ptak R, Hammarskjold ML, Rekosh D.  Heterocyclic compounds that inhibit Rev-RRE function and human immunodeficiency virus type 1 replication. Antimicrob Agents Chemother. 2008 Sep;52(9):3169-79. doi: 10.1128/AAC.00274-08. Epub 2008 Jul 14.

PubMed Listings for this Faculty Member

Contact Information
Office Address: PO Box 800734, Jordan Hall, Room 7088,
Office Phone: 434-982-1599, 434-982-1597
Fax Phone: 434-982-1590